Brodmann map — where each semiology localizes
0  signs per area
Frontopolar cortex10Dorsomedial & dorsolateral prefrontal cortex (superior frontal gyrus)9Frontal eye field (posterior area 8)8Premotor cortex & supplementary motor area (SMA)6Primary motor cortex (precentral gyrus)4Primary somatosensory cortex (area 3)3Primary somatosensory cortex (area 1)1Primary somatosensory cortex (area 2)2Somatosensory association cortex (anterior superior parietal lobule)5Posterior superior parietal lobule & precuneus7Dorsolateral prefrontal cortex (middle frontal gyrus)46Supramarginal gyrus40Angular gyrus (temporo-parietal junction)39Frontopolar cortex10Dorsomedial & dorsolateral prefrontal cortex (superior frontal gyrus)9Frontal eye field (posterior area 8)8Premotor cortex & supplementary motor area (SMA)6Primary motor cortex (precentral gyrus)4Primary somatosensory cortex (area 3)3Primary somatosensory cortex (area 1)1Primary somatosensory cortex (area 2)2Somatosensory association cortex (anterior superior parietal lobule)5Posterior superior parietal lobule & precuneus7Dorsolateral prefrontal cortex (middle frontal gyrus)46Supramarginal gyrus40Angular gyrus (temporo-parietal junction)39anteriorFrontopolar cortex10Orbitofrontal cortex11Frontal eye field (posterior area 8)8Premotor cortex & supplementary motor area (SMA)6Dorsomedial & dorsolateral prefrontal cortex (superior frontal gyrus)9Dorsolateral prefrontal cortex (middle frontal gyrus)46Pars orbitalis / lateral orbitofrontal cortex47Pars triangularis (Broca's area)45Pars opercularis (Broca's area)44Primary motor cortex (precentral gyrus)4Primary somatosensory cortex (area 3)3Primary somatosensory cortex (area 1)1Primary somatosensory cortex (area 2)2Subcentral area / parietal operculum (S2, gustatory)43Somatosensory association cortex (anterior superior parietal lobule)5Supramarginal gyrus40Posterior superior parietal lobule & precuneus7Angular gyrus (temporo-parietal junction)39Associative visual cortex (V3/V4/V5-MT)19Secondary visual cortex (V2)18Primary visual cortex (V1, calcarine)17Temporal pole38Superior temporal gyrus (Wernicke's area posteriorly)22Middle temporal gyrus21Inferior temporal gyrus20Fusiform / occipitotemporal gyrus37Primary auditory cortex (Heschl's gyrus)41Auditory association cortex (planum temporale)42Parainsular area 5252anteriorFrontopolar cortex10Dorsomedial & dorsolateral prefrontal cortex (superior frontal gyrus)9Frontal eye field (posterior area 8)8Premotor cortex & supplementary motor area (SMA)6Primary motor cortex (precentral gyrus)4Primary somatosensory cortex (area 3)3Somatosensory association cortex (anterior superior parietal lobule)5Posterior superior parietal lobule & precuneus7Dorsal posterior cingulate31Ventral posterior cingulate cortex23Anterior & mid-cingulate cortex24Dorsal anterior cingulate (area 32)32Subgenual cingulate (area 25)25Orbitofrontal cortex11Associative visual cortex (V3/V4/V5-MT)19Primary visual cortex (V1, calcarine)17Secondary visual cortex (V2)18Temporal pole38Uncus / periamygdaloid cortex34Entorhinal cortex28Perirhinal cortex35Parahippocampal / ectorhinal cortex36Fusiform / occipitotemporal gyrus37Inferior temporal gyrus20Orbitofrontal area 12 (rostromedial orbital)12Ectosplenial area 2626Piriform / presubicular cortex (area 27)27Retrosplenial granular cortex (area 29)29Retrosplenial agranular cortex (area 30)30Pregenual anterior cingulate (area 33)33anteriorOrbitofrontal cortex11Pars orbitalis / lateral orbitofrontal cortex47Temporal pole38Uncus / periamygdaloid cortex34Entorhinal cortex28Perirhinal cortex35Parahippocampal / ectorhinal cortex36Fusiform / occipitotemporal gyrus37Inferior temporal gyrus20Associative visual cortex (V3/V4/V5-MT)19Secondary visual cortex (V2)18Primary visual cortex (V1, calcarine)17Orbitofrontal cortex11Pars orbitalis / lateral orbitofrontal cortex47Temporal pole38Uncus / periamygdaloid cortex34Entorhinal cortex28Perirhinal cortex35Parahippocampal / ectorhinal cortex36Fusiform / occipitotemporal gyrus37Inferior temporal gyrus20Associative visual cortex (V3/V4/V5-MT)19Secondary visual cortex (V2)18Primary visual cortex (V1, calcarine)17anterior
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Region colors identify anatomy only; they do not indicate evidence strength.

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Weighted-Evidence Summary
460 signs have a reported relationship on this axis. Each row keeps the manuscripts, findings, and reported values for that sign together. Clinical relationship labels come directly from the reviewed evidence. Manuscript weights summarize support; they never create or remove an anatomical or lateralizing relationship.
How weighting works

Class I (3) applies to an exact-row guideline/consensus or a systematic review/meta-analysis contributing its own synthesis; class II (2) requires an approved primary-study design (CASE_SERIES, DIAGNOSTIC_STUDY, PROSPECTIVE_COHORT, RETROSPECTIVE_COHORT) and an independent primary result in that row; class III (1) covers case observations, narrative or educational evidence, and cited restatements.

Directness multipliers: Postoperative outcome 1.50; SEEG 1.50; Other intracranial EEG 1.35; Video EEG 1.20; Imaging concordance 1.15; Scalp EEG 1.10; Review 1.00; No direct confirmation 0.90.

Directness and the capped sample-size factor apply only to an exact-row independent primary contribution. Unresolved structured design remains visible with numerical weight 0.

All 77 reviewed reports are accounted for and represent 73 distinct manuscripts after duplicate files and report versions are combined. 69 manuscripts contribute weighted evidence; 3 await evidence-weight review; and 1 provide context without a sign-specific localization or lateralization result.

Source-reported directions, regions, percentages, and denominators remain attached to their exact findings. They are displayed below each row and are not converted into a new pooled target percentage.

Colored chips show reviewed relationships, not calculated percentages 1, 2, or 3+ contributing manuscripts (volume only)Weights summarize support; they are not reliability, certainty, sensitivity, or specificity.
Somatosensory aura (tingling, numbness, paresthesia - contralateral, somatotopic)Source terms: Somatosensory auraReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side27 manuscripts · 102 findings · 93 reported values
Weighted evidence supportevidence weight 58.02 across 27 manuscripts · 1 manuscript weight pending · 5 independent primary study · 6 systematic review or meta-analysis · 4 case report or observation · 11 narrative, educational, or cited context · 1 structured design not resolved

Contralateral somatosensory manifestations were the predominant or joint-predominant directional category in both TL and T+ groups, with ipsilateral and bilateral manifestations also reported. The review describes elementary sensory aura in pure fronto-opercular epilepsy as mainly contralateral to the epileptogenic zone. The review reports contralateral non-painful paresthesia in the compared fronto-opercular and pure-insular contexts. This alternate-version atomic row restates contralateral somatosensory aura at 38% in the first cited parietal surgical series. This alternate-version atomic row restates contralateral somatosensory aura at 38% in the second cited parietal surgical series. The review states that seizures from primary sensory cortex in the postcentral gyrus tend to begin with contralateral tingling or numbness. The review describes unilateral sensory aura as contralateral to the cerebral hemisphere of seizure onset. In the illustrated case, painful tingling in the left hand was contralateral to right-insular seizure onset. The source explicitly classifies the assessed somatic-aura category as non-lateralizing. Table 3 explicitly classifies somatic aura as non-lateralizing and reports a 5.9–10.5% study-level range. Table 4 explicitly labels the somatic aura non-lateralizing and reports odds of occurrence of 0.09 (95% CI 0.03–0.31). The source explicitly labels the modeled somatic-aura category as non-lateralizing. The modeled somatic-aura category is explicitly source-labeled non-lateralizing. Table 5 repeats the 5.9–10.5% lateral-TLE range for the source-labeled non-lateralizing somatic aura. The source explicitly classifies the somatic aura category as non-lateralizing and reports a mesial-TLE prevalence range of 0–18.8%. The chapter restates that painful sensation has been described more frequently in the nondominant hemisphere. The reported unilateral somatosensory manifestations were contralateral (upper limb or hemibody), and ipsilateral paresthesia was not observed. Tingling or numbness was contralateral to the epileptogenic zone in 51 of 52 patients. One of 52 patients with tingling or numbness had a bilateral distribution. For stimulation-evoked sensations involving midline face or trunk, responses were predominantly bilateral (68.2%), with contralateral (24.2%) and ipsilateral (7.6%) exceptions. After insular stimulation, limb responses were predominantly contralateral (94%), whereas midline face/trunk responses were mostly bilateral (68.2%); ipsilateral responses were uncommon in both subgroups. Somatosensory aura in insular seizures is described over contralateral limbs, while a widely distributed bilateral painful non-Jacksonian pattern is a specific phenotype favoring posterior insular involvement. Somatosensory auras are described as usually contralateral to the focus; right hemibody pain in the illustrative case suggested a left focus. The cited-study restatement reports predominantly contralateral onset (89%) for seizures with unilateral somatosensory aura, with ipsilateral onset in a minority. Unilateral somatosensory phenomena are described as predominantly contralateral to the focus, with occasional ipsilateral or bilateral distributions, particularly with insular, SMA, or secondary sensory involvement. The reproduced table lists contralateral somatosensory aura for primary somatosensory cortex and SSMA, but ipsilateral aura when unilateral for secondary somatosensory cortex. The review describes unilateral distal somatosensory aura as contralateral, bilateral or widespread sensations as potentially arising from SSMA or S2, and poorly localized all-body sensations as nonlateralizing. The review reports contralateral somatosensory aura as the most common aura in two cited parietal surgical series, at 38% in each. One of six typical anterior cingulate cases had a source-explicit contralateral indistinct somatosensory aura. The review assigns contralateral discrete-body-part symptoms to SI, bilateral or ipsilateral symptoms to SII, and primarily contralateral proximal poorly localized symptoms to SSMA. The review links somatosensory body-schema illusions, specifically, to nondominant inferior parietal or TPO activation. In one patient, a right-foot sensory aura preceded bilateral asymmetric tonic posturing and generalized tonic-clonic seizures. Unilateral somatosensory aura is described as usually contralateral to the suspected epileptogenic zone, with ipsilateral auras reported as a minority exception. The cited study reported unilateral somatosensory auras contralateral to the suspected epileptogenic zone when a lesion was known. In the cited cohort restatement, the suspected epileptogenic zone was contralateral to the sensory aura in 46%, ipsilateral in 6%, not lateralized in 25%, and had no identifiable unilateral lesion in 24%. No hemisphere-direction relationship is reported. The fronto-opercular onset prevalence reports no hemisphere direction. The prefrontal-operculum subgroup count reports no hemisphere direction. The precentral Rolandic-operculum subgroup count reports no hemisphere direction. The cited pure-insular series reports no hemisphere direction. The cited anterior-insular subgroup count reports no hemisphere direction. The posterior-insular subgroup count reports no hemisphere direction. The cited pure-insular series reports no hemisphere direction for face and hand paresthesia. The somatosensory frequencies report no body-side or hemisphere direction. The review table specifies no hemisphere or body-side direction for tingling or numbness. The source term hemisensory is preserved, but no side relation is reported. The stimulation statement reports no side direction. The cited insular stimulation result reports no hemisphere direction. The cited stimulation synthesis reports no hemisphere direction. A left hemibody sensory manifestation is reported, but no relation between body side and seizure-onset side is claimed. The combined somatosensory and auditory aura observation reports no hemisphere direction. No hemisphere or side-relative direction is reported. The qualitative review table reports no hemispheric direction for somatosensory symptoms. No hemisphere or body-side direction is reported. The table aggregate does not report side. Laterality is assessed elsewhere and is absent from this aggregate. The finding reports no cerebral lateralization. No hemisphere or body-side relationship is reported. The case reports right-sided symptoms but no relation to a seizure-onset hemisphere. The propagation model reports no hemisphere direction. No side or hemisphere relation is reported. No lateralization relationship is reported. The localizing probability reports no hemisphere direction. The localization confidence interval reports no hemisphere direction. The parietal localizing odds ratio reports no hemisphere direction. The insular localizing odds ratio reports no hemisphere direction. The insular odds-ratio interval reports no hemisphere direction. The basal-temporal somatosensory prevalence reports no hemisphere direction. The review does not state the side of the facial manifestations. The Table 3 somatosensory prevalence reports no hemisphere direction. The table does not report side. The restricted basal-temporal subset prevalence reports no hemisphere direction. The nonthermal, nonpainful response subtype reports no body-side direction. No lateralizing direction is reported. The symptom is described as lateralized, but no body side or hemisphere relation is reported. No hemisphere or body-side relationship is assigned. No seizure lateralization is reported. The cited parietal cohort prevalence reports no hemisphere direction. The cited parietal-cohort prevalence reports no hemisphere direction. This atomic finding reports regional associations and symptom frequencies but no hemisphere direction. The review synthesis reports no hemisphere direction for the aura combination or propagation pathway. A clearly defined body region is required, but no side-to-hemisphere relationship is reported.

Source-defined result groups 44
Localization: InsularSource-defined values retained separatelyAll reported · somato-sensory response body territory1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyprimary somatosensory/parietal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 18.2%contralateral upper limb · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyMidline face/trunk · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 15.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 16.7%All reported · other typical anterior patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: BilateralObserved proportion 1.9%All reported · contralateral distribution · patients with tingling or numbness1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyLimbs · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Lateralization: nonlateralizingSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyMidline face/trunk · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLimbs · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyinsular localization given somatosensory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyMidline face/trunk · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyLimbs · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyLimbs · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelysomato-sensory response analysis set · all other stimulated contacts, including non-eloquent contacts · stimulation contact1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyparietal localization given somatosensory aura · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLimbs · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyipsilateral paresthesia · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLimbs · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ 26.1% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 9.1%contralateral hemibody · patient1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyMidline face/trunk · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyTalairach z coordinate · all other stimulated contacts · stimulation contact1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · somato-sensory response body territory1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 66.7%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyinsular localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 11.9% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 11.9% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 98.1%All reported · ipsilateral or bilateral aura · patients with tingling or numbness1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 26.1% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given somatosensory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given somatosensory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: nonlateralizingSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 8.7% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 8.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: nonlateralizingSource-defined values retained separatelyMesial TLE patients assessed for Non-lateralizing somatic aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 26.1% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyMidline face/trunk · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyMidline face/trunk · midline body regions versus limbs; laterality categories · body-region-specific somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · thermal and painful somato-sensory subtypes · evoked somato-sensory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 16.9% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyTalairach y coordinate · all other stimulated contacts · stimulation contact1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 27

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 15 findings · 7 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • somatosensoryTable 1 defines or exemplifies the the source's own semiology category “somatosensory” as Tingling or touch sensation.PDF p.7, Table 1 Semiology descriptions and frequencies
  • somatosensorySomatosensory semiology comprised 2.9% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • somatosensory; Figure 3 all-data subsetFigure 3 reports N = 629 for the all-data somatosensory panel.PDF p.9, Figure 3 and caption
  • somatosensory; Figure 3 non-topological subsetFigure 3 reports N = 102 for the non-topological somatosensory panel.PDF p.9, Figure 3 and caption
  • somatosensory aura; frontal lobeUndifferentiated somatosensory auras implicated the frontal lobe in 23%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; frontal lobeThe 95% CI for somatosensory aura; frontal lobe was 15%–32%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; temporal lobeUndifferentiated somatosensory auras implicated the temporal lobe in 31%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; temporal lobeThe 95% CI for somatosensory aura; temporal lobe was 21%–42%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; parietal lobeUndifferentiated somatosensory auras implicated the parietal lobe in 38%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; parietal lobeThe 95% CI for somatosensory aura; parietal lobe was 28%–48%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; insulasomatosensory aura indicated insular localization in 59%.PDF p.8, Seizure semiology localizing values
  • somatosensory aura; primary somatosensory cortex/parietalSomatosensory auras had an intrinsic localizing OR of 7.6 for primary somatosensory cortex within the parietal lobe.PDF p.8, Relative localizing values of semiologies
  • somatosensory aura; primary somatosensory cortex/parietalThe 95% CI for somatosensory aura; primary somatosensory cortex/parietal was 5.1–11.3.PDF p.8, Relative localizing values of semiologies
  • somatosensory aura; insulaSomatosensory symptoms had an intrinsic localizing OR of 1.9 for the insula.PDF p.8, Relative localizing values of semiologies
  • somatosensory aura; insulaThe 95% CI for somatosensory aura; insula was 0.7–4.9.PDF p.8, Relative localizing values of semiologies
Reported values
  • somatosensory 2.9%somatosensoryPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • somatosensory aura; frontal lobe 23%somatosensory aura; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • somatosensory aura; temporal lobe 31%somatosensory aura; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • somatosensory aura; parietal lobe 38%somatosensory aura; parietal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • somatosensory aura; insula 59%somatosensory aura; insulaPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 7.6somatosensory aura; primary somatosensory cortex/parietalOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 1.9somatosensory aura; insulaOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior contralateral somatosensory auraOne typical anterior patient had a contralateral indistinct somatosensory aura.PDF p.3, Clinical Presentation
Reported values
  • 1/6 contralateral indistinct somatosensory auratypical anterior contralateral somatosensory auraProportion · n/N 1/6 · 6 typical anterior cingulate cases · auraPDF p.3, Clinical Presentation
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfNarrative, educational, or cited context · 7 findings · 7 reported values
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • Bartolomei et al. 2011 somatosensory auraTable 1 reports 58% somatosensory aura in the cited Bartolomei et al. 2011 cohort.PDF p.3, Table 1
  • Salanova et al. 1995a somatosensory auraTable 1 reports 63.4% somatosensory aura in the cited Salanova et al. 1995a cohort.PDF p.3, Table 1
  • Salanova et al. 1995b somatosensory auraTable 1 reports 62% somatosensory aura in the cited Salanova et al. 1995b cohort.PDF p.3, Table 1
  • Kim et al. 2004b somatosensory auraTable 1 reports 32.5% somatosensory aura in the cited Kim et al. 2004b cohort.PDF p.3, Table 1
  • Kim et al. 2004a somatosensory auraTable 1 reports 31.6% somatosensory aura in the cited Kim et al. 2004a cohort.PDF p.3, Table 1
  • Francione et al. 2015 somatosensory auraTable 1 reports 62.5% somatosensory aura in the cited Francione et al. 2015 cohort.PDF p.3, Table 1
  • Asadollahi et al. 2017 (this study) somatosensory auraTable 1 reports 38.8% somatosensory aura in the cited Asadollahi et al. 2017 (this study) cohort.PDF p.3, Table 1
Reported values
  • 58% somatosensory auraBartolomei et al. 2011 somatosensory auraPercentage · Bartolomei et al. 2011 cohort · auraPDF p.3, Table 1
  • 63.4% somatosensory auraSalanova et al. 1995a somatosensory auraPercentage · Salanova et al. 1995a cohort · auraPDF p.3, Table 1
  • 62% somatosensory auraSalanova et al. 1995b somatosensory auraPercentage · Salanova et al. 1995b cohort · auraPDF p.3, Table 1
  • 32.5% somatosensory auraKim et al. 2004b somatosensory auraPercentage · Kim et al. 2004b cohort · auraPDF p.3, Table 1
  • 31.6% somatosensory auraKim et al. 2004a somatosensory auraPercentage · Kim et al. 2004a cohort · auraPDF p.3, Table 1
  • 62.5% somatosensory auraFrancione et al. 2015 somatosensory auraPercentage · Francione et al. 2015 cohort · auraPDF p.3, Table 1
  • 38.8% somatosensory auraAsadollahi et al. 2017 (this study) somatosensory auraPercentage · Asadollahi et al. 2017 (this study) cohort · auraPDF p.3, Table 1
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 9 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • somatosensory auraSomatosensory auras did not differ significantly between TL and T+ groups across the source's ipsilateral, contralateral, and bilateral subcategories.PDF p.6, Table 2
Reported values
  • TL 16.9%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • T+ 8.7%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • T+ 26.1%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 11.9%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • P=0.3somatosensory auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
  • TL 11.9%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • TL 15.3%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • T+ 26.1%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • T+ 26.1%somatosensory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 6 findings · 6 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • somatosensory sensationsSomatosensory sensations accounted for 2% of the sensory manifestations in the narrative summary.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • facial somatomotor or sensory modificationsFacial somatomotor or sensory modifications were reported in 10% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Somato-sensory (Table 3)Table 3 reports somato-sensory symptoms in 2 cases (2%), with propagation timing marked uncertain.PDF p.6, Table 3
  • Facial somato-sensory or motor (Table 3)Table 3 reports facial somato-sensory or motor signs in 8 cases (10%), more during propagation.PDF p.6, Table 3
  • Somato-sensory (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports somato-sensory symptoms in 1 case (2%).PDF p.7, Table 4
  • Facial somato-sensory or motor (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports facial somato-sensory or motor signs in 3 cases (5%).PDF p.7, Table 4
Reported values
  • 2% somatosensory sensationssomatosensory sensationsPercentage · reviewed basal temporal seizure cases · ictal propagation uncertain in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 10% facial somatomotor or sensory modificationsfacial somatomotor or sensory modificationsPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 2 cases (2%)Somato-sensory (Table 3)Percentage · Table 3 basal temporal seizure cases · propagation?PDF p.6, Table 3
  • 8 cases (10%)Facial somato-sensory or motor (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 1/60 (2%)Somato-sensory (Table 4)Percentage · n/N 1/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
  • 3/60 (5%)Facial somato-sensory or motor (Table 4)Percentage · n/N 3/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Somatosensory symptomsTable 1 reports somatosensory symptoms as rare in temporal lobe seizures and common in frontal lobe seizures.PDF p.2, Table 1
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • sensory phenomena; sensory aura; paresthesiaSensory phenomena associated with SMA epilepsy may be diffuse and poorly localized, including nonspecific cephalic sensations, paresthesia, or a sense of impending movement.PDF p.7, Discussion
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfCase report or observation · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • perisylvian sensorimotor–sensory sequenceThe review gives a perisylvian example in which initial tingling in cheek, tongue, or throat is followed by hemifacial twitching or facial disgust with hypersalivation, then auditory hallucinations or language deficit; intracerebral recordings are described as showing repetitive spikes moving from one area to the next with strict anatomo-clinical correlations.PDF p.4, section 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 7 findings · 4 reported values
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • contralateral somatosensory auraIn one of two larger surgical series of parietal lobe epilepsy, contralateral somatosensory aura was the most commonly reported aura in 38% of cases.PDF p.7, Parietal lobe seizures
  • contralateral somatosensory auraIn the second larger surgical series of parietal lobe epilepsy, contralateral somatosensory aura was also reported in 38% of cases.PDF p.7, Parietal lobe seizures
  • primary sensory cortex; contralateral tingling and numbnessSeizures arising from primary sensory cortex in the postcentral gyrus tend to start with contralateral tingling or numbness, which may spread along adjacent body parts through the sensory homunculus; pain or altered thermal sensation may also occur and propagation to the frontal lobe may produce clonic activity with tonic posturing.PDF p.7, Primary sensory cortex; PDF p.3, Figure 1
  • unilateral sensory auraUnilateral sensory aura is described as a contralateral sign.PDF p.10, Lateralising signs
  • contralateral somatosensory auraIn two of the larger surgical series of patients with parietal lobe epilepsy, the most commonly reported aura was a contralateral somatosensory aura, reported in 38% in both series.PDF p.7, Parietal lobe seizures
  • tingling; numbness auraTable 3 lists tingling or numbness as localising to primary or secondary somatosensory cortex, supplementary motor area, or insula.PDF p.10, Table 3
  • hippocampal propagation to insula; complex visceral and somatosensory auraThe review states that seizures arising from hippocampus almost always propagate to the insula, so abdominal aura is also common in mesiotemporal seizures; nevertheless, the combination of complex visceral and somatosensory auras points toward insular onset.PDF p.8, Insular seizures; PDF p.9, Insular seizures
Reported values
  • contralateral somatosensory aura 38%contralateral somatosensory auraPercentage · one larger surgical series of parietal lobe epilepsy · aura/early ictalPDF p.7, Parietal lobe seizures
  • contralateral somatosensory aura 38%contralateral somatosensory auraPercentage · second larger surgical series of parietal lobe epilepsy · aura/early ictalPDF p.7, Parietal lobe seizures
  • Contralateral somatosensory aura 38% in second cited surgical seriescontralateral somatosensory auraPercentage · Patients in two surgical series of parietal lobe epilepsy · Second cited large parietal surgical series · AuraPDF p.7, Parietal lobe seizures
  • Contralateral somatosensory aura 38% in first cited surgical seriescontralateral somatosensory auraPercentage · Patients in two surgical series of parietal lobe epilepsy · First cited large parietal surgical series · AuraPDF p.7, Parietal lobe seizures
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.37 · 1 × 0.9 × 1.521
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • somatosensory and auditory aura; frontal subgroupOne frontal-subgroup aura combined a nonpainful somatosensory aura with an auditory sensation.PDF p.3, Aura
Reported values
  • 1 patientsomatosensory and auditory aura; frontal subgroupCount · n/N 1/11 · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Non-lateralizing somatic auraTable 3 reports 2 studies assessing Non-lateralizing somatic aura.PDF p.6, Table 3
  • Non-lateralizing somatic auraTable 3 reports 36 patients assessed for Non-lateralizing somatic aura.PDF p.6, Table 3
  • Non-lateralizing somatic auraTable 3 reports 5.9–10.5% as the percentage range or value for Non-lateralizing somatic aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Non-lateralizing somatic auraTable 4 reports overall odds of 0.09 for occurrence of Non-lateralizing somatic aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Non-lateralizing somatic auraTable 4 reports a 95% confidence interval of 0.03–0.31 for the overall odds of Non-lateralizing somatic aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Non-lateralizing somatic auraThe heterogeneity test for the Table 4 odds estimate for Non-lateralizing somatic aura has p=0.6194.PDF p.7, Table 4
  • Non-lateralizing somatic aura; lateral versus mesial comparisonTable 5 reports 2 studies comparing Non-lateralizing somatic aura in lateral and mesial TLE.PDF p.9, Table 5
  • Non-lateralizing somatic aura; lateral TLE patient denominatorTable 5 reports 36 lateral-TLE patients assessed for Non-lateralizing somatic aura.PDF p.9, Table 5
  • Non-lateralizing somatic aura; mesial TLE patient denominatorTable 5 reports 36 mesial-TLE patients assessed for Non-lateralizing somatic aura.PDF p.9, Table 5
  • Non-lateralizing somatic aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 5.9–10.5% for Non-lateralizing somatic aura.PDF p.9, Table 5
  • Non-lateralizing somatic aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–18.8% for Non-lateralizing somatic aura.PDF p.9, Table 5
Reported values
  • 5.9–10.5%Non-lateralizing somatic auraPercentage Range · Lateral temporal epilepsy patients assessed for Non-lateralizing somatic aura · ictalPDF p.6, Table 3
  • odds 0.09odds of occurrence; Non-lateralizing somatic auraOdds · Lateral temporal epilepsy patients assessed for Non-lateralizing somatic aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 5.9–10.5%Non-lateralizing somatic aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Non-lateralizing somatic aura · Lateral TLE patients assessed for Non-lateralizing somatic aura · ictalPDF p.9, Table 5
  • 0–18.8%Non-lateralizing somatic aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Non-lateralizing somatic aura · Mesial TLE patients assessed for Non-lateralizing somatic aura · ictalPDF p.9, Table 5
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfStructured design not resolved · 1 finding
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Somatosensory aura and parietal localizationThe source authors state that a somatosensory aura is the main feature localizing to the parietal lobe, whereas other symptoms may result from spread to frontal or temporal lobes.PDF p.5, §6.2
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 2 findings
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • somatosensory aurasSomatosensory auras arising from SI involve discrete body parts contralateral to the ictal discharge; SII produces similar symptoms that may be bilateral or ipsilateral to the seizure focus; and SSMA symptoms are poorly localized and primarily involve contralateral proximal body parts. The source table likewise lists SI and SSMA as mainly contralateral and SII as ipsilateral when unilateral.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
  • well-localized somatosensory auras and somatosensory illusionsWell-localized somatosensory auras that evolve to motor features are usually associated with a perirolandic epileptogenic zone close to the symptomatogenic zone, whereas illusions of swelling, shrinking, or movement of body parts are often elicited by activation of the nondominant inferior parietal lobe or TPO junction.PDF p.2, section 3.1 Auras
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • lateralized paresthesia followed by SP1 or SP2A lateralized paresthesia evolved into SP1 or SP2 in all of the frontal SHE cases described by the authors, suggesting a more posterior frontal seizure organization.PDF p.8, section 4.3
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 11 findings · 7 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • contralateral elementary sensory aura; somatosensory auraSeizures originating in the fronto-opercular region are described as commonly associated with contralateral elementary sensory aura, especially for the Rolandic operculum.PDF p.1, Abstract; PDF p.2, Key points
  • insular epilepsy; opercular epilepsy; non-painful paresthesiaThe source states that non-painful paresthesia does not discriminate between insular and frontal-opercular involvement, although pure-insular series described more extensive, variable, or multi-territory paresthesia than the face/upper-limb pattern in the review.PDF p.8, Discussion
  • somatosensory aura; precentral Rolandic operculum; prefrontal operculumThe source reports that the only significant semiological difference between prefrontal and precentral Rolandic operculum groups was the more frequent somatosensory aura in the Rolandic group.PDF p.6, Anatomical and clinical correlations; PDF p.8, Discussion
  • Somatosensory (arm and/or face)Table 2 reports 7/21 (33%) for Somatosensory (arm and/or face); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Somatosensory (arm and/or face)Table 2 reports 1/12 patients with Somatosensory (arm and/or face) in the prefrontal operculum group.PDF p.7, Table 2
  • Somatosensory (arm and/or face)Table 2 reports 6/9 patients with Somatosensory (arm and/or face) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Somatosensory (arm and/or face)Fisher's exact comparison of Somatosensory (arm and/or face) between the prefrontal and precentral Rolandic operculum groups has p=0.016.PDF p.7, Table 2
  • non-painful paresthesia; pure insular epilepsyThe cited Peltola series reported non-painful paresthesia in 8 of 11 patients (72%).PDF p.8, Discussion
  • non-painful paresthesia; anterior insulaWithin the cited Peltola series, four patients with non-painful paresthesia had an EZ in the anterior insula.PDF p.8, Discussion
  • non-painful paresthesia; posterior insulaWithin the cited Peltola series, four patients with non-painful paresthesia had an EZ in the posterior insula.PDF p.8, Discussion
  • face and hand paresthesia; pure insular epilepsyThe cited Singh series reported face and hand paresthesia in 3 of 9 patients.PDF p.8, Discussion
Reported values
  • 7/21 (33%)Somatosensory (arm and/or face)Percentage · n/N 7/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 1/12 patientsSomatosensory (arm and/or face)Proportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 6/9 patientsSomatosensory (arm and/or face)Proportion · n/N 6/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
  • 8/11 (72%)non-painful paresthesia; pure insular epilepsyPercentage · n/N 8/11 · 11 patients in the cited Peltola pure-insular series · 11 patients in the cited Peltola pure-insular series · ictal onsetPDF p.8, Discussion
  • 4 patientsnon-painful paresthesia; anterior insulaCount · n/N 4/8 · Peltola patients with non-painful paresthesia · ictal onsetPDF p.8, Discussion
  • 4 patientsnon-painful paresthesia; posterior insulaCount · n/N 4/8 · Peltola patients with non-painful paresthesia · ictal onsetPDF p.8, Discussion
  • three (33%) patientsface and hand paresthesia; pure insular epilepsyPercentage · n/N 3/9 · 9 patients in the cited Singh pure-insular series · 9 patients in the cited Singh pure-insular series · ictal onsetPDF p.8, Discussion
jobst-insula-and-its-epilepsies-2019.pdfCase report or observation · 6 findings · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • Figure 3 painful tingling in left handThe patient in Figure 3 described a painful tingling sensation in the left hand after right-insular onset.PDF p.4, Figure 3B
  • hemisensory symptoms in perisylvian spreadHemisensory symptoms follow the perioral symptoms in the source-described perisylvian propagation sequence.PDF p.1, Abstract
  • central-sulcus insular stimulation paresthesiasElectrical stimulation around the central sulcus of the insula produces paresthesias.PDF p.1, Abstract; PDF p.5, Somatosensory Sensations
  • somatosensory stimulation responsesSomatosensory sensations accounted for 335 of 550 evoked symptoms (61%) in the cited insular stimulation series.PDF p.5, Somatosensory Sensations
  • paresthesias most frequent somatosensory responseParesthesias were the most frequent somatosensory response in the cited insular stimulation series.PDF p.5, Somatosensory Sensations
  • left hemibody sensory seizures in SUDEP-related caseA 33-year-old patient in a SUDEP-related case had left hemibody sensory seizures.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
Reported values
  • 335/550 (61%) somatosensory sensationssomatosensory stimulation responsesPercentage · n/N 335/550 · 550 positive responses in the cited insular stimulation series · stimulation-evoked semiologyPDF p.5, Somatosensory Sensations
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal sensory (somatosensory)Focal sensory (somatosensory) semiology occurred in 6/61 individuals (10%) as initial semiology and 9/61 (15%) in the combined set-of-semiology.PDF p.3, Results; PDF p.5, Table 2
Reported values
  • Combined 9/61 (15%)Focal sensory (somatosensory)Percentage · n/N 9/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
  • Initial 6/61 (10%)Focal sensory (somatosensory)Percentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 4 findings · 4 reported values
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Unilateral somatosensory auraThe review reports unilateral somatosensory auras in less than 10% of LTM series, with 89% of seizures having contralateral onset; a clear sensory march in a well-localized area increases sign reliability.PDF p.7, section 1.15
  • Somatosensory phenomena by region and distributionThe review states that somatosensory phenomena can arise from mesial temporal structures, insula, secondary somatosensory region, or SSMA; unilateral phenomena are predominantly contralateral but may be ipsilateral or bilateral, particularly with insular, SMA, or secondary sensory involvement, and secondary sensory involvement is more likely to affect face and distal extremities with proximal sparing.PDF p.7, section 1.15
  • Somatosensory aura in Table 2Table 2 associates somatosensory aura with primary somatosensory cortex (BA 1, 2, 3b), secondary somatosensory areas (parietal operculum/SSII), and SSMA; it lists contralateral lateralisation to primary cortex, ipsilateral lateralisation if unilateral for secondary somatosensory cortex, and contralateral lateralisation for SSMA.PDF p.3, Table 2
  • Somatosensory aura symptomsIn large cohort studies, somatosensory auras were present in 12%; 77% of patients with somatosensory auras reported tingling, while pain or thermal changes were less common and more suggestive of secondary somatosensory area involvement; somatosensory auras correlated with centroparietal epilepsy, particularly with a clear march, but also occurred in temporal-lobe, mesial-frontal, and multifocal epilepsy.PDF p.7, section 1.15
Reported values
  • Contralateral onset in 89% of seizuresUnilateral somatosensory auraPercentage · LTM series; seizures with unilateral somatosensory aura · Seizures with unilateral somatosensory aura · ictal auraPDF p.7, section 1.15
  • Unilateral somatosensory auras in <10% of LTM seriesUnilateral somatosensory auraPercentage · LTM series; seizures with unilateral somatosensory aura · LTM series · ictal auraPDF p.7, section 1.15
  • 77% tingling among patients with somatosensory aurasSomatosensory aura symptomsPercentage · Large cohort studies; patients with somatosensory auras · patients with somatosensory auras · ictal auraPDF p.7, section 1.15
  • 12% aura prevalenceSomatosensory aura symptomsPercentage · Large cohort studies; patients with somatosensory auras · large cohort studies · ictal auraPDF p.7, section 1.15
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 11 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Somatosensory auraThe review describes unilateral somatosensory auras as generally pointing to a contralateral suspected epileptogenic zone, with greater reliability when the aura is well localized to a distal extremity and associated with a sensory march; ipsilateral sensory auras have also been reported.PDF p.2, section 2.1 Sensory auras; PDF p.2, section 2.1.1 Mechanism; PDF p.12, Table 1
  • Somatosensory auraMauguiere and Courjon described 127 patients with somatosensory auras selected among an epilepsy population of 8938; all except one had unilateral symptoms, and all patients with a known lesion and unilateral auras had symptoms contralateral to the suspected epileptogenic zone.PDF p.2, section 2.1 Sensory auras
  • Somatosensory auraTuxhorn et al. reviewed 600 patients and found 72 patients with sensory auras; among the reported suspected-zone classifications, 46% were contralateral to the aura, 6% ipsilateral, 24% had no identifiable unilateral lesion, and 25% were not lateralized.PDF p.2, section 2.1 Sensory auras
Reported values
  • frequency 1–60% of patientsSomatosensory auraRange · Patients with epilepsy or focal epilepsy as summarized by the review · reviewed populations · Ictal auraPDF p.2, section 2.1 Sensory auras; PDF p.2, section 2.1.1 Mechanism; PDF p.12, Table 1
  • 89% contralateralSomatosensory auraPercentage · Patients with epilepsy or focal epilepsy as summarized by the review · unilateral somatosensory auras · Ictal auraPDF p.2, section 2.1 Sensory auras; PDF p.2, section 2.1.1 Mechanism; PDF p.12, Table 1
  • 6.1% of epilepsy patientsSomatosensory auraPercentage · Patients with epilepsy or focal epilepsy as summarized by the review · epilepsy patients · Ictal auraPDF p.2, section 2.1 Sensory auras; PDF p.2, section 2.1.1 Mechanism; PDF p.12, Table 1
  • 92 with structural lesionSomatosensory auraCount · 127 patients selected among 8938 patients with epilepsy; 92 had an identifiable structural lesion and 32 had EEG seizures recorded · structural lesion · Ictal auraPDF p.2, section 2.1 Sensory auras
  • 127 patients among 8938Somatosensory auraPercentage · n/N 127/8938 · 127 patients selected among 8938 patients with epilepsy; 92 had an identifiable structural lesion and 32 had EEG seizures recorded · somatosensory aura patients · Ictal auraPDF p.2, section 2.1 Sensory auras
  • 32 with EEG seizuresSomatosensory auraCount · 127 patients selected among 8938 patients with epilepsy; 92 had an identifiable structural lesion and 32 had EEG seizures recorded · EEG seizures recorded · Ictal auraPDF p.2, section 2.1 Sensory auras
  • Not lateralized 25% of 72Somatosensory auraPercentage · 600 reviewed patients; 72 patients with sensory auras · Not lateralized · Ictal auraPDF p.2, section 2.1 Sensory auras
  • Suspected zone ipsilateral to aura 6% of 72Somatosensory auraPercentage · 600 reviewed patients; 72 patients with sensory auras · Ipsilateral · Ictal auraPDF p.2, section 2.1 Sensory auras
  • Sensory auras 72/600 (12%)Somatosensory auraPercentage · n/N 72/600 · 600 reviewed patients; 72 patients with sensory auras · Ictal auraPDF p.2, section 2.1 Sensory auras
  • Suspected zone contralateral to aura 46% of 72Somatosensory auraPercentage · 600 reviewed patients; 72 patients with sensory auras · Contralateral · Ictal auraPDF p.2, section 2.1 Sensory auras
  • No identifiable unilateral lesion 24% of 72Somatosensory auraPercentage · 600 reviewed patients; 72 patients with sensory auras · No identifiable unilateral lesion · Ictal auraPDF p.2, section 2.1 Sensory auras
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Somatosensory auraSomatosensory auras are abnormal somatosensory sensations or paresthesias limited to a clearly defined somatosensory region of the body; poorly localized or vague sensations are classified only as unclassifiable auras.PDF p.3, Auras, subsection Somatosensory auras; PDF p.2, Table 1
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 4 findings · 12 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • somato-sensory skin territory sizeThe median skin territory involved by somato-sensory sensations after insula stimulation was 3% of total skin surface, with a range of 0.1%-100%.PDF p.4, Somato-sensory Responses
  • somato-sensory response lateralization by body regionWhen the midline body was involved, face or trunk sensations were mostly bilateral, whereas limb sensations were predominantly contralateral to stimulation.PDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • somato-sensory responsesSomato-sensory response sites were broadly distributed across the insular cortex but were preferentially located in the postero-superior insula.PDF p.4, Somato-sensory Responses and Fig. 3; PDF p.7, Somato-sensory Responses
  • somato-sensory nonthermal and nonpainful sensationsNonthermal and nonpainful somato-sensory responses numbered 214 (39%), were described as neutral or unpleasant tingling, light touch, or slight electric current, and arose from sites distributed mainly across the posterior three quarters of the insular cortex.PDF p.3, Results; PDF p.4, Somato-sensory Responses and Fig. 3A
Reported values
  • range 0.1%–100%somato-sensory skin territory sizeRange · Somato-sensory responses evoked by insular stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses
  • median involved skin territory 3% of total skin surfacesomato-sensory skin territory sizeMedian · Somato-sensory responses evoked by insular stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses
  • Limbs 94%somato-sensory response lateralization by body regionPercentage · Somato-sensory responses involving the midline body or limbs after insular stimulation · Limbs · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Midline face/trunk 24.2%somato-sensory response lateralization by body regionPercentage · Somato-sensory responses involving the midline body or limbs after insular stimulation · Midline face/trunk · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Midline face/trunk 7.6%somato-sensory response lateralization by body regionPercentage · Somato-sensory responses involving the midline body or limbs after insular stimulation · Midline face/trunk · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Midline face/trunk 68.2%somato-sensory response lateralization by body regionPercentage · Somato-sensory responses involving the midline body or limbs after insular stimulation · Midline face/trunk · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Limbs 3%somato-sensory response lateralization by body regionPercentage · Somato-sensory responses involving the midline body or limbs after insular stimulation · Limbs · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Limbs 3%somato-sensory response lateralization by body regionPercentage · Somato-sensory responses involving the midline body or limbs after insular stimulation · Limbs · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • 335somato-sensory responsesCount · 335 insular contacts or responses classified as somato-sensory in the stimulation series · somato-sensory response analysis set · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses and Fig. 3; PDF p.7, Somato-sensory Responses
  • OR=0.98somato-sensory responsesOdds ratio · 335 insular contacts or responses classified as somato-sensory in the stimulation series · Talairach y coordinate · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses and Fig. 3; PDF p.7, Somato-sensory Responses
  • OR=1.05somato-sensory responsesOdds ratio · 335 insular contacts or responses classified as somato-sensory in the stimulation series · Talairach z coordinate · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses and Fig. 3; PDF p.7, Somato-sensory Responses
  • 214 responses (39% of 550 clinically eloquent responses)somato-sensory nonthermal and nonpainful sensationsPercentage · 214 nonthermal and nonpainful somato-sensory responses in the 550-response series · stimulation-evoked somato-sensory responsePDF p.3, Results; PDF p.4, Somato-sensory Responses and Fig. 3A
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 3 findings
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • somatosensory auraThe source describes somatosensory aura as the most common aura in insular seizures, with tingling, electrical-current, warmth, or painful sensations over contralateral limbs; a widely distributed, bilateral, painful, non-Jacksonian aura and/or accompanying sensory auras favors posterior two-thirds insular involvement over a parietal onset.PDF p.5, Ictal Semiology; PDF p.13, What localizations are suggested by the seizure semiology?
  • painful somatosensory seizure and contralateral auraIn the Case 2 discussion, the source states that somatosensory auras are usually localized to primary sensory cortex, secondary somatosensory cortex in the parietal operculum, or the posterior third of the insular cortex; painful seizures likely arise in the same regions, although supplementary motor, inferior parietal, and cingulate localizations have been proposed, and somatosensory auras are usually contralateral to the epileptic focus even when the insula is involved.PDF p.13, What localizations are suggested by the seizure semiology?
  • stimulation-evoked somatosensory, auditory, vestibular, olfactory, gustatory, and viscerosensory symptomsThe chapter reports that electrical stimulation studies evoked somatosensory symptoms, including pain, from the posterior two-thirds of the insula; auditory and vestibular symptoms from the posterior insula; and olfactory, gustatory, and viscerosensory symptoms, including laryngeal constriction, from the midinsula, whereas stimulation of the most anterior portion rarely evoked symptoms unless a larger network seizure was elicited.PDF p.3, insular functional differentiation and electrical cortical stimulation
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 8 findings · 6 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • contralateral tingling or numbnessTingling or numbness was contralateral to the epileptogenic zone in 51 of the 52 patients with this reported somatosensory aura.PDF p.3, Results, Aurae
  • bilateral tingling or numbnessOne patient with tingling or numbness had a bilateral distribution.PDF p.3, Results, Aurae
  • somatosensory aura entries in Table 1Table 1 lists 63 source-reported somatosensory aura entries and notes that aura entries can exceed patient counts because some patients had multiple aurae.PDF p.4, Table 1
  • tingling or numbness in extremitiesTingling or numbness in the extremities was reported by 52 patients, corresponding to 63% of the cohort.PDF p.3, Results, Aurae; PDF p.8, Discussion
  • epigastric aura preceded by foot numbnessOne patient had an epigastric aura preceded by numbness in one foot.PDF p.4, Results, Aurae
  • tingling as common reproduced auraThe most common stimulation-reproduced habitual aura was a tingling sensation.PDF p.5, Electrical cortical stimulation
  • right-fingertip tingling and pain in Fig. 1Figure 1 shows an aura of tingling and pain in the fingertips of the right hand followed by rightward head deviation and right-arm tonic posturing.PDF p.4, Fig. 1
  • somatosensory aura after spread to post-central gyrusThe source states that somatosensory aurae can occur with lesions limited to parietal association cortex, suggesting ictal spread to the more eloquent somatosensory cortex.PDF p.8, Discussion
Reported values
  • 51/52 patientscontralateral tingling or numbnessProportion · n/N 51/52 · 52 patients with tingling or numbness · aura or seizure onsetPDF p.3, Results, Aurae
  • 1/52 patientsbilateral tingling or numbnessProportion · n/N 1/52 · 52 patients with tingling or numbness · aura or seizure onsetPDF p.3, Results, Aurae
  • 63 source-reported aura entriessomatosensory aura entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 52/82 (63%) patientstingling or numbness in extremitiesPercentage · n/N 52/82 · 82 patients with parietal lobe epilepsy · aura or seizure onsetPDF p.3, Results, Aurae; PDF p.8, Discussion
  • 1 patientepigastric aura preceded by foot numbnessCount · 82-patient parietal epilepsy series · aura sequencePDF p.4, Results, Aurae
  • 1 caseright-fingertip tingling and pain in Fig. 1Count · n/N 1/1 · patient 7 (M.B.) · aura and ictal evolutionPDF p.4, Fig. 1
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • reflex seizures; hypermotor seizures; right foot sensory auraIn this patient, the two seizure types were hypermotor seizures and a right-foot sensory aura followed by bilateral asymmetric tonic posturing and generalized tonic-clonic seizures; the latter occurred spontaneously and was also provoked by loud sounds, more commonly by somatosensory stimulation of the right foot, and reflex seizures were exaggerated by sudden unexpected stimulation.PDF p.1, Case Report; PDF p.3, Discussion
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • anesthesia; paresthesia; thermic dispersion; painful sensationThe source reports anesthesia, paresthesia, or thermic dispersion mainly with parietal stimulation, with the main effect in postcentral gyrus but additional involvement of precuneus and posterior cingulum; insular stimulation induced paresthesias and localized warmth, and painful sensations were preferentially associated with the posterior two thirds of the insula and were more frequently described in the nondominant hemisphere.PDF p.14, Somato-sensory sensations and pain
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • somatosensory aurasThe review states that unilateral distal somatosensory auras confined to a clearly defined body region usually correspond to the contralateral primary sensory cortex, whereas bilateral or widespread sensations can arise from the supplementary sensorimotor area or S2; S2 stimulation can produce heat or pain, and poorly localized or lateralized “all body sensations” have no localizing or lateralizing value. Low-intensity motor-area stimulation may be perceived as a somatosensory aura when contractions do not produce actual movement.PDF p.1, Somatosensory auras; PDF p.2, Somatosensory auras (continued)
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 2 findings · 11 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • somatosensory and viscerosensory manifestationsThe reported manifestations included unpleasant nonpainful paresthesia in the contralateral upper limb, indescribable sensations in the contralateral hemibody or whole body, head/face/perioral paresthesia, auditory phenomena, epigastric sensation, and pharyngolaryngeal numbness or constriction; painful aura and ipsilateral paresthesia were not observed.PDF p.3, Results—Seizure semiology
  • autonomic; somatosensory/viscerosensory symptomsIn the 22-patient SEEG-defined insulo-opercular epilepsy series, autonomic symptoms and somatosensory/viscerosensory symptoms, separately or in combination, were the most prevalent auras and/or early seizure semiologies.PDF p.3, Results—Seizure semiology
Reported values
  • 6/22 (27%)somatosensory and viscerosensory manifestationsPercentage · n/N 6/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · head, face, or perioral · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · whole body · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • not observedsomatosensory and viscerosensory manifestationsCount · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · ipsilateral paresthesia · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 2/22 (9%)somatosensory and viscerosensory manifestationsPercentage · n/N 2/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · contralateral hemibody · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · epigastric · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 4/22 (18%)somatosensory and viscerosensory manifestationsPercentage · n/N 4/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · contralateral upper limb · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · pharyngolaryngeal · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • not observedsomatosensory and viscerosensory manifestationsCount · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · painful aura · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · auditory · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • Autonomic symptoms 7/22 (32%)autonomic; somatosensory/viscerosensory symptomsPercentage · n/N 7/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • Somatosensory/viscerosensory symptoms 13/22 (59%)autonomic; somatosensory/viscerosensory symptomsPercentage · n/N 13/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology

27 contributing manuscripts; source-reported values remain separate and are not pooled.

Abdominal / visceral pain sensation (interoceptive)Source terms: Abdominal auraReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere27 manuscripts · 90 findings · 86 reported values
Weighted evidence supportevidence weight 56.85 across 27 manuscripts · 2 manuscript weight pending · 6 independent primary study · 6 systematic review or meta-analysis · 11 narrative, educational, or cited context · 2 case report or observation · 2 structured design not resolved

In one case with a left amygdala/hippocampal cavernoma and left temporal EEG onset, right head/eye version and a figure-of-4 posture preceded rare focal-to-bilateral tonic-clonic seizures. The reported unilateral somatosensory manifestations were contralateral (upper limb or hemibody), and ipsilateral paresthesia was not observed. The reproduced table explicitly describes abdominal aura as non-lateralising. Right head/eye version and right-arm extension in the figure-of-4 posture were contralateral to the case's left-hemisphere onset. The review states that an abdominal aura combined with vomiting suggests a nondominant temporal epileptogenic zone. Epigastric aura occurred in 4 of 10 right-temporal patients versus 1 of 9 left-temporal patients. The review reports temporal abnormalities as unilateral or bilateral and provides no fixed hemisphere direction for abdominal-pain seizures. The 71% digestive-symptom frequency gives no body-side or hemisphere information. No hemisphere or body-side direction is reported. The cited comparison contains no lateralization information. The finding reports no cerebral lateralization. The probability statement contains no lateralization information. The mesiotemporal-versus-lateral temporal comparison contains no hemisphere direction. The stimulation-response frequency contains no lateralization information. The stimulation-site count contains no lateralization information. The visceral response description contains no body-side or hemisphere information. The cited stimulation response provides no hemispheric direction. The single-case observation contains no lateralization information. The mesial-versus-lateral temporal comparison provides no hemispheric direction. No hemispheric lateralization is supplied. The heterogeneity test contains no lateralization information. The study count contains no lateralization information. The denominator contains no lateralization information. The case description gives no body-side or hemisphere information. No lateralizing direction is reported. The educational epigastric definition gives no hemisphere or lateralization direction. The panel denominator carries no hemisphere or lateralization information. The non-topological probability contains no lateralization information. The confidence interval contains no lateralization information. The mesial-temporal probability contains no lateralization information. The insular percentage contains no lateralization information. This finding reports temporal localization but no cerebral lateralization. The odds-ratio confidence interval contains no lateralization information. The mesial-temporal odds ratio contains no lateralization information. The prevalence restatement contains no lateralization information. The prevalence summary contains no lateralization information. The restricted-subset prevalence contains no lateralization information. The source reports no significant difference in evoked-sensation type between right- and left-insular stimulation. No hemisphere or body-side relation to a cerebral reference is reported. The stimulation responses contain no lateralization information. No lateralization information is supplied. The cited anterior-versus-posterior insular comparison provides no lateralizing information. No seizure lateralization is reported. No hemisphere or body-side relationship is reported. The probability estimates contain no lateralization information. No hemisphere direction is reported. The review synthesis reports no hemisphere direction for the aura combination or propagation pathway. The patient-level falling, gustatory, and abdominal aura entry gives no body-side or hemisphere information. The case lists déjà vu, jamais vu, and abdominal aura terms without a side or lateralization direction. No hemisphere or lateralizing direction is reported. The temporo-polar frequency contains no lateralization information. The reported range contains no lateralization information. The sequential aura finding contains no lateralization information. The frequency and symptom-quality report gives no body-side or hemisphere information.

Source-defined result groups 41
Localization: FrontalObserved proportion 23.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 18.2%contralateral upper limb · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 50.0%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 7.5%All reported · other visceral response subtypes · evoked constrictive response1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 45.8%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization relative to the EUD-Loc prior · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 7.7%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyFrontal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 22.2%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 23.1%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: medio-lateral rapid temporo-lateral/temporo-mesial propagationSource-defined values retained separatelyAll reported · other Table 6 medio-lateral sign frequencies · Table 6 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 11.1%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 14.9%All reported · all other stimulation sites · evoked visceral response1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyTemporal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyOperculoinsular SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyipsilateral paresthesia · patient1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyWithin visceral responses · all other stimulation sites · evoked visceral response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelymesial temporal localization relative to prior distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyVisceral-response contacts versus other stimulation sites · All other stimulation sites · stimulation contact1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 9.1%contralateral hemibody · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 8.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal lobe localization given epigastric aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: OccipitalObserved proportion 14.3%All reported · no epigastric sensation after visual aura · patients1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · other visceral response subtypes · evoked constrictive response1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 25.0%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyWithin visceral responses · all other stimulation sites · evoked visceral response1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 11.1%LTL · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 9.5%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 17.1%Visceral responses · viscero-psychic symptom presentations · evoked visceral response1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyTemporal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyinsular localization given epigastric aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 50.0%Viscero-psychic responses · viscero-psychic symptom presentations · evoked viscero-psychic response1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyFrontal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelymesial temporal localization given epigastric aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 79.2%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyWithin visceral responses · all other stimulation sites · evoked visceral response1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 40.0%RTL · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.9%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 50.0%Viscero-psychic responses · viscero-psychic symptom presentations · evoked viscero-psychic response1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 27

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 13 findings · 6 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • epigastricTable 1 defines or exemplifies the the source's own semiology category “epigastric” as Abdominal rising sensation, for example a butterfly sensation.PDF p.7, Table 1 Semiology descriptions and frequencies
  • epigastricEpigastric semiology comprised 6.1% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • epigastric; Figure 3 all-data subsetFigure 3 reports N = 740 for the all-data epigastric panel.PDF p.9, Figure 3 and caption
  • epigastric; Figure 3 non-topological subsetFigure 3 reports N = 214 for the non-topological epigastric panel.PDF p.9, Figure 3 and caption
  • epigastric aura; temporal lobeAn epigastric aura was associated with an 83% probability that the seizure originated from the temporal lobe in the non-topological analysis.PDF p.8, Seizure semiology localizing values
  • epigastric aura; temporal lobeThe 95% CI for the temporal-lobe probability given an epigastric aura was 72%–94%.PDF p.8, Seizure semiology localizing values
  • epigastric aura; mesial temporal structuresAn epigastric aura was associated with a 61% probability of mesial temporal localization.PDF p.8, Seizure semiology localizing values
  • epigastric aura; mesial temporal structuresThe 95% CI for mesial temporal localization given an epigastric aura was 52%–71%.PDF p.8, Seizure semiology localizing values
  • epigastric aura; insulaepigastric aura indicated insular localization in 10%.PDF p.8, Seizure semiology localizing values
  • epigastric aura; temporal lobeEpigastric aura had an intrinsic localizing OR of 2.4 for temporal-lobe localization.PDF p.8, Relative localizing values of semiologies
  • epigastric aura; temporal lobeThe 95% CI for epigastric aura; temporal lobe was 1.9–2.9.PDF p.8, Relative localizing values of semiologies
  • epigastric aura; mesial temporal structuresThe abstract reports an OR of 2.8 for mesial temporal structures given an epigastric aura.PDF p.1, Abstract; PDF p.12, Relative localizing values using odds ratios
  • epigastric aura; mesial temporal structuresThe 95% CI for the mesial-temporal OR given an epigastric aura was 2.3–2.9.PDF p.1, Abstract; PDF p.12, Relative localizing values using odds ratios
Reported values
  • epigastric 6.1%epigastricPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • epigastric aura; temporal lobe 83%epigastric aura; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • epigastric aura; mesial temporal structures 61%epigastric aura; mesial temporal structuresPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • epigastric aura; insula 10%epigastric aura; insulaPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 2.4epigastric aura; temporal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 2.8epigastric aura; mesial temporal structuresOdds ratio · non-topological EUD-Loc comparisonPDF p.1, Abstract; PDF p.12, Relative localizing values using odds ratios
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 3 findings · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • posterior cingulate abdominal auraThe source reports 2 posterior cingulate patients with abdominal aura.PDF p.5, Clinical Presentation
  • patient 12 falling/gustatory/abdominal auraFalling, gustatory, and abdominal aura terms were listed for patient 12.PDF p.4, Figure 3
  • patient 13 déjà/jamais/abdominal auraDéjà vu, jamais vu, and abdominal aura terms were listed for patient 13.PDF p.4, Figure 3
Reported values
  • 2/4 abdominal auraposterior cingulate abdominal auraProportion · n/N 2/4 · 4 posterior cingulate cases · auraPDF p.5, Clinical Presentation
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • epigastric auraOne patient reported an epigastric aura.PDF p.2, Results
Reported values
  • 1/18 (5.5%) epigastric auraepigastric auraPercentage · n/N 1/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 3 findings · 11 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • digestive auraThe source states that the auras were mainly characterized by digestive symptoms, reported in 71% of the analyzed aura events.PDF p.5, Seizure clinical semiology; PDF p.7, Auras
  • digestive auraDigestive auras overall were more frequent in TL than T+ seizures (71.2% versus 43.5%, P=0.02); the source is internally inconsistent about which digestive subcategory carries P=0.05, so no subcategory-specific effect is resolved.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • abdominal auraThe source states that previous reports found abdominal aura more common in TL seizures than in other seizure types, especially in mesio-temporal lobe epilepsy with hippocampal sclerosis.PDF p.7, Auras
Reported values
  • digestive symptoms 71%digestive auraPercentage · 80 analyzed seizures, one typical seizure per patient · ictal onsetPDF p.5, Seizure clinical semiology; PDF p.7, Auras
  • overall digestive aura TL 71.2%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • Table 2 first component T+ 13%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • Table 2 third component T+ 4.3%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • Table 2 second component T+ 30.4%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • Table 2 second component TL 54.2%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • P=0.02digestive auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • Table 2 first component TL 16.9%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • Table 2 third component TL 6.8%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • P=0.05digestive auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
  • overall digestive aura T+ 43.5%digestive auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3 and Auras
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • epigastric sensationsThe narrative describes epigastric sensations as rare, at 5%.PDF p.4, Semiology and clinical features
  • Epigastric (Table 3)Table 3 reports epigastric symptoms in 3 cases (4%), more at seizure onset.PDF p.6, Table 3
  • Epigastric (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports epigastric symptoms in 4 cases (7%).PDF p.7, Table 4
Reported values
  • 5% epigastric sensationsepigastric sensationsPercentage · reviewed basal temporal seizure cases · ictal onsetPDF p.4, Semiology and clinical features
  • 3 cases (4%)Epigastric (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 4/60 (7%)Epigastric (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 8 findings · 5 reported values
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • psychic aura; abdominal aura; automotor seizure; figure-of-4 signIn an illustrative 36-year-old right-handed man with a left amygdala/hippocampal cavernoma, seizures began with déjà vu and epigastric rising, evolved to automotor features and rarely focal-to-bilateral tonic-clonic seizures, and showed right head/eye version plus a figure-of-4 posture before generalisation; left temporal EEG onset and the posture were consistent with left hemispheric onset.PDF p.5, Video case 3; PDF p.6, Video case 3 and Figure 4 caption
  • psychic and abdominal aura; figure-of-4 signIn video case 3, a 36-year-old right-handed man with a left amygdala/hippocampal-head cavernoma had déjà vu and epigastric rising followed by oral and manual automatisms and loss of awareness; before generalization, right head and eye version and a figure-of-4 posture with the left arm flexed and right arm extended lateralised onset to the left hemisphere, concordant with left temporal EEG onset.PDF p.6, Video case 3 and Figure 4
  • abdominal auraAn abdominal aura, including a rising epigastric sensation or abdominal discomfort, is reported as highly associated with temporal lobe epilepsy with a probability of 74%.PDF p.5, Auras
  • abdominal aura evolving to automotor seizureThe review states that evolution of an abdominal aura into an automotor seizure increases the probability of temporal lobe epilepsy to 98%.PDF p.5, Auras
  • abdominal aura; experiential phenomena; elemental auditory auraIn a cited study of 187 temporal lobe seizures assessed with intracranial stereo-EEG, abdominal aura and experiential phenomena such as fear, déjà vu, and jamais vu indicated mesiotemporal seizures, whereas elemental auditory aura indicated lateral onset involving Heschl’s gyrus/primary auditory cortex.PDF p.5, Auras
  • abdominal aura; automotor evolutionAn abdominal aura, such as a rising epigastric sensation or abdominal discomfort, is reported as highly associated with temporal lobe epilepsy with a probability of 74%, and evolution of the abdominal aura into an automotor seizure increases the probability to 98%.PDF p.5, Auras
  • abdominal aura; experiential phenomena; elemental auditory auraIn a cited study of 187 temporal lobe seizures assessed by intracranial stereo-EEG, abdominal aura and experiential phenomena including fear, déjà vu, and jamais vu indicated mesiotemporal seizures, whereas elemental auditory aura indicated lateral onset involving Heschl’s gyrus or primary auditory cortex.PDF p.5, Auras
  • hippocampal propagation to insula; complex visceral and somatosensory auraThe review states that seizures arising from hippocampus almost always propagate to the insula, so abdominal aura is also common in mesiotemporal seizures; nevertheless, the combination of complex visceral and somatosensory auras points toward insular onset.PDF p.8, Insular seizures; PDF p.9, Insular seizures
Reported values
  • probability of temporal lobe epilepsy 74%abdominal auraPercentage · focal epilepsy patients with abdominal aura in the cited study · aura/early ictalPDF p.5, Auras
  • probability of temporal lobe epilepsy 98%abdominal aura evolving to automotor seizurePercentage · focal epilepsy patients with abdominal aura in the cited study · aura to ictal evolutionPDF p.5, Auras
  • 98%abdominal aura; automotor evolutionPercentage · Patients with focal epilepsies in the cited study; exact cohort Not reported · abdominal aura evolving into automotor seizure · Aura and subsequent ictal automotor evolutionPDF p.5, Auras
  • 74%abdominal aura; automotor evolutionPercentage · Patients with focal epilepsies in the cited study; exact cohort Not reported · abdominal aura alone · Aura and subsequent ictal automotor evolutionPDF p.5, Auras
  • Qualitative association in 187 seizuresabdominal aura; experiential phenomena; elemental auditory auraCount · 187 temporal lobe seizures assessed by intracranial stereo-EEG · Aura and ictal onsetPDF p.5, Auras
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.37 · 1 × 0.9 × 1.521
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • epigastric aura; frontal subgroupOne frontal-subgroup aura was an epigastric sensation.PDF p.3, Aura
Reported values
  • 1 patientepigastric aura; frontal subgroupCount · n/N 1/11 · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 12 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • epigastric aura; olfactory/gustatory auraThe source states that absence of epigastric or olfactory/gustatory auras may be more indicative of lateral than mesial temporal seizures, whereas their presence points toward mesial rather than lateral onset.PDF p.7, Discussion; PDF p.10, Conclusions
  • Epigastric auraTable 3 reports 4 studies assessing Epigastric aura.PDF p.6, Table 3
  • Epigastric auraTable 3 reports 66 patients assessed for Epigastric aura.PDF p.6, Table 3
  • Epigastric auraTable 3 reports 0–13.6% as the percentage range or value for Epigastric aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Epigastric auraTable 4 reports overall odds of 0.11 for occurrence of Epigastric aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Epigastric auraTable 4 reports a 95% confidence interval of 0.04–0.26 for the overall odds of Epigastric aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Epigastric auraThe heterogeneity test for the Table 4 odds estimate for Epigastric aura has p=0.6299.PDF p.7, Table 4
  • Epigastric aura; lateral versus mesial comparisonTable 5 reports 3 studies comparing Epigastric aura in lateral and mesial TLE.PDF p.9, Table 5
  • Epigastric aura; lateral TLE patient denominatorTable 5 reports 44 lateral-TLE patients assessed for Epigastric aura.PDF p.9, Table 5
  • Epigastric aura; mesial TLE patient denominatorTable 5 reports 56 mesial-TLE patients assessed for Epigastric aura.PDF p.9, Table 5
  • Epigastric aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0–12.5% for Epigastric aura.PDF p.9, Table 5
  • Epigastric aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 31.3–40% for Epigastric aura.PDF p.9, Table 5
Reported values
  • 0–13.6%Epigastric auraPercentage Range · Lateral temporal epilepsy patients assessed for Epigastric aura · ictalPDF p.6, Table 3
  • odds 0.11odds of occurrence; Epigastric auraOdds · Lateral temporal epilepsy patients assessed for Epigastric aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0–12.5%Epigastric aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Epigastric aura · Lateral TLE patients assessed for Epigastric aura · ictalPDF p.9, Table 5
  • 31.3–40%Epigastric aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Epigastric aura · Mesial TLE patients assessed for Epigastric aura · ictalPDF p.9, Table 5
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.5
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Epigastric auraAn epigastric aura occurred in 4 RTL patients and 1 LTL patient.PDF p.4, numbered clinical-feature results
Reported values
  • LTL patients with epigastric aura 1/9Epigastric auraPercentage · n/N 1/9 · 10 RTL/RTLE patients and 9 LTL/LTLE patients · LTL · Preictal auraPDF p.4, numbered clinical-feature results
  • RTL patients with epigastric aura 4/10Epigastric auraPercentage · n/N 4/10 · 10 RTL/RTLE patients and 9 LTL/LTLE patients · RTL · Preictal auraPDF p.4, numbered clinical-feature results
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • abdominal aurasAbdominal auras are described as the most common autonomic aura and are localized to the anterior insula, frontal operculum, mesial temporal structures, and SSMA. In isolation they carry a reported 74% probability of TLE, rising to 98% when they evolve into an automotor component; when combined with vomiting they suggest an epileptogenic zone in the nondominant temporal lobe.PDF p.3, section 3.1 Auras; PDF p.2, Table 1
Reported values
  • TLE probability with isolated abdominal aura 74%abdominal aurasPercentage · patients with focal epilepsy; review-reported abdominal-aura series · Isolated abdominal aura · isolated aura versus evolution to automotor component; vomiting-associated auraPDF p.3, section 3.1 Auras; PDF p.2, Table 1
  • TLE probability when abdominal aura evolves to automotor component 98%abdominal aurasPercentage · patients with focal epilepsy; review-reported abdominal-aura series · Abdominal aura evolving to automotor component · isolated aura versus evolution to automotor component; vomiting-associated auraPDF p.3, section 3.1 Auras; PDF p.2, Table 1
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 5 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • epigastric and autonomic manifestationsTable 2 lists epigastric manifestations as n=8 frontal, n=3 temporal, and n=2 operculoinsular, with no posterior entry; it lists autonomic manifestations as n=6 frontal and n=2 temporal, with no operculoinsular or posterior entry. The narrative states that epigastric and autonomic features were present in all but the posterior subgroup.PDF p.6, Table 2; PDF p.7, section 3.3
Reported values
  • Autonomic manifestations, temporal n=2epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Temporal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Epigastric manifestations, temporal n=3epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Temporal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Epigastric manifestations, operculoinsular n=2epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Operculoinsular SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Epigastric manifestations, frontal n=8epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Frontal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Autonomic manifestations, frontal n=6epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Frontal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 8 findings · 6 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Viscero-sensoryTable 2 reports 5/21 (24%) for Viscero-sensory; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Viscero-sensoryTable 2 reports 3/12 patients with Viscero-sensory in the prefrontal operculum group.PDF p.7, Table 2
  • Viscero-sensoryTable 2 reports 2/9 patients with Viscero-sensory in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Viscero-sensoryFisher's exact comparison of Viscero-sensory between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
  • EpigastricTable 2 reports 2/21 (10%) for Epigastric; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • EpigastricTable 2 reports 1/12 patients with Epigastric in the prefrontal operculum group.PDF p.7, Table 2
  • EpigastricTable 2 reports 1/9 patients with Epigastric in the precentral Rolandic operculum group.PDF p.7, Table 2
  • EpigastricFisher's exact comparison of Epigastric between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 5/21 (24%)Viscero-sensoryPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 3/12 patientsViscero-sensoryProportion · n/N 3/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 2/9 patientsViscero-sensoryProportion · n/N 2/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
  • 2/21 (10%)EpigastricPercentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 1/12 patientsEpigastricProportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 1/9 patientsEpigastricProportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 3 findings · 3 reported values
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • abdominal-pain seizure localizationThe review states that interictal scalp EEG abnormalities in abdominal epilepsy most commonly involve temporal lobes, unilaterally or bilaterally, with case reports of ictal temporal abnormalities; parietal foci are less common, and insula or operculum should be considered as mimics or possible sources of the sensations.PDF p.2, Table 1; PDF p.5, Abdominal Pain as a Symptom of Seizures, Localization; PDF p.6, Localization (continued)
  • ictal abdominal painThe review reports ictal abdominal pain in 2 of 4,736 patients with epilepsy evaluated at a tertiary epilepsy center; it distinguishes true abdominal pain from common epigastric rising sensations and describes ictal episodes as usually shorter than 10 minutes, sometimes clustered, with sharp or colicky discomfort.PDF p.2, Table 1; PDF p.5, Abdominal Pain as a Symptom of Seizures, Description
  • insular electrical stimulation and abdominal sensationsThe review reports that the largest published study of insular electrical stimulation elicited visceral sensations of abdominal heaviness and constriction in several insular regions.PDF p.6, Abdominal Pain as a Symptom of Seizures, Localization
Reported values
  • episodes usually less than 10 minutes and may clusterictal abdominal painCount · n/N 2/4736 · 4,736 patients with epilepsy evaluated at a tertiary epilepsy center · IctalPDF p.2, Table 1; PDF p.5, Abdominal Pain as a Symptom of Seizures, Description
  • 2/4,736 patientsictal abdominal painCount · n/N 2/4736 · 4,736 patients with epilepsy evaluated at a tertiary epilepsy center · IctalPDF p.2, Table 1; PDF p.5, Abdominal Pain as a Symptom of Seizures, Description
  • sharp or colicky qualityictal abdominal painCount · n/N 2/4736 · 4,736 patients with epilepsy evaluated at a tertiary epilepsy center · IctalPDF p.2, Table 1; PDF p.5, Abdominal Pain as a Symptom of Seizures, Description
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • epigastric uncomfortable sensation and nauseaThe patient described occasional epigastric discomfort and nausea before loss of awareness.PDF p.2, Materials and Methods
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 9 findings · 3 reported values
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • visceral sensations after insular stimulationVisceral sensations are described as the next most common response after insular stimulation.PDF p.1, Abstract; PDF p.5, Visceral Symptoms
  • viscerosensory auraViscerosensory auras are among the reported clinical manifestations of insular seizures.PDF p.2, Clinical Features
  • visceral stimulation responsesVisceral symptoms accounted for 82 of 550 positive insular stimulation responses (15%).PDF p.5, Visceral Symptoms
  • constrictive visceral sensationsConstrictive sensations were observed at 41 electrical stimulation sites.PDF p.5, Visceral Symptoms
  • abdominal constrictive sensationAbdominal constrictive sensations were among the locations of constrictive responses.PDF p.5, Visceral Symptoms
  • constrictive sensation rangeConstrictive visceral responses ranged from simple discomfort to a frightening sensation of strangulation.PDF p.5, Visceral Symptoms
  • viscero-psychic responsesViscero-psychic symptoms were elicited at 14 insular stimulation sites.PDF p.5, Visceral Symptoms
  • abdominal heavinessAbdominal heaviness was one of the viscero-psychic symptoms elicited by insular stimulation.PDF p.5, Visceral Symptoms
  • fear associated with viscero-psychic symptomsThoracic or abdominal heaviness was associated with a feeling of fear in viscero-psychic responses.PDF p.5, Visceral Symptoms
Reported values
  • 82/550 (15%) visceral symptomsvisceral stimulation responsesPercentage · n/N 82/550 · 550 positive responses in the cited insular stimulation series · stimulation-evoked semiologyPDF p.5, Visceral Symptoms
  • 41 stimulation sites with constrictive sensationsconstrictive visceral sensationsCount · visceral responses in the cited insular stimulation series · stimulation-evoked visceral semiologyPDF p.5, Visceral Symptoms
  • 14 stimulation sites with viscero-psychic symptomsviscero-psychic responsesCount · visceral responses in the cited insular stimulation series · stimulation-evoked autonomic/affective semiologyPDF p.5, Visceral Symptoms
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Abdominal auraTable 2 associates abdominal aura with anterior insula, frontal operculum, mesial temporal lobe, and SSMA and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Abdominal auraThe authors state that patients with temporal lobe epilepsy frequently have abdominal sensations; some abdominal auras most probably reflect increased abdominal peristalsis and belong to the autonomic group, whereas others may reflect activation of sensory cortical areas of the abdominal viscera, and the category is retained independently because of its close relation to temporal lobe epilepsy.PDF p.3, Auras, subsection Abdominal auras; PDF p.2, Table 1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 3 findings · 6 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • viscerosensory symptomsInitial viscerosensory symptoms were more frequent in M than ML and especially L patients.PDF p.5, Semiologic analysis and Table 2
  • epigastric sensationInitial epigastric sensation was more frequent in M and ML than L patients, but the comparison did not reach the source’s p<0.05 threshold.PDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Viscerosensory sensations, epigastric sensation
  • prior diagnostic value of viscerosensory and epigastric sensationsThe discussion restates that prior authors reported diagnostic value for initial viscerosensory sensations, especially epigastric sensation, in differentiating medial temporal lobe epilepsy from lateral temporal lobe epilepsy.PDF p.7, Viscerosensory sensations, epigastric sensation
Reported values
  • M 19/24 (79.2%)viscerosensory symptomsPercentage · n/N 19/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Semiologic analysis and Table 2
  • ML 9/18 (50%)viscerosensory symptomsPercentage · n/N 9/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Semiologic analysis and Table 2
  • L 3/13 (23.1%)viscerosensory symptomsPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Semiologic analysis and Table 2
  • 1/13 (7.7%)epigastric sensationPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Viscerosensory sensations, epigastric sensation
  • 11/24 (45.8%)epigastric sensationPercentage · n/N 11/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Viscerosensory sensations, epigastric sensation
  • 7/18 (38.9%)epigastric sensationPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Viscerosensory sensations, epigastric sensation
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 4 findings · 10 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • viscero-sensitive sensationsVisceral sensations were the second major response group, occurring in 82 responses (14.9%) and comprising constrictive, viscero-vegetative, and viscero-psychic responses; their contacts were significantly more anterior than other stimulation sites, especially around or rostral to the central insular sulcus.PDF p.3, Results; PDF p.4, Visceral Sensations and Fig. 4; PDF p.7, Visceral Sensations
  • constrictive sensationsConstrictive sensations occurred in 41 responses (reported in the discussion as 7.4% of evoked responses), were located in pharyngo-laryngeal, retrosternal, or abdominal regions, and ranged from simple discomfort to frightening strangulation.PDF p.4, Visceral Sensations; PDF p.5, continuation of Visceral Sensations; PDF p.7, Visceral Sensations
  • viscero-psychic symptomsThe 14 viscero-psychic responses combined a visceral sensation with anxiety or fear; thoracic or abdominal constriction/heaviness accompanied anxiety in 7 of 14, and anxiety ranged from mild to panic and could be isolated in 7 of 14 cases.PDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
  • visceral responses and temporal-lobe seizure auraRestating observations attributed to Penfield and Faulk, the source reports a high frequency of visceral responses from the antero-inferior insular quadrant exposed after temporal-operculum removal, with patients describing those symptoms as identical to their ictal aura during surgery for temporal-lobe epilepsy.PDF p.7, Visceral Sensations
Reported values
  • 14 viscero-psychic responsesviscero-sensitive sensationsCount · 82 visceral responses in the 550-response series · Within visceral responses · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.4, Visceral Sensations and Fig. 4; PDF p.7, Visceral Sensations
  • 41 constrictive responsesviscero-sensitive sensationsCount · 82 visceral responses in the 550-response series · Within visceral responses · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.4, Visceral Sensations and Fig. 4; PDF p.7, Visceral Sensations
  • y-coordinate OR=1.045viscero-sensitive sensationsOdds ratio · 82 visceral responses in the 550-response series · Visceral-response contacts versus other stimulation sites · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.4, Visceral Sensations and Fig. 4; PDF p.7, Visceral Sensations
  • 27 viscero-vegetative responsesviscero-sensitive sensationsCount · 82 visceral responses in the 550-response series · Within visceral responses · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.4, Visceral Sensations and Fig. 4; PDF p.7, Visceral Sensations
  • Visceral responses 82/550 (14.9%)viscero-sensitive sensationsPercentage · n/N 82/550 · 82 visceral responses in the 550-response series · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.4, Visceral Sensations and Fig. 4; PDF p.7, Visceral Sensations
  • 41 constrictive responsesconstrictive sensationsCount · n/N 41/550 · 41 constrictive responses within the 82 visceral responses · stimulation-evoked visceral sensationPDF p.4, Visceral Sensations; PDF p.5, continuation of Visceral Sensations; PDF p.7, Visceral Sensations
  • source reports 7.4% of evoked responses in Discussionconstrictive sensationsPercentage · 41 constrictive responses within the 82 visceral responses · stimulation-evoked visceral sensationPDF p.4, Visceral Sensations; PDF p.5, continuation of Visceral Sensations; PDF p.7, Visceral Sensations
  • Isolated anxiety 7/14viscero-psychic symptomsCount · n/N 7/14 · 14 viscero-psychic responses within the 82 visceral responses · Viscero-psychic responses · stimulation-evoked visceral and affective sensationPDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
  • 14 viscero-psychic responses within 82 visceral responsesviscero-psychic symptomsCount · n/N 14/82 · 14 viscero-psychic responses within the 82 visceral responses · Visceral responses · stimulation-evoked visceral and affective sensationPDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
  • Thoracic/abdominal constriction or heaviness with anxiety 7/14viscero-psychic symptomsCount · n/N 7/14 · 14 viscero-psychic responses within the 82 visceral responses · Viscero-psychic responses · stimulation-evoked visceral and affective sensationPDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 2 findings
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • stimulation-evoked somatosensory, auditory, vestibular, olfactory, gustatory, and viscerosensory symptomsThe chapter reports that electrical stimulation studies evoked somatosensory symptoms, including pain, from the posterior two-thirds of the insula; auditory and vestibular symptoms from the posterior insula; and olfactory, gustatory, and viscerosensory symptoms, including laryngeal constriction, from the midinsula, whereas stimulation of the most anterior portion rarely evoked symptoms unless a larger network seizure was elicited.PDF p.3, insular functional differentiation and electrical cortical stimulation
  • viscerosensory auraViscerosensory aura is described as the second most common aura in insular seizures; abdominal, epigastric, or chest sensations may be indistinguishable from medial temporal lobe epilepsy, whereas pharyngo-laryngeal constriction, strangulation, or suffocation is presented as more specific, and the aura generally suggests ictal involvement of the middle insula.PDF p.5, Ictal Semiology; PDF p.14, What locations should be sampled based on semiology and EEG findings?
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • epigastric sensation after elementary hallucinationIn six patients, elementary visual hallucinations were followed by an epigastric sensation.PDF p.6, Results, Visual auras
Reported values
  • 6 patientsepigastric sensation after elementary hallucinationCount · n/N 6/42 · 42-patient cohort · seizure evolution from visual auraPDF p.6, Results, Visual auras
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfCase report or observation · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • epigastric aura preceded by foot numbnessOne patient had an epigastric aura preceded by numbness in one foot.PDF p.4, Results, Aurae
Reported values
  • 1 patientepigastric aura preceded by foot numbnessCount · 82-patient parietal epilepsy series · aura sequencePDF p.4, Results, Aurae
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 5 findings · 4 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • epigastric sensation; dreamy states; oro-alimentary automatisms; long seizure durationThe source states that focal-aware epigastric sensation, dreamy states, oro-alimentary automatisms, and long seizure duration are shared with medial temporal seizures.PDF p.5, Discussion
  • epigastric auraTable 3 reports epigastric aura in 22% of the temporo-polar synthesis (evidence grade Low).PDF p.5, Table 3
  • epigastric auraTable 3 reports a 0–43% range for epigastric aura across the temporo-polar reports (evidence grade Low).PDF p.5, Table 3
  • viscerosensory auraTable 6 reports viscerosensory aura in 73% of the medio-lateral synthesis (evidence grade Low).PDF p.6, Table 6
  • viscerosensory auraTable 6 reports a 50–85% range for viscerosensory aura across the medio-lateral reports (evidence grade Low).PDF p.6, Table 6
Reported values
  • 22%epigastric auraPercentage · Temporo-polar semiology synthesis represented in Table 3 · clinical onsetPDF p.5, Table 3
  • range 0–43%epigastric auraPercentage Range · Temporo-polar semiology synthesis represented in Table 3 · clinical onsetPDF p.5, Table 3
  • 73%viscerosensory auraPercentage · Medio-lateral temporal seizure semiology synthesis represented in Table 6 · earlyPDF p.6, Table 6
  • range 50–85%viscerosensory auraPercentage Range · Medio-lateral temporal seizure semiology synthesis represented in Table 6 · earlyPDF p.6, Table 6
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • epigastric, retrosternal, and oropharyngeal digestive sensationsThe source associates epigastric sensations with temporal pole BA 38, hippocampus, amygdala, and anterior cingulate cortex; retrosternal sensations preferentially with anterior cingulate cortex; and oropharyngeal sensations mainly with suprasylvian opercular cortex and insula. It emphasizes substantial variability and a widely distributed region for induced digestive and associated symptoms.PDF p.14, Digestive sensations
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • abdominal aurasThe review states that abdominal auras are frequent and usually secondary to temporal lobe epilepsy, but can occasionally be triggered by extratemporal epilepsy, mainly frontal or insular. The sensation usually begins in the epigastrium or midline stomach and may rise to the chest, throat, head, or face; when it rises to the neck or face, loss of consciousness is described as almost invariable. The review also reports that Van Buren's balloon studies found no gastromotor effect except rare gastric inhibition, and that stimulation has elicited similar sensations from the insula and other structures, with spread-related afterdischarges not excluded.PDF p.2, Abdominal auras
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 9 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • somatosensory and viscerosensory manifestationsThe reported manifestations included unpleasant nonpainful paresthesia in the contralateral upper limb, indescribable sensations in the contralateral hemibody or whole body, head/face/perioral paresthesia, auditory phenomena, epigastric sensation, and pharyngolaryngeal numbness or constriction; painful aura and ipsilateral paresthesia were not observed.PDF p.3, Results—Seizure semiology
Reported values
  • 6/22 (27%)somatosensory and viscerosensory manifestationsPercentage · n/N 6/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · head, face, or perioral · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · whole body · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • not observedsomatosensory and viscerosensory manifestationsCount · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · ipsilateral paresthesia · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 2/22 (9%)somatosensory and viscerosensory manifestationsPercentage · n/N 2/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · contralateral hemibody · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · epigastric · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 4/22 (18%)somatosensory and viscerosensory manifestationsPercentage · n/N 4/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · contralateral upper limb · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · pharyngolaryngeal · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • not observedsomatosensory and viscerosensory manifestationsCount · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · painful aura · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • 1/22 (5%)somatosensory and viscerosensory manifestationsPercentage · n/N 1/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · auditory · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology

27 contributing manuscripts; source-reported values remain separate and are not pooled.

Oral automatisms (lip smacking, chewing, swallowing, licking)Source terms: Oral automatismsReported: BilateralAlso reported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere22 manuscripts · 110 findings · 92 reported values
Weighted evidence supportevidence weight 55.35 across 22 manuscripts · 2 manuscript weight pending · 6 independent primary study · 2 case report or observation · 6 narrative, educational, or cited context · 6 systematic review or meta-analysis · 2 structured design not resolved

This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. The case observation records right-sided version during habitual partial seizures. Patient 8 had sudden stiffening of the left arm with oral automatisms. The cited review restates early facial activity and contralateral motor activity as suggestive of neocortical temporal epilepsy. Oroalimentary automatisms did not differ significantly between right and left temporal-lobe seizures. The cited Chassoux series restatement includes bilateral tonic-clonic seizures alongside oro-alimentary, salivation, dystonic, and head-deviation phenomena. This record provides no seizure lateralization. No lateralizing direction is reported for the visual-aura-to-automatism phenotype. No hemisphere or body-side direction is reported. No lateralizing direction is reported. No hemisphere direction is asserted. No seizure lateralization is reported. No lateralization axis information is reported for oro-alimentary automatisms in the restricted-OFC cases. No lateralization axis information is reported for non-HkB oro-alimentary automatisms. No lateralization axis information is reported for the entire OFC-involving group. No lateralization axis information is reported for the restricted-OFC EZN group. No lateralization axis information is reported for the oral-automatisms comparison. The row reports the number of studies with onset-timing data, not lateralization evidence. No lateralization axis information is reported for the oral-automatism onset latency. No lateralization axis information is reported for the oral-automatism odds result. No hemisphere direction is reported. The row reports a heterogeneity p value, not lateralization evidence. The row reports the number of comparison studies, not lateralization evidence. The row reports a lateral-TLE sample size, not lateralization evidence. The row reports a mesial-TLE sample size, not lateralization evidence. No lateralization axis information is reported for the lateral-TLE oral-automatism prevalence range. No lateralization axis information is reported for the mesial-TLE oral-automatism prevalence range. No lateralization axis information is reported for oral-automatism sensitivity. No lateralization axis information is reported for oral-automatism specificity. No source-supported hemispheric lateralization is reported. The semiology category definition contains no lateralization evidence. The row reports an all-data panel sample size, not lateralization evidence. The row reports a non-topological panel sample size, not lateralization evidence. No lateralization axis information is reported for oral and manual automatisms in the cingulate context. No lateralization axis information is reported. No hemisphere or lateralizing direction is reported. No lateralization axis information is reported for motor gestural/oro-alimentary automatisms. The row reports an overall association grade, not lateralization evidence. No lateralization axis information is reported for the Figure 4 oro-alimentary-automatism rate. No lateralization axis information is reported for motor gestural/oral automatisms. No lateralization axis information is reported for the restated oro-alimentary-automatism rate. No lateralization axis information is reported for oro-alimentary automatisms versus affective/autonomic aura. Figure 6 reports OR 13.3 for Affective/autonomic aura relative to Oro-alimentary automatisms, with no hemisphere or lateralization direction. No lateralization axis information is reported for smacking and swallowing. No body-side, seizure-onset side, or seizure-lateralization direction is reported.

Source-defined result groups 18
Localization: TemporalSource-defined values retained separately3 diagnostic-accuracy studies comparing lateral and mesial TLE for Oral automatism · lateral TLE versus mesial TLE · random-effects diagnostic-accuracy estimate1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 62.5%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 61.1%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 58.3%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Oral automatisms · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 22.2%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 55.6%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 27.8%RTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 15.4%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 15.4%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Oral automatisms · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separately3 diagnostic-accuracy studies comparing lateral and mesial TLE for Oral automatism · lateral TLE versus mesial TLE · random-effects diagnostic-accuracy estimate1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 7.7%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 19.2%LTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 25.0%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyanterior temporal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 22

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 12 findings · 5 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • oral and manual automatismsTable 1 defines or exemplifies the the source's own semiology category “oral and manual automatisms” as Upper-limb automatisms, automotor stereotyped distal limb movements, fiddling, pedal automatisms, lip smacking, chewing, oro-alimentary/orofacial automatisms, ictal drinking, or ictal swallowing.PDF p.7, Table 1 Semiology descriptions and frequencies
  • oral and manual automatismsOral and manual automatisms comprised 9.7% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • oral and manual automatisms; Figure 3 all-data subsetFigure 3 reports N = 2298 for the all-data oral and manual automatisms panel.PDF p.9, Figure 3 and caption
  • oral and manual automatisms; Figure 3 non-topological subsetFigure 3 reports N = 342 for the non-topological oral and manual automatisms panel.PDF p.9, Figure 3 and caption
  • oral and manual automatisms; temporal lobeOral and manual automatisms were temporal in origin in 47%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; temporal lobeThe 95% CI for oral and manual automatisms; temporal lobe was 40%–53%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; frontal lobeOral and manual automatisms were frontal in origin in 31%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; frontal lobeThe 95% CI for oral and manual automatisms; frontal lobe was 25%–36%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; cingulateoral and manual automatisms semiology was cingulate in 10%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; cingulateThe 95% CI for oral and manual automatisms; cingulate was 7%–13%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; anterior temporalOral and manual automatisms had an intrinsic OR of 2.4 for the anterior temporal subregion.PDF p.8, Relative localizing values of semiologies
  • oral and manual automatisms; anterior temporalThe 95% CI for oral and manual automatisms; anterior temporal was 1.7–3.3.PDF p.8, Relative localizing values of semiologies
Reported values
  • oral and manual automatisms 9.7%oral and manual automatismsPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • oral and manual automatisms; temporal lobe 47%oral and manual automatisms; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; frontal lobe 31%oral and manual automatisms; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; cingulate 10%oral and manual automatisms; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 2.4oral and manual automatisms; anterior temporalOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 8 left-arm stiffening and oral automatismsSudden stiffening of the left arm and oral automatisms were listed for patient 8.PDF p.4, Figure 3
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 3 findings · 7 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.86 · 2 × 1.5 × 1.952
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • oroalimentary automatismsComplex behaviours were common and mainly consisted of oroalimentary automatisms, reported in 75% of analyzed seizures.PDF p.5, Seizure clinical semiology
  • oroalimentary automatismsOroalimentary automatisms did not differ significantly between TL and T+ groups across chewing and swallowing.PDF p.6, Table 2; PDF p.7, Table 3
  • chewing automatisms and amygdalaThe source states that the amygdala appears to play a pivotal role in ictal chewing and suggests that it might also contribute to rapid bilateralization of TL discharges when chewing automatisms accompany post-ictal amnesia.PDF p.9, Post-ictal signs
Reported values
  • oroalimentary automatisms 75%oroalimentary automatismsPercentage · 80 analyzed seizures, one typical seizure per patient · ictalPDF p.5, Seizure clinical semiology
  • TL 76.3%oroalimentary automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2; PDF p.7, Table 3
  • TL 27.1%oroalimentary automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2; PDF p.7, Table 3
  • TL 59.3%oroalimentary automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2; PDF p.7, Table 3
  • T+ 56.5%oroalimentary automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2; PDF p.7, Table 3
  • T+ 13%oroalimentary automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2; PDF p.7, Table 3
  • T+ 65.2%oroalimentary automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2; PDF p.7, Table 3
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 4 findings · 4 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • oro-alimentary automatismsOro-alimentary automatisms were reported in 7% of reviewed cases and were described as the least frequent objective ictal sign in the narrative summary.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Oro-alimentary automatisms (Table 3)Table 3 reports oro-alimentary automatisms in 6 cases (7%), more during propagation.PDF p.6, Table 3
  • Oro-alimentary automatisms (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports oro-alimentary automatisms in 23 cases (38%).PDF p.7, Table 4
  • oro-alimentary automatisms plus aphasiaThe co-occurrence analysis identified oro-alimentary automatisms with aphasia in 22% of the 18-patient detailed-data set.PDF p.7, Figure 2 discussion
Reported values
  • 7% oro-alimentary automatismsoro-alimentary automatismsPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 6 cases (7%)Oro-alimentary automatisms (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 23/60 (38%)Oro-alimentary automatisms (Table 4)Percentage · n/N 23/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
  • 22% co-occurrenceoro-alimentary automatisms plus aphasiaPercentage · 18 patients with detailed semiology data · ictal; timing not otherwise reportedPDF p.7, Figure 2 discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Hand and mouth automatisms in mesial temporal onsetAutomatisms occur in almost two thirds of CPSs of mesial temporal lobe onset and often involve the hands, including fumbling, picking, or fidgeting, or the mouth, including chewing, lip smacking, or swallowing.PDF p.3, section 2.5 Automatisms
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 32 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • motor gestural/oro-alimentary automatismsThe source reports a frequency of 43% for motor gestural/oro-alimentary automatisms.PDF p.13, Table 3
  • motor gestural/oro-alimentary automatisms; reported frequency rangeThe source reports a frequency range of 0–91% for motor gestural/oro-alimentary automatisms.PDF p.13, Table 3
  • motor gestural/oro-alimentary automatisms; ACC association gradeTable 3 assigns the source's High overall association grade to motor gestural/oro-alimentary automatisms.PDF p.13, Table 3
  • oro-alimentary automatisms; Figure 4 rateFigure 4 displays a 8.6% rate for oro-alimentary automatisms.PDF p.10, Figure 4
  • motor gestural/oral automatismsMotor gestural/oral automatisms were reported in 43% of patients.PDF p.9, Objective symptomatology
  • oro-alimentary automatismsOro-alimentary automatisms were reported in 9% of patients.PDF p.9, Objective symptomatology
  • pairwise OR: Oro-alimentary automatisms relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Affective/autonomic auraFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Autonomic signsFigure 6 reports an odds ratio of 0.1 for Oro-alimentary automatisms relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Facial expression changeFigure 6 reports an odds ratio of 0.1 for Oro-alimentary automatisms relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.1 for Oro-alimentary automatisms relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.2 for Oro-alimentary automatisms relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.2 for Oro-alimentary automatisms relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.4 for Oro-alimentary automatisms relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Dystonic posturingFigure 6 reports an odds ratio of 0.4 for Oro-alimentary automatisms relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Head-eye deviationFigure 6 reports an odds ratio of 0.6 for Oro-alimentary automatisms relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to LaughterFigure 6 reports an odds ratio of 0.9 for Oro-alimentary automatisms relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 16.5 for Vocalization/verbalization relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 15.6 for Hypermotor-complex motor behavior relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 13.3 for Affective/autonomic aura relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 9.8 for Autonomic signs relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 9 for Facial expression change relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 7.9 for Motor (gestural) automatisms relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 5.8 for Loss of consciousness relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 4.6 for Post-ictal confusion/behavior change disinhibition relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 2.7 for Chapeau de gendarme relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 2.5 for Dystonic posturing relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.7 for Head-eye deviation relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.1 for Laughter relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.1 for Tonic-clonic relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 0.6 for F to BTC relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Tonic-clonicFigure 6 reports an odds ratio of 1.9 for Oro-alimentary automatisms relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to F to BTCFigure 6 reports an odds ratio of 1.9 for Oro-alimentary automatisms relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 43% (frequency range 0–91%)motor gestural/oro-alimentary automatismsPercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.13, Table 3
  • 8.6%oro-alimentary automatisms; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.10, Figure 4
  • 43%motor gestural/oral automatismsPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • 9%oro-alimentary automatismsPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Oro-alimentary automatisms relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Oro-alimentary automatisms relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Oro-alimentary automatisms relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Oro-alimentary automatisms relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Oro-alimentary automatisms relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Oro-alimentary automatisms relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Oro-alimentary automatisms relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Oro-alimentary automatisms relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Oro-alimentary automatisms relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 16.5pairwise OR: Vocalization/verbalization relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 15.6pairwise OR: Hypermotor-complex motor behavior relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.3pairwise OR: Affective/autonomic aura relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.8pairwise OR: Autonomic signs relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9pairwise OR: Facial expression change relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.9pairwise OR: Motor (gestural) automatisms relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.8pairwise OR: Loss of consciousness relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Chapeau de gendarme relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.5pairwise OR: Dystonic posturing relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Head-eye deviation relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Laughter relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Tonic-clonic relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: F to BTC relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Oro-alimentary automatisms relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Oro-alimentary automatisms relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • behavioural arrest; manual and oral automatismsTemporal lobe seizures are described as typically comprising behavioural arrest and manual and oral automatisms in two thirds of cases, with variable loss of awareness and postictal confusion.PDF p.4, Temporal lobe seizures
Reported values
  • behavioural arrest and manual/oral automatisms in two thirdsbehavioural arrest; manual and oral automatismsProportion · temporal lobe seizure literature · ictal and postictalPDF p.4, Temporal lobe seizures
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 11 findings · 9 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • OFC + group (EZN extending beyond OFC); aura; oro-alimentary automatisms; gestural automatismsThe source characterizes EZN extending beyond the OFC as having richer semiological profiles, with temporal extension more often associated with aura, oro-alimentary automatisms, and sleep.PDF p.6, Semiological profile; PDF p.7, Conclusion
  • oro-alimentary automatismsOro-alimentary automatisms may indicate an EZN extending beyond the OFC into the temporal lobe, but the source also reports them with an EZN restricted to the OFC.PDF p.3, Complex motor phenomena—automatisms
  • oro-alimentary automatismsOro-alimentary automatisms were reported in six of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • oro-alimentary automatisms; HkB subgroupOne of the 14 HkB cases had oro-alimentary automatisms.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • oro-alimentary automatisms; non-HkB subgroupSix of the non-HkB cases had oro-alimentary automatisms.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • oro-alimentary automatisms; entire groupThe source reports 18% for oro-alimentary automatisms in the entire ofc-involving group.PDF p.3, Complex motor phenomena—automatisms
  • oro-alimentary automatisms; OFC-restricted EZNThe source reports 27% for oro-alimentary automatisms in the ofc-restricted ezn group.PDF p.3, Complex motor phenomena—automatisms
  • oro-alimentary automatisms; OFC-extended EZNThe source reports 12% for oro-alimentary automatisms in the ofc-extended ezn group.PDF p.3, Complex motor phenomena—automatisms
  • oro-alimentary automatisms; temporal subgroupThe source reports 33% for oro-alimentary automatisms in the temporal subgroup of ofc-extended ezn.PDF p.3, Complex motor phenomena—automatisms
  • oro-alimentary automatisms; insular subgroupThe source reports 0% for oro-alimentary automatisms in the insular subgroup of ofc-extended ezn.PDF p.3, Complex motor phenomena—automatisms
  • oro-alimentary automatisms; frontal subgroupThe source reports 0% for oro-alimentary automatisms in the frontal subgroup of ofc-extended ezn.PDF p.3, Complex motor phenomena—automatisms
Reported values
  • 6/26 (23%)oro-alimentary automatismsPercentage · n/N 6/26 · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 1/14 patientsoro-alimentary automatisms; HkB subgroupCount · n/N 1/14 · HkB subgroup within OFC-restricted EZN · HkB subgroup within OFC-restricted EZN · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 6/12 (50%)oro-alimentary automatisms; non-HkB subgroupPercentage · n/N 6/12 · Non-HkB subgroup within OFC-restricted EZN · Non-HkB subgroup within OFC-restricted EZN · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 18%oro-alimentary automatisms; entire groupPercentage · Entire OFC-involving group · Entire OFC-involving group · ictalPDF p.3, Complex motor phenomena—automatisms
  • 27%oro-alimentary automatisms; OFC-restricted EZNPercentage · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.3, Complex motor phenomena—automatisms
  • 12%oro-alimentary automatisms; OFC-extended EZNPercentage · OFC-extended EZN group · OFC-extended EZN group · ictalPDF p.3, Complex motor phenomena—automatisms
  • 33%oro-alimentary automatisms; temporal subgroupPercentage · Temporal subgroup of OFC-extended EZN · Temporal subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—automatisms
  • 0%oro-alimentary automatisms; insular subgroupPercentage · Insular subgroup of OFC-extended EZN · Insular subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—automatisms
  • 0%oro-alimentary automatisms; frontal subgroupPercentage · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—automatisms
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 20 findings · 7 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • oral automatisms; manual automatisms; behavioral arrestThe source identifies oral automatisms, manual automatisms, and behavioral arrests as the most common semiologies in lateral temporal epilepsy, while noting that they likely emerge during propagation rather than at seizure onset.PDF p.1, Abstract; PDF p.4, Anatomo-clinical correlations; PDF p.8, Discussion
  • Oral automatismsTable 3 reports 3 studies assessing Oral automatisms.PDF p.6, Table 3
  • Oral automatismsTable 3 reports 51 patients assessed for Oral automatisms.PDF p.6, Table 3
  • Oral automatismsTable 3 reports 29.4–73.3% as the percentage range or value for Oral automatisms; the overall association grade is Low.PDF p.6, Table 3
  • Oral automatismsTable 3 reports 1 study with onset timing for Oral automatisms.PDF p.6, Table 3
  • Oral automatismsTable 3 reports an onset latency of 11 s for Oral automatisms.PDF p.6, Table 3
  • odds of occurrence; Oral automatismsTable 4 reports overall odds of 0.98 for occurrence of Oral automatisms in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Oral automatismsTable 4 reports a 95% confidence interval of 0.36–2.68 for the overall odds of Oral automatisms.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Oral automatismsThe heterogeneity test for the Table 4 odds estimate for Oral automatisms has p=0.0571.PDF p.7, Table 4
  • Oral automatisms; lateral versus mesial comparisonTable 5 reports 3 studies comparing Oral automatisms in lateral and mesial TLE.PDF p.9, Table 5
  • Oral automatisms; lateral TLE patient denominatorTable 5 reports 51 lateral-TLE patients assessed for Oral automatisms.PDF p.9, Table 5
  • Oral automatisms; mesial TLE patient denominatorTable 5 reports 67 mesial-TLE patients assessed for Oral automatisms.PDF p.9, Table 5
  • Oral automatisms; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 29.4–73.3% for Oral automatisms.PDF p.9, Table 5
  • Oral automatisms; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 31.3–80.6% for Oral automatisms.PDF p.9, Table 5
  • Oral automatism; diagnostic sensitivityTable 6 reports overall sensitivity 0.50 for Oral automatism in 3 studies comparing lateral with mesial TLE.PDF p.9, Table 6
  • Oral automatism; diagnostic sensitivity confidence intervalTable 6 reports a 95% confidence interval of 0.27–0.73 for sensitivity of Oral automatism.PDF p.9, Table 6
  • Oral automatism; sensitivity heterogeneityThe heterogeneity test for sensitivity of Oral automatism has p=0.0571.PDF p.9, Table 6
  • Oral automatism; diagnostic specificityTable 6 reports overall specificity 0.21 for Oral automatism in 3 studies comparing lateral with mesial TLE.PDF p.9, Table 6
  • Oral automatism; diagnostic specificity confidence intervalTable 6 reports a 95% confidence interval of 0.13–0.32 for specificity of Oral automatism.PDF p.9, Table 6
  • Oral automatism; specificity heterogeneityThe heterogeneity test for specificity of Oral automatism has p=0.8975.PDF p.9, Table 6
Reported values
  • 29.4–73.3%Oral automatismsPercentage Range · Lateral temporal epilepsy patients assessed for Oral automatisms · ictalPDF p.6, Table 3
  • median onset latency 11 sOral automatismsMedian · Lateral temporal epilepsy study reporting onset timing for Oral automatisms · ictal onsetPDF p.6, Table 3
  • odds 0.98odds of occurrence; Oral automatismsOdds · Lateral temporal epilepsy patients assessed for Oral automatisms · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 29.4–73.3%Oral automatisms; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Oral automatisms · Lateral TLE patients assessed for Oral automatisms · ictalPDF p.9, Table 5
  • 31.3–80.6%Oral automatisms; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Oral automatisms · Mesial TLE patients assessed for Oral automatisms · ictalPDF p.9, Table 5
  • sensitivity 0.50Oral automatism; diagnostic sensitivitySensitivity · 3 diagnostic-accuracy studies comparing lateral and mesial TLE for Oral automatism · 3 diagnostic-accuracy studies comparing lateral and mesial TLE for Oral automatism · ictal sign presencePDF p.9, Table 6
  • specificity 0.21Oral automatism; diagnostic specificitySpecificity · 3 diagnostic-accuracy studies comparing lateral and mesial TLE for Oral automatism · 3 diagnostic-accuracy studies comparing lateral and mesial TLE for Oral automatism · ictal sign presencePDF p.9, Table 6
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Oroalimentary automatismsOroalimentary automatisms did not differ significantly between RTL and LTL seizures.PDF p.4, Table 5; PDF p.4, numbered clinical-feature results
Reported values
  • 14/73 (25%)Oroalimentary automatismsPercentage · n/N 14/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.4, Table 5; PDF p.4, numbered clinical-feature results
  • 15/54 (29%)Oroalimentary automatismsPercentage · n/N 15/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.4, Table 5; PDF p.4, numbered clinical-feature results
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEDystonic limb posturing within 20 seconds of seizure onset was reported more often in MTLE than NTLE, 52% versus 26%, and oral automatisms were reported 69% versus 11%, respectively. Early facial grimacing or twitching and contralateral motor activity were suggestive of NTLE.PDF p.6, section 8.1 Neocortical temporal lobe epilepsy
Reported values
  • Oral automatisms in MTLE 69%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · MTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Early dystonic posturing in NTLE 26%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · NTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Early dystonic posturing in MTLE 52%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · MTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Oral automatisms in NTLE 11%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · NTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • oroalimentary automatismsTemporal-like insular seizures may include oroalimentary automatisms.PDF p.2, Clinical Features
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 4 findings · 12 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • oroalimentary automatismsOroalimentary automatisms over the whole seizure course were more frequent in M and ML than L patients.PDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Oroalimentary automatisms
  • early oroalimentary automatismsEarly oroalimentary automatisms, occurring during the first half of the seizure, were more frequent in ML than M or L patients.PDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Oroalimentary automatisms
  • late oroalimentary automatismsLate oroalimentary automatisms, occurring during the second half of the seizure, were more frequent in M than ML or L patients.PDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Oroalimentary automatisms
  • oroalimentary automatisms and medial-neocortical network involvementThe authors infer that the emergence of oroalimentary automatisms requires widespread dysfunction involving medial and temporal neocortical structures, with early occurrence characteristic of ML and late occurrence more characteristic of M after propagation.PDF p.8, Oroalimentary automatisms
Reported values
  • M=15/24 (62.5%)oroalimentary automatismsPercentage · n/N 15/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Oroalimentary automatisms
  • ML=11/18 (61.1%)oroalimentary automatismsPercentage · n/N 11/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Oroalimentary automatisms
  • p=0.014oroalimentary automatismsP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Oroalimentary automatisms
  • L=2/13 (15.4%)oroalimentary automatismsPercentage · n/N 2/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Oroalimentary automatisms
  • L=1/13 (7.7%)early oroalimentary automatismsPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Oroalimentary automatisms
  • M=6/24 (25%)early oroalimentary automatismsPercentage · n/N 6/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Oroalimentary automatisms
  • p=0.015early oroalimentary automatismsP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Oroalimentary automatisms
  • ML=10/18 (55.6%)early oroalimentary automatismsPercentage · n/N 10/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Oroalimentary automatisms
  • p=0.012late oroalimentary automatismsP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Oroalimentary automatisms
  • ML=4/18 (22.2%)late oroalimentary automatismsPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Oroalimentary automatisms
  • L=2/13 (15.4%)late oroalimentary automatismsPercentage · n/N 2/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Oroalimentary automatisms
  • M=14/24 (58.3%)late oroalimentary automatismsPercentage · n/N 14/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Oroalimentary automatisms
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 4 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • oro-alimentary automatisms (OAA)The review reports that Aupy et al. (2018) found increased coherence between mediobasal temporal structures and insulo-opercular cortex before the onset of rhythmic chewing movements in temporal-lobe seizures.PDF p.5, Table 1, Oro-alimentary automatisms row
  • oro-alimentary automatisms (OAA)In the summarized Aupy et al. study, increased coherence between mediobasal temporal structures and insulo-opercular cortex occurred before rhythmic chewing movements; the table states that 2 of 15 patients had seizures compared with and without OAA.PDF p.5, Table 1 (continued), Aupy et al. 2018 row; PDF p.11, mechanism 1
Reported values
  • 2 of 15oro-alimentary automatisms (OAA)Percentage · n/N 2/15 · 15 subjects with temporal-lobe epilepsy; 2 of 15 had seizures compared with and without oro-alimentary automatisms · within-patient comparison subset · Before onset of rhythmic chewing movementsPDF p.5, Table 1, Oro-alimentary automatisms row
  • 15 subjectsoro-alimentary automatisms (OAA)Count · 15 subjects with temporal-lobe epilepsy; 2 of 15 had seizures compared with and without oro-alimentary automatisms · temporal-lobe epilepsy study · Before onset of rhythmic chewing movementsPDF p.5, Table 1, Oro-alimentary automatisms row
  • 15 subjectsoro-alimentary automatisms (OAA)Count · 15 subjects with temporal-lobe epilepsy; 2/15 patients had seizures compared with and without OAA · Aupy et al. temporal-lobe epilepsy study · pre-onset of rhythmic chewing movements and ictal OAAPDF p.5, Table 1 (continued), Aupy et al. 2018 row; PDF p.11, mechanism 1
  • 2 of 15oro-alimentary automatisms (OAA)Percentage · n/N 2/15 · 15 subjects with temporal-lobe epilepsy; 2/15 patients had seizures compared with and without OAA · within-patient comparison subset · pre-onset of rhythmic chewing movements and ictal OAAPDF p.5, Table 1 (continued), Aupy et al. 2018 row; PDF p.11, mechanism 1
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • recurrent ictal speech utterances; oro-alimentary automatisms; right-sided versionIn the patient’s habitual partial seizures, an aura of nausea was followed by staring gaze, partial loss of consciousness, oro-alimentary automatisms, right-sided version, and postictal confusion; family reported recurrent stereotyped French or English sentence repetitions from age 18.PDF p.2, left column, paragraph beginning “Partial seizures began”; PDF p.2, right column, paragraph beginning “Five stereotyped and spontaneous electroclinical seizures”
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 2 findings · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • smacking and swallowing in Fig. 2The Figure 2 tracing labels smacking and swallowing during later seizure evolution.PDF p.14, Fig. 2
  • oral alimentary automatismsOral alimentary automatisms occurred in 21 of 42 patients.PDF p.6, Results, Non-visual manifestations
Reported values
  • 21/42 (50%) patientsoral alimentary automatismsPercentage · n/N 21/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal propagation or later ictal manifestationPDF p.6, Results, Non-visual manifestations
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • oral and gestural automatismsOral and gestural automatisms occurred in 17% of patients.PDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
Reported values
  • 17%oral and gestural automatismsPercentage · 82-patient parietal epilepsy series · ictal propagation or later ictal phasePDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • Chassoux cohort; oro-alimentary automatisms; salivation; dystonic signs; head deviation; bilateral tonic-clonic seizuresThe review restates that Chassoux et al. described 33 patients with oro-alimentary automatisms, salivation, motor signs including dystonia and head deviation, and bilateral tonic-clonic seizures in the medio-lateral context.PDF p.4, Medio-lateral temporal origin
  • epigastric sensation; dreamy states; oro-alimentary automatisms; long seizure durationThe source states that focal-aware epigastric sensation, dreamy states, oro-alimentary automatisms, and long seizure duration are shared with medial temporal seizures.PDF p.5, Discussion
simone-anatomo-functional-organization-insular-networks-2025.pdfStructured design not resolved · 1 finding
simone-anatomo-functional-organization-insular-networks-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The paper summarizes prior macaque ICMS mapping performed with 200-microsecond biphasic pulses at 50 Hz, 4 mA, for 3 seconds; a behavior entered the dataset when two observers recognized it and it was evoked in more than 50% of trials. The present analyses used ICMS maps and insular tracer injections in two male rhesus macaques (Mk1 and Mk2), indirect tracer data from 22 additional animals, and resting-state fMRI from 12 male macaques aged 4-8 years. The authors warped the ICMS maps and injection sites onto the INIA19 macaque template and delineated six insular fields. No seizure cohort, ictal or postictal observations, or clinical localization reference standard was studied.
Findings
  • emotional field; lip-smacking; discomfort reactionsThe macaque ventral middle insula was defined as an ICMS emotion-related field in which stimulation elicited lip-smacking, described as an affiliative gesture during emotionally salient social situations; intermingled stimulation sites also produced difficult-to-interpret discomfort reactions ranging from postural adjustments to psychomotor agitation. The discussion reports lip-smacking during direct eye contact with a specific experimenter and notes that the behavior can also occur during anxiety or fear.PDF p.5, Fig. 1C, E and caption; PDF p.10, Fig. 5B, C and caption; PDF p.12, §4.4.1; PDF p.19, §5.3
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 2 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • oro-alimentary automatismsOnly one patient in the series presented oro-alimentary automatisms.PDF p.4, Results—Seizure semiology; PDF p.5, Table 1; PDF p.8, Discussion
Reported values
  • 1 patientoro-alimentary automatismsCount · 22 patients with insulo-opercular epilepsy · ictal automatic behaviorPDF p.4, Results—Seizure semiology; PDF p.5, Table 1; PDF p.8, Discussion
  • no percentage reportedoro-alimentary automatismsCount · 22 patients with insulo-opercular epilepsy · ictal automatic behaviorPDF p.4, Results—Seizure semiology; PDF p.5, Table 1; PDF p.8, Discussion
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfNarrative, educational, or cited context · 1 finding
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • psychomotor semiology: oroalimentary automatismsTypical temporal psychomotor semiology included oroalimentary automatisms.PDF p.4, Seizure semiology on video-EEG recording
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 5 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • orolingual and hand automatismsOrolingual/hand automatisms occurred in 10 of 19 patients (52.6%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
  • visual aura to automatism phenotypePhenotype II is characterized primarily by oropharyngeal, limb, or verbal automatisms, with or without a preceding visual aura.PDF p.9, Phenotype II
  • oropharyngeal automatismsTable 2 records staring followed by oropharyngeal automatisms and eye blinking in a seizure sequence.PDF p.6, Table 2 Case 1 Sz2
  • chewing and swallowing automatismsTable 2 records orolimentary automatisms consisting of chewing and swallowing in Case 11.PDF p.7, Table 2 Case 11
Reported values
  • 10/19 (52.6%) orolingual/hand automatismsorolingual and hand automatismsPercentage · n/N 10/19 · 19 patients monitored with SEEG · ictal automatismsPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

22 contributing manuscripts; source-reported values remain separate and are not pooled.

Hypermotor seizures (explosive, bipedal/bimanual, thrashing, agitated)Source terms: Hypermotor seizure; Hypermotor seizuresReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side30 manuscripts · 144 findings · 101 reported values
Weighted evidence supportevidence weight 53.56 across 30 manuscripts · 3 manuscript weight pending · 5 independent primary study · 6 systematic review or meta-analysis · 3 structured design not resolved · 5 case report or observation · 11 narrative, educational, or cited context

No lateralizing direction is reported. No lateralization is reported for the behavioral-arrest phenotype. Source-reported giratory forms were predominantly ipsilateral: T+ 8.7% ipsilateral versus 4.3% contralateral, TL 3.4% ipsilateral versus 0% contralateral, and bilateral 0% in both cohorts. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. The source provides no lateralizing information for complex motor behavior with a hyperkinetic aspect. No lateralizing information is present. The case reports right orbitofrontal onset with later bilateral tonic propagation. The frontal-like hyperkinetic description provides no lateralizing information. The single reported case had left insular epilepsy with sleep-related hyperkinetic automatisms. The OFC-restricted EZN review statement reports no hemisphere or lateralization direction. The EZN-extension association provides no lateralizing information. The insular-subgroup frequency provides no lateralizing information. The hypermotor/hyperkinetic terminology statement provides no lateralizing information. No sign-specific lateralizing rule is present. The patient’s seizures had left anterior inferolateral temporal onset before frontal involvement and hypermotor behavior. The review classification of ictal feature categories reports no lateralizing direction. No hemisphere or body-side direction is reported for the clustered manifestations. The cited mechanistic network includes bilateral caudate nuclei and provides no hemisphere-specific onset direction. No lateralization information is reported. The whole-group hyperkinetic frequency provides no lateralizing information. The autonomic-hyperkinetic association coefficient provides no lateralizing information. The emotional-hyperkinetic association coefficient provides no lateralizing information. Emotional signs preceding hyperkinetic behavior provide no lateralizing information. Autonomic signs preceding hyperkinetic behavior provide no lateralizing information. No cerebral-hemisphere lateralizing direction is reported. The cited study reported bilateral hypermotor automatisms; bilateral describes motor behavior and does not identify a hemisphere. The sleep-related hypermotor phenotype record provides no lateralizing information. No resolved lateralization direction is reported. The cited anterior-versus-posterior insular comparison provides no lateralizing information. The ventral-versus-dorsal insular focus record provides no lateralizing information. Delayed hypermotor manifestation provides no lateralizing information. Right facial pain, right-ear ringing, right hemibody and foot manifestations predominated in the early sequence, while left-sided stiffening occurred in half of seizures. The table explicitly describes the hypermotor seizure pattern as non-lateralising. The hypermotor-seizure review record provides no lateralizing information. The case had right orbitofrontal onset and later bilateral tonic seizures after spread to supplementary motor area contacts. No seizure lateralization is reported. The cited emotional-expression statement reports no hemisphere or lateralization direction. left anterior/middle cingulate, central operculum, and insula on FDG-PET; hemisphere source-explicit Left-side context is not treated as a separate source-stated lateralization assertion. The review synthesis reports opposite lateralizing directions for rare body-axis rotation depending on preceding version: contralateral to the epileptogenic zone with version and ipsilateral without version. No hemisphere direction is reported. No hemisphere or body-side direction is reported. No lateralization evidence is reported. This finding provides no lateralization information. No directional head-eye side or hemisphere is reported. In one patient, a right-foot sensory aura preceded bilateral asymmetric tonic posturing and generalized tonic-clonic seizures. The hypermotor-seizure definition provides no lateralizing direction.

Source-defined result groups 35
Localization: Frontal / TemporalSource-defined values retained separatelyAll reported · whole group and other network subgroup · patients in the named network subgroup1 manuscript · 1 reported value · not pooled
Localization: ACC / cingulateSource-defined values retained separatelypatient-level frequency synthesized across eligible studies1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 50.0%All reported · typical psychomotor seizure characteristics · patients1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 18.2%All reported · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · scalp ictal rhythm1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%All reported · 6/61 (10%) combined · individuals1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 75.0%All reported · other hypermotor semiology features · patients1 manuscript · 1 reported value · not pooled
Localization: typical anterior cingulate lesionObserved proportion 100.0%All reported · atypical anterior group · patients1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 75.0%All reported · one patient with equal anterior-lateral and inferomesial involvement · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyAll reported · whole group and other network subgroup · patients in the named network subgroup1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 23.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: OFC-extended EZNSource-defined values retained separatelyOFC-extended EZN group · patients with HkB1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyFrontal subgroup of OFC-extended EZN · subgroup patients with HkB1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHypermotor-complex motor behavior · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTemporal subgroup of OFC-extended EZN · subgroup patients with HkB1 manuscript · 1 reported value · not pooled
Localization: entire OFC-involving groupSource-defined values retained separatelyEntire OFC-involving group · patients with HkB1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Table 3 point estimate 6% · Table 3 between-report frequency range1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other Table 3 temporo-polar sign estimates · Table 3 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalObserved proportion 100.0%All reported · seizures without hypermotor behavior · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft-sided stiffening · Early diurnal versus later nocturnal/postoperative semiology · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalObserved proportion 100.0%All reported · seizures without hypermotor behavior · seizures1 manuscript · 1 reported value · not pooled
Localization: SMA / pre-SMASource-defined values retained separatelyAll reported · patients with the ictal symptom1 manuscript · 1 reported value · not pooled
Localization: PCE / posterior cingulate onsetObserved proportion 14.3%All reported · bilateral asymmetric tonic, dialeptic, and automotor seizures · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 25.0%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 9.8%All reported · 0/61 (0%) initial · individuals1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 22.2%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: OFC-restricted EZNObserved proportion 53.8%OFC-restricted EZN cases · patients with HkB1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 30

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 8 findings · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.389
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior hypermotor seizuresAll six typical anterior patients had hypermotor seizures.PDF p.4, Clinical Presentation
  • typical anterior hypermotor feature: twisting aroundThe source lists twisting around as an example of the complex motor/hypermotor manifestations in the typical anterior group.PDF p.4, Clinical Presentation
  • typical anterior hypermotor feature: banging headThe source lists banging head as an example of the complex motor/hypermotor manifestations in the typical anterior group.PDF p.4, Clinical Presentation
  • typical anterior hypermotor feature: flailingThe source lists flailing as an example of the complex motor/hypermotor manifestations in the typical anterior group.PDF p.4, Clinical Presentation
  • typical anterior hypermotor feature: violent sweeping movementsThe source lists violent sweeping movements as an example of the complex motor/hypermotor manifestations in the typical anterior group.PDF p.4, Clinical Presentation
  • typical anterior hypermotor feature: runningThe source lists running as an example of the complex motor/hypermotor manifestations in the typical anterior group.PDF p.4, Clinical Presentation
  • atypical anterior hypermotor frequencyHypermotor seizures were infrequent or absent in the atypical anterior group.PDF p.5, Atypical Anterior Cingulate Epilepsy
  • anterior cingulate mostly nocturnal hypermotor patternAmong the 10 anterior cingulate cases, most presented with frequent, mostly nocturnal and predominantly hypermotor/hyperkinetic seizures with rare generalization, with or without fear, loud vocalization, or nonmirthful laughter.PDF p.6, Discussion
Reported values
  • 6/6 hypermotor seizurestypical anterior hypermotor seizuresProportion · n/N 6/6 · 6 typical anterior cingulate cases · ictal semiologyPDF p.4, Clinical Presentation
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 12 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • giratory motor signGiratory motor signs did not differ significantly between TL and T+ groups across ipsilateral, contralateral, and bilateral forms.PDF p.6, Table 2
  • hypermotor behavioursHypermotor behaviours did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL giratory 3.4%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • T+ ipsilateral 8.7%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
  • T+ bilateral 0%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
  • TL bilateral 0%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • T+ giratory 13%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
  • P=0.1giratory motor signP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • T+ contralateral 4.3%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
  • TL ipsilateral 3.4%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • TL contralateral 0%giratory motor signPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • T+ 43.5%hypermotor behavioursPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
  • TL 30.5%hypermotor behavioursPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • P=0.26hypermotor behavioursP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 6 findings · 5 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • hyperkinetic behaviorHyperkinetic behavior was reported in 13% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Hyperkinetic/Agitation (Table 3)Table 3 reports hyperkinetic/agitation signs in 11 cases (13%), more during propagation.PDF p.6, Table 3
  • Hyperkinetic/Agitation (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports hyperkinetic/agitation signs in 21 cases (35%).PDF p.7, Table 4
  • hyperkinetic/agitation plus gelastic behaviorThe co-occurrence analysis identified hyperkinetic/agitation with gelastic behavior in 22% of the 18-patient detailed-data set.PDF p.7, Figure 2 discussion
  • hypermotor bilateral automatisms (Mirandola study)Hypermotor bilateral automatisms were observed exclusively in the PIT group, in 6 patients (43%).PDF p.7, cited-study discussion
  • hypermotor bilateral automatisms group comparison (Mirandola study)The cited comparison of hypermotor bilateral automatisms is reported as statistically significant at p<.05.PDF p.7, cited-study discussion
Reported values
  • 13% hyperkinetic behaviorhyperkinetic behaviorPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 11 cases (13%)Hyperkinetic/Agitation (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 21/60 (35%)Hyperkinetic/Agitation (Table 4)Percentage · n/N 21/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
  • 22% co-occurrencehyperkinetic/agitation plus gelastic behaviorPercentage · 18 patients with detailed semiology data · ictal; timing not otherwise reportedPDF p.7, Figure 2 discussion
  • 6/14 patients (43%)hypermotor bilateral automatisms (Mirandola study)Percentage · n/N 6/14 · 14 PIT-lesion patients in the cited Mirandola comparison · ictalPDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Hypermotor activityTable 1 reports hypermotor activity as rare in temporal lobe seizures and common in frontal lobe seizures.PDF p.2, Table 1
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf; bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Consecutive presurgical SEEG series from Timone Hospital, Marseille, February 2000-November 2010: 54 patients in whom SEEG-defined EZ was within the frontal lobe, selected from 180 SEEG explorations; patients with inconclusive intracranial recording (n=1) or a nonpredominantly frontal EZ were excluded. All patients had noninvasive presurgical assessment and video-SEEG after complete or partial antiepileptic-drug withdrawal; 374 seizures were recorded and analyzed. The cohort included 22 male and 32 female patients, mean age 24.9 +/- 9.5 years, mean epilepsy duration 16.9 +/- 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed VEEG and electrical data; 31 ictal signs and 24 brain-area variables were scored 0-1-2 per patient, with rank-based PCA, hierarchical clustering, correlation matrices, and Kendall tests at p < 0.05. The source describes sampling 20 cortical regions in one methods passage and distinguishes the SEEG-defined EZ from the source-defined early spread network.
Findings
  • Fearful Group 4 pattern; type 1 hypermotor seizures (HMS1)The authors state that the Group 4 electroclinical pattern resembles type 1 hypermotor seizures (HMS1), with the important difference that movements were not invariably hyperkinetic in the present study, citing Rheims et al., 2008.PDF p.11, discussion of Group 4 and fearful seizures; PDF p.13, reference list
  • Hyperkinetic versus normokinetic gestural behaviorHyperkinetic and normokinetic gestural motor behavior could both occur within the same patient group and in the same patient from one seizure to another; the authors therefore judged hyperkinetic character per se not to be a useful indicator of seizure localization.PDF p.10, Electroclinical subgroups; PDF p.11, Electroclinical spectrum following a rostrocaudal gradient
Reported values
  • Group 4 (5 patients)Fearful Group 4 pattern; type 1 hypermotor seizures (HMS1)Count · n/N 5/54 · Current Group 4 (5 patients); cited comparison population Not reported · Group 4 · IctalPDF p.11, discussion of Group 4 and fearful seizures; PDF p.13, reference list
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • hyperkinetic patternTable 3 lists 3 patients for the the source's own ictal symptom “hyperkinetic pattern”; its table phase label is onset.PDF p.6, Table 3
  • hyperkinetic patternTable 3 reports a pooled prevalence of 1% for the the source's own ictal symptom “hyperkinetic pattern”; its table phase label is onset.PDF p.6, Table 3
Reported values
  • 1% pooled prevalencehyperkinetic patternPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 35 findings · 31 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • emotional and autonomic manifestations; vocalization; facial expression; hypermotor behaviorThe review identifies emotional/autonomic manifestations, vocalization, facial expression changes, complex automatisms, and hypermotor behavior with preserved awareness as the main ACC clinical features.PDF p.11, Anatomical and clinical correlations; PDF p.15, Conclusion
  • hypermotor-complex motor behaviorThe source reports a frequency of 60% for hypermotor-complex motor behavior.PDF p.13, Table 3
  • hypermotor-complex motor behavior; reported frequency rangeThe source reports a frequency range of 0–100% for hypermotor-complex motor behavior.PDF p.13, Table 3
  • hypermotor-complex motor behavior; ACC association gradeTable 3 assigns the source's High overall association grade to hypermotor-complex motor behavior.PDF p.13, Table 3
  • hypermotor-complex motor behavior; Figure 4 rateFigure 4 displays a 60% rate for hypermotor-complex motor behavior.PDF p.10, Figure 4
  • hypermotor-complex motor behavior typicalityHypermotor-complex motor behavior met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • hypermotor-complex motor behavior; pairwise odds-ratio significancehypermotor-complex motor behavior showed eight significant pairwise odds-ratio comparisons after Holm correction.PDF p.10, Statistical analysis of ictal semiology
  • pairwise OR: Hypermotor-complex motor behavior relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.9 for Hypermotor-complex motor behavior relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 1.1 for Vocalization/verbalization relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.8 for Affective/autonomic aura relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.6 for Autonomic signs relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.6 for Facial expression change relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.5 for Motor (gestural) automatisms relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.4 for Loss of consciousness relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.1 for Laughter relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Affective/autonomic auraFigure 6 reports an odds ratio of 1.2 for Hypermotor-complex motor behavior relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Autonomic signsFigure 6 reports an odds ratio of 1.6 for Hypermotor-complex motor behavior relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Facial expression changeFigure 6 reports an odds ratio of 1.7 for Hypermotor-complex motor behavior relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 2 for Hypermotor-complex motor behavior relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.7 for Hypermotor-complex motor behavior relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 3.4 for Hypermotor-complex motor behavior relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 5.8 for Hypermotor-complex motor behavior relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Dystonic posturingFigure 6 reports an odds ratio of 6.2 for Hypermotor-complex motor behavior relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Head-eye deviationFigure 6 reports an odds ratio of 9.1 for Hypermotor-complex motor behavior relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to LaughterFigure 6 reports an odds ratio of 13.7 for Hypermotor-complex motor behavior relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 15.6 for Hypermotor-complex motor behavior relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Tonic-clonicFigure 6 reports an odds ratio of 25.7 for Hypermotor-complex motor behavior relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to F to BTCFigure 6 reports an odds ratio of 25.7 for Hypermotor-complex motor behavior relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 60% (frequency range 0–100%)hypermotor-complex motor behaviorPercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.13, Table 3
  • 60%hypermotor-complex motor behavior; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.10, Figure 4
  • 8 significant pairwise comparisonshypermotor-complex motor behavior; pairwise odds-ratio significanceCount · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.10, Statistical analysis of ictal semiology
  • OR 0.9pairwise OR: Hypermotor-complex motor behavior relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Vocalization/verbalization relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Affective/autonomic aura relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Autonomic signs relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Facial expression change relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Motor (gestural) automatisms relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Loss of consciousness relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Dystonic posturing relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Laughter relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Hypermotor-complex motor behavior relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Hypermotor-complex motor behavior relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Hypermotor-complex motor behavior relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2pairwise OR: Hypermotor-complex motor behavior relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Hypermotor-complex motor behavior relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.4pairwise OR: Hypermotor-complex motor behavior relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.8pairwise OR: Hypermotor-complex motor behavior relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.2pairwise OR: Hypermotor-complex motor behavior relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.1pairwise OR: Hypermotor-complex motor behavior relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.7pairwise OR: Hypermotor-complex motor behavior relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 15.6pairwise OR: Hypermotor-complex motor behavior relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 25.7pairwise OR: Hypermotor-complex motor behavior relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 25.7pairwise OR: Hypermotor-complex motor behavior relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfCase report or observation · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • hyperkinetic seizure; bilateral tonic seizureIn an illustrative 24-year-old man with sleep-related hyperkinetic seizures, PET and stereo-EEG supported a right orbitofrontal source; seizures progressed to bilateral tonic seizures with loss of awareness, and the patient was seizure-free after right orbitofrontal resection.PDF p.4, Video case 2 and Figure 3 caption
  • hyperkinetic seizure; orbitofrontal onsetIn video case 2, a 24-year-old man had hyperkinetic seizures from sleep, right orbitofrontal PET hypometabolism, stereo-EEG onset in the right orbitofrontal region, progression to bilateral tonic seizures with loss of awareness when the seizure spread to the supplementary motor area, and seizure freedom after right orbitofrontal resection.PDF p.4, Video case 2; PDF p.5, Figure 3
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 10 findings · 7 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • OFC group (EZN restricted to OFC); hyperkinetic behavior; verbal automatisms; sleep-related seizuresThe source characterizes seizures with an EZN restricted to the OFC as having a relatively sparse semiological profile, mainly hyperkinetic behavior and verbal automatisms, often associated with sleep.PDF p.5, Semiological profiles; PDF p.7, Conclusion
  • frontal and insular EZN extension; hyperkinetic behavior; mimic automatisms; gestural automatismsFrontal and insular extensions are described as more likely to show hyperkinetic behavior, mimic automatisms, and gestural automatisms.PDF p.7, Conclusion
  • hyperkinetic behaviorThe review states that no specific association of hyperkinetic behavior with a particular OFC sublobar region has been identified.PDF p.3, Complex motor phenomena—hyperkinetic behavior
  • hyperkinetic behaviorHyperkinetic behavior was reported in 14 of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • hyperkinetic behavior; OFC-extended EZNHyperkinetic behavior was reported in 30% of the OFC-extended group.PDF p.3, Complex motor phenomena—hyperkinetic behavior
  • hyperkinetic behavior; entire OFC-involving groupHyperkinetic behavior was reported in 36% of the entire group.PDF p.3, Complex motor phenomena—hyperkinetic behavior
  • hyperkinetic behavior; temporal OFC-extended subgroupHyperkinetic behavior was reported in 8% of the temporal subgroup.PDF p.3, Complex motor phenomena—hyperkinetic behavior
  • hyperkinetic behavior; insular OFC-extended subgroupHyperkinetic behavior was reported in 40% of the insular subgroup.PDF p.3, Complex motor phenomena—hyperkinetic behavior
  • hyperkinetic behavior; frontal OFC-extended subgroupHyperkinetic behavior was reported in 45% of the frontal subgroup.PDF p.3, Complex motor phenomena—hyperkinetic behavior
  • hyperkinetic behavior; Chibane cited cohortChibane et al. were reported as having 62.5% hyperkinetic behavior.PDF p.3, Complex motor phenomena—hyperkinetic behavior
Reported values
  • 14/26 (53.8%)hyperkinetic behaviorPercentage · n/N 14/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 30%hyperkinetic behavior; OFC-extended EZNPercentage · OFC-extended EZN group · OFC-extended EZN group · ictalPDF p.3, Complex motor phenomena—hyperkinetic behavior
  • 36%hyperkinetic behavior; entire OFC-involving groupPercentage · Entire OFC-involving group · Entire OFC-involving group · ictalPDF p.3, Complex motor phenomena—hyperkinetic behavior
  • 8%hyperkinetic behavior; temporal OFC-extended subgroupPercentage · Temporal subgroup of OFC-extended EZN · Temporal subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—hyperkinetic behavior
  • 40%hyperkinetic behavior; insular OFC-extended subgroupPercentage · Insular subgroup of OFC-extended EZN · Insular subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—hyperkinetic behavior
  • 45%hyperkinetic behavior; frontal OFC-extended subgroupPercentage · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—hyperkinetic behavior
  • 62.5%hyperkinetic behavior; Chibane cited cohortPercentage · Chibane cited cohort · Chibane cited cohort · ictalPDF p.3, Complex motor phenomena—hyperkinetic behavior
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdfStructured design not resolved · 2 findings · 1 reported value
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.423
The study enrolled seven consecutive PCE patients; six had SEEG-identified posterior cingulate ictal onset and one had an MRI-identified postcingulate tumour. Four patients underwent CCEP. SEEG and scalp EEG were retrospectively analyzed with video-documented ictal semiology; the source used the Lüders seizure-classification scheme. The posterior cingulate was operationally defined caudal to the vertical posterior commissure line.
Findings
  • hypermotor seizure in PCEOne of seven PCE patients had hypermotor seizures.PDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
  • Case 1 hypermotor spreadCase 1 hypermotor seizures spread to the postcentral gyrus, ventrolateral premotor area, and orbitofrontal cortex.PDF p.5, Ictal semiology and SEEG findings; PDF p.3, Figure 1
Reported values
  • 1/7 hypermotor seizurehypermotor seizure in PCEProportion · n/N 1/7 · 7 PCE patients · ictal semiologyPDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • hypermotor seizuresHypermotor seizures with rapid, violent proximal-limb and trunk movements originate primarily in the frontal lobe and less commonly in the temporal lobe, posterior cortex, or insula. Ventromedial frontal seizures have more hypermotor features, while dorsolateral frontal seizures more often show head/eye version and complex gestural automatisms; sexual-quality hypermotor movements and rare body-axis rotation of at least 180 degrees suggest frontal origin. Rotation is usually contralateral to the epileptogenic zone when preceded by version and usually ipsilateral when not preceded by version.PDF p.3, section 3.3 Complex motor seizures; PDF p.2, Table 1
Reported values
  • Body-axis rotation of at least 180 degrees in rare caseshypermotor seizuresCount · patients with focal epilepsy · ictal motor; rotation with or without preceding versionPDF p.3, section 3.3 Complex motor seizures; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • nocturnal hyperkinetic seizures in TPENocturnal hyperkinetic seizures mimicking frontal lobe epilepsy are reported in TPE; the chapter interprets MTLE-like and FLE-like manifestations as potentially reflecting regional propagation toward mesial temporal or frontal structures.PDF p.10, Temporal pole or temporo-polar epilepsy
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • posterior SHE primitive and less-integrated hypermotor movementsThe posterior SHE group tended to exhibit more primitive and less-integrated hypermotor movements with SMA and central cingulate semiology.PDF p.8, section 4.2
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 7 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • complex motor behavior; hyperkinetic automatismsThe source states that complex motor behaviors with a hyperkinetic aspect are not specific to opercular involvement because they are also reported in frontal, parietal, temporal, and insular epilepsies.PDF p.9, Discussion
  • timing; nocturnal seizure; hyperkinetic seizureThe source states that very little timing information was provided across the included studies and specifically notes one patient with nocturnal hyperkinetic seizures in the Nobili study.PDF p.9, Discussion
  • Complex motor behavior (hyperkinetic automatisms)Table 2 reports 5/21 (24%) for Complex motor behavior (hyperkinetic automatisms); timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Moderate.PDF p.7, Table 2
  • Complex motor behavior (hyperkinetic automatisms)Table 2 reports 3/12 patients with Complex motor behavior (hyperkinetic automatisms) in the prefrontal operculum group.PDF p.7, Table 2
  • Complex motor behavior (hyperkinetic automatisms)Table 2 reports 2/9 patients with Complex motor behavior (hyperkinetic automatisms) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Complex motor behavior (hyperkinetic automatisms)Fisher's exact comparison of Complex motor behavior (hyperkinetic automatisms) between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 5/21 (24%)Complex motor behavior (hyperkinetic automatisms)Percentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 3/12 patientsComplex motor behavior (hyperkinetic automatisms)Proportion · n/N 3/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 2/9 patientsComplex motor behavior (hyperkinetic automatisms)Proportion · n/N 2/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfCase report or observation · 5 findings · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • hypermotor behaviorHypermotor behavior is among the clinical manifestations reported with insular seizures.PDF p.2, Clinical Features
  • hyperkinetic behavior frontal-like symptomFrontal-like insular seizures may include hyperkinetic behavior.PDF p.2, Clinical Features
  • hypermotor manifestations suggesting insular focusHypermotor manifestations are among the observed signs that suggest an insular focus.PDF p.3, Video EEG
  • CHRNB2 and CHRNA4 mutations with sleep-related hypermotor seizuresMutations in CHRNB2 and CHRNA4 were reported in two patients with sleep-related hypermotor seizures.PDF p.3, Genetic Testing
  • hyperkinetic automatisms in left insular SUDEP caseThe SEEG-proven left-insular case had hyperkinetic automatisms.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
Reported values
  • 2 patients with sleep-related hypermotor seizures and CHRNB2/CHRNA4 mutationsCHRNB2 and CHRNA4 mutations with sleep-related hypermotor seizuresCount · 2 patients with operculo-insular epilepsy cases · sleep-related ictal semiologyPDF p.3, Genetic Testing
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • HyperkineticHyperkinetic semiology was absent as initial semiology (0/61, 0%) and occurred in 6/61 individuals (10%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • 0/61 (0%) initialHyperkineticPercentage · n/N 0/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • 6/61 (10%) combinedHyperkineticPercentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Hypermotor seizure patternTable 2 associates hypermotor semiology with anterior cingulum, orbitofrontal, frontopolar, opercular-insular, and medial intermediate frontal regions and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Hypermotor seizureHypermotor seizures are complex motor seizures dominated by large movements of proximal limb segments and trunk; the movements imitate normal actions but are inappropriate and usually purposeless, may be stereotypically repeated in sequences such as pedaling, and consciousness may be preserved.PDF p.4, Complex motor seizures; PDF p.5, Complex motor seizures, Hypermotor seizures; PDF p.2, Table 1
mcgonigal-frontal-lobe-seizures-overview-update-2022.pdfNarrative, educational, or cited context · 1 finding
mcgonigal-frontal-lobe-seizures-overview-update-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This document is a review/Neurological Update and reports or synthesizes observations from multiple SEEG, intracerebral-recording, and other cited series rather than a single study population. It specifically describes a cited SEEG series of 54 patients with FLE and a cited series of 42 patients with prefrontal seizures for emotional prevalence; other cited cohort sizes, ascertainment details, reference standards, and region-specific denominators are not reported in the document. The review frames its electroclinical correlations as group-level aids for presurgical sublobar hypotheses. It states that both seizure onset and propagation contribute to semiological expression and distinguishes elementary motor signs from complex motor behavior.
Findings
  • sleep-related hypermotor phenotype with frontal and extra-frontal localizationsThe review states that many previously termed nocturnal frontal lobe epilepsy cases had confirmed frontal localizations on intracerebral EEG, including orbitofrontal cortex, anterior cingulate, and supplementary motor area, while similar sleep-related hypermotor seizure phenotypes may also arise from extra-frontal localizations including insula; it presents Sleep-Related Hypermotor Epilepsies as broader terminology reflecting this localization range.PDF p.5, Frontal seizures and genetics
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 6 findings · 8 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • vestibular symptoms; hyperkinetic motor behaviorThe review reports that Bartolomei et al. (2011) found seizures predominantly arising from the superior parietal lobule were often associated with vestibular symptoms, whereas hyperkinetic motor behavior was associated with inferior parietal involvement.PDF p.6, Table 2, Parietal lobe row
  • vestibular symptoms; hyperkinetic motor behaviorIn the summarized Bartolomei et al. study of parietal seizures, seizures predominantly arising from the superior parietal lobule were often associated with vestibular symptoms, whereas hyperkinetic motor behavior was associated with inferior parietal involvement.PDF p.6, Table 2, Bartolomei et al. 2011 row
  • antero-posterior rockingThe review reports that Zalta et al. (2020) associated delta-range rhythmic body rocking in a prefrontal seizure with cortical delta oscillatory activity and phase-coupled high-gamma energy.PDF p.5, Table 1, Antero-posterior rocking row
  • hyperkinetic seizure; automatismThe authors caution that “hyperkinetic seizure” conflates an individual semiologic feature with the description of the overall seizure and, although included in the current ILAE classification, does not correspond to a known localization, etiology, or pathophysiological correlation; they also identify “automatism” and “hyperkinetic” as terms with imprecise or nonconsensual meaning in some contexts.PDF p.12, Table 3; PDF p.13, paragraph 2
  • antero-posterior rocking; rhythmic body rockingIn the summarized Zalta et al. case, delta-range rhythmic body rocking in prefrontal seizures was associated with cortical delta oscillatory activity and phase-coupled high-gamma energy when compared with non-rocking seizures in the same patient.PDF p.5, Table 1 (continued), Zalta et al. 2020 row; PDF p.11, mechanism 4
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 17 subjectsvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy and 34 seizures · Seizure organization and semiologic expressionPDF p.6, Table 2, Parietal lobe row
  • 34 seizuresvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy and 34 seizures · Seizure organization and semiologic expressionPDF p.6, Table 2, Parietal lobe row
  • 34 seizuresvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy; 34 seizures · ictalPDF p.6, Table 2, Bartolomei et al. 2011 row
  • 17 subjectsvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy; 34 seizures · ictalPDF p.6, Table 2, Bartolomei et al. 2011 row
  • n=1 subjectantero-posterior rockingCount · 1 subject with frontal-lobe epilepsy · During antero-posterior rockingPDF p.5, Table 1, Antero-posterior rocking row
  • Patient in intraoperative stimulation study n=1antero-posterior rocking; rhythmic body rockingCount · 1 subject with frontal-lobe epilepsy; number of seizures Not reported · ictal, during antero-posterior rockingPDF p.5, Table 1 (continued), Zalta et al. 2020 row; PDF p.11, mechanism 4
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • supplementary negative motor and frontal hypermotor seizuresSupplementary sensorimotor seizures may produce ictal paralysis or other negative motor symptoms, often with no scalp EEG because of mesial frontal dipole orientation; bizarre hypermotor seizures can arise from cingulate or orbitofrontal regions or appear after extrafrontal spread, with unilateral posturing and axial rotation favoring mesial frontal origin, severe agitation favoring orbitofrontal localization, and a longer electrical-to-hypermotor latency suggesting extrafrontal onset.PDF p.52; PDF p.53
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfCase report or observation · 3 findings
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • affective ACC expressionStronger emotional expressions such as fear or menace, with open eyes, hypermotor, and autonomic features, were linked to the rostroventral “affective” ACC.PDF p.8, Discussion
  • figure 2 chapeau de gendarme caseFigure 2 describes a 16-year-old girl with sleep-related hypermotor epilepsy and the chapeau de gendarme sign.PDF p.7, Figure 2
  • persistence during hypermotor phaseThe chapeau de gendarme sign persisted during the hypermotor phase and correlated with extensive mesial frontal involvement in the Figure 2 case.PDF p.7, Figure 2
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 12 findings · 7 reported values
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • automatisms; elementary motor; hyperkinetic; autonomic; emotional; grimace; cognitive; other subjectiveThe source classifies ictal features into automatisms, elementary motor, hyperkinetic, autonomic, emotional, grimace, cognitive, and other subjective categories for the cluster and prevalence analyses.PDF p.4, Statistical analysis
  • emotional; autonomic; cognitive; grimacing; hyperkinetic behaviorThe source identifies a main cluster containing emotional, grimacing, autonomic, cognitive, and hyperkinetic manifestations across the whole group and both subgroups.PDF p.1, Abstract; PDF p.10, Figure 3
  • hyperkinetic behaviorThe source defines hyperkinetic behavior as an excessive amount and speed of motor movements with an increased rate in motor sequences.PDF p.12, Discussion
  • hyperkinetic behavior; dorsoanterior insula; mesial frontal lobes; SMA; MCC; caudate nucleiThe source describes a reported hyperkinetic-behavior network involving coupling changes between dorsoanterior insula, mesial frontal lobes including SMA/MCC, and bilateral caudate heads.PDF p.12, Discussion
  • emotional; autonomic; automatisms; hyperkinetic behavior; grimaceAcross groups, the source places autonomic and emotional features at seizure onset, while automatisms, hyperkinetic behavior, and grimace are associated with propagation.PDF p.2, Key points; PDF p.9, Seizure semiology
  • hyperkinetic behavior; whole groupHyperkinetic behavior was reported in 39% of the whole review group.PDF p.5, All group; PDF p.9, Figure 2
  • hyperkinetic behavior; fronto-temporal subgroupHyperkinetic behavior was reported in 21% of the fronto-temporal subgroup (33 patients).PDF p.5, Fronto-temporal subgroup
  • hyperkinetic behavior; temporo-frontal subgroupHyperkinetic behavior was reported in 46% of the temporo-frontal subgroup (76 patients).PDF p.5, Temporo-frontal subgroup
  • association coefficient; autonomic and hyperkineticThe source reports an association coefficient of 0.606 for autonomic and hyperkinetic in the whole group.PDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient; emotional and hyperkineticThe source reports an association coefficient of 0.879 for emotional and hyperkinetic in the fronto-temporal subgroup.PDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
  • hyperkinetic behavior preceded by emotional signsThe source states that hyperkinetic behavior could be preceded by emotional signs in 31% of cases.PDF p.12, Discussion
  • hyperkinetic behavior preceded by autonomic signsThe source states that hyperkinetic behavior could be preceded by autonomic signs in 38% of cases.PDF p.12, Discussion
Reported values
  • 39%hyperkinetic behavior; whole groupPercentage · 109 review patients, whole group · ictal propagationPDF p.5, All group; PDF p.9, Figure 2
  • 21%hyperkinetic behavior; fronto-temporal subgroupPercentage · 33 patients, fronto-temporal subgroup · ictal propagationPDF p.5, Fronto-temporal subgroup
  • 46%hyperkinetic behavior; temporo-frontal subgroupPercentage · 76 patients, temporo-frontal subgroup · ictal propagationPDF p.5, Temporo-frontal subgroup
  • association coefficient 0.606association coefficient; autonomic and hyperkineticAssociation Coefficient · 109 review patients · ictal symptom co-occurrencePDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient 0.879association coefficient; emotional and hyperkineticAssociation Coefficient · 33 fronto-temporal subgroup patients · ictal symptom co-occurrencePDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
  • 31%hyperkinetic behavior preceded by emotional signsPercentage · Source-described hyperkinetic-behavior cases · ictal onset before hyperkinetic propagationPDF p.12, Discussion
  • 38%hyperkinetic behavior preceded by autonomic signsPercentage · Source-described hyperkinetic-behavior cases · ictal onset before hyperkinetic propagationPDF p.12, Discussion
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 3 findings · 7 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • focal nonmotor unaware seizures; hyperkinetic features; asymmetric tonic posturing; elementary facial contractionsThe source relates more ventrally located insular foci to focal nonmotor unaware seizures and more dorsally located foci to motor manifestations caused by propagation toward frontal areas, including often sleep-related hyperkinetic features, asymmetric tonic posturing, or elementary facial contractions; patients are frequently unaware of these manifestations.PDF p.5, Ictal Semiology; PDF p.16, Summary
  • delayed hypermotor manifestationIn hypermotor seizures, the chapter identifies a delay from seizure onset to the hypermotor manifestation, averaging 20 seconds with a reported range of 5 to 40 seconds in one study, together with previously described auras during wakefulness, as features suggesting an insular rather than primary frontal origin.PDF p.5, Ictal Semiology
  • Case 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyCase 2 was a 46-year-old right-handed man whose seizures began with lancinating right facial pain followed within 2 seconds by high-pitched right-ear ringing descending along the right hemibody to the foot, sometimes with right-foot tremor, witnessed erratic right-sided and truncal movements, and left-sided stiffening in half the seizures; he was usually conscious without postictal paresis, had 10–15-second events up to 100 times per day triggered by sounds, and could develop hypersalivation, speech difficulty, later nocturnal hypermotor seizures, and urinary incontinence.PDF p.11, Case 2; PDF p.13, continuation of Case 2
Reported values
  • Average delay 20 secondsdelayed hypermotor manifestationCount · Patients in one cited study of hypermotor seizures; cohort size not reported here · Ictal; interval from seizure onset to hypermotor manifestationPDF p.5, Ictal Semiology
  • range 5–40 secondsdelayed hypermotor manifestationCount · Patients in one cited study of hypermotor seizures; cohort size not reported here · Ictal; interval from seizure onset to hypermotor manifestationPDF p.5, Ictal Semiology
  • within 2 secondsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyDuration · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · early sensory sequence · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 10–15-second eventsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · habitual events · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 2–3 per monthCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · youth · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • in half the seizuresCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyOther reported value · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · left-sided stiffening · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • up to 100 times per dayCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyFrequency · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · later high-frequency period · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 2 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • hypermotor semiology; temporal pole propagation; frontal onsetThe source cautions that hypermotor semiology may arise through temporal-pole propagation rather than indicating a primary frontal onset.PDF p.6, Discussion
  • hypermotorTable 3 reports hypermotor semiology in 6% of the temporo-polar synthesis (evidence grade Low).PDF p.5, Table 3
  • hypermotorTable 3 reports a 0–50% range for hypermotor semiology across the temporo-polar reports (evidence grade Low).PDF p.5, Table 3
Reported values
  • 6%hypermotorPercentage · Temporo-polar semiology synthesis represented in Table 3 · clinical onset or laterPDF p.5, Table 3
  • range 0–50%hypermotorPercentage Range · Temporo-polar semiology synthesis represented in Table 3 · clinical onset or laterPDF p.5, Table 3
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • reflex seizures; hypermotor seizures; right foot sensory auraIn this patient, the two seizure types were hypermotor seizures and a right-foot sensory aura followed by bilateral asymmetric tonic posturing and generalized tonic-clonic seizures; the latter occurred spontaneously and was also provoked by loud sounds, more commonly by somatosensory stimulation of the right foot, and reflex seizures were exaggerated by sudden unexpected stimulation.PDF p.1, Case Report; PDF p.3, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • hypermotor seizuresThe review describes hypermotor seizures as complex multijoint movements involving the trunk and proximal limbs, often occurring during sleep with possible preserved consciousness. Most are stated to originate from orbital or mesial frontal regions, although temporal and insular epilepsies can also produce them; some consist of sexual-activity-like automatisms with pelvic, limb, groin, or genital movements.PDF p.4, Complex motor seizures; PDF p.5, Hypermotor seizures
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 1 reported value
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • hypermotor behaviorHypermotor behavior was detected in four patients.PDF p.4, Results—Seizure semiology; PDF p.10, Discussion
Reported values
  • 4/22 (18%)hypermotor behaviorPercentage · n/N 4/22 · 22 patients with insulo-opercular epilepsy · ictal complex motor behaviorPDF p.4, Results—Seizure semiology; PDF p.10, Discussion
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 23 findings · 10 reported values
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.452
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • thrashing or upper-extremity flexion-extensionAmong the four hypermotor patients, the source reports three hypermotor patients with thrashing or flexion and extension of upper extremities.PDF p.4, Seizure semiology on video-EEG recording
  • hypermotor and hyperkinetic terminologyThe introduction describes the pattern as “hypermotor” and notes that the 2006 ILAE Classification Core uses the term “hyperkinetic.”PDF p.2, Introduction
  • hypermotor feature: thrashingThe source lists thrashing among repetitive complex movements involving proximal limbs and trunk in hypermotor seizures.PDF p.2, Introduction
  • hypermotor feature: body rockingThe source lists body rocking among repetitive complex movements involving proximal limbs and trunk in hypermotor seizures.PDF p.2, Introduction
  • temporal pole lesions and hypermotor seizuresThe article investigates and concludes that hypermotor seizures occur frequently in patients with lesions involving the temporal pole.PDF p.1, Summary and Conclusion; PDF p.5, Discussion
  • hypermotor seizure semiologyFour of eight patients with temporal pole lesions exhibited hypermotor seizure semiology.PDF p.1, Summary; PDF p.4, Results; PDF p.5, Discussion
  • anterior lateral temporal scalp ictal activity in hypermotor seizuresThree of four hypermotor patients had 4–5 Hz rhythmic scalp ictal activity in the anterior lateral temporal region that later spread to the inferomesial temporal region.PDF p.4, EEG findings
  • orbitofrontal spread in hypermotor seizuresOne patient had rapid spread through temporal and lateral orbitofrontal areas in two complex partial seizures with hypermotor manifestation.PDF p.4, EEG findings
  • hypermotor behavior with orbitofrontal involvementIn both seizures described in that patient, hypermotor behavior began in conjunction with involvement of the orbitofrontal region.PDF p.4, EEG findings
  • absence of orbitofrontal spread without hypermotor behaviorSeizures without hypermotor behavior did not spread to the orbitofrontal region in the described comparison.PDF p.4, EEG findings
  • left anterior inferolateral temporal onset in 10 hypermotor seizuresIn one patient with 10 hypermotor seizures, ictal onset was from the left anterior inferolateral temporal region.PDF p.4, EEG findings; PDF p.5, Figure 2
  • spread to lateral temporal regionsThose seizures spread rapidly to other lateral temporal regions.PDF p.4, EEG findings
  • spread to basal temporal cortexThose seizures also spread to basal temporal cortex.PDF p.4, EEG findings
  • spread to orbitofrontal regionThose seizures also spread to the orbitofrontal region.PDF p.4, EEG findings
  • delayed onset of hypermotor behaviorThe onset of hypermotor behavior was delayed after the onset of frontal involvement in the described 10-seizure patient.PDF p.4, EEG findings; PDF p.5, Figure 2
  • hypermotor behavior with orbitofrontal delta activityHypermotor behavior usually corresponded to the end of ictal activity in lateral temporal cortex and development of prominent delta activity in the orbitofrontal region.PDF p.4, EEG findings; PDF p.5, Figure 2
  • hypermotor semiology in temporal lobe epilepsy cited estimateThe discussion cites studies indicating that 2–3% of patients with hippocampal or extrahippocampal temporal lobe epilepsy manifest hypermotor semiology.PDF p.5, Discussion
  • hypermotor neocortical versus mesial temporal estimateThe discussion cites a 6% hypermotor rate in neocortical temporal lobe epilepsy versus 1% in mesial temporal lobe epilepsy.PDF p.5, Discussion
  • cited hypermotor temporal lobe countThe discussion cites a study with nine hypermotor-seizure patients among 502 patients with temporal lobe epilepsy of any etiology.PDF p.5, Discussion
  • reported frontal structures associated with hypermotor onsetThe discussion states that earlier studies suggested origin from the medial frontal gyrus, anterior cingulate cortex, or orbitofrontal and frontal polar regions.PDF p.5, Discussion
  • orbitofrontal involvement with hypermotor behaviorIn both patients studied with subdural grids, orbitofrontal involvement was always present with the hypermotor behavior.PDF p.5, Discussion
  • temporal pole onset inferred from subdural gridsIn the two subdural-grid patients, localization of seizure onset to the temporal pole was inferred from ictal discharge at the anterior edge of the grids.PDF p.5, Discussion
  • temporal-pole-to-frontal spread hypothesisThe authors state that their data support the hypothesis that hypermotor manifestations associated with temporal pole lesions arise from direct spread from the pole to the frontal lobe.PDF p.6, Discussion
Reported values
  • 3/4 thrashing or upper-extremity flexion-extensionthrashing or upper-extremity flexion-extensionProportion · n/N 3/4 · 4 patients with hypermotor seizure semiology · ictal semiologyPDF p.4, Seizure semiology on video-EEG recording
  • 4/8 (50%) hypermotor seizure semiologyhypermotor seizure semiologyPercentage · n/N 4/8 · 8-patient temporal pole lesion cohort · ictal semiologyPDF p.1, Summary; PDF p.4, Results; PDF p.5, Discussion
  • 4–5 Hz rhythmic scalp ictal activityanterior lateral temporal scalp ictal activity in hypermotor seizuresRate range · 4 hypermotor patients · ictal onset and spreadPDF p.4, EEG findings
  • 3/4 hypermotor patients with anterior lateral temporal scalp ictal activityanterior lateral temporal scalp ictal activity in hypermotor seizuresProportion · n/N 3/4 · 4 hypermotor patients · ictal onset and spreadPDF p.4, EEG findings
  • 2 seizures with rapid temporal-to-lateral-orbitofrontal spreadorbitofrontal spread in hypermotor seizuresCount · n/N 2/2 · one hypermotor patient; two recorded seizures · seizure spreadPDF p.4, EEG findings
  • 2/2 seizures with hypermotor behavior beginning with orbitofrontal involvementhypermotor behavior with orbitofrontal involvementProportion · n/N 2/2 · two hypermotor seizures in one patient · seizure evolutionPDF p.4, EEG findings
  • 2–3% hypermotor semiologyhypermotor semiology in temporal lobe epilepsy cited estimatePercentage Range · cited temporal lobe epilepsy populations · ictal semiologyPDF p.5, Discussion
  • 6% neocorticalhypermotor neocortical versus mesial temporal estimatePercentage · cited neocortical temporal epilepsy population · neocortical temporal epilepsy · ictal semiologyPDF p.5, Discussion
  • 1% mesialhypermotor neocortical versus mesial temporal estimatePercentage · cited mesial temporal epilepsy population · mesial temporal epilepsy · ictal semiologyPDF p.5, Discussion
  • 9/502 hypermotor seizurescited hypermotor temporal lobe countProportion · n/N 9/502 · cited temporal lobe epilepsy population · ictal semiologyPDF p.5, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • behavioral-arrest onset phenotypePhenotype V begins with behavioral arrest and progresses to oculomotor or motor signs, including limb tonic or hypermotor activity, with a tendency to evolve into GTCS.PDF p.9, Phenotype V

30 contributing manuscripts; source-reported values remain separate and are not pooled.

Contralateral dystonic limb posturingSource terms: Dystonic limb posturingReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere23 manuscripts · 99 findings · 116 reported values
Weighted evidence supportevidence weight 51.89 across 23 manuscripts · 1 manuscript weight pending · 5 independent primary study · 1 structured design not resolved · 6 systematic review or meta-analysis · 10 narrative, educational, or cited context · 1 case report or observation

The discussion restates greater lateralizing value for dystonic than tonic posturing without stating the lateralizing direction. The review describes early upper-limb and orofacial elementary motor signs as mainly contralateral tonic, clonic, or dystonic manifestations. At onset, 8/21 fronto-opercular epilepsy patients had contralateral brachial tonic, clonic, or dystonic posturing. Four of 12 prefrontal-operculum patients had contralateral brachial tonic, clonic, or dystonic posturing at onset. Four of nine precentral Rolandic-operculum patients had contralateral brachial tonic, clonic, or dystonic posturing at onset. This row restates the Fisher exact test for the contralateral brachial combined-sign comparison. Table 3 reports three studies assessing contralateral dystonic posturing. Table 3 reports 45 patients assessed for contralateral dystonic posturing. Across included lateral-temporal studies, contralateral dystonic posturing ranged from 0–60%. Table 3 reports one study contributing onset timing for contralateral dystonic posturing. One lateral-temporal study reported median onset of contralateral dystonic posturing at 26 seconds. The random-effects odds of contralateral dystonic posturing occurrence in lateral TLE were 0.15. The overall odds estimate for contralateral dystonic posturing has a 95% confidence interval of 0.01–2.95. The heterogeneity test for the contralateral dystonic-posturing odds estimate is p=0.0037. Table 5 reports three studies comparing contralateral dystonic posturing across lateral and mesial TLE. Table 5 reports 45 lateral-TLE patients assessed for contralateral dystonic posturing. Table 5 reports 96 mesial-TLE patients assessed for contralateral dystonic posturing. Study-level lateral-TLE prevalence of contralateral dystonic posturing ranged from 0–60%. Study-level mesial-TLE prevalence of contralateral dystonic posturing ranged from 40–74.2%. The review restates that dystonic limb posturing reliably predicts seizure onset in the contralateral hemisphere. The educational tables label ictal dystonia as contralateral. The cited series includes delayed motor signs, including source-described contralateral dystonia, without a reported onset-side direction. The review synthesis describes early upper-extremity dystonic and clonic activity as contralateral to the temporal seizure focus. Right-sided motor manifestations accompanied a case interpreted as left mesial temporal epilepsy. The review describes automatisms with dystonia as a strong but direction-unspecified lateralisation clue and preserves the ictal/postictal distinction. The table restates dystonic posturing as contralateral. The review states that dystonic posturing tends to occur contralateral to seizure onset. The review restates that the dystonic limb is contralateral to the epileptogenic zone in more than 90% of cases. The cited review restates early facial activity and contralateral motor activity as suggestive of neocortical temporal epilepsy. The cited Chassoux series restatement includes bilateral tonic-clonic seizures alongside oro-alimentary, salivation, dystonic, and head-deviation phenomena. Dystonic posturing in the reviewed ACC cases was reported as contralateral to seizure onset and occurred later in ictal propagation. The paper restates that ictal dystonia in temporal lobe epilepsy is almost always contralateral to the hemisphere or epileptogenic focus. The review describes ictal dystonic posturing as contralateral to seizure onset and basal-ganglia hyperperfusion as contralateral to the posturing. The table reports ipsilateral, contralateral, and bilateral dystonic posturing, but it does not define what those labels are relative to. All 34 seizures with unilateral dystonia placed it contralateral to the EEG seizure-onset focus; none were ipsilateral. The review associates mesial-temporal automatisms with hand or mouth movements, ictal speech with nondominant seizures, and unilateral dystonic posturing with a contralateral seizure-onset relation. Cerebral lateralization: these signs are contralateral to seizure onset; target lobe is not differentiated by these signs alone. Table 3 reports one study assessing ipsilateral dystonic posturing. Table 3 reports 13 patients assessed for ipsilateral dystonic posturing. Ipsilateral dystonic posturing was reported in 23.1% of the lateral-temporal population represented in the table. Table 5 reports one study comparing ipsilateral dystonic posturing across lateral and mesial TLE. Table 5 reports 13 lateral-TLE patients assessed for ipsilateral dystonic posturing. Table 5 reports 45 mesial-TLE patients assessed for ipsilateral dystonic posturing. Ipsilateral dystonic posturing occurred in 23.1% of the reported lateral-TLE subgroup. Ipsilateral dystonic posturing occurred in 2.2% of the reported mesial-TLE subgroup. Unilateral dystonic posturing predicted the epileptogenic zone contralateral to the postured limb with a reported PPV of 75%. Among five patients with upper-limb dystonia, three were labeled contralateral and two ipsilateral, a slight contralateral numerical predominance. The review distinguishes right-temporal tendencies for selected automatisms or well-formed ictal language, contralateral nonmanipulative movements and dystonia, ipsilateral early head turning with dystonia, and predominantly contralateral late or versive turning. The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. The review describes head/eye deviation as suggesting an ipsilateral focus and other listed unilateral motor signs as usually indicating a contralateral focus. The review reports unilateral dystonic posturing as predominantly contralateral to the epileptogenic zone. Unilateral dystonic posturing was overwhelmingly contralateral to seizure onset in the cited series. The review reports unilateral dystonic posturing as contralateral to the epileptogenic zone in 96% of 29 affected patients, with one ipsilateral exception. The cited Dupont series is restated as predominantly ipsilateral automatisms in mesial TLE, exclusively contralateral automatisms in neocortical TLE, and contralateral dystonia plus ipsilateral automatisms only in mesial TLE. This finding provides no lateralization information. The category definition reports no lateralizing direction. The 3.4% value is composition of non-topological data and reports no lateralizing direction. The all-data panel count supplies no lateralizing direction. The non-topological panel count supplies no lateralizing direction. No lateralization axis information is reported for dystonic posturing versus affective/autonomic aura. No hemisphere or body-side direction is reported. No lateralization evidence is reported. Figure 6 reports OR 5.2 for Affective/autonomic aura relative to Dystonic posturing, with no hemisphere or lateralization direction. No lateralizing direction is reported.

Source-defined result groups 63
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelycontralateral upper limb dystonia · ipsilateral · patient1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyT+ · TL 30.5% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyT+ · TL 3.4% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyTL · T+ 17.4% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyT+ · TL 0% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: anterior cingulate cortex/cingulate seizure casesSource-defined values retained separatelypatient-level frequency synthesized across eligible studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTemporal lobe epilepsy; all observed cases · seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%All reported · individual1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · propagation timing · seconds from seizure onset1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyLateral TLE patients assessed for Ipsilateral dystonic posturing · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Table 3 point estimate 19% · Table 3 between-report frequency range1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyTL · T+ 21.7% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Contralateral dystonic posturing · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyMesial TLE patients assessed for Contralateral dystonic posturing · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · propagation timing · seconds from seizure onset1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 3.3%All reported · individual1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyTL · T+ 4.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Ipsilateral dystonic posturing · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other Table 3 temporo-polar sign estimates · Table 3 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft sphenoidal · left versus right temporal/sphenoidal recording maxima · source-defined interictal sharp-wave observations and single-case seizure observations1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Ipsilateral dystonic posturing · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHypermotor-complex motor behavior · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyT+ · TL 27.1% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyAutonomic signs · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given dystonic seizure · localizing data point1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyright sphenoidal · left versus right temporal/sphenoidal recording maxima · source-defined interictal sharp-wave observations and single-case seizure observations1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 0.0%ipsilateral to EEG focus · 34 contralateral seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft anterior temporal · left versus right temporal/sphenoidal recording maxima · source-defined interictal sharp-wave observations and single-case seizure observations1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyDystonic posturing · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyipsilateral upper limb dystonia · contralateral · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: orbitofrontal cortex-restricted epileptogenic-zone networkSource-defined values retained separatelyOFC-restricted EZN cases · patients1 manuscript · 1 reported value · not pooled
Localization: T+ / TLSource-defined values retained separatelyTL · T+ 0% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 29.3%contralateral to EEG focus · 0 ipsilateral seizures · seizures1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyDystonic posturing · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Contralateral dystonic posturing · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: cingulateSource-defined values retained separatelycingulate localization · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTemporal lobe epilepsy; all observed cases · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyLateral TLE patients assessed for Contralateral dystonic posturing · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyOverall; all observed cases were temporal · sign-positive lateralization1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyMesial TLE patients assessed for Ipsilateral dystonic posturing · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 23

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 8 findings · 3 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • dystonicTable 1 defines or exemplifies the the source's own semiology category “dystonic” as Twisted posture or reported dystonia.PDF p.7, Table 1 Semiology descriptions and frequencies
  • dystonicDystonic semiology comprised 3.4% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • dystonic; Figure 3 all-data subsetFigure 3 reports N = 634 for the all-data dystonic panel.PDF p.9, Figure 3 and caption
  • dystonic; Figure 3 non-topological subsetFigure 3 reports N = 120 for the non-topological dystonic panel.PDF p.9, Figure 3 and caption
  • dystonic; frontal lobeDystonic seizures originated mainly from the frontal lobe in 53%.PDF p.8, Seizure semiology localizing values
  • dystonic; frontal lobeThe 95% CI for dystonic; frontal lobe was 40%–66%.PDF p.8, Seizure semiology localizing values
  • dystonic; cingulatedystonic semiology was cingulate in 5%.PDF p.8, Seizure semiology localizing values
  • dystonic; cingulateThe 95% CI for dystonic; cingulate was 2%–9%.PDF p.8, Seizure semiology localizing values
Reported values
  • dystonic 3.4%dystonicPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • dystonic; frontal lobe 53%dystonic; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • dystonic; cingulate 5%dystonic; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 9 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • dystonic posturingDystonic posturing did not differ significantly between TL and T+ groups across ipsilateral, contralateral, and bilateral forms.PDF p.6, Table 2
Reported values
  • T+ 0%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • P=0.43dystonic posturingP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • T+ 17.4%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 30.5%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • TL 27.1%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 4.3%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 3.4%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 21.7%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 0%dystonic posturingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • delayed motor signs (Duchowny study)The cited Duchowny series is described as having behavioral arrest and delayed motor signs including version, contralateral dystonia, clonic jerks, and automatisms.PDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Dystonic limb posturingDystonic posturing of the arms and legs is described as reliably predicting seizure onset in the contralateral hemisphere.PDF p.4, Table 2; PDF p.4, section 4; PDF p.5, dystonic-posturing paragraph
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 31 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • dystonic posturing; contralateral to seizure onsetDystonic posturing occurred in 19% of patients and was contralateral to seizure onset.PDF p.9, Objective symptomatology
  • dystonic posturing; head-eye deviation; tonic-clonic manifestationsThe review links dystonic posturing, head/eye deviation, and tonic-clonic manifestations to propagation rather than the earliest seizure phase.PDF p.11, Anatomical and clinical correlations
  • dystonic posturingThe source reports a frequency of 19% for dystonic posturing.PDF p.13, Table 3
  • dystonic posturing; reported frequency rangeThe source reports a frequency range of 0–60% for dystonic posturing.PDF p.13, Table 3
  • dystonic posturing; ACC association gradeTable 3 assigns the source's Moderate overall association grade to dystonic posturing.PDF p.13, Table 3
  • dystonic posturing; Figure 4 rateFigure 4 displays a 19.4% rate for dystonic posturing.PDF p.10, Figure 4
  • pairwise OR: Dystonic posturing relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Autonomic signsFigure 6 reports an odds ratio of 0.3 for Dystonic posturing relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Facial expression changeFigure 6 reports an odds ratio of 0.3 for Dystonic posturing relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.3 for Dystonic posturing relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.4 for Dystonic posturing relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.5 for Dystonic posturing relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.9 for Dystonic posturing relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Dystonic posturingFigure 6 reports an odds ratio of 6.5 for Vocalization/verbalization relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Dystonic posturingFigure 6 reports an odds ratio of 6.2 for Hypermotor-complex motor behavior relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Dystonic posturingFigure 6 reports an odds ratio of 5.2 for Affective/autonomic aura relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Dystonic posturingFigure 6 reports an odds ratio of 3.9 for Autonomic signs relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Dystonic posturingFigure 6 reports an odds ratio of 3.6 for Facial expression change relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Dystonic posturingFigure 6 reports an odds ratio of 3.1 for Motor (gestural) automatisms relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Dystonic posturingFigure 6 reports an odds ratio of 2.3 for Loss of consciousness relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Dystonic posturingFigure 6 reports an odds ratio of 1.8 for Post-ictal confusion/behavior change disinhibition relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Dystonic posturingFigure 6 reports an odds ratio of 1.1 for Chapeau de gendarme relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Dystonic posturingFigure 6 reports an odds ratio of 0.7 for Head-eye deviation relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Dystonic posturingFigure 6 reports an odds ratio of 0.6 for Laughter relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Dystonic posturingFigure 6 reports an odds ratio of 0.4 for Oro-alimentary automatisms relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Dystonic posturingFigure 6 reports an odds ratio of 0.4 for Tonic-clonic relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Dystonic posturingFigure 6 reports an odds ratio of 0.2 for F to BTC relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Head-eye deviationFigure 6 reports an odds ratio of 1.5 for Dystonic posturing relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to LaughterFigure 6 reports an odds ratio of 2.2 for Dystonic posturing relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 2.5 for Dystonic posturing relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Tonic-clonicFigure 6 reports an odds ratio of 4.2 for Dystonic posturing relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to F to BTCFigure 6 reports an odds ratio of 4.2 for Dystonic posturing relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 19%dystonic posturing; contralateral to seizure onsetPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • 19% (frequency range 0–60%)dystonic posturingPercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.13, Table 3
  • 19.4%dystonic posturing; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.10, Figure 4
  • OR 0.2pairwise OR: Dystonic posturing relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Dystonic posturing relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Dystonic posturing relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Dystonic posturing relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Dystonic posturing relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Dystonic posturing relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Dystonic posturing relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Dystonic posturing relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Dystonic posturing relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.5pairwise OR: Vocalization/verbalization relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.2pairwise OR: Hypermotor-complex motor behavior relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.2pairwise OR: Affective/autonomic aura relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.9pairwise OR: Autonomic signs relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Facial expression change relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.1pairwise OR: Motor (gestural) automatisms relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.3pairwise OR: Loss of consciousness relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.8pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Chapeau de gendarme relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Head-eye deviation relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Laughter relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Oro-alimentary automatisms relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Tonic-clonic relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: F to BTC relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Dystonic posturing relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.2pairwise OR: Dystonic posturing relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.5pairwise OR: Dystonic posturing relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.2pairwise OR: Dystonic posturing relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.2pairwise OR: Dystonic posturing relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • mesial temporal automatisms; ictal speech; unilateral dystonic posturingMesial temporal automatisms often involve the hands or mouth; less common vocalisations and ictal speech are associated with non-dominant seizures; unilateral dystonic posturing can occur and is described as a contralateral sign.PDF p.5, Mesial temporal lobe including hippocampus
  • unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionThe review describes unilateral clonic movements, unilateral tonic or dystonic posturing, and early forced head version as robust lateralising motor signs with positive predictive value greater than 80%, and states that these signs are contralateral to the side of seizure onset.PDF p.10, Lateralising signs
Reported values
  • positive predictive value >80%unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionPositive predictive value · focal seizure literature · ictal onset/early ictalPDF p.10, Lateralising signs
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • dystonic elementary motor phenomenonOne restricted-OFC case had a dystonic elementary motor phenomenon.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 1 patientdystonic elementary motor phenomenonCount · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 21 findings · 8 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Contralateral dystonic posturingTable 3 reports 3 studies assessing Contralateral dystonic posturing.PDF p.6, Table 3
  • Contralateral dystonic posturingTable 3 reports 45 patients assessed for Contralateral dystonic posturing.PDF p.6, Table 3
  • Contralateral dystonic posturingTable 3 reports 0–60% as the percentage range or value for Contralateral dystonic posturing; the overall association grade is Low.PDF p.6, Table 3
  • Contralateral dystonic posturingTable 3 reports 1 study with onset timing for Contralateral dystonic posturing.PDF p.6, Table 3
  • Contralateral dystonic posturingTable 3 reports an onset latency of 26 s for Contralateral dystonic posturing.PDF p.6, Table 3
  • odds of occurrence; Contralateral dystonic posturingTable 4 reports overall odds of 0.15 for occurrence of Contralateral dystonic posturing in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Contralateral dystonic posturingTable 4 reports a 95% confidence interval of 0.01–2.95 for the overall odds of Contralateral dystonic posturing.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Contralateral dystonic posturingThe heterogeneity test for the Table 4 odds estimate for Contralateral dystonic posturing has p=0.0037.PDF p.7, Table 4
  • Contralateral dystonic posturing; lateral versus mesial comparisonTable 5 reports 3 studies comparing Contralateral dystonic posturing in lateral and mesial TLE.PDF p.9, Table 5
  • Contralateral dystonic posturing; lateral TLE patient denominatorTable 5 reports 45 lateral-TLE patients assessed for Contralateral dystonic posturing.PDF p.9, Table 5
  • Contralateral dystonic posturing; mesial TLE patient denominatorTable 5 reports 96 mesial-TLE patients assessed for Contralateral dystonic posturing.PDF p.9, Table 5
  • Contralateral dystonic posturing; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0–60% for Contralateral dystonic posturing.PDF p.9, Table 5
  • Contralateral dystonic posturing; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 40–74.2% for Contralateral dystonic posturing.PDF p.9, Table 5
  • Ipsilateral dystonic posturingTable 3 reports 1 studies assessing Ipsilateral dystonic posturing.PDF p.6, Table 3
  • Ipsilateral dystonic posturingTable 3 reports 13 patients assessed for Ipsilateral dystonic posturing.PDF p.6, Table 3
  • Ipsilateral dystonic posturingTable 3 reports 23.1% as the percentage range or value for Ipsilateral dystonic posturing; the overall association grade is Low.PDF p.6, Table 3
  • Ipsilateral dystonic posturing; lateral versus mesial comparisonTable 5 reports 1 studies comparing Ipsilateral dystonic posturing in lateral and mesial TLE.PDF p.9, Table 5
  • Ipsilateral dystonic posturing; lateral TLE patient denominatorTable 5 reports 13 lateral-TLE patients assessed for Ipsilateral dystonic posturing.PDF p.9, Table 5
  • Ipsilateral dystonic posturing; mesial TLE patient denominatorTable 5 reports 45 mesial-TLE patients assessed for Ipsilateral dystonic posturing.PDF p.9, Table 5
  • Ipsilateral dystonic posturing; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 23.1% for Ipsilateral dystonic posturing.PDF p.9, Table 5
  • Ipsilateral dystonic posturing; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 2.2% for Ipsilateral dystonic posturing.PDF p.9, Table 5
Reported values
  • 0–60%Contralateral dystonic posturingPercentage Range · Lateral temporal epilepsy patients assessed for Contralateral dystonic posturing · ictalPDF p.6, Table 3
  • median onset latency 26 sContralateral dystonic posturingMedian · Lateral temporal epilepsy study reporting onset timing for Contralateral dystonic posturing · ictal onsetPDF p.6, Table 3
  • odds 0.15odds of occurrence; Contralateral dystonic posturingOdds · Lateral temporal epilepsy patients assessed for Contralateral dystonic posturing · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0–60%Contralateral dystonic posturing; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Contralateral dystonic posturing · Lateral TLE patients assessed for Contralateral dystonic posturing · ictalPDF p.9, Table 5
  • 40–74.2%Contralateral dystonic posturing; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Contralateral dystonic posturing · Mesial TLE patients assessed for Contralateral dystonic posturing · ictalPDF p.9, Table 5
  • 23.1%Ipsilateral dystonic posturingPercentage · Lateral temporal epilepsy patients assessed for Ipsilateral dystonic posturing · ictalPDF p.6, Table 3
  • 23.1%Ipsilateral dystonic posturing; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Ipsilateral dystonic posturing · Lateral TLE patients assessed for Ipsilateral dystonic posturing · ictalPDF p.9, Table 5
  • 2.2%Ipsilateral dystonic posturing; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Ipsilateral dystonic posturing · Mesial TLE patients assessed for Ipsilateral dystonic posturing · ictalPDF p.9, Table 5
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 4 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Unilateral dystonic posturingUnilateral dystonic posturing was reported as a contralateral lateralizing sign with 75% PPV and inter-observer kappa of 0.80, and was observed only in temporal lobe epilepsy.PDF p.3, Table 1; PDF p.3, §5.1
Reported values
  • inter-observer kappa 0.80Unilateral dystonic posturingKappa · Sign-positive occurrences included 8 seizures in 7 patients, all in temporal lobe epilepsy. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 8 seizures with unilateral dystonic posturingUnilateral dystonic posturingCount · Sign-positive occurrences included 8 seizures in 7 patients, all in temporal lobe epilepsy. · Temporal lobe epilepsy; all observed cases · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 7 patients with unilateral dystonic posturingUnilateral dystonic posturingCount · Sign-positive occurrences included 8 seizures in 7 patients, all in temporal lobe epilepsy. · Temporal lobe epilepsy; all observed cases · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • PPV 75% (contralateral)Unilateral dystonic posturingPositive predictive value · Sign-positive occurrences included 8 seizures in 7 patients, all in temporal lobe epilepsy. · Overall; all observed cases were temporal · IctalPDF p.3, Table 1; PDF p.3, §5.1
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Ictal dystoniaBoth tables list Ictal dystonia as Contralateral.PDF p.2, Lateralizing signs/Localization table row "Ictal dystonia" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Ictal dystonia" (printed p.5)
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfCase report or observation · 2 findings · 3 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • contralateral upper-extremity dystonic and clonic activityIn a series comparing mesial and neocortical temporal seizure semiology, automatisms and dystonic posturing of the contralateral upper extremity early in the seizure were more common in mesial temporal epilepsy, whereas early clonic activity of the contralateral upper extremity or facial grimacing suggested neocortical temporal origin.PDF p.4, temporal seizure semiology paragraph beginning "In series comparing mesial"
  • Case Study 1 olfactory aura, dystonic posturing, and left temporal findingsIn Case Study 1, a right-handed woman had recurrent unusual-odor auras without initial loss of consciousness, later seizures with loss of awareness, oral/manual automatisms, unintelligible speech, left-hand automatisms, right-arm dystonic posturing, and head version to the right. Interictal sharp waves were maximal at the left sphenoidal electrode in 90% of the source-defined observations versus 5% at the left anterior temporal and 5% at the right sphenoidal electrode, and ictal rhythmic delta followed by repetitive spiking was maximal in the left temporal region; the chapter's discussion interpreted the combined history and testing as left mesial temporal lobe epilepsy.PDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
Reported values
  • 5% right sphenoidalCase Study 1 olfactory aura, dystonic posturing, and left temporal findingsPercentage · Single illustrative case, 31-year-old right-handed woman with poorly controlled seizures · right sphenoidal · aura, ictal, and interictalPDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
  • 90% left sphenoidalCase Study 1 olfactory aura, dystonic posturing, and left temporal findingsPercentage · Single illustrative case, 31-year-old right-handed woman with poorly controlled seizures · left sphenoidal · aura, ictal, and interictalPDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
  • 5% left anterior temporalCase Study 1 olfactory aura, dystonic posturing, and left temporal findingsPercentage · Single illustrative case, 31-year-old right-handed woman with poorly controlled seizures · left anterior temporal · aura, ictal, and interictalPDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 2 findings · 5 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • dystonic limb posturingDystonic limb posturing is more common in TLE than EXTLE, typically follows bilateral manual automatisms or occurs with automatisms in the other upper limb, and is contralateral to the epileptogenic zone in more than 90% of cases. When accompanied by manual automatisms and ipsilateral head turning, it is highly suggestive of MTLE.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEDystonic limb posturing within 20 seconds of seizure onset was reported more often in MTLE than NTLE, 52% versus 26%, and oral automatisms were reported 69% versus 11%, respectively. Early facial grimacing or twitching and contralateral motor activity were suggestive of NTLE.PDF p.6, section 8.1 Neocortical temporal lobe epilepsy
Reported values
  • More than 90% contralateral to EZdystonic limb posturingPercentage · patients with focal epilepsy, including TLE and EXTLE · ictal motor, following or accompanying automatismsPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • Oral automatisms in MTLE 69%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · MTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Early dystonic posturing in NTLE 26%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · NTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Early dystonic posturing in MTLE 52%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · MTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Oral automatisms in NTLE 11%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · NTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 2 findings
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal SPECT, dystonic posturing, focal aware seizures, and network propagationIctal contralateral dystonic posturing is associated with hyperperfused basal ganglia in the hemisphere contralateral to the posturing, whereas ictal SPECT has lower sensitivity for temporal focal aware seizures; SPECT can show early propagation through network connectivity but is not routinely used for MTLE-HS when video-EEG and structural MRI already provide the needed localizing information and is mainly helpful for restricting areas for SEEG in MRI-normal cases.PDF p.20, Ictal SPECT in TLE; PDF p.21, Ictal SPECT in TLE
  • unilateral dystonic posturing, head/eye deviation, clonic or tonic movements, and hypokinesiaSecondary motor signs related to propagation outside the temporal lobe may lateralize the seizure-onset zone: unilateral dystonic posturing is usually contralateral to the focus, head or eye deviation suggests an ipsilateral focus, and other unilateral clonic or tonic movements or limb immobility usually indicate a contralateral focus.PDF p.8, Focal impaired awareness seizures
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; orofacial; brachial; tonic; clonic; dystonicElementary motor symptoms were described as early, mainly involving the orofacial regions and/or arms; arm manifestations were mainly contralateral tonic, clonic, or dystonic seizures or postures.PDF p.6, Anatomical and clinical correlations; PDF p.8, Discussion
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 8/21 (38%) for Brachial contralateral (tonic and/or clonic or dystonic posture); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Moderate.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 4/12 patients with Brachial contralateral (tonic and/or clonic or dystonic posture) in the prefrontal operculum group.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 4/9 patients with Brachial contralateral (tonic and/or clonic or dystonic posture) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Fisher's exact comparison of Brachial contralateral (tonic and/or clonic or dystonic posture) between the prefrontal and precentral Rolandic operculum groups has p=0.673.PDF p.7, Table 2
Reported values
  • 8/21 (38%)Brachial contralateral (tonic and/or clonic or dystonic posture)Percentage · n/N 8/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsBrachial contralateral (tonic and/or clonic or dystonic posture)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 4/9 patientsBrachial contralateral (tonic and/or clonic or dystonic posture)Proportion · n/N 4/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal motor (dystonic)Focal motor (dystonic) semiology was absent as initial semiology (0/61, 0%) and occurred in 2/61 individuals (3%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 0/61 (0%)Focal motor (dystonic)Percentage · n/N 0/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 2/61 (3%)Focal motor (dystonic)Percentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Automatisms with dystoniaThe review states that automatisms may be ictal or postictal and provide strong lateralisation clues when associated with dystonia; manipulative automatisms may be more common postictally, and EEG can help distinguish ictal from postictal automatisms.PDF p.4, section 1.6
  • Dystonic posturingTable 3 associates dystonic posturing with basal ganglia involvement and contralateral lateralisation.PDF p.4, Table 3
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 4 findings · 12 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral dystonic posturingUnilateral dystonic posturing in temporal lobe epilepsy lateralizes predominantly to the contralateral epileptogenic zone.PDF p.6, section 3.8; PDF p.12, Table 1
  • unilateral dystonic posturingIn Kotagal et al., unilateral dystonic posturing was always contralateral to seizure onset.PDF p.6, section 3.8
  • unilateral dystonic posturingYen et al. found unilateral dystonic posturing contralateral in 96%, with one ipsilateral exception.PDF p.6, section 3.8; PDF p.12, Table 1
  • unilateral motor automatisms with dystonic posturingDupont et al. reported predominantly ipsilateral automatisms in mesial TLE, exclusively contralateral automatisms in neocortical TLE, and the combination of contralateral dystonia with ipsilateral automatisms only in mesial TLE.PDF p.6, section 3.9
Reported values
  • Unilateral dystonic posturing contralateral in 100%unilateral dystonic posturingPercentage · patients with temporal lobe epilepsy and unilateral dystonic posturing · Selected table evidence · ictalPDF p.6, section 3.8; PDF p.12, Table 1
  • Reported ipsilateral exception n=1unilateral dystonic posturingCount · patients with temporal lobe epilepsy and unilateral dystonic posturing · Yen report · ictalPDF p.6, section 3.8; PDF p.12, Table 1
  • Unilateral dystonic posturing in 43.9% of TLEunilateral dystonic posturingPercentage · patients with temporal lobe epilepsy and unilateral dystonic posturing · Temporal lobe epilepsy · ictalPDF p.6, section 3.8; PDF p.12, Table 1
  • 100% contralateralunilateral dystonic posturingPercentage · 31 consecutive patients seizure free after temporal lobectomy plus 10 patients evaluated by video/EEG; 118 seizures reviewed · unilateral dystonic posturing · ictalPDF p.6, section 3.8
  • 41 seizuresunilateral dystonic posturingCount · n/N 41/118 · 31 consecutive patients seizure free after temporal lobectomy plus 10 patients evaluated by video/EEG; 118 seizures reviewed · reviewed seizures · ictalPDF p.6, section 3.8
  • 118 seizuresunilateral dystonic posturingCount · 31 consecutive patients seizure free after temporal lobectomy plus 10 patients evaluated by video/EEG; 118 seizures reviewed · reviewed seizures · ictalPDF p.6, section 3.8
  • 18 patientsunilateral dystonic posturingCount · 31 consecutive patients seizure free after temporal lobectomy plus 10 patients evaluated by video/EEG; 118 seizures reviewed · patients with unilateral dystonic posturing · ictalPDF p.6, section 3.8
  • 31 consecutive patientsunilateral dystonic posturingCount · 31 consecutive patients seizure free after temporal lobectomy plus 10 patients evaluated by video/EEG; 118 seizures reviewed · seizure-free after temporal lobectomy · ictalPDF p.6, section 3.8
  • 96% contralateralunilateral dystonic posturingPercentage · 83 patients seizure free after temporal lobectomy, including 29 with dystonic posturing · patients with dystonic posturing · ictalPDF p.6, section 3.8; PDF p.12, Table 1
  • 29/83 had dystonic posturingunilateral dystonic posturingPercentage · n/N 29/83 · 83 patients seizure free after temporal lobectomy, including 29 with dystonic posturing · unilateral dystonic posturing · ictalPDF p.6, section 3.8; PDF p.12, Table 1
  • 1 of 29 ipsilateralunilateral dystonic posturingPercentage · n/N 1/29 · 83 patients seizure free after temporal lobectomy, including 29 with dystonic posturing · ipsilateral exception · ictalPDF p.6, section 3.8; PDF p.12, Table 1
  • 26/60 had unilateral motor automatismsunilateral motor automatisms with dystonic posturingCount · n/N 26/60 · 60 patients with temporal lobe epilepsy, including 26 with unilateral motor automatisms · ictalPDF p.6, section 3.9
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 2 findings · 24 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • ictal dystoniaThe current paper reports that ictal dystonia, as described in the cited literature, almost always lateralizes to the contralateral hemisphere in temporal lobe epilepsy, and that Rusu et al. described the earliest and/or most marked dystonic posturing as contralateral to the epileptogenic focus, mainly involving the hand.PDF p.8, cited dystonia value and study definition; PDF p.12, discussion of cited duration and lateralization; PDF p.13, discussion of the cited Rusu result
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • temporal automatisms, dystonic posturing, and head turningOroalimentary automatisms suggest temporal involvement but are not specific; spitting, drinking, and preserved responsiveness during automatisms favor right temporal localization; manipulative automatisms alone do not lateralize, whereas nonmanipulative distal or proximal movements tend to be contralateral and may precede contralateral dystonic posturing; dystonic posturing is usually contralateral, early head turning with dystonia tends ipsilateral, late head turning is more often contralateral, and versive head turning is almost always contralateral.PDF p.50; PDF p.51
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 2 findings · 4 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • dystonic versus tonic posturingThe discussion distinguishes tonic from dystonic posturing, states that dystonia has greater lateralizing value, and reports that Kotagal et al. (1989) observed unilateral dystonia in 15% of patients with TLE.PDF p.5, Discussion
  • unilateral dystoniaIn the unilateral TLE cohort, unilateral dystonia occurred only on the side contralateral to the EEG seizure focus.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
Reported values
  • 15% of patients with TLE, as reported for Kotagal et al. (1989)dystonic versus tonic posturingPercentage · Cited TLE study as described by the current source; not independently reviewed · ictal motor posturingPDF p.5, Discussion
  • 0 ipsilateral seizuresunilateral dystoniaCount · n/N 0/116 · 19 patients with unilateral TLE; dystonia occurred in 12 patients · ipsilateral to EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 34 contralateral seizures (30% of all 116 seizures)unilateral dystoniaPercentage · n/N 34/116 · 19 patients with unilateral TLE; dystonia occurred in 12 patients · contralateral to EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 12 patientsunilateral dystoniaCount · n/N 12/19 · 19 patients with unilateral TLE; dystonia occurred in 12 patients · patients with unilateral dystonia · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 2 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • Chassoux cohort; oro-alimentary automatisms; salivation; dystonic signs; head deviation; bilateral tonic-clonic seizuresThe review restates that Chassoux et al. described 33 patients with oro-alimentary automatisms, salivation, motor signs including dystonia and head deviation, and bilateral tonic-clonic seizures in the medio-lateral context.PDF p.4, Medio-lateral temporal origin
  • dystonicTable 3 reports dystonic signs in 19% of the temporo-polar synthesis (evidence grade Low).PDF p.5, Table 3
  • dystonicTable 3 reports a 0–100% range for dystonic signs across the temporo-polar reports (evidence grade Low).PDF p.5, Table 3
Reported values
  • 19%dystonicPercentage · Temporo-polar semiology synthesis represented in Table 3 · later after propagation to symptomatogenic areasPDF p.5, Table 3
  • range 0–100%dystonicPercentage Range · Temporo-polar semiology synthesis represented in Table 3 · later after propagation to symptomatogenic areasPDF p.5, Table 3
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • dystonic posturingThe review defines dystonic posturing as sustained, longer-than-10-second, forced, unnatural positioning of one upper extremity with a clear rotational component and states that, in temporal lobe epilepsy, it reliably lateralizes to the contralateral hemisphere; it can also occur in extratemporal epilepsy. The review relates it to basal-ganglia activation through spread and cites ictal SPECT evidence of basal-ganglia involvement.PDF p.5, Additional lateralizing signs/Dystonic posturing; PDF p.6, Dystonic posturing (continued)
Reported values
  • Sustained >10 secdystonic posturingCount · Patients with temporal lobe and extratemporal epilepsy; no cohort reported · Ictal, sustained >10 secPDF p.5, Additional lateralizing signs/Dystonic posturing; PDF p.6, Dystonic posturing (continued)
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 3 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • upper limb dystoniaUpper limb dystonia occurred in five patients; it was contralateral in three and ipsilateral in two, and could involve the whole arm or be limited to the hand.PDF p.3, Results—Seizure semiology; PDF p.5, Table 1
Reported values
  • five patients (23%)upper limb dystoniaPercentage · n/N 5/22 · 22 patients with insulo-opercular epilepsy · all upper limb dystonia · ictal motor semiologyPDF p.3, Results—Seizure semiology; PDF p.5, Table 1
  • three patientsupper limb dystoniaCount · 22 patients with insulo-opercular epilepsy · contralateral upper limb dystonia · ictal motor semiologyPDF p.3, Results—Seizure semiology; PDF p.5, Table 1
  • two patientsupper limb dystoniaCount · 22 patients with insulo-opercular epilepsy · ipsilateral upper limb dystonia · ictal motor semiologyPDF p.3, Results—Seizure semiology; PDF p.5, Table 1

23 contributing manuscripts; source-reported values remain separate and are not pooled.

Vertiginous aura / ictal vestibular sensationSource terms: Vertiginous auraReported: IpsilateralAlso reported: Right hemisphere20 manuscripts · 42 findings · 42 reported values
Weighted evidence supportevidence weight 49.49 across 20 manuscripts · 1 manuscript weight pending · 7 independent primary study · 7 narrative, educational, or cited context · 5 systematic review or meta-analysis · 1 structured design not resolved

The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. The cited table describes vertiginous aura as not-lateralising but often right. No lateralizing direction is reported. No hemisphere or body-side direction is reported. Gustatory aura was associated with the TS subgroup and vestibular aura with the TPO subgroup; no lateralization is reported. No seizure lateralization is reported. The cited vertigo observations do not report a hemisphere or lateralizing direction. No cerebral direction or body-side result is reported. No lateralization relationship is reported. The primary table's dizziness/cephalic-aura result reports no hemisphere or lateralization direction. The primary odds result for Dizziness/cephalic aura reports no hemisphere or lateralization direction. The primary lateral-TLE percentage range for Dizziness/cephalic aura reports no hemisphere or lateralization direction. The primary mesial-TLE percentage range for Dizziness/cephalic aura reports no hemisphere or lateralization direction. No lateralization axis information is reported for the nine vertiginous-sensation patients. No lateralization axis information is reported for the 11 vertiginous-sensation entries. No lateralizing direction is reported for the dizzy aura reproduced at electrode 8. The educational stimulation statement contains no lateralization evidence. No lateralization axis information is reported for the review's vertigo frequency. The review table reports vertigo in seven basal-temporal cases (8%) with no hemisphere or lateralizing direction. The review reports vertigo in 4/60 high- or very-high-confidence basal-temporal EZ cases (7%) with no hemisphere or lateralizing direction. No lateralization axis information is reported for stimulation-evoked vestibular sensations. This record provides no seizure lateralization. No lateralization axis information is reported for the typical anterior freezing/lightheadedness aura. No lateralizing direction is reported for the posterior-cingulate falling aura. The patient-level falling, gustatory, and abdominal aura entry gives no body-side or hemisphere information. The primary result reports no lateralization; vertigo frequencies did not differ significantly across the M, ML, and L temporal-onset groups. The primary comparison reports no hemisphere-level lateralization; it compares M, ML, and L temporal-onset subtypes. The review places fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo between lateral and medial temporal patterns.

Source-defined result groups 25
Localization: Insular / ParietalObserved proportion 100.0%pain at seizure onset · other SOZ · patient1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · no vertiginous sensation · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 8.3%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 7.5%All reported · other insular stimulation sites and vestibular description categories · evoked vestibular response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: Insular / ParietalObserved proportion 100.0%choking sensation · other SOZ · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Dizziness/cephalic aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 12.5%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: falling aura / posterior cingulate lesionObserved proportion 25.0%All reported · other posterior aura terms · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Dizziness/cephalic aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 11.1%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 33.3%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 84.6%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyVestibular-response contacts · other insular stimulation sites and vestibular description categories · stimulation contact1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 15.4%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyVestibular-response contacts · other insular stimulation sites and vestibular description categories · stimulation contact1 manuscript · 1 reported value · not pooled
Localization: Insular / ParietalObserved proportion 100.0%vertigo or falling sensation · other SOZ · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · other aura categories · aura entries1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 20

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 3 findings · 2 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior freezing/lightheadedness auraOne typical anterior patient had a subjective sensation of freezing with or without lightheadedness.PDF p.3, Clinical Presentation
  • posterior cingulate falling auraThe source reports 1 posterior cingulate patient with falling aura.PDF p.5, Clinical Presentation
  • patient 12 falling/gustatory/abdominal auraFalling, gustatory, and abdominal aura terms were listed for patient 12.PDF p.4, Figure 3
Reported values
  • 1/6 subjective freezing aura with or without lightheadednesstypical anterior freezing/lightheadedness auraProportion · n/N 1/6 · 6 typical anterior cingulate cases · auraPDF p.3, Clinical Presentation
  • 1/4 falling auraposterior cingulate falling auraProportion · n/N 1/4 · 4 posterior cingulate cases · auraPDF p.5, Clinical Presentation
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • dizzinessTwo patients reported dizziness.PDF p.2, Results
Reported values
  • 2/18 (11%) dizzinessdizzinessPercentage · n/N 2/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 4 findings · 8 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • vestibular auraVestibular auras were more frequent in T+ than TL seizures, driven in the table by rotatory rather than non-rotatory symptoms.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • T+ subgroup associations for gustatory and vestibular aurasAmong T+ cases, gustatory auras were significantly associated with the TS subgroup and vestibular auras with the TPO subgroup.PDF p.5, Seizure clinical semiology; PDF p.7, Auras
  • gustatory, vestibular, and auditory symptomsThe source states that the localizing significance of gustatory, vestibular, and auditory symptoms remains uncertain in the cited literature.PDF p.7, Auras
  • rotatory vestibular symptomThe source states that a cited case report described epileptic rotatory vertigo arising from the temporo-parieto-occipital junction and that a cortical electrical stimulation study identified a lateral temporoparietal area from which rotatory sensations were easily elicited.PDF p.7, Auras
Reported values
  • TL 1.7%vestibular auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • T+ 13%vestibular auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • TL 0%vestibular auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • T+ 8.7%vestibular auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • T+ 4.3%vestibular auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • TL 1.7%vestibular auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • P=0.02T+ subgroup associations for gustatory and vestibular aurasP value · T+ subgroup patients and their one analyzed typical seizure; TS n=7 and TPO n=6 · TPO subgroup · ictal onsetPDF p.5, Seizure clinical semiology; PDF p.7, Auras
  • P=0.009T+ subgroup associations for gustatory and vestibular aurasP value · T+ subgroup patients and their one analyzed typical seizure; TS n=7 and TPO n=6 · TS subgroup · ictal onsetPDF p.5, Seizure clinical semiology; PDF p.7, Auras
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • vertigoVertigo accounted for 8% of the sensory manifestations in the narrative summary.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Vertigo (Table 3)Table 3 reports vertigo in 7 cases (8%), more at seizure onset.PDF p.6, Table 3
  • Vertigo (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports vertigo in 4 cases (7%).PDF p.7, Table 4
Reported values
  • 8% vertigovertigoPercentage · reviewed basal temporal seizure cases · ictal onsetPDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 7 cases (8%)Vertigo (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 4/60 (7%)Vertigo (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • gustatory; olfactory; vestibular; autonomic auraTable 3 maps gustatory aura to insula or mesiotemporal regions, olfactory aura to insula, mesiotemporal, or orbitofrontal regions, vestibular aura to posterior temporal or parietal regions, and autonomic aura to insula, amygdala, or cingulate regions.PDF p.10, Table 3; PDF p.3, Figure 1
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Dizziness/cephalic auraTable 3 reports 3 studies assessing Dizziness/cephalic aura.PDF p.6, Table 3
  • Dizziness/cephalic auraTable 3 reports 47 patients assessed for Dizziness/cephalic aura.PDF p.6, Table 3
  • Dizziness/cephalic auraTable 3 reports 11.8–50% as the percentage range or value for Dizziness/cephalic aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Dizziness/cephalic auraTable 4 reports overall odds of 0.31 for occurrence of Dizziness/cephalic aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Dizziness/cephalic auraTable 4 reports a 95% confidence interval of 0.10–0.93 for the overall odds of Dizziness/cephalic aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Dizziness/cephalic auraThe heterogeneity test for the Table 4 odds estimate for Dizziness/cephalic aura has p=0.1134.PDF p.7, Table 4
  • Dizziness/cephalic aura; lateral versus mesial comparisonTable 5 reports 2 studies comparing Dizziness/cephalic aura in lateral and mesial TLE.PDF p.9, Table 5
  • Dizziness/cephalic aura; lateral TLE patient denominatorTable 5 reports 25 lateral-TLE patients assessed for Dizziness/cephalic aura.PDF p.9, Table 5
  • Dizziness/cephalic aura; mesial TLE patient denominatorTable 5 reports 40 mesial-TLE patients assessed for Dizziness/cephalic aura.PDF p.9, Table 5
  • Dizziness/cephalic aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 11.8–50% for Dizziness/cephalic aura.PDF p.9, Table 5
  • Dizziness/cephalic aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–40% for Dizziness/cephalic aura.PDF p.9, Table 5
Reported values
  • 11.8–50%Dizziness/cephalic auraPercentage Range · Lateral temporal epilepsy patients assessed for Dizziness/cephalic aura · ictalPDF p.6, Table 3
  • odds 0.31odds of occurrence; Dizziness/cephalic auraOdds · Lateral temporal epilepsy patients assessed for Dizziness/cephalic aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 11.8–50%Dizziness/cephalic aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Dizziness/cephalic aura · Lateral TLE patients assessed for Dizziness/cephalic aura · ictalPDF p.9, Table 5
  • 0–40%Dizziness/cephalic aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Dizziness/cephalic aura · Mesial TLE patients assessed for Dizziness/cephalic aura · ictalPDF p.9, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • vertiginous aurasVertiginous auras with sensations of rotation or movement are usually associated with visual or auditory symptoms and a symptomatogenic zone near the visual and auditory association areas at the temporoparietal junction. Electrical stimulation readily elicits vestibular or rotatory sensations from a lateral temporoparietal region spanning the Sylvian fissure, including the parietal operculum and middle and posterior superior and middle temporal gyri.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • visual and vestibular illusions, including vertigoVisual and vestibular illusions, especially vertigo, are reported particularly in posterior LTLE, but the chapter states that they probably rely on propagation of ictal activity to occipital or parietal regions.PDF p.9, Focal aware seizures
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 3 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.90 · 2 × 1.5 × 1.301
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • pain, choking sensation, vertigo, and falling sensationAll four patients with pain at seizure onset and all three patients with a choking sensation had an insular SOZ, while all three patients with either vertigo or a falling sensation had a parietal SOZ.PDF p.6, section 3.3
Reported values
  • all four patientspain, choking sensation, vertigo, and falling sensationPercentage · n/N 4/4 · SHE patients with the specified sensory manifestations; source reports four pain cases, three choking cases, and three vertigo/falling cases · pain at seizure onset · at the beginning of the seizure/early sensory onsetPDF p.6, section 3.3
  • all three patientspain, choking sensation, vertigo, and falling sensationPercentage · n/N 3/3 · SHE patients with the specified sensory manifestations; source reports four pain cases, three choking cases, and three vertigo/falling cases · vertigo or falling sensation · at the beginning of the seizure/early sensory onsetPDF p.6, section 3.3
  • all three patientspain, choking sensation, vertigo, and falling sensationPercentage · n/N 3/3 · SHE patients with the specified sensory manifestations; source reports four pain cases, three choking cases, and three vertigo/falling cases · choking sensation · at the beginning of the seizure/early sensory onsetPDF p.6, section 3.3
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • vestibular body-motion sensationLess common vestibular responses were described as a feeling of body motion.PDF p.5, Other Insular Responses
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal sensory (vestibular)Focal sensory (vestibular) semiology occurred in 1/61 individuals (2%) both as initial semiology and in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Combined 1/61 (2%)Focal sensory (vestibular)Percentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Initial 1/61 (2%)Focal sensory (vestibular)Percentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Vertiginous auraTable 2 associates vertiginous aura with the temporo-parieto-occipital junction, including superior temporal and inferior parietal regions, and describes it as not-lateralising, often right.PDF p.3, Table 2
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 7 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • vertigoVertigo frequencies did not differ significantly across M, ML, and L groups.PDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • sensory hallucination or illusion (visual, auditory, vestibular)The combined category of visual, auditory, or vestibular sensory hallucination or illusion was more frequent in L than M or ML patients.PDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
Reported values
  • p=0.86vertigoP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • L=2/13 (15.4%)vertigoPercentage · n/N 2/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • M=2/24 (8.3%)vertigoPercentage · n/N 2/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • ML=2/18 (11.1%)vertigoPercentage · n/N 2/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • 6/18 (33.3%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 6/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
  • 3/24 (12.5%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
  • 11/13 (84.6%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 11/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 5 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • vestibular sensationsVestibular sensations occurred in 41 of 550 clinically eloquent stimulations (7.5%), were mainly localized to the medium and posterior-superior insula, and were described as body motion in 39/41 responses or movement of the visual environment in 2/41.PDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5B
Reported values
  • z-coordinate OR=0.84vestibular sensationsOdds ratio · 41 vestibular responses in the 550-response series · Vestibular-response contacts · stimulation-evoked vestibular responsePDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5B
  • Visual environment moving 2/41 (4.9%)vestibular sensationsPercentage · n/N 2/41 · 41 vestibular responses in the 550-response series · Vestibular responses · stimulation-evoked vestibular responsePDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5B
  • Vestibular responses 41/550 (7.5%)vestibular sensationsPercentage · n/N 41/550 · 41 vestibular responses in the 550-response series · stimulation-evoked vestibular responsePDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5B
  • y-coordinate OR=0.9vestibular sensationsOdds ratio · 41 vestibular responses in the 550-response series · Vestibular-response contacts · stimulation-evoked vestibular responsePDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5B
  • Body motion 39/41 (95.1%)vestibular sensationsPercentage · n/N 39/41 · 41 vestibular responses in the 550-response series · Vestibular responses · stimulation-evoked vestibular responsePDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5B
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 4 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • vestibular symptoms; hyperkinetic motor behaviorThe review reports that Bartolomei et al. (2011) found seizures predominantly arising from the superior parietal lobule were often associated with vestibular symptoms, whereas hyperkinetic motor behavior was associated with inferior parietal involvement.PDF p.6, Table 2, Parietal lobe row
  • vestibular symptoms; hyperkinetic motor behaviorIn the summarized Bartolomei et al. study of parietal seizures, seizures predominantly arising from the superior parietal lobule were often associated with vestibular symptoms, whereas hyperkinetic motor behavior was associated with inferior parietal involvement.PDF p.6, Table 2, Bartolomei et al. 2011 row
Reported values
  • 17 subjectsvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy and 34 seizures · Seizure organization and semiologic expressionPDF p.6, Table 2, Parietal lobe row
  • 34 seizuresvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy and 34 seizures · Seizure organization and semiologic expressionPDF p.6, Table 2, Parietal lobe row
  • 34 seizuresvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy; 34 seizures · ictalPDF p.6, Table 2, Bartolomei et al. 2011 row
  • 17 subjectsvestibular symptoms; hyperkinetic motor behaviorCount · 17 subjects with parietal-lobe epilepsy; 34 seizures · ictalPDF p.6, Table 2, Bartolomei et al. 2011 row
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • stimulation-evoked somatosensory, auditory, vestibular, olfactory, gustatory, and viscerosensory symptomsThe chapter reports that electrical stimulation studies evoked somatosensory symptoms, including pain, from the posterior two-thirds of the insula; auditory and vestibular symptoms from the posterior insula; and olfactory, gustatory, and viscerosensory symptoms, including laryngeal constriction, from the midinsula, whereas stimulation of the most anterior portion rarely evoked symptoms unless a larger network seizure was elicited.PDF p.3, insular functional differentiation and electrical cortical stimulation
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 4 findings · 3 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • vertiginous sensationVertiginous sensations were reported by nine patients in the narrative results.PDF p.3, Results, Aurae
  • vertiginous sensation entries in Table 1Table 1 lists 11 vertiginous-sensation aura entries.PDF p.4, Table 1
  • dizzy aura reproduced at electrode 8In Figure 2, stimulation of electrode 8 reproduced a dizzy aura that the patient described as feeling like swaying rather than things going round.PDF p.7, Fig. 2
  • vertigo at temporo-parietal borderThe source states that vertiginous aurae are elicited predominantly from the temporo-parietal border in cited stimulation work.PDF p.9, Discussion
Reported values
  • 9 patientsvertiginous sensationCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae
  • 11 source-reported aura entriesvertiginous sensation entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 1 casedizzy aura reproduced at electrode 8Count · n/N 1/1 · patient 49 (M.Mc.) · stimulation responsePDF p.7, Fig. 2
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • fear; auditory hallucinations; gustatory hallucinations; sensory hallucinations; vertigoThe source describes fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo as intermediate features between lateral and medial temporal patterns.PDF p.5, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • dizziness with or without colored lightsTable 2 records dizziness with or without colored lights as an aura in Case 13.PDF p.7, Table 2 Case 13

20 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal head versionReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphereNo single reliable side21 manuscripts · 98 findings · 125 reported values
Weighted evidence supportevidence weight 48.16 across 21 manuscripts · 2 manuscript weight pending · 6 independent primary study · 7 narrative, educational, or cited context · 2 structured design not resolved · 5 systematic review or meta-analysis · 1 case report or observation

Source reports contralateral limb posturing in a sequential occipital-onset phenotype. The source describes visual aura followed by head-eye deviation and contralateral tonic posturing as activity propagates through dorsal parietal nodes toward premotor areas. The seizure contains a leftward head/eye deviation, preserved as a body-side observation without cerebral lateralization inference. Table 2 records rightward head, eye, and body deviation in a case with source-reported right occipital onset. MCC stimulation elicited ipsilateral rightward head turning within a composite experience whose table distribution was labeled bilateral. In the unilateral TLE cohort, head version occurred only contralateral to the EEG seizure focus. Head turning occurred in both directions relative to the EEG seizure-onset focus: 15 ipsilateral and 17 contralateral seizures; the card also reports 5 ipsilateral-turning and 6 contralateral-turning patients. The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. Two recorded bilateral tonic-clonic seizures began with left head deviation despite generalized bifrontally predominant EEG activity; an earlier event reportedly turned right, so head direction was not proof of focal epilepsy. The reproduced table lists head turning with ipsilateral lateralization while also retaining contralateral-space neglect and propagation-to-basal-ganglia contexts. The reproduced table associates head version with a contralateral direction. The current paper restates that version has high positive predictive value for the side of ictal onset without specifying a left/right or ipsi/contra direction. Cited evidence is conflicting: some reports found no lateralizing value, whereas Wyllie et al. reported contralateral onset when deviation was forced, involuntary, and sustained. The cited Chassoux series restatement includes bilateral tonic-clonic seizures alongside oro-alimentary, salivation, dystonic, and head-deviation phenomena. The source reports head and eye deviation in 14% of patients and describes it as contralateral to seizure onset. Cited reports found ipsiversion in 50% and 48% of seizures with head/eye turning and concluded that forced turning at onset had no localizing or lateralizing value. The cited study reports 4/16 ipsiversion in a selected series; no cerebral reference frame is resolved. The cited series reported ipsiversion incidence of 3% in a larger series and 4/16 (25%) in a selected series. The cited series reports contraversive head and eye movements in 29% of 55 patients without a resolved cerebral reference frame. The review synthesis states that the ictal focus was contralateral to the direction of head turning in reviewed occipital-lobe epilepsy reports. The Figure 2 tracing shows rightward head deviation during the illustrated depth-recorded seizure. The primary result reports contralateral head deviation relative to the focus in 21/42 patients (50%). Both depth-studied patients had contralateral head and eye deviation. One patient had ipsilateral head deviation relative to the focus. The review restates that late forced head and eye version can be ipsilateral when initial contraversion ends during generalization, but can remain contralateral when initial contraversion persists. In the cited Wyllie series, late deviation was contralateral when initial contraversion persisted and ipsilateral when initial contraversion ended. The cited series reports late ipsiversion after an initial contraversive movement in 6 of 38 selected patients, always ipsilateral to the epilepsy focus. No lateralizing direction is reported for the visual-aura sequence. No hemisphere or body-side direction is reported. No lateralization axis information is reported for temporal psychomotor head turning. No lateralization axis information is reported for the head-turning study count. No lateralization axis information is reported for the 15-patient head-turning denominator. No lateralization axis information is reported for the 14-second head-turning onset value. No lateralization axis information is reported for the head-turning study comparison. No lateralization axis information is reported for the 15 lateral-TLE head-turning patients. No lateralization axis information is reported for the 31 mesial-TLE head-turning patients. No lateralization axis information is reported for the 41% head-and-eye-deviation frequency. The educational definition of head version gives no hemisphere or lateralizing direction. No lateralization axis information is reported for the 4.3% head-version frequency. The all-data head-version panel sample size N=597 provides no lateralization result. The non-topological head-version panel sample size N=151 provides no lateralization result. No lateralization axis information is reported for head version with temporal-lobe localization. No lateralization axis information is reported for head version with frontal-lobe localization. No lateralization axis information is reported for the conditional frontal head-version probability. No lateralization axis information is reported for the conditional temporal head-version probability. No lateralization axis information is reported for the frontal head-version odds interval. No lateralization axis information is reported for the temporal head-version odds interval. No cerebral lateralization axis information is reported for head version or orientation. No cerebral lateralization axis information is reported for the 25 head-orientation cases. No cerebral lateralization axis information is reported for the 15/60 head-orientation cases. The primary comparison reports no lateralization; head and/or eye deviation over the whole seizure course did not differ significantly across M, ML, and L temporal-onset groups. The primary result reports no lateralization; late head and/or eye deviation did not differ significantly across M, ML, and L temporal-onset groups. This finding provides no lateralization information. Frequency only; no lateralization is reported. No lateralization axis information is reported for the 0–50% head-eye-deviation range. No lateralization axis information is reported for the moderate head-eye-deviation association grade. No lateralization is reported. No seizure lateralization is reported. No directional head-eye side or hemisphere is reported. No lateralization axis information is reported for head-eye deviation versus affective/autonomic aura. No lateralization axis information is reported for head-eye deviation versus autonomic signs. This record provides no seizure lateralization. No lateralization evidence is reported. Figure 6 reports OR 7.7 for Affective/autonomic aura relative to Head-eye deviation, with no hemisphere or lateralization direction. Figure 6 reports OR 5.7 for Autonomic signs relative to Head-eye deviation, with no hemisphere or lateralization direction. No lateralizing direction is reported. No lateralizing semiology is reported for the tonic-clonic versus head-eye-deviation odds comparison. No lateralizing semiology is reported for the reciprocal head-eye-deviation versus tonic-clonic odds comparison. No independent lateralization axis record is present; the card concerns the timing of contraversive movement relative to onset region.

Source-defined result groups 29
Localization: TemporalObserved proportion 33.3%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization relative to EUD-Loc · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 37.5%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelycontralateral · ipsilateral versus contralateral head turning relative to EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: OccipitalObserved proportion 100.0%All reported · seizure spread beyond occipital lobe · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization relative to EUD-Loc · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion range 12.9–46.9% (median 29.9%)ipsilateral · ipsilateral versus contralateral head turning relative to EEG focus · seizure, with patient count in parentheses1 manuscript · 2 reported values · not pooled
Localization: Frontal / Occipital / Parietal / TemporalObserved proportion 86.5%frontal · onset regions and preceding ictal event categories · seizure; patient counts in parentheses in Table 21 manuscript · 1 reported value · not pooled
Localization: Frontal / Occipital / Parietal / TemporalObserved proportion 57.4%total · onset regions and preceding ictal event categories · seizure; patient counts in parentheses in Table 21 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Head turning · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given head version · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyipsilateral · ipsilateral versus contralateral head turning relative to EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 33.3%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 23.1%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given head version · localizing data point1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyDystonic posturing · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion range 14.7–53.1% (median 33.9%)contralateral · ipsilateral versus contralateral head turning relative to EEG focus · seizure, with patient count in parentheses1 manuscript · 2 reported values · not pooled
Localization: TemporalObserved proportion 50.0%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 50.0%All reported · no contralateral head deviation · patients1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%All reported · seizure spread beyond occipital lobe · cases1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.5%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Head turning · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 21

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 16 findings · 7 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • head versionTable 1 defines or exemplifies the the source's own semiology category “head version” as Forced head deviation over the shoulder or extreme head turn.PDF p.7, Table 1 Semiology descriptions and frequencies
  • head versionHead version comprised 4.3% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • head version; Figure 3 all-data subsetFigure 3 reports N = 597 for the all-data head version panel.PDF p.9, Figure 3 and caption
  • head version; Figure 3 non-topological subsetFigure 3 reports N = 151 for the non-topological head version panel.PDF p.9, Figure 3 and caption
  • head version; temporal lobeHead version implicated the temporal lobe in 46%.PDF p.8, Seizure semiology localizing values
  • head version; temporal lobeThe 95% CI for head version; temporal lobe was 36%–57%.PDF p.8, Seizure semiology localizing values
  • head version; frontal lobeHead version implicated the frontal lobe in 33%.PDF p.8, Seizure semiology localizing values
  • head version; frontal lobeThe 95% CI for head version; frontal lobe was 24%–41%.PDF p.8, Seizure semiology localizing values
  • head version; frontal lobeHead version had a probability of 0.33 for frontal localization in the non-topological estimate.PDF p.8, Relative localizing values
  • head version; frontal lobeThe interval for the head-version frontal localization given head version probability was 0.24–0.41.PDF p.8, Relative localizing values
  • head version; temporal lobeHead version had a probability of 0.46 for temporal localization in the non-topological estimate.PDF p.8, Relative localizing values
  • head version; temporal lobeThe interval for the head-version temporal localization given head version probability was 0.36–0.57.PDF p.8, Relative localizing values
  • head version; frontal lobeHead version had an OR of 0.9 for frontal localization relative to the EUD-Loc prior.PDF p.8, Relative localizing values of semiologies
  • head version; frontal lobeThe 95% CI for head version; frontal lobe was 0.7–1.2.PDF p.8, Relative localizing values of semiologies
  • head version; temporal lobeHead version had an OR of 1.21 for temporal localization relative to the EUD-Loc prior.PDF p.8, Relative localizing values of semiologies
  • head version; temporal lobeThe 95% CI for head version; temporal lobe was 0.9–1.6.PDF p.8, Relative localizing values of semiologies
Reported values
  • head version 4.3%head versionPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • head version; temporal lobe 46%head version; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • head version; frontal lobe 33%head version; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • probability 0.33head version; frontal lobeProbability · non-topological localizing data pointsPDF p.8, Relative localizing values
  • probability 0.46head version; temporal lobeProbability · non-topological localizing data pointsPDF p.8, Relative localizing values
  • OR 0.9head version; frontal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 1.21head version; temporal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • head version and ictal SPECT hyperperfusionThe source reports an ictal SPECT study in which head version was related to multiple hyperperfusion areas in frontal, temporal, and basal ganglia regions.PDF p.8, Motor signs
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • head version or orientationHead version or orientation was reported in 30% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Head orientation (Table 3)Table 3 reports head orientation in 25 cases (30%), more during propagation.PDF p.6, Table 3
  • Head orientation (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports head orientation in 15 cases (25%).PDF p.7, Table 4
Reported values
  • 30% head orientationhead version or orientationPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 25 cases (30%)Head orientation (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 15/60 (25%)Head orientation (Table 4)Percentage · n/N 15/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 31 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • head-eye deviation; contralateral to seizure onsetHead and eye deviation occurred in 14% of patients and was contralateral to seizure onset.PDF p.9, Objective symptomatology
  • dystonic posturing; head-eye deviation; tonic-clonic manifestationsThe review links dystonic posturing, head/eye deviation, and tonic-clonic manifestations to propagation rather than the earliest seizure phase.PDF p.11, Anatomical and clinical correlations
  • head-eye deviationThe source reports a frequency of 14% for head-eye deviation.PDF p.13, Table 3
  • head-eye deviation; reported frequency rangeThe source reports a frequency range of 0–50% for head-eye deviation.PDF p.13, Table 3
  • head-eye deviation; ACC association gradeTable 3 assigns the source's Moderate overall association grade to head-eye deviation.PDF p.13, Table 3
  • head-eye deviation; Figure 4 rateFigure 4 displays a 14% rate for head-eye deviation.PDF p.10, Figure 4
  • pairwise OR: Head-eye deviation relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Autonomic signsFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Facial expression changeFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.3 for Head-eye deviation relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.4 for Head-eye deviation relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.6 for Head-eye deviation relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Dystonic posturingFigure 6 reports an odds ratio of 0.7 for Head-eye deviation relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Head-eye deviationFigure 6 reports an odds ratio of 9.6 for Vocalization/verbalization relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Head-eye deviationFigure 6 reports an odds ratio of 9.1 for Hypermotor-complex motor behavior relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Head-eye deviationFigure 6 reports an odds ratio of 7.7 for Affective/autonomic aura relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Head-eye deviationFigure 6 reports an odds ratio of 5.7 for Autonomic signs relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Head-eye deviationFigure 6 reports an odds ratio of 5.2 for Facial expression change relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Head-eye deviationFigure 6 reports an odds ratio of 4.6 for Motor (gestural) automatisms relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Head-eye deviationFigure 6 reports an odds ratio of 3.4 for Loss of consciousness relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Head-eye deviationFigure 6 reports an odds ratio of 2.7 for Post-ictal confusion/behavior change disinhibition relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Head-eye deviationFigure 6 reports an odds ratio of 1.6 for Chapeau de gendarme relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Head-eye deviationFigure 6 reports an odds ratio of 1.5 for Dystonic posturing relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Head-eye deviationFigure 6 reports an odds ratio of 0.9 for Laughter relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Head-eye deviationFigure 6 reports an odds ratio of 0.6 for Oro-alimentary automatisms relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Head-eye deviationFigure 6 reports an odds ratio of 0.6 for Tonic-clonic relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Head-eye deviationFigure 6 reports an odds ratio of 0.4 for F to BTC relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to LaughterFigure 6 reports an odds ratio of 1.5 for Head-eye deviation relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.7 for Head-eye deviation relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Tonic-clonicFigure 6 reports an odds ratio of 2.8 for Head-eye deviation relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to F to BTCFigure 6 reports an odds ratio of 2.8 for Head-eye deviation relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 14%head-eye deviation; contralateral to seizure onsetPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • 14% (frequency range 0–50%)head-eye deviationPercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.13, Table 3
  • 14%head-eye deviation; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.10, Figure 4
  • OR 0.1pairwise OR: Head-eye deviation relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Head-eye deviation relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Head-eye deviation relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Head-eye deviation relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Head-eye deviation relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Vocalization/verbalization relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.1pairwise OR: Hypermotor-complex motor behavior relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.7pairwise OR: Affective/autonomic aura relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.7pairwise OR: Autonomic signs relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.2pairwise OR: Facial expression change relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.6pairwise OR: Motor (gestural) automatisms relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.4pairwise OR: Loss of consciousness relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Chapeau de gendarme relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Dystonic posturing relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Laughter relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Oro-alimentary automatisms relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Tonic-clonic relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: F to BTC relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Head-eye deviation relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Head-eye deviation relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.8pairwise OR: Head-eye deviation relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.8pairwise OR: Head-eye deviation relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 10 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Head turningTable 3 reports 1 studies assessing Head turning.PDF p.6, Table 3
  • Head turningTable 3 reports 15 patients assessed for Head turning.PDF p.6, Table 3
  • Head turningTable 3 reports 60% as the percentage range or value for Head turning; the overall association grade is Low.PDF p.6, Table 3
  • Head turningTable 3 reports 1 study with onset timing for Head turning.PDF p.6, Table 3
  • Head turningTable 3 reports an onset latency of 14 s for Head turning.PDF p.6, Table 3
  • Head turning; lateral versus mesial comparisonTable 5 reports 1 studies comparing Head turning in lateral and mesial TLE.PDF p.9, Table 5
  • Head turning; lateral TLE patient denominatorTable 5 reports 15 lateral-TLE patients assessed for Head turning.PDF p.9, Table 5
  • Head turning; mesial TLE patient denominatorTable 5 reports 31 mesial-TLE patients assessed for Head turning.PDF p.9, Table 5
  • Head turning; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 60% for Head turning.PDF p.9, Table 5
  • Head turning; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 64.5% for Head turning.PDF p.9, Table 5
Reported values
  • 60%Head turningPercentage · Lateral temporal epilepsy patients assessed for Head turning · ictalPDF p.6, Table 3
  • median onset latency 14 sHead turningMedian · Lateral temporal epilepsy study reporting onset timing for Head turning · ictal onsetPDF p.6, Table 3
  • 60%Head turning; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Head turning · Lateral TLE patients assessed for Head turning · ictalPDF p.9, Table 5
  • 64.5%Head turning; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Head turning · Mesial TLE patients assessed for Head turning · ictalPDF p.9, Table 5
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal head deviation in cited studiesThe current paper reports conflicting cited evidence on ictal head deviation: Robillard et al. (1983) and Ochs et al. (1984) indicated no lateralizing value, whereas Wyllie et al. (1986) found seizure onset lateralized to the contralateral hemisphere when head and eye deviation was defined as unquestionably forced, involuntary, and sustained.PDF p.6, Discussion, tonic-head-deviation paragraph
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 2 findings · 4 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Head/Body turnHead/Body turn semiology occurred in 3/61 individuals (5%) as initial semiology and 6/61 (10%) in the combined set-of-semiology.PDF p.5, Table 2
  • Head versionHead-version semiology occurred in 1/61 individuals (2%) as initial semiology and 12/61 (20%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Combined 6/61 (10%)Head/Body turnPercentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Initial 3/61 (5%)Head/Body turnPercentage · n/N 3/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Initial 1/61 (2%)Head versionPercentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 12/61 (20%)Head versionPercentage · n/N 12/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Head turningTable 3 associates head turning with exhaustion of the epileptogenic hemisphere, propagation to basal ganglia, or neglect of contralateral space and lists ipsilateral lateralisation.PDF p.4, Table 3
  • Head versionTable 3 associates head version during secondary generalized tonic-clonic seizures with premotor area (BA 6 and 8) and contralateral lateralisation.PDF p.4, Table 3
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfNarrative, educational, or cited context · 1 finding
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • head/eye versionThe methods section characterizes version as a well-recognized lateralizing sign with good interobserver agreement and high positive predictive value for the side of ictal onset.PDF p.2, Methods—definition and comparison of version
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Late ipsiversionThe review identifies ipsilateral forced head and eye version at the end of a generalized tonic-clonic seizure as a distinct lateralizing sign, especially when an initial contraversion ends during the generalized phase; if initial contraversion persists, late version can remain contralateral.PDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversionIn Wyllie et al., a study of 61 seizures in 27 patients with version, 9 patients had a late versive movement; when initial contraversion persisted, late deviation was contralateral in 3 patients, and when initial contraversion ended, late version was ipsilateral in 6 patients.PDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversionChee et al. found late ipsiversion after an initial contraversive movement before generalization in 6 of 38 selected patients, always ipsilateral to the epilepsy focus as determined by ictal EEG.PDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
Reported values
  • 6 patients had ipsilateral late versionLate ipsiversionCount · 27 patients with 61 seizures and version; 9 patients with late versive movement · initial contraversion ended · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • 3 patients had contralateral late deviationLate ipsiversionCount · 27 patients with 61 seizures and version; 9 patients with late versive movement · initial contraversion persisted · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • 61 seizuresLate ipsiversionCount · 27 patients with 61 seizures and version; 9 patients with late versive movement · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • 9/27 patients had late movementLate ipsiversionPercentage · n/N 9/27 · 27 patients with 61 seizures and version; 9 patients with late versive movement · late versive movement · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversion in 6/38 patientsLate ipsiversionPercentage · n/N 6/38 · 38 selected patients with frontal and temporal lobe epilepsy; 6 with late ipsiversion · Before or at the end of generalizationPDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversion ipsilateral to epilepsy focus 6/6Late ipsiversionPercentage · n/N 6/6 · 38 selected patients with frontal and temporal lobe epilepsy; 6 with late ipsiversion · Patients with late ipsiversion · Before or at the end of generalizationPDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 7 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • head and/or eyes deviationHead and/or eyes deviation over the whole seizure course did not differ significantly across M, ML, and L groups.PDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • late head and/or eyes deviationLate head and/or eyes deviation did not differ significantly across M, ML, and L groups.PDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
Reported values
  • ML=9/18 (50%)head and/or eyes deviationPercentage · n/N 9/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • L=5/13 (38.5%)head and/or eyes deviationPercentage · n/N 5/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • M=9/24 (37.5%)head and/or eyes deviationPercentage · n/N 9/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • p=0.69head and/or eyes deviationP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • 6/18 (33.3%)late head and/or eyes deviationPercentage · n/N 6/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
  • 8/24 (33.3%)late head and/or eyes deviationPercentage · n/N 8/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
  • 3/13 (23.1%)late head and/or eyes deviationPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding · 4 reported values
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • generalized epilepsy with ictal head deviationIn the illustrated adult case, two recorded bilateral tonic-clonic seizures began with head deviation to the left, but the EEG began with generalized bifrontally predominant rhythmic 12 Hz activity and 4-4.5 Hz spike-and-wave activity; an earlier witnessed event reportedly turned to the right, and the case was diagnosed as adult-onset idiopathic generalized epilepsy, illustrating that head direction at onset is not by itself proof of focal epilepsy.PDF p.380; PDF p.381; PDF p.386
Reported values
  • 4–4.5 Hz spike-and-wave activitygeneralized epilepsy with ictal head deviationRange · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
  • two recorded bilateral tonic-clonic seizuresgeneralized epilepsy with ictal head deviationCount · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · illustrated adult case · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
  • up to 60% of primary generalized seizures may have head deviationgeneralized epilepsy with ictal head deviationPercentage · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · primary generalized seizures · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
  • generalized bifrontally predominant rhythmic 12 Hz activitygeneralized epilepsy with ictal head deviationFrequency · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • head turns to the right, detaches from the neck, and sees himself from outsideMCC stimulation S12 in Patient 7 elicited a composite body-perception experience in which the head turned to the right, was felt likely to detach from the neck after a sensation that it would explode, and was followed by a visual hallucination of seeing himself from outside from all angles without a secondary body.PDF p.5, Section 3.1 Clinical effects; PDF p.6, continuation of Section 3.1; PDF p.7, Table 2
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 2 findings · 9 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • head versionIn the unilateral TLE cohort, head version occurred only on the side contralateral to the EEG seizure focus.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • head turningHead turning occurred in both directions relative to the EEG seizure focus, with 15 seizures ipsilateral and 17 contralateral.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
Reported values
  • 6 patientshead versionCount · n/N 6/19 · 19 patients with unilateral TLE; head version occurred in 6 patients · patients with head version · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 0 ipsilateral seizureshead versionCount · n/N 0/116 · 19 patients with unilateral TLE; head version occurred in 6 patients · ipsilateral to EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 14 contralateral seizures (12% of all 116 seizures)head versionPercentage · n/N 14/116 · 19 patients with unilateral TLE; head version occurred in 6 patients · contralateral to EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 17 contralateral seizures (53.1% of 32 head-turning seizures)head turningPercentage · n/N 17/32 · 19 patients with unilateral TLE; head turning occurred in 11 patients according to Table 1 patient counts · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
  • 17 contralateral seizures (15% of all 116)head turningPercentage · n/N 17/116 · 19 patients with unilateral TLE; head turning occurred in 11 patients according to Table 1 patient counts · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
  • 5 patients with ipsilateral head turninghead turningCount · 19 patients with unilateral TLE; head turning occurred in 11 patients according to Table 1 patient counts · ipsilateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
  • 15 ipsilateral seizures (46.9% of 32 head-turning seizures)head turningPercentage · n/N 15/32 · 19 patients with unilateral TLE; head turning occurred in 11 patients according to Table 1 patient counts · ipsilateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
  • 6 patients with contralateral head turninghead turningCount · 19 patients with unilateral TLE; head turning occurred in 11 patients according to Table 1 patient counts · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
  • 15 ipsilateral seizures (13% of all 116)head turningPercentage · n/N 15/116 · 19 patients with unilateral TLE; head turning occurred in 11 patients according to Table 1 patient counts · ipsilateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.5, Discussion
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 6 findings · 4 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • contraversive head and eye movement in Ludwig and Ajmone-MarsanThe source reports contraversive head and eye movements in 29% of 55 patients in the cited Ludwig and Ajmone-Marsan series.PDF p.20, Discussion
  • focus contralateral to direction of head turningThe source states that reviewed reports of occipital lobe epilepsy found the ictal focus contralateral to the direction of head turning.PDF p.20, Discussion
  • head deviation in Fig. 2The Figure 2 tracing labels head deviation to the right during the illustrated depth-recorded seizure.PDF p.14, Fig. 2
  • contralateral head deviationContralateral head deviation occurred in 21 of 42 patients.PDF p.6, Results, Non-visual manifestations
  • contralateral head and eye deviation with occipital-localized seizureTwo depth-studied patients had contralateral head and eye deviation while the seizure remained localized to the occipital lobe.PDF p.6, Results, Non-visual manifestations
  • ipsilateral head deviationOne patient had ipsilateral head deviation.PDF p.6, Results, Non-visual manifestations
Reported values
  • 29% of 55 patientscontraversive head and eye movement in Ludwig and Ajmone-MarsanPercentage · cited Ludwig and Ajmone-Marsan occipital epilepsy series · ictal manifestationPDF p.20, Discussion
  • 21/42 (50%) patientscontralateral head deviationPercentage · n/N 21/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.6, Results, Non-visual manifestations
  • 2 casescontralateral head and eye deviation with occipital-localized seizureCount · n/N 2/2 · two depth-studied cohort patients · ictal onset and early evolutionPDF p.6, Results, Non-visual manifestations
  • 1 patientipsilateral head deviationCount · n/N 1/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.6, Results, Non-visual manifestations
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • head and eye deviationHead and eye deviation occurred in 41% of patients.PDF p.4, Results, Other seizure characteristics
Reported values
  • 41%head and eye deviationPercentage · 82-patient parietal epilepsy series · ictal motor or oculomotor phasePDF p.4, Results, Other seizure characteristics
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • Chassoux cohort; oro-alimentary automatisms; salivation; dystonic signs; head deviation; bilateral tonic-clonic seizuresThe review restates that Chassoux et al. described 33 patients with oro-alimentary automatisms, salivation, motor signs including dystonia and head deviation, and bilateral tonic-clonic seizures in the medio-lateral context.PDF p.4, Medio-lateral temporal origin
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfNarrative, educational, or cited context · 1 finding
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • psychomotor semiology: head turningTypical temporal psychomotor semiology included head turning.PDF p.4, Seizure semiology on video-EEG recording
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 5 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • dorsal parietal to premotor motor evolutionThe authors link rapid motor evolution after visual aura to propagation to dorsal parietal nodes and then premotor areas.PDF p.13, Phenotype III discussion
  • head and eye deviation to the leftTable 2 records head and eye deviation to the left in a seizure that followed left-upper-limb tonic posturing.PDF p.6, Table 2 Case 1 Sz1
  • head-eye-body deviation to the rightTable 2 records head, eye, and body deviation to the right in Case 5.PDF p.6, Table 2 Case 5
  • visual aura to head-eye deviation or pursuitIn Phenotype III, a visual aura rapidly progresses to head-eye deviation or eye pursuit.PDF p.9, Phenotype III; PDF p.13, Phenotype III discussion
wyllie1986.pdfStructured design not resolved · 4 findings · 45 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • ipsiversion in Ochs and Robillard seriesThe current paper reports that Ochs et al. and Robillard et al. found ipsiversion in 50% and 48%, respectively, of seizures with head and eye turning and concluded that forced head turning at clinical seizure onset had no localizing or lateralizing value.PDF p.3, discussion paragraph comparing Ochs and Robillard; PDF p.5, references 31-32
  • ipsiversion in Ajmone Marsan and Abraham seriesThe current paper reports that Ajmone Marsan and Abraham found ipsiversion in 4 of 16 pentylenetetrazol-induced seizures with version and lateralized ictal EEG, but cautions that the seizures were selected to illustrate other electroclinical features and the 25% incidence may not have been representative.PDF p.4, paragraph beginning “Ajmone Marsan and Abraham”; PDF p.6, reference 39
  • ipsiversion in Ajmone Marsan and Ralston seriesThe current paper reports a 3% incidence of ipsiversion in a larger series of pentylenetetrazol-induced seizures by Ajmone Marsan and Ralston and suggests that this may have been a more accurate assessment than the 25% incidence in the selected Ajmone Marsan and Abraham series.PDF p.4, paragraph comparing the 3% and 25% incidences; PDF p.6, reference 38
  • ictal events preceding contraversive head and eye movementThirty-five of 61 versive seizures (57%) began with the versive movement; these were predominantly frontal-onset (91%) and none was temporal-onset, whereas the other versive seizures were preceded by quiet staring or staring with automatisms as detailed in Table 2.PDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
Reported values
  • 50%ipsiversion in Ochs and Robillard seriesPercentage · Seizures with head and eye turning in the cited Ochs report; cohort details not reported here · Ochs et al. · Head turning at clinical seizure onsetPDF p.3, discussion paragraph comparing Ochs and Robillard; PDF p.5, references 31-32
  • 48%ipsiversion in Ochs and Robillard seriesPercentage · Seizures with head and eye turning in the cited Robillard report; cohort details not reported here · Robillard et al. · Head turning at clinical seizure onsetPDF p.3, discussion paragraph comparing Ochs and Robillard; PDF p.5, references 31-32
  • Ipsiversion 4 of 16 seizures (25%)ipsiversion in Ajmone Marsan and Abraham seriesPercentage · n/N 4/16 · Pentylenetetrazol-induced seizures selected to illustrate other electroclinical features in the cited series · Ictal head and eye turningPDF p.4, paragraph beginning “Ajmone Marsan and Abraham”; PDF p.6, reference 39
  • Ipsiversion incidence 3% in larger cited seriesipsiversion in Ajmone Marsan and Ralston seriesPercentage · Larger pentylenetetrazol-induced seizure series cited by the current paper · Larger Ajmone Marsan and Ralston series · Ictal head and eye turningPDF p.4, paragraph comparing the 3% and 25% incidences; PDF p.6, reference 38
  • Ipsiversion incidence 4/16 (25%) in selected cited seriesipsiversion in Ajmone Marsan and Ralston seriesPercentage · n/N 4/16 · Larger pentylenetetrazol-induced seizure series cited by the current paper · Selected Ajmone Marsan and Abraham series · Ictal head and eye turningPDF p.4, paragraph comparing the 3% and 25% incidences; PDF p.6, reference 38
  • frontal all versive seizures: 37 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by staring with automatisms: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by staring with automatisms: 14 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal all versive seizures: 10 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by quiet staring: 5 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by quiet staring: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by quiet staring: 1 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by quiet staring: 2 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by quiet staring: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by staring with automatisms: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total all versive seizures: 27 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by staring with automatisms: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total all versive seizures: 61 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total version at onset 35/61 (57%)ictal events preceding contraversive head and eye movementPercentage · n/N 35/61 · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal no preceding ictal event; version at onset: 1 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal no preceding ictal event; version at onset: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total no preceding ictal event; version at onset: 12 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by quiet staring: 8 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by staring with automatisms: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by quiet staring: 8 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by quiet staring: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by quiet staring: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal no preceding ictal event; version at onset: 10 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by quiet staring: 5 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital no preceding ictal event; version at onset: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal no preceding ictal event; version at onset: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by staring with automatisms: 18 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal all versive seizures: 20 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal all versive seizures: 2 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by staring with automatisms: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital all versive seizures: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital no preceding ictal event; version at onset: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal all versive seizures: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal all versive seizures: 14 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal version at onset 32/37 (91%)ictal events preceding contraversive head and eye movementPercentage · n/N 32/37 · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal no preceding ictal event; version at onset: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by staring with automatisms: 18 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by staring with automatisms: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by staring with automatisms: 14 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital all versive seizures: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion

21 contributing manuscripts; source-reported values remain separate and are not pooled.

clonic jerking (rhythmic, somatotopic distribution)Source terms: Focal clonic jerkingReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere23 manuscripts · 41 findings · 94 reported values
Weighted evidence supportevidence weight 44.62 across 23 manuscripts · 2 manuscript weight pending · 6 independent primary study · 2 structured design not resolved · 3 systematic review or meta-analysis · 12 narrative, educational, or cited context

Case 17 had right mouth, face, neck, and upper-limb clonic movements with a source-described left LG/FuG/PCu/SPL pathway. Ipsilateral, contralateral, and bilateral clonic motor forms occurred in both TL and T+ groups, without significant between-group differences. All 24 seizures with clonic jerking were contralateral to the EEG seizure-onset focus; no ipsilateral events were reported. The review describes early upper-limb and orofacial elementary motor signs as mainly contralateral tonic, clonic, or dystonic manifestations. At onset, 8/21 fronto-opercular epilepsy patients had contralateral brachial tonic, clonic, or dystonic posturing. Four of 12 prefrontal-operculum patients had contralateral brachial tonic, clonic, or dystonic posturing at onset. Four of nine precentral Rolandic-operculum patients had contralateral brachial tonic, clonic, or dystonic posturing at onset. This row restates the Fisher exact test for the contralateral brachial combined-sign comparison. The review states that focal clonic activity may have lateralizing value without specifying a direction. Cerebral lateralization: these signs are contralateral to seizure onset; target lobe is not differentiated by these signs alone. Unilateral clonic activity was contralateral to the epileptogenic zone with reported PPV 100% and kappa 0.81. The last clonic jerk was predominantly ipsilateral to the epileptogenic zone, with 86% overall PPV and kappa 0.85. The review table lists focal clonic jerking contralateral to a perirolandic focus. Focal motor clonic activity occurred contralateral to the epileptogenic zone in 57% of the parietal-epilepsy cohort. The cited series includes delayed motor signs, including source-described contralateral dystonia, without a reported onset-side direction. The review synthesis describes early upper-extremity dystonic and clonic activity as contralateral to the temporal seizure focus. The cited table lists clonic semiology as contralateral. The review describes unilateral clonic seizures as highly contralateralizing, while separately noting possible ipsilateral terminal paradoxical clonus. Longer terminal clonus in a secondarily generalized tonic-clonic seizure is described as ipsilateral to the epileptogenic focus. In this case, right head version and right-arm extension were contralateral to left onset, while the left last clonic jerk was ipsilateral to left onset. The review describes SSMA seizures as usually involving bilateral clonic activity with tonic posturing. Late focal jerking was contralateral to seizure onset and occurred more often in left temporal seizures (22/73) than right temporal seizures (6/54), p=0.02. The co-occurring progression pattern was described as more frequent in left temporal seizures. The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. The review describes head/eye deviation as suggesting an ipsilateral focus and other listed unilateral motor signs as usually indicating a contralateral focus. Unilateral clonic activity usually points contralaterally to the seizure focus, with ipsilateral exceptions; a cited frontal cohort estimate gave 83% contralateral direction. In a cited seizure-free frontal-lobe surgical cohort, unilateral clonic activity was contralateral in 10 patients and ipsilateral in 2. The review describes the last clonic jerk at an asymmetric generalized-seizure ending as usually ipsilateral to the seizure-onset hemisphere. Among 30 patients with asymmetric ending, the last jerk was ipsilateral to onset in 25, with PPV 83.3%. The focal clonic head jerks have no reported movement direction; bilateral applies only to the recorded pathway. No lateralizing information is supplied. No lateralization information is reported. No lateralizing direction is reported for the tonic-to-clonic propagation description. The cited anterior-versus-posterior insular comparison provides no lateralizing information.

Source-defined result groups 44
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · no focal motor clonic activity · patients1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyparietal · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyIpsilateral to EEG seizure focus · Contralateral to EEG seizure focus · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyoverall · incorrect direction · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Left hemisphereObserved proportion 30.1%LTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelytemporal · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyfrontal · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Left hemisphereObserved proportion 11.1%RTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 20.7%Contralateral to EEG seizure focus · seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 55.6%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · sign-positive lateralization1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 42.9%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 36.8%Contralateral to EEG seizure focus · Ipsilateral to EEG seizure focus · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 23

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 8 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • clonic motor signsClonic motor signs did not differ significantly between TL and T+ groups across ipsilateral, contralateral, and bilateral forms.PDF p.6, Table 2
Reported values
  • TL 25.4%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • TL 18.6%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 13%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • T+ 13%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 33.9%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 21.7%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • T+ 21.7%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 20.3%clonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • delayed motor signs (Duchowny study)The cited Duchowny series is described as having behavioral arrest and delayed motor signs including version, contralateral dystonia, clonic jerks, and automatisms.PDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Focal clonic jerkingFocal clonic jerking is listed as localizing to a contralateral perirolandic focus.PDF p.4, Table 2
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • tonic posturing; clonic jerksThe source describes clonic jerks following focal tonic manifestations as likely reflecting propagation from the SMA to the primary motor area.PDF p.7, Discussion
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionThe review describes unilateral clonic movements, unilateral tonic or dystonic posturing, and early forced head version as robust lateralising motor signs with positive predictive value greater than 80%, and states that these signs are contralateral to the side of seizure onset.PDF p.10, Lateralising signs
  • head version; figure-of-4 sign; last clonic jerkIn video case 7, a 33-year-old man with left temporal hypometabolism had head version to the right followed by right-arm extension in a figure-of-4 posture, indicating left hemispheric onset; in one seizure the last clonic jerk was on the left, also pointing to left onset, while ictal EEG was non-localisable in one seizure and lateralised left in another.PDF p.10, Video case 7
Reported values
  • positive predictive value >80%unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionPositive predictive value · focal seizure literature · ictal onset/early ictalPDF p.10, Lateralising signs
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 2 findings · 27 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Unilateral clonicIn the surgical cohort, unilateral clonic activity was reported as a contralateral lateralizing sign with 100% PPV and inter-observer kappa of 0.81.PDF p.3, Table 1; PDF p.3, §5.1
  • Last clonic jerkThe last clonic jerk was reported as an ipsilateral lateralizing sign with 86% PPV and inter-observer kappa of 0.85 overall.PDF p.3, Table 1; PDF p.3, §5.1
Reported values
  • inter-observer kappa 0.81Unilateral clonicKappa · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 3 patients in Occipital lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Occipital lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 12 patients overallUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Overall · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 17 seizures overallUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Overall · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 6 seizures in Occipital lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Occipital lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 patients in Temporal lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Temporal lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 seizures in Temporal lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Temporal lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 seizures in Parietal lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Parietal lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • PPV 100% (contralateral)Unilateral clonicPositive predictive value · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 patients in Parietal lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Parietal lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 5 patients in Frontal lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Frontal lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 7 seizures in Frontal lobe epilepsyUnilateral clonicCount · Sign-positive occurrences included 17 seizures in 12 patients overall; temporal 2 seizures/2 patients, frontal 7/5, parietal 2/2, and occipital 6/3. · Frontal lobe epilepsy · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 patientsLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · temporal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 3 seizuresLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · frontal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 0 seizuresLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · occipital · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 2 seizuresLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · temporal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 86% overall PPVLast clonic jerkPositive predictive value · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · overall · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 2 patientsLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · parietal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 7 patientsLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · overall sign-positive occurrences · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 2 seizuresLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · parietal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 7 seizuresLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · overall sign-positive occurrences · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 0 patientsLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · occipital · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 67% PPVLast clonic jerkPositive predictive value · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · frontal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 100% PPVLast clonic jerkPositive predictive value · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · temporal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • kappa 0.85Last clonic jerkKappa · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · overall · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 3 patientsLast clonic jerkCount · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · frontal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
  • 100% PPVLast clonic jerkPositive predictive value · Sign-positive occurrences included 7 seizures in 7 patients overall; temporal 2/2, frontal 3/3, parietal 2/2, and occipital 0/0. · parietal · Ictal or terminal ictal motor phase.PDF p.3, Table 1; PDF p.3, §5.1
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 2 findings · 3 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Contralateral focal jerkingLate contralateral focal jerking was more common in LTL than RTL seizures.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • Co-occurrence of tonic head deviation, focal jerking, and secondary generalizationThe authors state that tonic head deviation, focal jerking, and secondarily generalized seizures often occurred together and probably represented further spread of the seizure discharge.PDF p.6, Discussion
Reported values
  • p=0.02Contralateral focal jerkingP value · RTL seizure group, n=54, versus LTL seizure group, n=73 · Late ictal phasePDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • RTL 6/54 seizures (11%)Contralateral focal jerkingPercentage · n/N 6/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · Late ictal phasePDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • LTL 22/73 seizures (30%)Contralateral focal jerkingPercentage · n/N 22/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · Late ictal phasePDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • contralateral upper-extremity dystonic and clonic activityIn a series comparing mesial and neocortical temporal seizure semiology, automatisms and dystonic posturing of the contralateral upper extremity early in the seizure were more common in mesial temporal epilepsy, whereas early clonic activity of the contralateral upper extremity or facial grimacing suggested neocortical temporal origin.PDF p.4, temporal seizure semiology paragraph beginning "In series comparing mesial"
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • clonic seizuresClonic activity reflects propagation over the motor cortex when it spreads from distal to proximal regions. In FLE it tends to occur early with consciousness preserved; in TLE it usually involves the face or upper extremity after an automotor phase; parietal-origin seizures are typically preceded by somatosensory disturbance, occipital-origin seizures by visual auras or versive head/eye movements, and SSMA seizures by bilateral clonic activity with tonic posturing.PDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
Reported values
  • Clonic contractions recur at 0.2–5 per secondclonic seizuresCount · patients with focal epilepsy and focal epilepsy subgroups · ictal sequencePDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • unilateral dystonic posturing, head/eye deviation, clonic or tonic movements, and hypokinesiaSecondary motor signs related to propagation outside the temporal lobe may lateralize the seizure-onset zone: unilateral dystonic posturing is usually contralateral to the focus, head or eye deviation suggests an ipsilateral focus, and other unilateral clonic or tonic movements or limb immobility usually indicate a contralateral focus.PDF p.8, Focal impaired awareness seizures
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 9 findings · 6 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; orofacial; brachial; tonic; clonic; dystonicElementary motor symptoms were described as early, mainly involving the orofacial regions and/or arms; arm manifestations were mainly contralateral tonic, clonic, or dystonic seizures or postures.PDF p.6, Anatomical and clinical correlations; PDF p.8, Discussion
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 8/21 (38%) for Brachial contralateral (tonic and/or clonic or dystonic posture); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Moderate.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 4/12 patients with Brachial contralateral (tonic and/or clonic or dystonic posture) in the prefrontal operculum group.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 4/9 patients with Brachial contralateral (tonic and/or clonic or dystonic posture) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Fisher's exact comparison of Brachial contralateral (tonic and/or clonic or dystonic posture) between the prefrontal and precentral Rolandic operculum groups has p=0.673.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 9/21 (43%) for Elementary motor: orofacial (tonic and/or clonic, grimace); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 4/12 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the prefrontal operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 5/9 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Fisher's exact comparison of Elementary motor: orofacial (tonic and/or clonic, grimace) between the prefrontal and precentral Rolandic operculum groups has p=0.396.PDF p.7, Table 2
Reported values
  • 8/21 (38%)Brachial contralateral (tonic and/or clonic or dystonic posture)Percentage · n/N 8/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsBrachial contralateral (tonic and/or clonic or dystonic posture)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 4/9 patientsBrachial contralateral (tonic and/or clonic or dystonic posture)Proportion · n/N 4/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
  • 9/21 (43%)Elementary motor: orofacial (tonic and/or clonic, grimace)Percentage · n/N 9/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 5/9 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 5/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • clonic motor manifestationClonic motor manifestations are among the clinical manifestations reported with insular seizures.PDF p.2, Clinical Features
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 2 findings · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • focal clonic activityThe authors state that focal clonic activity can be characteristic of frontal-lobe involvement and may have lateralising value, but does not always localise to a specific frontal-lobe region.PDF p.5, Discussion
  • Focal motor (clonic)Focal motor (clonic) semiology occurred in 2/61 individuals (3%) as initial semiology and 7/61 (11%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 2/61 (3%)Focal motor (clonic)Percentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 7/61 (11%)Focal motor (clonic)Percentage · n/N 7/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Clonic seizure patternTable 2 associates clonic semiology with primary motor cortex, premotor cortex, and SSMA and lists contralateral lateralisation.PDF p.3, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 4 findings · 13 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Unilateral clonic activityThe review presents unilateral clonic activity as a frequent lateralizing sign that usually points contralaterally to the seizure focus, while noting that ipsilateral jerking can occur, in part through the last-clonic-jerk phenomenon.PDF p.4, section 3.3 Unilateral clonic activity; PDF p.5, section 3.3.1 Mechanism; PDF p.12, Table 1
  • Unilateral clonic activityJanszky et al. found unilateral clonic activity in 33% of patients with frontal lobe epilepsy rendered seizure free after surgery; clonic activity was ipsilateral to the seizure focus in 2 and contralateral in 10 patients.PDF p.4, section 3.3 Unilateral clonic activity
  • Last clonic jerk and asymmetric endingThe review describes asymmetric ending of a generalized tonic-clonic seizure, particularly a last clonic jerk ipsilateral to the hemisphere of seizure onset, as a lateralizing sign with high reported observer agreement in the cited series.PDF p.5, section 3.4 Significance of last clonic jerk
  • Last clonic jerkLeutmezer et al. investigated 70 patients with mesial temporal lobe epilepsy due to hippocampal sclerosis and Engel class I or II outcome after 1 year; asymmetric ending occurred in 30 of 43 patients with secondary generalized tonic-clonic seizures, and the last jerk was ipsilateral to seizure onset in 25 of 30, with a positive predictive value of 83.3%.PDF p.5, section 3.4 Significance of last clonic jerk
Reported values
  • 44.4%Unilateral clonic activityPercentage · Patients with focal or frontal lobe epilepsy · frontal lobe epilepsy · Ictal clonic phasePDF p.12, Table 1
  • 56%Unilateral clonic activityPercentage · Patients with focal or frontal lobe epilepsy · epileptic seizures · Ictal clonic phasePDF p.4, section 3.3 Unilateral clonic activity; PDF p.5, section 3.3.1 Mechanism; PDF p.12, Table 1
  • 83%Unilateral clonic activityPercentage · Patients with focal or frontal lobe epilepsy · frontal lobe epilepsy patients with unilateral clonic activity · Ictal clonic phasePDF p.12, Table 1
  • 33% of patients had unilateral clonic activityUnilateral clonic activityPercentage · Patients with frontal lobe epilepsy rendered seizure free after epilepsy surgery · frontal-lobe epilepsy seizure-free surgical cohort · Ictal clonic phasePDF p.4, section 3.3 Unilateral clonic activity
  • 2 patients ipsilateralUnilateral clonic activityCount · Patients with frontal lobe epilepsy rendered seizure free after epilepsy surgery · ipsilateral · Ictal clonic phasePDF p.4, section 3.3 Unilateral clonic activity
  • 10 patients contralateralUnilateral clonic activityCount · Patients with frontal lobe epilepsy rendered seizure free after epilepsy surgery · contralateral · Ictal clonic phasePDF p.4, section 3.3 Unilateral clonic activity
  • Table 1 does not list this signLast clonic jerk and asymmetric endingCount · n/N 25/30 · Patients with mesial or temporal lobe epilepsy and generalized tonic-clonic seizures · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • specific series are reported in F012 and F013Last clonic jerk and asymmetric endingCount · n/N 25/30 · Patients with mesial or temporal lobe epilepsy and generalized tonic-clonic seizures · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 43 patientsLast clonic jerkCount · n/N 43/70 · 70 patients with mesial temporal lobe epilepsy due to hippocampal sclerosis and Engel class I or II outcome after 1 year; 43 with secondary generalized tonic-clonic seizures · secondary generalized tonic-clonic seizures · End of secondary generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 25 of 30Last clonic jerkCount · n/N 25/30 · 70 patients with mesial temporal lobe epilepsy due to hippocampal sclerosis and Engel class I or II outcome after 1 year; 43 with secondary generalized tonic-clonic seizures · asymmetric ending · End of secondary generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 83.3%Last clonic jerkPositive predictive value · n/N 25/30 · 70 patients with mesial temporal lobe epilepsy due to hippocampal sclerosis and Engel class I or II outcome after 1 year; 43 with secondary generalized tonic-clonic seizures · asymmetric ending · End of secondary generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 96.7%Last clonic jerkOther reported value · 70 patients with mesial temporal lobe epilepsy due to hippocampal sclerosis and Engel class I or II outcome after 1 year; 43 with secondary generalized tonic-clonic seizures · last-clonic-jerk assessment · End of secondary generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 30 of 43Last clonic jerkCount · n/N 30/43 · 70 patients with mesial temporal lobe epilepsy due to hippocampal sclerosis and Engel class I or II outcome after 1 year; 43 with secondary generalized tonic-clonic seizures · asymmetric ending · End of secondary generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • clonic seizureThe source defines clonic seizures as a series of myoclonic contractions that recur regularly at a rate of 0.2–5 per second.PDF p.4, Simple motor seizures
  • Clonic seizureClonic seizures are a series of myoclonic contractions that recur regularly at a rate of 0.2 to 5 per second.PDF p.4, Simple motor seizures, Clonic seizures; PDF p.2, Table 1
Reported values
  • recurrent contraction rate 0.2–5/sclonic seizureRate range · ictalPDF p.4, Simple motor seizures
  • 0.2-5/s recurrence rateClonic seizureCount · IctalPDF p.4, Simple motor seizures, Clonic seizures; PDF p.2, Table 1
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 1 finding · 24 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 1 finding · 3 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • clonic jerkingIn the unilateral TLE cohort, clonic jerking occurred only on the side contralateral to the EEG seizure focus.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
Reported values
  • 24/116 contralateral seizures (21%)clonic jerkingPercentage · n/N 24/116 · 19 patients with unilateral TLE; clonic jerking occurred in 7 patients · Contralateral to EEG seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 0 ipsilateral seizuresclonic jerkingCount · 19 patients with unilateral TLE; clonic jerking occurred in 7 patients · Ipsilateral to EEG seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 7 patients with contralateral clonic jerkingclonic jerkingCount · n/N 7/19 · 19 patients with unilateral TLE; clonic jerking occurred in 7 patients · Contralateral to EEG seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • focal motor clonic activityFocal motor clonic activity occurred in 57% of patients and was contralateral to the epileptogenic zone in the source description.PDF p.4, Results, Other seizure characteristics
Reported values
  • 57%focal motor clonic activityPercentage · 82-patient parietal epilepsy series · ictal motor phasePDF p.4, Results, Other seizure characteristics
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • focal clonic movement; negative motor responses; tonic posturing; palilaliaThe source reports that central-region pulse or short-train stimulation is used to induce focal clonic movement, that negative motor responses are seen in the pre-SMA region, and that SMA-proper stimulation induces positive motor behaviors such as tonic posturing or palilalia.PDF p.13, Motor Behaviors
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • clonic seizuresThe review states that clonic contractions recur at 0.2-5 per second and that the symptomatogenic zone is usually the primary motor strip. In temporal lobe epilepsy, the face, frontal eye field, and hand areas tend to be affected earlier than the legs; when clonus without altered consciousness is the first seizure sign, the epileptogenic zone is usually at or near the primary motor strip. Unilateral clonic seizures have high lateralizing value toward the contralateral hemisphere.PDF p.4, Clonic seizures
  • end of seizure paradoxical clonusIn secondarily generalized tonic-clonic seizures, the review states that clonic activity may persist longer on the side ipsilateral to the epileptogenic focus; it calls this “end of seizure paradoxical clonus” a highly reliable lateralizing sign and states that asymmetric seizure termination is relatively unusual in generalized epilepsy.PDF p.4, Clonic seizures
Reported values
  • Regular recurrence rate 0.2-5 per secondclonic seizuresCount · Patients with focal epilepsy, including temporal lobe epilepsy; no cohort reported · Ictal; first sign and early propagation emphasizedPDF p.4, Clonic seizures
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • right-sided clonic mouth-face-neck-upper-limb movementsTable 2 records right-sided clonic movements involving the mouth, face, neck, and upper limb in Case 17.PDF p.8, Table 2 Case 17
  • focal clonic head jerksTable 2 records evolution to focal clonic jerks of the head in Case 19.PDF p.8, Table 2 Case 19

23 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal aphasia / speech arrest during seizureSource terms: Ictal aphasia / speech arrestReported: ContralateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side25 manuscripts · 74 findings · 76 reported values
Weighted evidence supportevidence weight 43.31 across 25 manuscripts · 2 manuscript weight pending · 2 structured design not resolved · 4 systematic review or meta-analysis · 4 independent primary study · 11 narrative, educational, or cited context · 4 case report or observation

Speech arrest occurred with equal frequency in the dominant- and nondominant-hemisphere seizure-onset groups. Dysphasia was reported in 4 DHS seizures from 3 patients versus 1 NHS seizure/patient, with p=0.002, supporting a dominant-hemisphere tendency in the study's classified ictal-language result. The discussion restates nondominant temporal onset for ictal normal speech and dominant-hemisphere onset for dysphasia. The review states that anarthria alone is insufficient for hemispheric lateralization. The educational statement says dominant-hemisphere seizures can produce the same phonatory symptoms as non-dominant seizures, with dysphasia additionally possible in dominant-hemisphere seizures. The review links early ictal dysphasia to dominant-hemisphere involvement and unilateral elementary auditory aura to contralateral seizure onset. The illustrative case reports left temporal ictal EEG onset and a left-sided structural/metabolic temporal extension. The review links ictal or postictal dysphasia to the dominant hemisphere, formed nonsensical ictal speech to the nondominant hemisphere, and explicitly describes speech arrest as non-lateralising. Speech arrest is restated as an insular-stimulation speech impairment in a series spanning dominant and nondominant language hemispheres. The review restates opposite language-sign directions for aphasia and ictal speech/verbalization, with paraphasia described as not clearly lateralizing. The review restates left temporal resection association for dysphasia and a non-lateralizing result for speech automatisms. The cited study is restated as finding anterior/posterior aphasia lateralizing and vocal disturbances without lateralizing value. The cited stimulation series describes left superior temporal stimulation effects that vary by task and subregion, including auditory phenomena, phonological errors, and naming or reading deficits. The cited source associates ictal speech arrest at onset with dominant-hemisphere seizure origin. Two patients had difficulty speaking at onset with epileptogenic zones in the speech-dominant parietal lobe. Three aphasic-aura entries are listed, with dominant-side information not aggregated. Aphasic seizure was reproduced by stimulation of the left supramarginal gyrus in one patient. The source educational statement associates aphasic aurae with seizures originating in the dominant parietal lobe. Early naming difficulties are associated with a left epileptogenic zone, while late comprehension deficits are associated with posterior basal temporal involvement. The cited mapping study is restated as producing two speech arrests in the dominant inferior parietal lobule after more than 1,000 low-frequency ECS stimulations. The review reports speech- or language-induced aphasic seizures in a dominant temporal-lobe seizure-origin context. The case reports left temporooccipital lateralized periodic discharges during aphasic status epilepticus. A single case caption reports left temporal rhythmic 4–6/sec EEG activity during a focal seizure with restlessness, aphasia, and eye blinking. The cited series restates ictal dysphasia in 16 of 33 patients with dominant temporal-lobe lesions and in none of 24 patients with recessive temporal-lobe lesions. The cited Hecaen and Angelergues report describes 32 ictal speech-automatism cases among 208 patients: EEG focus was left in 11, right in 13, and undecided in 8; 176/208 remaining cases were dysphasic. The cited review associates temporal verbal automatisms with the non-dominant language hemisphere and describes speech arrest/vocalization in cortical language areas. Right facial pain, right-ear ringing, right hemibody and foot manifestations predominated in the early sequence, while left-sided stiffening occurred in half of seizures. The review describes ictal or postictal dys/aphasia as having approximately 90% lateralisation value but gives no direction and says its localisation value is poor. The review states that ictal and postictal aphasia point primarily to dominant-hemisphere involvement, while acknowledging non-dominant onset and poor localization after spread. The review associates memory/language deficits with dominant temporal seizures. The cited review associates aphasic seizures with dominant-hemisphere lateralization despite preserved awareness and memory. Dysphasia was much more frequent in dominant-origin temporal-lobe seizures (27 seizures in 12 patients) than in nondominant-origin seizures (3 seizures in 2 patients), with all nondominant events being isolated paraphasias. The cited Bingley report restates ictal dysphasia in 48% of 33 patients with dominant temporal-lobe lesions versus 0/24 with nondominant temporal-lobe lesions. The cited source reports significantly more paroxysmal expressive dysphasia or speech arrest with left-sided discharges than with right-sided discharges in right-handed patients. A single video case describes ictal dysphasia with left temporal/neocortical onset-related findings and dominant-language impairment affecting verbal commands, expressive language, and reading. The review distinguishes dominant-hemisphere dysphasia, nondominant ictal speech or preserved awareness, contralateral RINCH motions, and nonlateralizing speech arrest. The cited study is restated as finding speech arrest nonspecific and not significantly different between LTL- and RTL-origin seizures. The review summarizes prior association of aphasic fits with left-hemisphere lesions in right-handed patients and temporal-lobe seizures. Table I reports 13 aphasic-fit cases with left epileptic dysfunction and 0 with right dysfunction, with P<0.01 stated in the text and summary. The primary result reports speech arrest equally on the left and right, four cases each, with no significant laterality. The primary result reports sensory aphasia in two left postero-temporal cases and one left anterotemporal case. The cited report restates left-sided seizure patterns in four cases with aphasic fits. The cited Penfield restatement associates aphasic fits with left temporal seizure patterns based on cerebral stimulation. The review discusses aphasic focal aware seizures in dominant-hemisphere temporal-plus epilepsy and does not assign a fixed anatomic side beyond functional dominance. The cited cohort restates aphasic seizures in 80% of patients with left-hemisphere temporo-polar encephaloceles. The case reports a right temporal seizure focus with right-sided language dominance, a dominant-temporal exception to the usual nondominant pattern. The review and table identify the language-dominant hemisphere as the usual side for ictal aphasia or dysphasia. The cited series is restated as having 16 of 17 surgically confirmed epileptogenic zones on the left. Speech arrest occurred with nondominant temporal-lobe onset in two seizures and dominant temporal-lobe onset in one seizure. The source attributes to Hecaen the statement that ictal paraphasia/Jargon aphasia is present in the dominant hemisphere. No hemisphere or body-side direction is reported. The primary focal-cognitive-semiology prevalence result reports no hemisphere or lateralization direction. No hemisphere, dominance, or side-relative direction is reported. No lateralization relationship is reported. No lateralizing direction is reported for medial-frontal speech arrest and oral motor phenomena. No lateralizing direction is reported for isolated aphasia. No lateralizing direction is reported for aphasia as a sole manifestation or for the listed additional seizure types. No lateralizing direction is reported for aphasic status epilepticus. No lateralizing direction is reported for the stimulus-induced ictal language disturbances. No lateralization information is reported. No lateralizing direction is reported for jargonaphasia in the basal temporal language area network. No lateralizing direction is reported for speech inhibition or speech arrest. No lateralizing direction is reported for the the source's own speech-inhibition count. The pooled speech-inhibition prevalence result provides no hemispheric direction. The heterogeneity result for pooled speech inhibition provides no hemispheric direction. No lateralizing direction is reported for the speech-inhibition heterogeneity result. No lateralizing direction is reported for global aphasia during propagation. No lateralizing direction is reported for the cited speech manifestation frequency. The late-dysphasia comparison reports no lateralization. No lateralizing direction is reported for the aphasic-seizure definition. No lateralizing semiology is reported; the row concerns scalp and depth-electrode detection during aphasic fits. Either hemisphere is reported, but no side is specified for the speech-arrest observation. The aphasia-related EEG focus comparison provides no hemispheric direction. No lateralizing direction is reported for the educational aphasic-seizure definition.

Source-defined result groups 27
Lateralization: Does not lateralizeObserved proportion 5.3%DHS · 1 NHS patient · patients1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyDominant temporal-lobe onset · Nondominant temporal-lobe onset · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Right hemisphereObserved proportion 100.0%All reported · usual nondominant-hemisphere association · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin; first patient · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / right:0Observed proportion 0.0%Right · case1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyNondominant temporal-lobe onset · Dominant temporal-lobe onset · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphereSource-defined values retained separatelyAll reported · no aphasic aura · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft postero-temporal · Postero-temporal versus anterotemporal region · case/patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin; second patient · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Localization: SMA / pre-SMA / speech inhibitionSource-defined values retained separatelyAll reported · patients with the ictal symptom1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphereObserved proportion 3.4%dominant-hemisphere onset · NHS versus DHS · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Lateralization: dominant side not aggregatedSource-defined values retained separatelyAll reported · other aura categories · aura entries1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 2 reported values · not pooled
Lateralization: Left hemisphere / right:0Observed proportion 100.0%Left · case1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyspeech arrest · right side · case/patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelydominant-origin · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeObserved proportion 5.3%NHS · 1 DHS patient · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft anterotemporal · Postero-temporal versus anterotemporal region · case/patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · usual nondominant-hemisphere association · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphereObserved proportion 0.9%nondominant-hemisphere onset · NHS versus DHS · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyspeech arrest · left side · case/patient1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · no aphasic aura · patients1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft-sided stiffening · Early diurnal versus later nocturnal/postoperative semiology · seizure1 manuscript · 1 reported value · not pooled
Localization: ParietalObserved proportion 1.2%All reported · no reproduced aphasic seizure · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelydominant-origin · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphereSource-defined values retained separatelydominant-hemisphere onset · NHS versus DHS · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphereSource-defined values retained separatelynondominant-hemisphere onset · NHS versus DHS · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 25

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 3 findings · 7 reported values
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • dominant inferior parietal speech arrestThe review reports that Balestrini et al. obtained only two speech arrests in the dominant inferior parietal lobule after more than a thousand low-frequency ECS delivered through sEEG electrodes.PDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • speech arrest during ecological language tasksIn the review's account of de Ribaupierre et al., speech arrest occurred at 8 of 184 depth-electrode contacts in 3 patients during 2-5 mA stimulation, while 6 mA with 0.3 ms phase duration was the maximum stimulation for negative contacts.PDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1
  • medial frontal speech arrest and mouth or tongue motor phenomenaThe review reports that medial frontal ECS can produce speech arrest, sometimes with positive or negative motor phenomena of the mouth or tongue, and relates this finding to a phonological-articulatory network between supplementary motor area and ALA.PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG
Reported values
  • 172 subjectsdominant inferior parietal speech arrestCount · 172-subject Balestrini et al. study listed in Table 1; parietal sEEG exploration · Balestrini et al. study · low-frequency ECS during parietal language mappingPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • two speech arrests after more than 1,000 ECSdominant inferior parietal speech arrestCount · n/N 2/>1,000 ECS · 172-subject Balestrini et al. study listed in Table 1; parietal sEEG exploration · dominant inferior parietal lobule · low-frequency ECS during parietal language mappingPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • 6 mAspeech arrest during ecological language tasksOther reported value · 3 patients for the narrative speech-arrest observation; Table 1 lists 8 subjects for the de Ribaupierre et al. study · negative contacts · ECS during ecological language production such as counting, reading aloud, or spontaneous speechPDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1
  • 8 subjectsspeech arrest during ecological language tasksCount · 3 patients for the narrative speech-arrest observation; Table 1 lists 8 subjects for the de Ribaupierre et al. study · de Ribaupierre et al. study total in Table 1 · ECS during ecological language production such as counting, reading aloud, or spontaneous speechPDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1
  • 0.3 msspeech arrest during ecological language tasksDuration · 3 patients for the narrative speech-arrest observation; Table 1 lists 8 subjects for the de Ribaupierre et al. study · maximum stimulation for negative contacts · ECS during ecological language production such as counting, reading aloud, or spontaneous speechPDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1
  • 2–5 mAspeech arrest during ecological language tasksRange · 3 patients for the narrative speech-arrest observation; Table 1 lists 8 subjects for the de Ribaupierre et al. study · contacts producing speech arrest · ECS during ecological language production such as counting, reading aloud, or spontaneous speechPDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1
  • 8 of 184 depth-electrode contactsspeech arrest during ecological language tasksCount · n/N 8/184 · 3 patients for the narrative speech-arrest observation; Table 1 lists 8 subjects for the de Ribaupierre et al. study · contacts producing speech arrest · ECS during ecological language production such as counting, reading aloud, or spontaneous speechPDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • early naming and late comprehensionThe review states that early naming difficulties are strongly associated with a left epileptogenic zone, whereas late comprehension deficits are more likely associated with posterior basal temporal involvement.PDF p.9, Discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal speech arrestSpeech arrest at seizure onset before altered consciousness, or inability to speak despite clear attempts with later recall, is described as implying dominant-hemisphere seizure origin; the source attributes possible mechanisms to Wernicke’s area, Broca’s area, or the dominant basotemporal area.PDF p.4, Table 2; PDF p.5, language-disturbances paragraph
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 5 findings · 2 reported values
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • speech inhibition; speech arrestIctal speech inhibition is described as a well-documented SMA epilepsy manifestation; stimulation studies may produce speech arrest without affecting consciousness.PDF p.7, Discussion
  • speech inhibitionTable 3 lists 7 patients for the the source's own ictal symptom “speech inhibition”; its table phase label is onset.PDF p.6, Table 3
  • speech inhibitionTable 3 reports a pooled prevalence of 10% for the the source's own ictal symptom “speech inhibition”; its table phase label is onset.PDF p.6, Table 3
  • speech inhibition; between-study heterogeneityThe source reports I2 heterogeneity of 0.51% for pooled speech inhibition prevalence.PDF p.5, Results
  • speech inhibition; heterogeneity testThe source reports p = 0.45 for the between-study heterogeneity test of pooled speech inhibition prevalence.PDF p.5, Results
Reported values
  • 10% pooled prevalencespeech inhibitionPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
  • I2 = 0.51%speech inhibition; between-study heterogeneityHeterogeneity I2 · Patients with SMA or pre-SMA epilepsy in the selected studies · ictal symptom prevalence analysisPDF p.5, Results
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 3 findings
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • ictal speech arrest, vocalization, and verbal automatismsThe review states that most seizures involving cortical language areas reduce to speech arrest or vocalization depending on the involved area and its distance from ventral central regions; verbal automatisms occur in temporal seizures and are associated with the non-dominant language hemisphere, while aphasia-like abnormal production is less frequent.PDF p.7, section 8
  • pre-SMA speech and movement arrest / negative motor areasSeizures arising from rostral SMA or pre-SMA may consist of speech arrest, optional quavering vocalization, movement arrest, or subtle leg repositioning; when the examiner raises the arms they gradually drop back, a negative motor phenomenon associated with dorsal or ventral premotor areas.PDF p.3, section 4
  • jargonaphasia and basal temporal language areaJargonaphasia is reported in seizures originating from the basal temporal language area, with fast discharges occurring simultaneously in BTLA and posterior superior temporal gyrus including Heschl’s gyrus and planum temporale; the review interprets desynchronization as a functional disconnection between language comprehension and speech production.PDF p.7, section 8
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 5 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • lateral/neocortical temporal seizure; auditory aura; ictal dysphasiaLateral or neocortical temporal seizures are described as having fewer auras and often auditory or vertiginous features; elementary sounds such as humming, ringing, and buzzing indicate primary auditory cortex, complex sounds indicate auditory association areas, elementary unilateral auditory aura indicates contralateral onset, and early ictal dysphasia may indicate dominant-hemisphere involvement.PDF p.6, Lateral/neocortical temporal lobe; PDF p.3, Figure 1
  • psychic aura; ictal dysphasiaIn an illustrative 27-year-old woman with a non-lesional MRI and left temporal PET abnormality, seizures began with fear/anxiety and sometimes ear noise followed by difficulty speaking; she could follow visual but not verbal commands, and ictal EEG showed left temporal onset suggesting neocortical onset.PDF p.6, Video case 4; PDF p.6, Figure 5 caption
  • ictal/postictal dysphasia; speech arrest; ictal speechIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value; speech arrest is described as non-lateralising, whereas ictal speech consisting of formed nonsensical phrases is a non-dominant sign.PDF p.10, Lateralising signs
  • ictal dysphasia; neocortical temporal onsetIn video case 4, a 27-year-old woman with a psychic aura and occasional ear noise had ictal dysphasia; she could follow visual but not verbal commands, with expressive-language and reading impairment, and PET, statistical analysis, and ictal EEG indicated a left temporal neocortical onset extending toward the temporoparieto-occipital junction.PDF p.6, Video case 4; PDF p.7, Figure 5
  • ictal/postictal dysphasia; ictal speech; preserved awareness; RINCH motionsIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value and must be distinguished from non-lateralising speech arrest; formed nonsensical ictal speech and preserved awareness during ictal automatisms point to the nondominant hemisphere, while rhythmic ictal non-clonic hand motions may be contralateral in temporal lobe epilepsy and peri-ictal drinking, spitting, vomiting, or urge to urinate point to a nondominant focus.PDF p.10, Lateralising signs
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Speech arrest in a cited studyThe current paper reports that Gabr et al. (1989) found no significant difference in speech arrest between LTL- and RTL-origin seizures and argued that speech arrest is nonspecific and may result from a negative or positive motor effect or altered consciousness.PDF p.5, Discussion, speech-arrest paragraph
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • aphasic focal aware seizures in TPE and the basal temporal language areaAphasic focal aware seizures in dominant-hemisphere TPE are not necessarily explained by propagation through perisylvian language areas; the chapter also describes involvement of anterior temporo-basal structures, including a basal temporal language area 2–9 cm from the temporal tip and including the fusiform gyrus.PDF p.10, Temporal pole or temporo-polar epilepsy
  • aphasic seizures with left temporo-polar encephalocelesIn a cited cohort of patients with temporo-polar encephaloceles, 80% of patients with left-hemisphere lesions had aphasic seizures.PDF p.10, Temporal pole or temporo-polar epilepsy
Reported values
  • basal temporal language area located 2–9 cm from the temporal tipaphasic focal aware seizures in TPE and the basal temporal language areaCount · patients with dominant-hemisphere TPE or anterior temporo-basal lesions · focal aware ictalPDF p.10, Temporal pole or temporo-polar epilepsy
  • 80% of patients with left-hemisphere lesions had aphasic seizuresaphasic seizures with left temporo-polar encephalocelesPercentage · patients with temporo-polar encephaloceles and left-hemisphere lesions in the cited cohort · ictal focal awarePDF p.10, Temporal pole or temporo-polar epilepsy
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 5 findings · 19 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • dysphasiasDysphasias occurred in 30 seizures in 14 patients: 27 seizures in 12 patients with dominant-origin seizures and 3 seizures in 2 patients with nondominant-origin seizures; all three nondominant dysphasias were isolated paraphasias, one patient had 2 ictal seizures, the second had 1 postictal seizure, and all other dysphasias were postictal and arose from the dominant hemisphere.PDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • ictal dysphasiaThe source reports that Bingley found ictal dysphasia in 48% of 33 patients with dominant temporal-lobe lesions and epilepsy versus 0 of 24 patients with a lesion in the nondominant temporal lobe.PDF p.5, Discussion
  • paroxysmal expressive dysphasia or speech arrestThe source reports that McKeever and coworkers found significantly more paroxysmal expressive dysphasia or speech arrest in right-handed patients with left-sided discharges than in those with right-sided discharges (p <= 0.05).PDF p.5, Discussion
  • speech arrestSpeech arrest occurred in 3 seizures in 3 different patients: 2 episodes were ictal and 1 postictal; 1 seizure had dominant temporal-lobe onset and 2 had nondominant onset, and all patients appeared responsive during the arrest.PDF p.3, Table 3 and Results; PDF p.5, conclusion
  • expressive dysphasia/speech arrestThe source reports that McKeever and colleagues observed expressive dysphasia or speech arrest in at least one seizure in 94% of their cases.PDF p.5, Discussion
Reported values
  • 27 dominant-origin seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · dominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 2 ictal nondominant dysphasia seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin; first patient · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 14 patients with dysphasiadysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 3 nondominant-origin seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 2 nondominant-origin patientsdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 1 postictal nondominant dysphasia seizuredysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin; second patient · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 12 dominant-origin patientsdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · dominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 30 dysphasia seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • Dominant temporal-lesion patients with ictal dysphasia 48% of 33ictal dysphasiaPercentage · Patients with temporal-lobe lesions and epilepsy in the cited Bingley report · Dominant temporal-lobe lesion · ictalPDF p.5, Discussion
  • Nondominant temporal-lesion patients with ictal dysphasia 0/24ictal dysphasiaPercentage · n/N 0/24 · Patients with temporal-lobe lesions and epilepsy in the cited Bingley report · Nondominant temporal-lobe lesion · ictalPDF p.5, Discussion
  • p ≤ 0.05paroxysmal expressive dysphasia or speech arrestP value · Right-handed patients in the cited McKeever study · paroxysmal; exact ictal/postictal phase not reported in this restatementPDF p.5, Discussion
  • Responsive patients during speech arrest 3/3speech arrestPercentage · n/N 3/3 · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • Nondominant-origin speech-arrest seizures n=2speech arrestCount · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · Nondominant temporal-lobe onset · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • Ictal speech-arrest episodes n=2speech arrestCount · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · Ictal · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • Postictal speech-arrest episodes n=1speech arrestCount · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · Postictal · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • Speech-arrest seizures n=3speech arrestCount · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • Dominant-origin speech-arrest seizures n=1speech arrestCount · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · Dominant temporal-lobe onset · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • Patients with speech arrest n=3speech arrestCount · 3 patients and 3 seizures in the 35-patient temporal-lobe epilepsy cohort · 2 ictal episodes and 1 postictal episodePDF p.3, Table 3 and Results; PDF p.5, conclusion
  • 94% of cases with expressive dysphasia or speech arrest in at least one seizureexpressive dysphasia/speech arrestPercentage · Cases in the cited McKeever study; exact denominator not reported in this passage · ictal/seizure-related; exact phase not otherwise reported in this cited restatementPDF p.5, Discussion
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 3 findings
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • speech arrest; anarthria; dysarthria; dysphasiaThe source states that speech arrest, including anarthria or dysarthria, can be the first sign of seizures starting from the frontal operculum, while anarthria alone is not sufficient to assign hemispheric lateralization.PDF p.9, Discussion
  • dominant hemisphere; non-dominant hemisphere; dysphasia; postictal language disorderThe source states that seizures in dominant and non-dominant hemispheres can produce the same phonatory symptoms, while dominant-hemisphere seizures may additionally produce dysphasia that can persist postictally.PDF p.9, Discussion
  • speech arrest; motor aphasia; dysprosody; dysarthriaThe discussion reports that language disorders in the cited Peltola series combined motor aphasia, dysprosody, or dysarthria early in seizure semiology but not at initial onset, suggesting opercular spread.PDF p.9, Discussion
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 3 findings
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • aphasia; ictal speech; ictal verbalizationThe article states that aphasic seizures or aphasia are associated with dominant temporal/hemisphere seizures, whereas ictal speech or verbalization is generally interpreted as a non-dominant temporal/hemisphere sign.PDF p.2, Introduction; PDF p.3, Discussion
  • dysphasia; speech automatismsThe article reports that the Serafetinides and Falconer series described dysphasia as predominantly associated with left temporal resection, whereas speech automatisms did not show a lateralizing value.PDF p.3, Discussion
  • anterior and posterior aphasia; vocal disturbancesThe article reports that Dussaule et al. found anterior and posterior aphasia to be lateralizing language disturbances, whereas vocal disturbances showed no lateralizing value.PDF p.3, Discussion
ictal-speech-disturbance-cerebral-dominance.pdfIndependent primary study · 10 findings · 7 reported values
ictal-speech-disturbance-cerebral-dominance.pdf
Independent primary study · Class II · Evidence weight 3.42 · 2 × 1.1 × 1.557
The authors collected about 43 cases with ictal speech disturbances over 8 years. Interictal EEG was examined at least twice per case; laterality was defined by a spike or sharp-wave focus, unilateral dominant spike or sharp wave, or unilateral slow wave corresponding to same-region brain damage or tumor. Laterality was confirmed in 36 cases; 7 cases with independent foci, no laterality, or normal findings were excluded. The statistical report concerns 34 right-handed epileptics because 2 left-handed patients could not be tested statistically. A control pool comprised 243 right-handed patients with unilateral abnormal EEG findings, 136 left and 117 right, and was assessed by t test.
Findings
  • aphasic fitThe authors state that prior authors generally associated aphasic fits with temporal-lobe seizures and left-hemisphere epileptogenic lesions in right-handed patients, while the exact percentage remained controversial.PDF p.2, Introduction; PDF p.4, Discussion
  • aphasic fitIn the reported right-handed epileptic cases, aphasic fits were associated with left rather than right EEG-defined epileptic dysfunction, 13 cases versus 0, with statistical significance reported at P<0.01.PDF p.3, Results, Table I; PDF p.5, Summary item 1
  • speech arrestSpeech arrest showed no significant laterality in the reported right-handed epileptic cases, with 4 cases on the left and 4 on the right side of epileptic dysfunction.PDF p.3, Results, Table I; PDF p.4, Discussion; PDF p.5, Summary item 3
  • sensory aphasiaAmong the aphasic-fit cases, the authors report sensory aphasia in the left postero-temporal region in two cases and the left anterotemporal region in one case.PDF p.4, Results paragraph beginning “Three types with ictal speech disturbances”
  • aphasic fitThe current article reports that Alajouanine and Sabouraud observed seizure patterns on the left side in 4 cases with aphasic fits.PDF p.4, Discussion paragraph beginning “Alajouanine et al.”
  • aphasic fitThe current article reports that Penfield and coworkers assumed aphasic fits occurred in relation to left temporal seizure patterns based on cerebral stimulation.PDF p.4, Discussion paragraph beginning “Alajouanine et al.”
  • ictal paraphasia or Jargon aphasiaThe authors state that ictal paraphasia or Jargon aphasia has occasionally been mistaken for speech automatism and attribute to Hecaen the statement that ictal paraphasia is present in the dominant hemisphere.PDF p.5, Discussion paragraph beginning “The question of why”
  • aphasic fitThe current article reports that Ajmone Marsan and Abraham described cases in which scalp EEG did not change during an aphasic fit while seizure patterns appeared with depth electrodes.PDF p.4, Discussion paragraph beginning “Alajouanine et al.”
  • speech arrestThe current article reports that Penfield and coworkers found speech arrest caused by neural discharge involving the inferior Rolandic area or supplementary motor area of either hemisphere.PDF p.4, Discussion paragraph beginning “It seems that the side of focus”
  • aphasic fitThe current article reports from Brain that EEG findings varied from anterotemporal to posterotemporal focus depending on expressive versus comprehensive aphasic reciprocity.PDF p.4, Discussion final paragraph; PDF p.5, Discussion opening
Reported values
  • Aphasic-fit cases with right epileptic dysfunction n=0aphasic fitCount · n/N 0/13 · 34 right-handed epileptics in the report; 13 aphasic-fit cases in the Table II summation · Right · ictalPDF p.3, Results, Table I; PDF p.5, Summary item 1
  • Aphasic-fit cases with left epileptic dysfunction n=13aphasic fitCount · n/N 13/13 · 34 right-handed epileptics in the report; 13 aphasic-fit cases in the Table II summation · Left · ictalPDF p.3, Results, Table I; PDF p.5, Summary item 1
  • Right 4speech arrestCount · n/N 4/8 speech-arrest cases · 34 right-handed epileptics in the report; 8 speech-arrest cases in the Table II summation · speech arrest · ictalPDF p.3, Results, Table I; PDF p.4, Discussion; PDF p.5, Summary item 3
  • Left 4speech arrestCount · n/N 4/8 speech-arrest cases · 34 right-handed epileptics in the report; 8 speech-arrest cases in the Table II summation · speech arrest · ictalPDF p.3, Results, Table I; PDF p.4, Discussion; PDF p.5, Summary item 3
  • 1 left anterotemporal casesensory aphasiaCount · Aphasic-fit cases with sensory aphasia; exact subgroup denominator Not reported · left anterotemporal · ictalPDF p.4, Results paragraph beginning “Three types with ictal speech disturbances”
  • 2 left postero-temporal casessensory aphasiaCount · Aphasic-fit cases with sensory aphasia; exact subgroup denominator Not reported · left postero-temporal · ictalPDF p.4, Results paragraph beginning “Three types with ictal speech disturbances”
  • 4 cases with left-sided seizure patternsaphasic fitCount · 4 cited aphasic-fit cases; denominator Not reported · ictalPDF p.4, Discussion paragraph beginning “Alajouanine et al.”
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • speech arrest from insular stimulationSpeech arrest was one of the speech impairments evoked by insular stimulation.PDF p.5, Other Insular Responses
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal cognitive (aphasia)Focal cognitive (aphasia) semiology was present in 1/61 individuals (2%) as initial semiology and 3/61 (5%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 1/61 (2%)Focal cognitive (aphasia)Percentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 3/61 (5%)Focal cognitive (aphasia)Percentage · n/N 3/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 4 findings · 1 reported value
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Ictal or postictal dys/aphasiaThe review describes ictal or postictal dys/aphasia as a valuable finding with approximately 90% lateralisation value, while stating that its localisation value is poor.PDF p.5, section 1.9
  • Ictal aphasiaThe review states that ictal aphasia occurs only with dominant-hemisphere involvement, even when seizure onset is in the non-dominant hemisphere; one cited series associated ictal aphasia with parieto-occipital seizure onsets.PDF p.5, section 1.9
  • Memory, language, orientation, and expressive speech deficitsThe review states that dominant temporal lobe seizures result in memory and language deficits, whereas frontal seizures result in loss of orientation and expressive speech function.PDF p.3, section 1.3
  • Global aphasia with propagationThe review states that larger cortical-stimulation intensities engage more of the language network, resulting in global aphasia, and that this is typically what occurs in seizures undergoing propagation.PDF p.6, section 1.9
Reported values
  • Approximately 90% lateralisation valueIctal or postictal dys/aphasiaPercentage · Video-EEG seizure literature; exact population not reported · ictal or postictalPDF p.5, section 1.9
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfCase report or observation · 3 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • automatisms with preserved responsiveness and ictal dysphasiaJanszky et al. reported a dominant-temporal exception to the usual nondominant lateralization of preserved-responsive automatisms.PDF p.7, section 3.10; PDF p.12, Table 1
  • ictal dysphasia and aphasiaIctal dysphasia or aphasia lateralizes to the language-dominant hemisphere.PDF p.9, section 4.2; PDF p.12, Table 1
  • ictal dysphasiaSerafetinides and Falconer reported ictal dysphasia in 34 TLE patients and postoperative confirmation in 17, 16 of whom had left-sided zones.PDF p.9, section 4.2
Reported values
  • 1 caseautomatisms with preserved responsiveness and ictal dysphasiaCount · n/N 1/1 · one 25-year-old woman with right temporal lobe epilepsy · ictalPDF p.7, section 3.10; PDF p.12, Table 1
  • 100% dominantictal dysphasia and aphasiaPercentage · epilepsy monitoring unit patients with ictal dysphasia or aphasia · patients with ictal dysphasia or aphasia · ictalPDF p.9, section 4.2; PDF p.12, Table 1
  • 34.2% of EMU patientsictal dysphasia and aphasiaPercentage · epilepsy monitoring unit patients with ictal dysphasia or aphasia · EMU patients · ictalPDF p.9, section 4.2; PDF p.12, Table 1
  • TLE patients with ictal dysphasia n=34ictal dysphasiaCount · 34 patients with temporal lobe epilepsy and ictal dysphasia · ictalPDF p.9, section 4.2
  • Confirmed zones left-sided 16/17ictal dysphasiaPercentage · n/N 16/17 · 34 patients with temporal lobe epilepsy and ictal dysphasia · Postoperatively confirmed · ictalPDF p.9, section 4.2
  • Postoperative confirmation 17/34ictal dysphasiaPercentage · n/N 17/34 · 34 patients with temporal lobe epilepsy and ictal dysphasia · ictalPDF p.9, section 4.2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 2 findings
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • aphasic seizureAphasic seizures are described as episodes in which the patient cannot speak and often cannot understand spoken language; the source presents them as a probable negative phenomenon caused by activation of a cortical language center, analogous to cortical stimulation of language areas.PDF p.5, Special seizures
  • Aphasic seizureDuring aphasic seizures the patient cannot speak and often cannot understand spoken language; the source describes these as probably negative phenomena produced by epileptic activation of a cortical language center, analogous to cortical language-area stimulation.PDF p.5, Special seizures, Aphasic seizures; PDF p.2, Table 1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 4 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • late dysphasiaLate dysphasia did not differ significantly across M, ML, and L groups.PDF p.7, Table 5; PDF p.9, Nondifferentiating ictal characteristics
Reported values
  • L=0/13 (0%)late dysphasiaPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.9, Nondifferentiating ictal characteristics
  • ML=3/18 (16.7%)late dysphasiaPercentage · n/N 3/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.9, Nondifferentiating ictal characteristics
  • M=6/24 (25%)late dysphasiaPercentage · n/N 6/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.9, Nondifferentiating ictal characteristics
  • p=0.14late dysphasiaP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · late ictal, second half of seizurePDF p.7, Table 5; PDF p.9, Nondifferentiating ictal characteristics
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding · 5 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyCase 2 was a 46-year-old right-handed man whose seizures began with lancinating right facial pain followed within 2 seconds by high-pitched right-ear ringing descending along the right hemibody to the foot, sometimes with right-foot tremor, witnessed erratic right-sided and truncal movements, and left-sided stiffening in half the seizures; he was usually conscious without postictal paresis, had 10–15-second events up to 100 times per day triggered by sounds, and could develop hypersalivation, speech difficulty, later nocturnal hypermotor seizures, and urinary incontinence.PDF p.11, Case 2; PDF p.13, continuation of Case 2
Reported values
  • within 2 secondsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyDuration · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · early sensory sequence · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 10–15-second eventsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · habitual events · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 2–3 per monthCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · youth · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • in half the seizuresCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyOther reported value · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · left-sided stiffening · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • up to 100 times per dayCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyFrequency · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · later high-frequency period · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 3 findings · 10 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • speech arrestSpeech arrest occurred with equal frequency in dominant- and nondominant-hemisphere seizure-onset groups.PDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • dysphasiaDysphasia was more frequent in dominant-hemisphere than nondominant-hemisphere seizure-onset observations and was treated by the authors as a significant lateralizing feature.PDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • ictal normal speech and dysphasia in prior video/EEG reportsThe discussion states that prior video/EEG analyses confirmed the source’s directional language conclusion: ictal normal speech with nondominant temporal onset and dysphasia with dominant-hemisphere onset.PDF p.6, Discussion
Reported values
  • p=1speech arrestP value · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · ictalPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • 1 DHS patientspeech arrestCount · n/N 1/19 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · DHS · ictalPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • 1 NHS patientspeech arrestCount · n/N 1/19 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · NHS · ictalPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • NHS 1 seizure (1% of all 116 seizures)speech arrestPercentage · n/N 1/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · NHS · ictalPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • DHS 1 seizure (1% of all 116 seizures)speech arrestPercentage · n/N 1/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · DHS · ictalPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • p=0.002dysphasiaP value · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures; DHS dysphasia occurred in 3 patients · ictal language manifestation as classified by the studyPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • DHS 4 seizures (4% of all 116)dysphasiaPercentage · n/N 4/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures; DHS dysphasia occurred in 3 patients · dominant-hemisphere onset · ictal language manifestation as classified by the studyPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • 1 NHS patientdysphasiaCount · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures; DHS dysphasia occurred in 3 patients · nondominant-hemisphere onset · ictal language manifestation as classified by the studyPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • NHS 1 seizure (1% of all 116)dysphasiaPercentage · n/N 1/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures; DHS dysphasia occurred in 3 patients · nondominant-hemisphere onset · ictal language manifestation as classified by the studyPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • 3 DHS patientsdysphasiaCount · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures; DHS dysphasia occurred in 3 patients · dominant-hemisphere onset · ictal language manifestation as classified by the studyPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 4 findings · 3 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • aphasic auraTwo patients with epileptogenic zones in the speech-dominant parietal lobe had difficulty speaking at seizure onset.PDF p.3, Results, Aurae
  • aphasic aura entries in Table 1Table 1 lists three aphasic-aura entries.PDF p.4, Table 1
  • aphasic seizure reproduced from left supramarginal gyrusAn aphasic seizure was reproduced in one patient by stimulation of the left supramarginal gyrus.PDF p.5, Electrical cortical stimulation
  • aphasic aura and dominant parietal originThe source states that aphasic aurae occurred in a few patients whose seizures originated in the dominant parietal lobe.PDF p.9, Discussion
Reported values
  • 2 patientsaphasic auraCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae
  • 3 source-reported aura entriesaphasic aura entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 1 patientaphasic seizure reproduced from left supramarginal gyrusCount · n/N 1/80 · 80 stimulated patients · stimulation responsePDF p.5, Electrical cortical stimulation
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfNarrative, educational, or cited context · 2 findings · 7 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • ictal dysphasiaThe current article reports that Bingley found ictal dysphasia in 16/33 patients with a dominant temporal-lobe lesion and in 0/24 with a recessive temporal-lobe lesion.PDF p.10, discussion of prior dysphasia reports
  • ictal speech automatism; dysphasic speech disorderThe current article reports that Hecaen and Angelergues described 32 cases of ictal speech automatism among 208 epileptic patients with paroxysmal speech disorders; EEG focus was left-sided in 11, right-sided in 13, and undecided in 8, while the remaining 176 cases were dysphasic.PDF p.10, discussion of prior speech-automatism reports
Reported values
  • recessive lesion 0/24ictal dysphasiaPercentage · n/N 0/24 · Bingley’s cited patients with temporal-lobe lesions and epilepsy · recessive temporal-lobe lesion · Ictal dysphasiaPDF p.10, discussion of prior dysphasia reports
  • dominant lesion 16/33 (48%)ictal dysphasiaPercentage · n/N 16/33 · Bingley’s cited patients with temporal-lobe lesions and epilepsy · dominant temporal-lobe lesion · Ictal dysphasiaPDF p.10, discussion of prior dysphasia reports
  • 13 of 32ictal speech automatism; dysphasic speech disorderPercentage · n/N 13/32 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · speech automatism; right-sided EEG focus · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 8 of 32ictal speech automatism; dysphasic speech disorderPercentage · n/N 8/32 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · speech automatism; undecided EEG focus · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 32 cases ... among 208ictal speech automatism; dysphasic speech disorderPercentage · n/N 32/208 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · ictal speech automatism · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 176/208ictal speech automatism; dysphasic speech disorderPercentage · n/N 176/208 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · dysphasic speech disorder · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 11 of 32ictal speech automatism; dysphasic speech disorderPercentage · n/N 11/32 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · speech automatism; left-sided EEG focus · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 2 findings
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • hallucinations or illusions; auditory symptoms; articulatory or phonological errors; naming or reading deficitsIn the posterior left superior temporal region, the source reports task- and subregion-specific effects: word-repetition stimulation of Heschl’s gyrus induced hallucinations or illusions without language deficit; planum temporale stimulation induced auditory symptoms with comprehension deficit; left planum temporale or Spt stimulation during word or pseudoword repetition elicited articulatory or phonological errors and difficulty maintaining the phonological loop; and posterior left STS stimulation during naming or reading produced naming or reading deficits without positive auditory symptoms, including the source’s reported “graphene” decoding, comprehension, and “graphene to phoneme” deficits.PDF p.7, posterior left superior temporal gyrus paragraph; PDF p.8, Fig. 10.3 caption
  • task-specific language effects in medial and basal temporal regions; elementary speech arrest or slowing; semantic picture matchingThe source reports that naming or reading stimulation in medial and basal temporal regions was more likely to induce a language deficit than repetition or automatic speech; naming was described as most sensitive in the inferior frontal gyrus and mesial temporal anterior region, while the insula showed more elementary speech arrest or slowing during automatic speech. At a basal temporal site, stimulation disrupted naming while the same site and stimulation parameters allowed a semantic picture-matching task to be performed perfectly.PDF p.9, medial and basal temporal task paragraph; PDF p.9, basal temporal region paragraph; PDF p.17, Table 10.1, Semantic Processing
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • aphasic seizuresThe review states that aphasic seizures occur despite preserved awareness and memory, are often mixed aphasias, and lateralize the epilepsy to the dominant hemisphere; they can also present as status epilepticus.PDF p.5, Aphasic seizures
unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 7 findings · 1 reported value
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • speech- or language-induced aphasic seizuresThe review reports speech- or language-induced aphasic seizures all originating in the dominant temporal lobe.PDF p.2, §2.3
  • aphasic status epilepticus with left temporooccipital LPDsFigure 1 depicts a 75-year-old male with aphasic status epilepticus in structural focal epilepsy due to intracerebral bleeding and ictal left temporooccipital lateralized periodic discharges.PDF p.3, Fig.1 caption and EEG rendering
  • focal seizure with restlessness, aphasia, and eye blinkingFigure 2 depicts a 59-year-old female with a focal seizure involving restlessness, aphasia, and eye blinking, with a seizure pattern showing left temporal rhythmic 4–6/sec activity.PDF p.3, Fig.2 caption and EEG rendering
  • isolated aphasiaThe review states that isolated aphasia is reported to be a rare ictal phenomenon.PDF p.2, §2 opening paragraph
  • aphasia as sole manifestation and additional seizure typesThe review states that aphasia can occur as the sole manifestation of epileptic seizures, while additional seizure types are frequently reported; its Table 2 lists secondary generalized seizures, generalized tonic seizures, focal motor seizures/Epilepsia partialis continua, head turning, somato-sensory seizures, complex partial or psychic seizures, and various auras as additional types.PDF p.2, §2.1; PDF p.2, Table 2
  • aphasic status epilepticus (ASE)The review describes aphasia as a symptom of nonconvulsive status epilepticus and states that ASE may occur with or without additional seizure types; prolonged fluent aphasia seems rare, whereas most cases are characterized by deficit symptoms presenting as non-fluent aphasia.PDF p.2, §2.2
  • stimulus-induced ictal language disturbancesThe review describes telephone calls and watching television as triggers of speech arrest or aphasic seizures, photic stimulation as producing bleating vocalizations, and reading epilepsy as producing ictal dyslexia.PDF p.2, §2.3
Reported values
  • Rhythmic 4–6/sec EEG activityfocal seizure with restlessness, aphasia, and eye blinkingCount · Female, 59 years; focal seizure · ictalPDF p.3, Fig.2 caption and EEG rendering

25 contributing manuscripts; source-reported values remain separate and are not pooled.

motor signsReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere20 manuscripts · 45 findings · 71 reported values
Weighted evidence supportevidence weight 37.13 across 20 manuscripts · 4 manuscript weight pending · 4 independent primary study · 5 systematic review or meta-analysis · 4 structured design not resolved · 4 narrative, educational, or cited context · 3 case report or observation

The review describes early upper-limb and orofacial elementary motor signs as mainly contralateral tonic, clonic, or dystonic manifestations. Left focal motor seizures occurred in a patient with a right parietal BOSD and right-centroparietal interictal maximum. The case began with a right frontal ictal field and left facial twitching, then evolved through bilateral propagation and bilateral motor activity. Group 1 includes several source-labeled contralateral motor components, but the composite group also contains signs without a stated direction. Both reported simple motor signs were contralateral to the resected side. One typical anterior patient had equally frequent contralateral simple motor seizures along with hypermotor activity. The cited review restates early facial activity and contralateral motor activity as suggestive of neocortical temporal epilepsy. In Case 2, initial forced right eye deviation was ipsilateral to the right temporal epileptogenic region, whereas later left-arm tonic posturing and left facial clonia were contralateral motor signs. When arm or face motor activity accompanied contraversion, the source describes it as contralateral to the seizure focus. Contralateral focal motor activity occurred in 16 of 42 patients. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. The source reports no lateralizing direction for the network-propagation account of occipital-onset seizures. No lateralizing information is supplied. No lateralization information is reported. No hemispheric lateralization is reported. This record provides no hemispheric lateralization. The frontal motor hierarchy provides no lateralizing direction. The posterior cingulate epilepsy cohort included bilateral asymmetric tonic manifestations, but no side-of-onset relationship is reported. This record provides no seizure lateralization. The review classification of ictal feature categories reports no lateralizing direction. The prevalence estimate is not lateralizing. The subgroup occurrence estimate is not lateralizing. The co-occurrence coefficient is not lateralizing. The symptom co-occurrence coefficient is not lateralizing. The surgical-extent association is not lateralizing. The duplicate body-text statistic is not lateralizing. The cited coupling comparison provides no lateralizing information. The cited frontal rostrocaudal gradient is not lateralizing. No hemisphere or body-side direction is reported. The review mentions asymmetric, bilateral, and body-distribution features but provides no hemisphere-relative direction for a lateralizing conclusion. The cited coupling patterns provide no lateralizing information. The rostrocaudal cluster gradient is not lateralizing.

Source-defined result groups 30
Lateralization: ContralateralObserved proportion 38.1%All reported · no focal motor activity · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyparietal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyoccipital · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelytemporal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelytemporal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelytotal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalSource-defined values retained separatelyGroup 1 · other patient groups · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyfrontal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelyoccipital · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelytemporal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: FrontalObserved proportion 50.0%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyparietal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalObserved proportion 47.3%total · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyoccipital · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelytotal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyfrontal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelytotal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelyfrontal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Lateralization: ContralateralObserved proportion 11.1%All reported · ipsilateral resected side · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 55.6%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 52.5%total · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyparietal · arm versus face activity and temporal versus extratemporal onset · seizure; patient counts in parentheses in Table 31 manuscript · 2 reported values · not pooled
Localization: FrontalObserved proportion 42.9%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 33.3%All reported · seizure1 manuscript · 2 reported values · not pooled
Localization: FrontalObserved proportion 61.9%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 16.7%All reported · other typical anterior patients · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalSource-defined values retained separatelyGroup 1 early spread network · other patient groups/whole population · anatomical-area involvement1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 77.8%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · patients with the ictal symptom1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 20

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 2 findings · 2 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior contralateral simple motor seizuresOne typical anterior patient had equally frequent contralateral simple motor seizures along with hypermotor activity.PDF p.4, Clinical Presentation
  • posterior cingulate motor phenomenaMotor phenomena were observed in three of four posterior cingulate patients.PDF p.5, Clinical Presentation
Reported values
  • 1/6 with contralateral simple motor seizures accompanying hypermotor activitytypical anterior contralateral simple motor seizuresProportion · n/N 1/6 · 6 typical anterior cingulate cases · ictal semiologyPDF p.4, Clinical Presentation
  • 3/4 (75%) with motor phenomenaposterior cingulate motor phenomenaPercentage · n/N 3/4 · 4 posterior cingulate cases · ictal semiologyPDF p.5, Clinical Presentation
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • contralateral simple motor signsTwo patients had contralateral simple motor signs.PDF p.2, Results
Reported values
  • 2/18 (11%) contralateral simple motor signscontralateral simple motor signsPercentage · n/N 2/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • language disturbances and motor phenomenaThe abstract characterizes basal temporal seizures as frequently presenting with language disturbances and motor phenomena, with less pronounced emotional and sensory signs than other temporal lobe epilepsy forms.PDF p.1, Abstract; PDF p.2, Key points
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfStructured design not resolved · 1 finding · 2 reported values
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
This single-center presurgical series included 54 patients whose SEEG-defined epileptogenic zone (EZ) predominantly involved the frontal lobe, selected from 180 SEEG explorations performed from February 2000 through November 2010; one inconclusive exploration and nonpredominantly frontal cases were excluded. The cohort included 22 male and 32 female patients, mean age 24.9 ± 9.5 years, mean epilepsy duration 16.9 ± 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed all seizures and scored presence/absence of 31 ictal signs; each patient's sign was assigned 0, 1, or 2 according to reproducibility. The “early spread network” was the cortical tissue involved from electrical onset through completion of clinical semiology and was explicitly distinguished from the EZ. SEEG sampling is described as 20 frontal cortical regions, while the later matrices are described as containing 24 brain-area variables. Analyses used correlation matrices, Kendall tests with p < 0.05, PCA on rank-transformed sign scores, hierarchical clustering, and value-test ≥ 2 to identify characteristic variables.
Findings
  • Group 1 elementary motor signsGroup 1 comprised 16 patients and was characterized by one or more elementary motor signs, including clonic signs, contralateral tonic posture, contralateral versive signs, asymmetric tonic posture, secondary generalization, or asymmetric facial contraction; somesthetic localized aura and tonic vocalization could also occur. Gestural motor behavior and emotional features were absent. Its early spread network showed significant involvement of rolandic cortex (BA 4), rolandic operculum (low BA 4), and parietal cortex, with other caudal and premotor regions also possible; discharge could begin in medial or lateral premotor regions or propagate lateromedially.PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Group 1
Reported values
  • value-test > 2Group 1 elementary motor signsThreshold · Group 1, 16 patients · Group 1 early spread network · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Group 1
  • 16 patientsGroup 1 elementary motor signsCount · Group 1, 16 patients · Group 1 · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Group 1
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • elementary motor signsTable 3 lists 5 patients for the the source's own ictal symptom “elementary motor signs”; its table phase label is onset.PDF p.6, Table 3
  • elementary motor signsTable 3 reports a pooled prevalence of 4% for the the source's own ictal symptom “elementary motor signs”; its table phase label is onset.PDF p.6, Table 3
Reported values
  • 4% pooled prevalenceelementary motor signsPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • elementary motor sign; complex motor sign; gestural behaviourIntracranial stereo-EEG literature is summarized as placing elementary clonic, tonic, and versive signs in precentral and premotor regions; less-natural proximal stereotypies such as rocking and turning in premotor/posterior prefrontal regions; and more integrated natural gestural behaviour with distal stereotypies such as manual automatisms in more anterior prefrontal regions including orbitofrontal cortex, frontal pole, and anterior cingulate.PDF p.2, Frontal lobe seizures; PDF p.3, Figure 1
  • elementary motor signs; complex motor signs; gestural behaviourThe review reports that intracranial stereo-EEG studies associate elementary clonic, tonic, and versive signs with precentral and premotor regions; more complex motor signs with more rostral frontal regions; non-integrated proximal stereotypies such as rocking and turning with premotor and posterior prefrontal regions; and integrated distal stereotypies such as manual automatisms with anterior prefrontal regions including orbitofrontal cortex, frontal pole, and anterior cingulate.PDF p.2, Frontal lobe seizures
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • elementary motor phenomenaElementary motor phenomena were reported in two of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 2/26 (7.6%)elementary motor phenomenaPercentage · n/N 2/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdfStructured design not resolved · 1 finding · 1 reported value
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.423
The study enrolled seven consecutive PCE patients; six had SEEG-identified posterior cingulate ictal onset and one had an MRI-identified postcingulate tumour. Four patients underwent CCEP. SEEG and scalp EEG were retrospectively analyzed with video-documented ictal semiology; the source used the Lüders seizure-classification scheme. The posterior cingulate was operationally defined caudal to the vertical posterior commissure line.
Findings
  • motor manifestations in PCEThree of seven patients showed motor manifestations.PDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
Reported values
  • 3/7 motor manifestationsmotor manifestations in PCEProportion · n/N 3/7 · 7 PCE patients · ictal semiologyPDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEDystonic limb posturing within 20 seconds of seizure onset was reported more often in MTLE than NTLE, 52% versus 26%, and oral automatisms were reported 69% versus 11%, respectively. Early facial grimacing or twitching and contralateral motor activity were suggestive of NTLE.PDF p.6, section 8.1 Neocortical temporal lobe epilepsy
Reported values
  • Oral automatisms in MTLE 69%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · MTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Early dystonic posturing in NTLE 26%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · NTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Early dystonic posturing in MTLE 52%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · MTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
  • Oral automatisms in NTLE 11%early dystonia, oral automatisms, and early facial or contralateral motor activity in NTLE versus MTLEPercentage · patients with NTLE and MTLE · NTLE · within 20 seconds of seizure onset; early ictalPDF p.6, section 8.1 Neocortical temporal lobe epilepsy
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 10 findings · 6 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; orofacial; brachial; tonic; clonic; dystonicElementary motor symptoms were described as early, mainly involving the orofacial regions and/or arms; arm manifestations were mainly contralateral tonic, clonic, or dystonic seizures or postures.PDF p.6, Anatomical and clinical correlations; PDF p.8, Discussion
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 9/21 (43%) for Elementary motor: orofacial (tonic and/or clonic, grimace); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 4/12 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the prefrontal operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 5/9 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Fisher's exact comparison of Elementary motor: orofacial (tonic and/or clonic, grimace) between the prefrontal and precentral Rolandic operculum groups has p=0.396.PDF p.7, Table 2
  • Elementary motor: otherTable 2 reports 13/21 (62%) for Elementary motor: other; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Moderate.PDF p.7, Table 2
  • Elementary motor: otherTable 2 reports 6/12 patients with Elementary motor: other in the prefrontal operculum group.PDF p.7, Table 2
  • Elementary motor: otherTable 2 reports 7/9 patients with Elementary motor: other in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Elementary motor: otherFisher's exact comparison of Elementary motor: other between the prefrontal and precentral Rolandic operculum groups has p=0.367.PDF p.7, Table 2
Reported values
  • 9/21 (43%)Elementary motor: orofacial (tonic and/or clonic, grimace)Percentage · n/N 9/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 5/9 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 5/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
  • 13/21 (62%)Elementary motor: otherPercentage · n/N 13/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 6/12 patientsElementary motor: otherProportion · n/N 6/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 7/9 patientsElementary motor: otherProportion · n/N 7/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 1 finding
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • Gastaut syndrome headache-associated seizure semiologyThe review describes Gastaut syndrome as rare and usually occurring in the first decade; seizures begin with visual symptoms such as scintillating scotomas or hallucinations and eye deviation, then evolve to impaired awareness and focal motor activity, with migraine headaches common after seizures.PDF p.3, Localization; PDF p.4, Localization (continued)
jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdfCase report or observation · 1 finding
jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study included consecutive children with focal epilepsy and MRI-defined BOSD evaluated at The Hospital for Sick Children in Toronto between January 2007 and July 2019; patients with less than 1 year of postsurgical follow-up were excluded. Forty-one children were included. Medical-record data included seizure semiology, seizure frequency, age at seizure onset, antiseizure medications, and comorbidities. Mean age at surgery was 9.7 years (SD 4.5), 29 patients were male (70.7%), and mean age at seizure onset was 4.7 years (SD 3.5). Table 1 reported daily seizures in 30 of 41 patients (73.2%), weekly seizures in 9 (22.0%), monthly seizures in 1 (2.4%), yearly seizures in 1 (2.4%), and a history of focal status epilepticus requiring hospitalization in 8 (19.5%); these are cohort descriptors, not separate findings here. Presurgical evaluation included scalp video EEG, MEG, FDG-PET, and invasive video EEG when indicated. Thirty-seven patients underwent IVEEG, and 34 had available ictal data. Forty patients underwent MEG. MRI context included left-sided lesions in 23 of 41 patients (56.1%) and right-sided lesions in 18 (43.9%); lesion distributions were frontal 21 (51.2%), parietal 6 (14.6%), temporal 2 (4.9%), insular 4 (9.8%), and pre- or postcentral 8 (19.5%). These lesion-distribution and treatment details are contextual only and are not findings in this report.
Findings
  • frequent left focal motor seizuresFigure 2 describes a 13-year-old right-handed, developmentally normal female with frequent left focal motor seizures and a right parietal BOSD; interictal EEG showed characteristic EKG-like spike waves in the right centroparietal head region with fields in the left centroparietal region.PDF p.5, Figure 2 caption
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 4 findings · 11 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • motor signs; frontal semiologyThe review reports that Hagiwara et al. (2017) found strong couplings with mesial frontal and cingulate regions in the three patients with frontal semiology, whereas the two patients with insular semiology only showed couplings between the insula and cingulate regions.PDF p.5, Table 1, Motor signs row
  • elementary motor signs; gestural motor behavior; emotional expressionThe review reports that Bonini, McGonigal et al. (2014) identified four frontal-lobe semiologic groups along a rostro-caudal gradient: Group 1 had elementary motor signs without gestural motor behavior; Group 2 combined elementary and gestural motor signs, often with mainly proximal tonic signs and facial contraction; Group 3 had no elementary motor signs and often distal, integrated gestural behavior; and Group 4 had no elementary motor signs with integrated gestural behavior in an emotional, usually fearful, context.PDF p.6, Table 2, Frontal lobe row
  • motor signs; frontal semiology; insular semiologyIn the summarized Hagiwara et al. study, the three patients with frontal semiology showed strong couplings between insula and mesial frontal or cingulate regions, including medial orbitofrontal cortex, pre-SMA/SMA, and anterior-to-posterior cingulate, whereas the two patients with insular semiology only showed couplings between insula and cingulate regions.PDF p.5, Table 1 (continued), Hagiwara et al. 2017 row
  • elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresIn the summarized Bonini, McGonigal et al. study, automated clustering of clinical signs and brain areas involved in seizure onset and early propagation found a rostrocaudal frontal gradient with four groups: elementary motor signs without gestural behavior; elementary plus gestural signs with mainly proximal tonic signs and facial contraction; gestural behavior without elementary signs and often distal or integrated; and gestural behavior in an emotional, often fearful, context with an integrated appearance.PDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
Reported values
  • 2 patients with insular semiology onlymotor signs; frontal semiologyCount · 5 subjects with insular epilepsy; 3 with frontal semiology and 2 with insular semiology only · insular semiology only · Period of semiologic expressionPDF p.5, Table 1, Motor signs row
  • 3 patients with frontal semiologymotor signs; frontal semiologyCount · 5 subjects with insular epilepsy; 3 with frontal semiology and 2 with insular semiology only · frontal semiology · Period of semiologic expressionPDF p.5, Table 1, Motor signs row
  • n=5 subjectsmotor signs; frontal semiologyCount · 5 subjects with insular epilepsy; 3 with frontal semiology and 2 with insular semiology only · cited study · Period of semiologic expressionPDF p.5, Table 1, Motor signs row
  • 374 seizureselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • 54 subjectselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • 2 patients with insular semiology onlymotor signs; frontal semiology; insular semiologyCount · 5 subjects with insular epilepsy; 3 with frontal semiology and 2 with insular semiology only; number of seizures Not reported · insular semiology only · ictal, during motor semiologyPDF p.5, Table 1 (continued), Hagiwara et al. 2017 row
  • 3 patients with frontal semiologymotor signs; frontal semiology; insular semiologyCount · 5 subjects with insular epilepsy; 3 with frontal semiology and 2 with insular semiology only; number of seizures Not reported · frontal semiology · ictal, during motor semiologyPDF p.5, Table 1 (continued), Hagiwara et al. 2017 row
  • 5 subjects totalmotor signs; frontal semiology; insular semiologyCount · 5 subjects with insular epilepsy; 3 with frontal semiology and 2 with insular semiology only; number of seizures Not reported · cited study · ictal, during motor semiologyPDF p.5, Table 1 (continued), Hagiwara et al. 2017 row
  • Semiology clusters n=4elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Patients in semiology series n=54elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Seizures in semiology series n=374elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 2 findings
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • multifocal status with focal motor onset and bilateral propagationIn the illustrated new-onset refractory status case, initial right frontal focal ictal discharges with left facial twitching became more intense and spread to the right temporal region, then left frontal and left temporal regions; recurrent motor seizures progressed from left facial twitching to bifacial and bilateral upper-extremity jerking, while other multifocal ictal discharges had no visible motor correlate, leading the source to classify the course as focal motor status evolving to focal nonconvulsive status and then focal-onset bilateral convulsive status.PDF p.416; PDF p.417; PDF p.418; PDF p.420
  • frontal aura, primary motor, and supplementary motor semiologyFrontal auras are less common and less specific than temporal auras; abdominal sensations can arise from orbitofrontal or cingulate regions; forced thinking suggests dorsolateral frontal involvement; preserved-awareness clonic activity is most localizing to primary motor cortex, with lower-extremity signs suggesting mesial frontal and facial signs suggesting inferior frontal involvement; supplementary sensorimotor seizures tend to be brief, clustered, nocturnal, asymmetrical tonic or postural events with proximal predominance, and may include vocalization, startle precipitation, or bilateral symptoms without loss of consciousness.PDF p.51; PDF p.52; PDF p.53
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 9 findings · 8 reported values
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • automatisms; elementary motor; hyperkinetic; autonomic; emotional; grimace; cognitive; other subjectiveThe source classifies ictal features into automatisms, elementary motor, hyperkinetic, autonomic, emotional, grimace, cognitive, and other subjective categories for the cluster and prevalence analyses.PDF p.4, Statistical analysis
  • elementary motor signs; whole groupElementary motor signs were reported in 47% of the whole review group.PDF p.5, All group; PDF p.9, Figure 2
  • elementary motor signs; fronto-temporal subgroupElementary motor signs was reported in 24% of the fronto-temporal subgroup (33 patients).PDF p.5, Fronto-temporal subgroup
  • elementary motor signs; temporo-frontal subgroupElementary motor signs was reported in 57% of the temporo-frontal subgroup (76 patients).PDF p.5, Temporo-frontal subgroup
  • association coefficient; motor elementary and other clusterThe source reports an association coefficient of 0.553 for motor elementary and other cluster in the whole group.PDF p.9, Seizure semiology; PDF p.10, Figure 3A
  • association coefficient; motor elementary and other subjectiveThe source reports an association coefficient of 0.818 for motor elementary and other subjective in the fronto-temporal subgroup.PDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
  • elementary motor signs; multilobar resection; whole groupElementary motor signs were significantly more frequent among patients receiving multilobar resection in the whole-group analysis, with p=.022.PDF p.1, Abstract; PDF p.9, Seizure semiology
  • elementary motor signs; multilobar resection; fronto-temporal subgroupThe source reports a fronto-temporal subgroup p value for the association between elementary motor signs and multilobar resection as .0012 in the abstract.PDF p.1, Abstract
  • elementary motor signs; multilobar resection; fronto-temporal subgroupThe source reports a fronto-temporal subgroup p value for the association between elementary motor signs and multilobar resection as .12 in the body text.PDF p.9, Seizure semiology
Reported values
  • 47%elementary motor signs; whole groupPercentage · 109 review patients, whole group · ictalPDF p.5, All group; PDF p.9, Figure 2
  • 24%elementary motor signs; fronto-temporal subgroupPercentage · 33 patients, fronto-temporal subgroup · ictalPDF p.5, Fronto-temporal subgroup
  • 57%elementary motor signs; temporo-frontal subgroupPercentage · 76 patients, temporo-frontal subgroup · ictalPDF p.5, Temporo-frontal subgroup
  • association coefficient 0.553association coefficient; motor elementary and other clusterAssociation Coefficient · 109 review patients · ictal symptom co-occurrencePDF p.9, Seizure semiology; PDF p.10, Figure 3A
  • association coefficient 0.818association coefficient; motor elementary and other subjectiveAssociation Coefficient · 33 fronto-temporal subgroup patients · ictal symptom co-occurrencePDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
  • p=0.022elementary motor signs; multilobar resection; whole groupP value · Review patients undergoing surgery with whole-group sign/resection comparison · ictal sign associated with surgical extentPDF p.1, Abstract; PDF p.9, Seizure semiology
  • p=0.0012elementary motor signs; multilobar resection; fronto-temporal subgroupP value · Fronto-temporal subgroup patients undergoing surgery with sign/resection comparison · ictal sign associated with surgical extentPDF p.1, Abstract
  • p=0.12elementary motor signs; multilobar resection; fronto-temporal subgroupP value · Fronto-temporal subgroup patients undergoing surgery with sign/resection comparison · ictal sign associated with surgical extentPDF p.9, Seizure semiology
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 2 findings · 2 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • contralateral focal motor activityContralateral focal motor activity occurred in 16 of 42 patients.PDF p.6, Results, Non-visual manifestations
  • focal motor activity in cited reportsThe source reports focal motor activity in as many as 47% of patients in a cited occipital epilepsy series.PDF p.21, Discussion
Reported values
  • 16/42 (38%) patientscontralateral focal motor activityPercentage · n/N 16/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal propagation or later ictal manifestationPDF p.6, Results, Non-visual manifestations
  • up to 47%focal motor activity in cited reportsUpper-bound percentage · cited occipital lobe epilepsy reports · ictal propagation or later ictal manifestationPDF p.21, Discussion
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • ictal motor signs; elementary motor signs; complex motor behaviorAll patients had ictal motor signs; elementary tonic and/or dystonic motor signs occurred more commonly than complex motor behavior, although both could occur in the same seizure.PDF p.3, Results—Seizure semiology; PDF p.7, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • occipital onset with temporal-like automatism and motor expressionThe source concludes that occipital-onset seizures can produce temporal-like automatisms and frontal- or parietal-like motor symptoms through network propagation.PDF p.12, Key Findings and Phenotype-Propagation Pattern Correspondences; PDF p.14, Clinical Translation
wyllie1986.pdfStructured design not resolved · 1 finding · 30 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.893
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • ictal arm and face involvement on the side of contraversionDuring contraversion, arm and face motor activity occurred on the side toward which contraversion was directed: arm clonic movement or tonic posturing occurred in 32 of 61 versive seizures (52%), face tonic or clonic contraction in 26 of 55 seizures with continuously visible faces (47%), and arm and face involvement occurred with equal frequency in temporal and extratemporal onset seizures.PDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
Reported values
  • total arm activity: 17 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · total · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • frontal all versive seizures: 10 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · frontal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • temporal arm activity: 12 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · temporal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • parietal arm activity: 0 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · parietal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • total face activity 26/55 (47%)ictal arm and face involvement on the side of contraversionPercentage · n/N 26/55 · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · total · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • parietal all versive seizures: 2 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · parietal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • temporal all versive seizures: 14 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · temporal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • occipital arm activity: 0 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · occipital · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • occipital face activity: 0 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · occipital · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • parietal face activity: 1 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · parietal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • frontal arm activity: 20 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · frontal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • parietal all versive seizures: 2 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · parietal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • occipital arm activity: 0 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · occipital · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • total all versive seizures: 61 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · total · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • temporal face activity: 8 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · temporal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • frontal arm activity: 6 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · frontal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • temporal face activity: 7 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · temporal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • frontal face activity: 17 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · frontal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • parietal face activity: 1 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · parietal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • frontal all versive seizures: 37 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · frontal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • parietal arm activity: 0 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · parietal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • total all versive seizures: 27 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · total · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • occipital all versive seizures: 2 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · occipital · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • temporal all versive seizures: 20 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · temporal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • temporal arm activity: 11 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · temporal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • occipital all versive seizures: 1 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · occipital · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • occipital face activity: 0 seizuresictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · occipital · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • total arm activity 32/61 (52%)ictal arm and face involvement on the side of contraversionPercentage · n/N 32/61 · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · total · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • frontal face activity: 8 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · frontal · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
  • total face activity: 16 patientsictal arm and face involvement on the side of contraversionCount · 61 versive seizures from 27 patients; face analysis restricted to 55 seizures with continuous full facial visibility · total · During contraversion; focal motor activity began within 5 seconds after contraversion onsetPDF p.3, Table 3; PDF p.3, paragraphs describing arm/face activity and timing; PDF p.4, discussion of contralateral arm and face movement
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdfCase report or observation · 1 finding · 2 reported values
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a two-case report with no control or comparator group. Case-1 was a 24-year-old right-handed man; 32 habitual seizures were recorded during 3 days of scalp video-EEG, with two followed by secondary GTCS, and two right-hemisphere SEEG implantations were performed 4 months apart. Case-2 was a 19-year-old right-handed man; three habitual seizures were captured on video-EEG and right temporal neocortical, temporal-pole, and medial-structure regions were explored with SEEG. The source describes scalp EEG, MRI, FDG-PET, SEEG onset and propagation, anatomical reconstruction, cortical resection, and seizure-free follow-up of 17 months for Case-1 and 25 months for Case-2. Case-1 MRI/FDG-PET was reported unremarkable for an evaluable lesion; Case-2 MRI and PET findings were reported in the right middle-posterior inferior temporal/fusiform and medial temporal regions. No cohort-wide denominator for ipsiversive eye deviation, no control comparison, and no population-level frequency or diagnostic statistic are reported.
Findings
  • Case-2 forced right eye deviation with left motor signsIn Case-2, the reported habitual seizure chronology was eyes open and staring followed by forced deviation to the right, proximal left-arm tonic posturing with a clenched left fist, and left facial clonia in one seizure; the episodes included loss of consciousness.PDF p.5, Case-2 case presentation; PDF p.8-9, Discussion
Reported values
  • left facial clonia occurred in 1 of 3 captured habitual seizuresCase-2 forced right eye deviation with left motor signsCount · n/N 1/3 · Case-2; three habitual seizures were captured on video-EEG, but the source does not state that every listed component occurred in all three · ictal onset and progressionPDF p.5, Case-2 case presentation; PDF p.8-9, Discussion
  • Qualitative semiologic sequenceCase-2 forced right eye deviation with left motor signsCount · n/N 1/3 · Case-2; three habitual seizures were captured on video-EEG, but the source does not state that every listed component occurred in all three · ictal onset and progressionPDF p.5, Case-2 case presentation; PDF p.8-9, Discussion

20 contributing manuscripts; source-reported values remain separate and are not pooled.

Gustatory auraReported: IpsilateralAlso reported: Right hemisphereNo single reliable side17 manuscripts · 36 findings · 23 reported values
Weighted evidence supportevidence weight 36.98 across 17 manuscripts · 1 manuscript weight pending · 3 independent primary study · 8 narrative, educational, or cited context · 5 systematic review or meta-analysis · 1 structured design not resolved

The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. Gustatory aura is restated as non-lateralising. Gustatory auras are described as having no lateralizing value. Olfactory and gustatory auras are summarized as generally nonlateralizing. No source-supported hemispheric or body-side lateralization is reported. Gustatory aura was associated with the TS subgroup and vestibular aura with the TPO subgroup; no lateralization is reported. No seizure lateralization is reported. No lateralizing direction is reported for gustatory symptoms. No lateralizing direction is reported. No hemisphere or body-side direction is reported. The mesial-versus-lateral temporal comparison provides no hemispheric direction. The study-count record provides no hemispheric direction. This lateral-versus-mesial temporal statistic provides no hemispheric lateralization. The lateral-temporal prevalence result provides no hemispheric direction. The occurrence odds provide no hemispheric direction. The lateral-TLE prevalence result provides no hemispheric direction. The mesial-TLE prevalence range provides no hemispheric direction. No seizure lateralization is reported for the 7% gustatory-sensation summary. No seizure lateralization is reported for the 6-case, 7% gustatory-symptom entry. No seizure lateralization is reported for the 4/60 (7%) gustatory-symptom entry. No lateralizing direction is reported for gustatory sensations. The patient-level falling, gustatory, and abdominal aura entry gives no body-side or hemisphere information. The review places fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo between lateral and medial temporal patterns.

Source-defined result groups 15
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 40.0%not clearly identifiable · gustatory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Olfactory/gustatory aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: response frequencyObserved proportion 2.7%gustatory sensation · other evoked response types · evoked response1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 60.0%nasty or unpleasant · gustatory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Lateralization: description subtypeObserved proportion 60.0%nasty or unpleasant · gustatory response1 manuscript · 1 reported value · not pooled
Localization: L group / M group / ML groupObserved proportion 8.3%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: L group / M group / ML groupObserved proportion 0.0%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: L group / M group / ML groupObserved proportion 5.6%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Lateralization: description subtypeObserved proportion 40.0%not clearly identifiable · gustatory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Olfactory/gustatory aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 2.7%gustatory sensation · other evoked response types · evoked response1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 17

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 2 findings · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • posterior cingulate gustatory auraThe source reports 1 posterior cingulate patient with gustatory aura.PDF p.5, Clinical Presentation
  • patient 12 falling/gustatory/abdominal auraFalling, gustatory, and abdominal aura terms were listed for patient 12.PDF p.4, Figure 3
Reported values
  • 1/4 gustatory auraposterior cingulate gustatory auraProportion · n/N 1/4 · 4 posterior cingulate cases · auraPDF p.5, Clinical Presentation
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 4 findings · 5 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • gustatory hallucinationGustatory hallucinations were more frequent in T+ than TL seizures.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • T+ subgroup associations for gustatory and vestibular aurasAmong T+ cases, gustatory auras were significantly associated with the TS subgroup and vestibular auras with the TPO subgroup.PDF p.5, Seizure clinical semiology; PDF p.7, Auras
  • gustatory, vestibular, and auditory symptomsThe source states that the localizing significance of gustatory, vestibular, and auditory symptoms remains uncertain in the cited literature.PDF p.7, Auras
  • gustatory symptoms and insulo-opercular cortexThe source states that cortical electrical stimulation studies support a role for the suprasylvian opercular cortex and/or insula in the occurrence of gustatory symptoms.PDF p.7, Auras
Reported values
  • T+ 21.7%gustatory hallucinationPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • P=0.02gustatory hallucinationP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • TL 5.1%gustatory hallucinationPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Auras
  • P=0.02T+ subgroup associations for gustatory and vestibular aurasP value · T+ subgroup patients and their one analyzed typical seizure; TS n=7 and TPO n=6 · TPO subgroup · ictal onsetPDF p.5, Seizure clinical semiology; PDF p.7, Auras
  • P=0.009T+ subgroup associations for gustatory and vestibular aurasP value · T+ subgroup patients and their one analyzed typical seizure; TS n=7 and TPO n=6 · TS subgroup · ictal onsetPDF p.5, Seizure clinical semiology; PDF p.7, Auras
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • gustatory sensationsGustatory sensations accounted for 7% of the sensory manifestations in the narrative summary.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Gustatory (Table 3)Table 3 reports gustatory symptoms in 6 cases (7%), with propagation timing marked uncertain.PDF p.6, Table 3
  • Gustatory (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports gustatory symptoms in 4 cases (7%).PDF p.7, Table 4
Reported values
  • 7% gustatory sensationsgustatory sensationsPercentage · reviewed basal temporal seizure cases · ictal propagation uncertain in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 6 cases (7%)Gustatory (Table 3)Percentage · Table 3 basal temporal seizure cases · propagation?PDF p.6, Table 3
  • 4/60 (7%)Gustatory (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • gustatory; olfactory; vestibular; autonomic auraTable 3 maps gustatory aura to insula or mesiotemporal regions, olfactory aura to insula, mesiotemporal, or orbitofrontal regions, vestibular aura to posterior temporal or parietal regions, and autonomic aura to insula, amygdala, or cingulate regions.PDF p.10, Table 3; PDF p.3, Figure 1
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 12 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • epigastric aura; olfactory/gustatory auraThe source states that absence of epigastric or olfactory/gustatory auras may be more indicative of lateral than mesial temporal seizures, whereas their presence points toward mesial rather than lateral onset.PDF p.7, Discussion; PDF p.10, Conclusions
  • Olfactory/gustatory auraTable 3 reports 3 studies assessing Olfactory/gustatory aura.PDF p.6, Table 3
  • Olfactory/gustatory auraTable 3 reports 42 patients assessed for Olfactory/gustatory aura.PDF p.6, Table 3
  • Olfactory/gustatory auraTable 3 reports 0% as the percentage range or value for Olfactory/gustatory aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Olfactory/gustatory auraTable 4 reports overall odds of 0.04 for occurrence of Olfactory/gustatory aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Olfactory/gustatory auraTable 4 reports a 95% confidence interval of 0.01–0.19 for the overall odds of Olfactory/gustatory aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Olfactory/gustatory auraThe heterogeneity test for the Table 4 odds estimate for Olfactory/gustatory aura has p=0.9159.PDF p.7, Table 4
  • Olfactory/gustatory aura; lateral versus mesial comparisonTable 5 reports 3 studies comparing Olfactory/gustatory aura in lateral and mesial TLE.PDF p.9, Table 5
  • Olfactory/gustatory aura; lateral TLE patient denominatorTable 5 reports 42 lateral-TLE patients assessed for Olfactory/gustatory aura.PDF p.9, Table 5
  • Olfactory/gustatory aura; mesial TLE patient denominatorTable 5 reports 67 mesial-TLE patients assessed for Olfactory/gustatory aura.PDF p.9, Table 5
  • Olfactory/gustatory aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0% for Olfactory/gustatory aura.PDF p.9, Table 5
  • Olfactory/gustatory aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–18.8% for Olfactory/gustatory aura.PDF p.9, Table 5
Reported values
  • 0%Olfactory/gustatory auraPercentage · Lateral temporal epilepsy patients assessed for Olfactory/gustatory aura · ictalPDF p.6, Table 3
  • odds 0.04odds of occurrence; Olfactory/gustatory auraOdds · Lateral temporal epilepsy patients assessed for Olfactory/gustatory aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0%Olfactory/gustatory aura; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Olfactory/gustatory aura · Lateral TLE patients assessed for Olfactory/gustatory aura · ictalPDF p.9, Table 5
  • 0–18.8%Olfactory/gustatory aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Olfactory/gustatory aura · Mesial TLE patients assessed for Olfactory/gustatory aura · ictalPDF p.9, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • olfactory and gustatory aurasOlfactory auras are typically unpleasant and often associated with gustatory phenomena; stimulation of the amygdala, olfactory bulb, insula, or posterior orbitofrontal region can produce olfactory sensations or illusions. Gustatory auras can be difficult to distinguish from olfactory disturbances, and stimulation of the parietal operculum or mesiobasal temporal regions can produce gustatory hallucinations.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • olfactory and gustatory hallucinationsUnpleasant olfactory and gustatory hallucinations can result from seizures involving mesial temporal structures, particularly the amygdala, but are not pathognomonic because gustatory symptoms with hypersalivation and olfactory symptoms have also been reported with opercular and orbitofrontal seizures, respectively.PDF p.8, Focal sensory seizures; PDF p.10, Temporal plus epilepsy
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 3 findings · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • gustatory auraGustatory auras are among the reported clinical manifestations of insular seizures.PDF p.2, Clinical Features
  • gustatory aura as suggestive insular featureGustatory auras are described as highly suggestive of insular or insulo-opercular seizures.PDF p.2, Clinical Features
  • gustatory stimulation responsesGustatory sensations represented 2.7% of all responses in the cited insular stimulation series.PDF p.5, Other Insular Responses; PDF p.5, Figure 4 panel 5
Reported values
  • 2.7% gustatory responsesgustatory stimulation responsesPercentage · all responses in the cited insular stimulation series · stimulation-evoked semiologyPDF p.5, Other Insular Responses; PDF p.5, Figure 4 panel 5
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal sensory (gustatory)Focal sensory (gustatory) semiology occurred in 2/61 individuals (3%) both as initial semiology and in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • 2/61 (3%) initialFocal sensory (gustatory)Percentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • 2/61 (3%) combinedFocal sensory (gustatory)Percentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Gustatory auraTable 2 associates gustatory aura with Rolandic and parietal operculum, basal/mesial temporal regions, and insula and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Gustatory auraPerception of a taste as an epileptic phenomenon is a gustatory aura, but the term is applied only when the gustatory hallucination is the predominant symptom.PDF p.3, Auras, subsection Gustatory auras; PDF p.2, Table 1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 4 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • gustatory hallucinationGustatory hallucination frequencies did not differ significantly across M, ML, and L groups.PDF p.5, Table 2
Reported values
  • p=0.78gustatory hallucinationP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · initial ictal subjective symptomPDF p.5, Table 2
  • M=2/24 (8.3%)gustatory hallucinationPercentage · n/N 2/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2
  • ML=1/18 (5.6%)gustatory hallucinationPercentage · n/N 1/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2
  • L=0/13 (0%)gustatory hallucinationPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • gustatory sensationsGustatory sensations occurred in 15 responses (2.7%), were obtained exclusively from a relatively restricted medium-upper insular zone corresponding to the posterior short gyrus, and were described as nasty or unpleasant in 9 cases or not clearly identifiable in 6.PDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
Reported values
  • 9 casesgustatory sensationsCount · n/N 9/15 · 15 gustatory responses in the 550-response series · nasty or unpleasant · stimulation-evoked gustatory sensationPDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
  • 15 responses (2.7%)gustatory sensationsPercentage · n/N 15/550 · 15 gustatory responses in the 550-response series · gustatory sensation · stimulation-evoked gustatory sensationPDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
  • 6gustatory sensationsCount · n/N 6/15 · 15 gustatory responses in the 550-response series · not clearly identifiable · stimulation-evoked gustatory sensationPDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • stimulation-evoked somatosensory, auditory, vestibular, olfactory, gustatory, and viscerosensory symptomsThe chapter reports that electrical stimulation studies evoked somatosensory symptoms, including pain, from the posterior two-thirds of the insula; auditory and vestibular symptoms from the posterior insula; and olfactory, gustatory, and viscerosensory symptoms, including laryngeal constriction, from the midinsula, whereas stimulation of the most anterior portion rarely evoked symptoms unless a larger network seizure was elicited.PDF p.3, insular functional differentiation and electrical cortical stimulation
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • fear; auditory hallucinations; gustatory hallucinations; sensory hallucinations; vertigoThe source describes fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo as intermediate features between lateral and medial temporal patterns.PDF p.5, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • gustatory aurasThe review describes gustatory auras as unpleasant tastes, states that cortical stimulation studies identify the insula as a symptomatogenic zone, and states that these auras have no lateralizing value.PDF p.2, Gustatory auras

17 contributing manuscripts; source-reported values remain separate and are not pooled.

Late forced/tonic head version (>30s, sustained, contralateral)Source terms: Late forced/tonic head version; Late forced head versionReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side22 manuscripts · 52 findings · 138 reported values
Weighted evidence supportevidence weight 36.57 across 22 manuscripts · 3 manuscript weight pending · 4 independent primary study · 3 case report or observation · 9 narrative, educational, or cited context · 3 systematic review or meta-analysis · 3 structured design not resolved

The review restates that early nonforced head turning is usually ipsilateral, whereas later forceful involuntary version is most often contralateral to the seizure focus. In this case, right head version and right-arm extension were contralateral to left onset, while the left last clonic jerk was ipsilateral to left onset. In the cited study, late forced head deviation was contralateral in more than 90% of qualifying seizures. Two patients had one or two atypical post-tapering seizures with contralateral version; these observations were excluded from propagation-pattern classification. Version was more frequent in T+ than TL seizures, with TL 35.6% versus T+ 60.9% overall and a significant contralateral subtype association (P=0.001); ipsilateral and bilateral categories remain separately recorded. The cited restatement describes contralateral versive manifestations, more frequent association with T+ epilepsy, and occurrence in temporal-origin seizures. The case observation records right-sided version during habitual partial seizures. Version was reported as contralateral with 100% PPV and inter-observer kappa 0.74; sign-positive occurrences were distributed across temporal, frontal, parietal, and occipital cohorts. The educational tables label forced head version as contralateral. The cited series includes delayed motor signs, including source-described contralateral dystonia, without a reported onset-side direction. The review restates contralateral frontal-eye-field involvement for versive seizures and possible SMA involvement for asymmetric tonic posturing. Versive seizures are described as highly lateralizing toward the contralateral hemisphere, especially shortly before secondary generalization, with reliability depending on the source-defined conditions. Version occurred in 9/16 TLE and 8/15 XTLE patients and was contralateral to ictal onset in all patients with version in each subgroup. Version occurred in 13/26 Group II patients and was contralateral to ictal onset in all 13 patients with version. The review states that sustained pre-GTCS head/eye version is contralateral to the seizure-onset hemisphere and distinguishes earlier frontal from later impaired-awareness temporal version. The review restates greater-than-90% contralateral head version immediately before SGTCS, up to 15–20% ipsilateral version at the end, and an ipsilateral-nonversive to contralateral-versive temporal sequence. Tonic head deviation was predominantly contralateral to seizure onset, with 19/21 pooled episodes contralateral; LTL had 16/73 (22%) late contralateral episodes versus RTL 3/54 (6%). The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. Version-first and version-plus-tonic sequence counts are reported, with correct EZ lateralization in 3/4 tonic-start/asymmetric-clonic sequences and 1/1 M2e-to-clonic sequence, but no direction is stated. The review restates contralateral lateralization above 90% under specified timing/quality conditions and 100% under other cited conditions. All 61 versive seizures were contralateral to onset and none ipsilateral, while nonversive turning was nearly evenly split (6/13 contralateral, 7/13 ipsilateral) and nonlocalizing. Head-and-eye version or eye-only version was contralateral to seizure onset; head and eyes moved together in 40/61 versive seizures, with separate head-only, eye-only, frontal-onset, and occipital-onset counts. Versive movement was contraversive relative to seizure-onset hemisphere regardless of whether it was smooth (40/61) or jerking (21/61). Contraversive head/eye movement persisted into the generalized phase in 8/27 seizures, while 12/27 generalized seizures ended with ipsiversion. The review describes forced sustained head and eye version as generally contralateral to seizure onset and particularly reliable in specified late or tonic-clonic contexts. The cited Wyllie series reviewed 74 seizures in 37 patients and described versive movements as always contralateral to seizure onset. The cited study is restated as finding a lateralizing value for version, with high reliability only under specified conditions and no direction reported here. No lateralizing direction is reported for overall versive manifestations. No source-supported hemispheric or body-side lateralization is reported. Lateral-temporal versus mesial-temporal is a localization comparison, not a cerebral hemisphere direction. No lateralizing direction is reported for version. No hemisphere or body-side direction is reported. No lateralizing direction is reported for version heterogeneity. Patient 9 had forced tonic head-and-eye deviation to the right, but the onset hemisphere is not supplied. Patient 14 had right version followed by a generalized tonic-clonic or dialeptic seizure. No seizure lateralization is reported. The supplied evidence identifies the subsequent contraversion as directed contralateral to the hemisphere of seizure onset. The educational definition describes sustained extreme movement to one side, but does not provide a seizure-onset hemisphere.

Source-defined result groups 61
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%Staring with automatisms · quiet staring versus staring with automatisms before contraversion · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 0% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 75.0%Correct EZ lateralization among tonic-start/asymmetric-clonic sequences · Version-first versus non-version-first order; variable sequence patterns · representative seizure (source also uses patient labels)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 21.9%LTL; contralateral late deviation · RTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%XTLE with version · TLE versus XTLE · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyversion first; temporal · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 100.0%Correct EZ lateralization in M2e-to-clonic sequence · Version-first versus non-version-first order; variable sequence patterns · representative seizure (source also uses patient labels)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 2.7%LTL; ipsilateral late deviation · RTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelywaning after return to midline · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeObserved proportion 100.0%Versive; contralateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 35.6% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyFrontal onset; Nonversive contralateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeObserved proportion 53.8%Nonversive; ipsilateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 90.5%Pooled tonic-head-deviation episodes · RTL versus LTL and contralateral versus ipsilateral relation to onset · episode1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 43.5% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 65.6%smooth versive movement · jerking versive movement · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Table 3 point estimate 6% · Table 3 between-report frequency range1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelynon-version first; extra-temporal · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyversion first · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other Table 3 temporo-polar sign estimates · Table 3 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelywaning · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Versive seizure · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyTemporal onset; Nonversive contralateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeObserved proportion 0.0%Versive; ipsilateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 44.4%end of generalized seizure · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeObserved proportion 46.2%Nonversive; contralateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyQuiet staring; extratemporal origin · Temporal origin · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyQuiet staring; temporal origin · Extratemporal origin · seizure1 manuscript · 1 reported value · not pooled
Localization: Frontal / OccipitalSource-defined values retained separatelyoccipital onset · combined head-and-eye movement versus head-only or eye-only version · seizure and patient for the explicitly reported patient counts1 manuscript · 2 reported values · not pooled
Localization: TemporalSource-defined values retained separatelynon-version first; temporal · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 5.6%RTL; contralateral late deviation · LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyVersive; contralateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 4 reported values · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Versive seizure · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 30.4% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 34.4%jerking versive movement · smooth versive movement · seizure1 manuscript · 1 reported value · not pooled
Localization: Frontal / OccipitalSource-defined values retained separatelyfrontal onset · combined head-and-eye movement versus head-only or eye-only version · seizure and patient for the explicitly reported patient counts1 manuscript · 2 reported values · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelypersistent contraversion · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 10.2% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 60.9% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 32.2% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyversion first; extra-temporal · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 29.6%persistent contraversion · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · Seizure and patient counts for sign occurrence; PPV analysis unit not otherwise reported.1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 0.0%RTL; ipsilateral late deviation · LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%Group II · patient with version1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyTemporal onset; Nonversive ipsilateral · versive versus nonversive lateral head and eye movement · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelynon-version first · Version-first versus non-version-first; temporal versus extra-temporal origin · seizure, one representative seizure per patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelypersistent contraversion · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelycontinued throughout · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 2 reported values · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelywaning after return to midline · contraversion persistence versus waning or continuation; temporal versus extratemporal onset · seizure; patient counts reported for the waning and continuing subsets1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 22

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 2 findings
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 9 forced right head/eye deviationHead and eyes forced tonic deviation to the right was listed for patient 9.PDF p.4, Figure 3
  • patient 14 right version evolutionRight version followed by generalized tonic-clonic or dialeptic seizure was listed for patient 14.PDF p.4, Figure 3
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 3 findings · 11 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • version of head and/or eyesVersion of the head and/or eyes was more frequent in T+ than TL seizures, with the significant subtype association occurring for contralateral version.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • versive manifestationsThe source states that versive manifestations of the eyes and head have extratemporal localizing associations in prior reports but have also been observed in seizures of TL origin.PDF p.8, Motor signs
  • versive manifestationsSimple motor signs were common and included versive manifestations, reported in 43.7% of analyzed seizures.PDF p.5, Seizure clinical semiology
Reported values
  • TL 10.2%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL 0%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL 35.6%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ 43.5%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ 0%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL 32.2%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • P=0.04version of head and/or eyesP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • P=0.001version of head and/or eyesP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ 30.4%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ 60.9%version of head and/or eyesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • versive manifestations 43.7%versive manifestationsPercentage · 80 analyzed seizures, one typical seizure per patient · ictalPDF p.5, Seizure clinical semiology
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • delayed motor signs (Duchowny study)The cited Duchowny series is described as having behavioral arrest and delayed motor signs including version, contralateral dystonia, clonic jerks, and automatisms.PDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Early head turn and late versionAn early nonforced head turn or head tilt, especially with preserved consciousness, is usually ipsilateral to seizure onset, whereas later, more forceful involuntary version is most often contralateral to the seizure focus.PDF p.4, Table 2; PDF p.4, section 4 Lateralizing Features in Temporal Lobe Epilepsy
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 5 findings · 2 reported values
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • versionThe discussion identifies version as a possible early localizing sign in SMA epilepsy because it was mostly reported at seizure onset.PDF p.8, Discussion
  • versionTable 3 lists 11 patients for the the source's own ictal symptom “version”; its table phase label is onset.PDF p.6, Table 3
  • versionTable 3 reports a pooled prevalence of 23% for the the source's own ictal symptom “version”; its table phase label is onset.PDF p.6, Table 3
  • version; between-study heterogeneityThe source reports I2 heterogeneity of 0.00% for pooled version prevalence.PDF p.4, Results
  • version; heterogeneity testThe source reports p = 0.47 for the between-study heterogeneity test of pooled version prevalence.PDF p.4, Results
Reported values
  • 23% pooled prevalenceversionPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
  • I2 = 0.00%version; between-study heterogeneityHeterogeneity I2 · Patients with SMA or pre-SMA epilepsy in the selected studies · ictal symptom prevalence analysisPDF p.4, Results
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfCase report or observation · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • head version; figure-of-4 sign; last clonic jerkIn video case 7, a 33-year-old man with left temporal hypometabolism had head version to the right followed by right-arm extension in a figure-of-4 posture, indicating left hemispheric onset; in one seizure the last clonic jerk was on the left, also pointing to left onset, while ictal EEG was non-localisable in one seizure and lateralised left in another.PDF p.10, Video case 7
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • versive elementary motor phenomenonOne restricted-OFC case had a versive elementary motor phenomenon.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 1 patientversive elementary motor phenomenonCount · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Versive seizureTable 3 reports 2 studies assessing Versive seizure.PDF p.6, Table 3
  • Versive seizureTable 3 reports 39 patients assessed for Versive seizure.PDF p.6, Table 3
  • Versive seizureTable 3 reports 0–13.6% as the percentage range or value for Versive seizure; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Versive seizureTable 4 reports overall odds of 0.11 for occurrence of Versive seizure in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Versive seizureTable 4 reports a 95% confidence interval of 0.03–0.43 for the overall odds of Versive seizure.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Versive seizureThe heterogeneity test for the Table 4 odds estimate for Versive seizure has p=0.2741.PDF p.7, Table 4
  • Versive seizure; lateral versus mesial comparisonTable 5 reports 1 studies comparing Versive seizure in lateral and mesial TLE.PDF p.9, Table 5
  • Versive seizure; lateral TLE patient denominatorTable 5 reports 17 lateral-TLE patients assessed for Versive seizure.PDF p.9, Table 5
  • Versive seizure; mesial TLE patient denominatorTable 5 reports 20 mesial-TLE patients assessed for Versive seizure.PDF p.9, Table 5
  • Versive seizure; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0% for Versive seizure.PDF p.9, Table 5
  • Versive seizure; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0% for Versive seizure.PDF p.9, Table 5
Reported values
  • 0–13.6%Versive seizurePercentage Range · Lateral temporal epilepsy patients assessed for Versive seizure · ictalPDF p.6, Table 3
  • odds 0.11odds of occurrence; Versive seizureOdds · Lateral temporal epilepsy patients assessed for Versive seizure · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0%Versive seizure; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Versive seizure · Lateral TLE patients assessed for Versive seizure · ictalPDF p.9, Table 5
  • 0%Versive seizure; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Versive seizure · Mesial TLE patients assessed for Versive seizure · ictalPDF p.9, Table 5
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 4 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • VersionIn the surgical cohort, version was reported as a contralateral lateralizing sign with 100% PPV for seizure lateralization and inter-observer kappa of 0.74.PDF p.3, Table 1; PDF p.3, §5.1
Reported values
  • PPV 100% (contralateral)VersionPositive predictive value · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 2 seizures/1 patient, frontal 8/6, parietal 6/4, and occipital 6/3. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 22 seizures with versionVersionCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 2 seizures/1 patient, frontal 8/6, parietal 6/4, and occipital 6/3. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 14 patients with versionVersionCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 2 seizures/1 patient, frontal 8/6, parietal 6/4, and occipital 6/3. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • inter-observer kappa 0.74VersionKappa · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 2 seizures/1 patient, frontal 8/6, parietal 6/4, and occipital 6/3. · IctalPDF p.3, Table 1; PDF p.3, §5.1
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Forced head versionBoth tables list Forced head version as Contralateral.PDF p.2, Lateralizing signs/Localization table row "Forced head version" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Forced head version" (printed p.5)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 5 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Tonic head deviationTonic head deviation, predominantly contralateral to the hemisphere of seizure origin, was more common in LTL than RTL seizures; across 21 episodes it was contralateral to seizure onset in 19 (90%).PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
Reported values
  • RTL ipsilateral late tonic head deviation 0/54Tonic head deviationPercentage · n/N 0/54 · RTL seizure group, n=54, versus LTL seizure group, n=73; pooled tonic-head-deviation episodes n=21 · RTL; ipsilateral late deviation · Late ictal phase; source states it most often occurred before secondary generalizationPDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL contralateral late tonic head deviation 16/73 (22%)Tonic head deviationPercentage · n/N 16/73 · RTL seizure group, n=54, versus LTL seizure group, n=73; pooled tonic-head-deviation episodes n=21 · LTL; contralateral late deviation · Late ictal phase; source states it most often occurred before secondary generalizationPDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • Contralateral to seizure onset 19/21 episodes (90%)Tonic head deviationPercentage · n/N 19/21 · RTL seizure group, n=54, versus LTL seizure group, n=73; pooled tonic-head-deviation episodes n=21 · Pooled tonic-head-deviation episodes · Late ictal phase; source states it most often occurred before secondary generalizationPDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL contralateral late tonic head deviation 3/54 (6%)Tonic head deviationPercentage · n/N 3/54 · RTL seizure group, n=54, versus LTL seizure group, n=73; pooled tonic-head-deviation episodes n=21 · RTL; contralateral late deviation · Late ictal phase; source states it most often occurred before secondary generalizationPDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL ipsilateral late tonic head deviation 2/73 (3%)Tonic head deviationPercentage · n/N 2/73 · RTL seizure group, n=54, versus LTL seizure group, n=73; pooled tonic-head-deviation episodes n=21 · LTL; ipsilateral late deviation · Late ictal phase; source states it most often occurred before secondary generalizationPDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 2 findings · 3 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • versive seizuresSustained forced turning of the head or eyes, usually with same-side mouth deviation and head hyperextension, is contralateral to the hemisphere of seizure onset when it occurs immediately before a GTCS. In temporal lobe seizures version occurs later while consciousness is impaired, unlike the earlier pattern described in FLE.PDF p.3, section 3.2 Simple motor seizures
  • head version during SGTCSHead version is contralateral to the epileptogenic zone in more than 90% of cases, especially when it occurs in the 10 seconds preceding an SGTCS. Ipsilateral head version at the end of an SGTCS occurs in as many as 15–20% of patients with focal seizures and is more common in FLE than TLE; in temporal-lobe seizures, brief initial ipsilateral nonversive turning often precedes contralateral version immediately before SGTCS.PDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
Reported values
  • in the 10 seconds preceding an SGTCShead version during SGTCSOther reported value · patients with focal seizures, including FLE and TLE · pre-SGTCS · initial phase of generalization; particularly 10 seconds before SGTCS; end of SGTCSPDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
  • ipsilateral end-of-SGTCS version up to 15–20%head version during SGTCSRange · patients with focal seizures, including FLE and TLE · end-of-SGTCS · initial phase of generalization; particularly 10 seconds before SGTCS; end of SGTCSPDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
  • more than 90% contralateralhead version during SGTCSPercentage · patients with focal seizures, including FLE and TLE · pre-SGTCS head version · initial phase of generalization; particularly 10 seconds before SGTCS; end of SGTCSPDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Versive seizures and asymmetric tonic posturingThe review states that electrical stimulation of M1 and SMA produces myoclonic, tonic, clonic, tonic-clonic, or version responses; versive seizures indicate contralateral frontal eye field involvement, and asymmetric tonic posturing can indicate SMA involvement.PDF p.4, section 1.6
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 2 findings · 6 reported values
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.707
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • versionIn Group I, version occurred in 9 of 16 TLE patients (56.3%) and 8 of 15 XTLE patients (53.3%), and was contralateral to ictal onset in all patients with version in each subgroup.PDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group I
  • versionIn Group II, version occurred in 13 of 26 patients (50%) and was contralateral to ictal onset in all 13 patients with version.PDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group II
Reported values
  • TLE occurrence 9/16 (56.3%)versionPercentage · n/N 9/16 · Group I patients with seizures progressing to secondary generalization; TLE and XTLE subgroups · TLEPDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group I
  • XTLE occurrence 8/15 (53.3%)versionPercentage · n/N 8/15 · Group I patients with seizures progressing to secondary generalization; TLE and XTLE subgroups · XTLEPDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group I
  • XTLE lateralization 8/8 (100%)versionPercentage · n/N 8/8 · Group I patients with seizures progressing to secondary generalization; TLE and XTLE subgroups · XTLE with versionPDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group I
  • TLE lateralization 9/9 (100%)versionPercentage · n/N 9/9 · Group I patients with seizures progressing to secondary generalization; TLE and XTLE subgroups · TLEPDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group I
  • 13/13 (100%)versionPercentage · n/N 13/13 · Group II patients · Group IIPDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group II
  • 13/26 (50%)versionPercentage · n/N 13/26 · Group II patients · Group IIPDF p.3, Table 1—Patients with version and Patients with version contralateral to focus; PDF p.3, Results—Group II
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 4 findings · 8 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Forced head deviationKernan et al. found forced head deviation contralateral in more than 90% of seizures when the seizure developed into a generalized tonic-clonic seizure or occurred within 10 seconds before generalization.PDF p.4, section 3.1 Version
  • VersionThe review treats forced, involuntary, sustained head and eye version as a lateralizing sign that is generally contralateral to seizure onset and particularly reliable immediately before the tonic-clonic phase, with neck extension, or with late ipsiversion.PDF p.4, section 3.1 Version; PDF p.4, section 3.1.1 Mechanism; PDF p.12, Table 1
  • Versive head and eye movementWyllie et al. reviewed 74 seizures in 37 patients and defined version as a forced and involuntary movement resulting in sustained unnatural positioning; only versive movements were lateralizing and they were always contralateral to seizure onset as determined by EEG.PDF p.4, section 3.1 Version
  • VersionChee et al. found version in 45% of 38 selected patients with frontal and temporal lobe epilepsy, with a positive predictive value of 94%; the review states reliability was 100% under specified conditions including immediate pre-tonic-clonic version, neck extension, or association with late ipsiversion.PDF p.4, section 3.1 Version
Reported values
  • More than 90% contralateralForced head deviationPercentage · Patients with seizures developing into generalized tonic-clonic seizures or occurring within 10 seconds before generalization · Immediately before or during generalizationPDF p.4, section 3.1 Version
  • Version in 22.2% of frontal-lobe epilepsy patientsVersionPercentage · Patients with focal seizures and frontal or temporal lobe epilepsy as summarized by the review · Frontal lobe epilepsy · Ictal; immediately before or during secondary generalizationPDF p.4, section 3.1 Version; PDF p.4, section 3.1.1 Mechanism; PDF p.12, Table 1
  • Version contralateral in 100%VersionPercentage · Patients with focal seizures and frontal or temporal lobe epilepsy as summarized by the review · Version · Ictal; immediately before or during secondary generalizationPDF p.4, section 3.1 Version; PDF p.4, section 3.1.1 Mechanism; PDF p.12, Table 1
  • 37 patientsVersive head and eye movementCount · 37 patients with 74 seizures and lateral head and eye movements · Wyllie et al. cohort · IctalPDF p.4, section 3.1 Version
  • 74 seizuresVersive head and eye movementCount · 37 patients with 74 seizures and lateral head and eye movements · Wyllie et al. cohort · IctalPDF p.4, section 3.1 Version
  • Version PPV 94%VersionPositive predictive value · 38 selected patients with frontal and temporal lobe epilepsy · Ictal; immediately before tonic-clonic phase or with late ipsiversionPDF p.4, section 3.1 Version
  • Reliability 100% under specified version conditionsVersionPercentage · 38 selected patients with frontal and temporal lobe epilepsy · Immediate pre-tonic-clonic version, neck extension, or late ipsiversion · Ictal; immediately before tonic-clonic phase or with late ipsiversionPDF p.4, section 3.1 Version
  • Version in 45% of 38 selected patientsVersionPercentage · 38 selected patients with frontal and temporal lobe epilepsy · Ictal; immediately before tonic-clonic phase or with late ipsiversionPDF p.4, section 3.1 Version
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Versive seizureVersive seizures involve sustained and extreme conjugate eye movement or lateral movement of the head, and sometimes the whole body, to one side; eye movements may combine smooth tonic deviation with superimposed saccades, body version replaces saccades with small clonic lateral movements, and the body may complete one or more 360-degree turns.PDF p.4, Simple motor seizures, Versive seizures; PDF p.2, Table 1
Reported values
  • One or more 360-degree turns may occurVersive seizureCount · IctalPDF p.4, Simple motor seizures, Versive seizures; PDF p.2, Table 1
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 4 findings · 47 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • version-first ictal motor sequence; version plus tonic and/or M2e progressionAmong the 38 sequence seizures, version was the first motor sign in 29/38; among those 29 version-first seizures, M2e followed in 15/29 and tonic posturing in 7/29, which the authors combine as version followed by a tonic seizure in 22/29 because they treat M2e as a special tonic form. One seizure had simultaneous version and tonic posturing as the first sign followed by secondary generalization and asymmetric clonic ending; three of the remaining non-version-first seizures showed version plus tonic activity in a different order; in total 33/38 showed version plus tonic activity in variable order. Version was absent in 5/38, four seizures started with tonic activity and ended with asymmetric clonic ending, three of those lateralized the EZ correctly, and one M2e-to-clonic sequence lateralized the EZ correctly.PDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • version; versive head and eye movementsThe current paper reports that defined versive head and eye deviation lateralized the EZ to the contralateral hemisphere, describes a value above 90% when version occurred within 10 seconds or less before motor generalization, and reports 100% contralateral lateralization under the cited conditions of neck extension and late ipsiversion after the end of a generalized tonic-clonic seizure.PDF p.7, Version definition and cited value; PDF p.13, discussion of version; PDF p.14, discussion of cited version conditions
  • version as the initial sign versus non-version as the initial signTable 2 compares 29 seizures with version as the first sign (15 temporal and 14 extra-temporal) with 9 seizures without version as the first sign (4 temporal and 5 extra-temporal) and reports no statistically significant difference in temporal versus extra-temporal origin, with p=0.693.PDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • Correct EZ lateralization in M2e-to-clonic sequence 1/1version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/1 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Correct EZ lateralization in M2e-to-clonic sequence · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2e-to-clonic sequence 1/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · M2e-to-clonic sequence · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version absent 5/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 5/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version absent · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version as second sign in non-version-first seizures 4/9version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 4/9 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version as second sign in non-version-first seizures · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Non-version-first with version plus tonic in different order 3/9version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 3/9 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Non-version-first with version plus tonic in different order · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version plus tonic in variable order 33/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 33/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version plus tonic in variable order · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Tonic start with asymmetric clonic ending 4/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 4/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Tonic start with asymmetric clonic ending · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Tonic posturing second after version 7/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 7/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Tonic posturing second after version · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version followed by tonic including M2e 22/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 22/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version followed by tonic including M2e · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version first 29/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 29/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version first · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2e second after version 15/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 15/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · M2e second after version · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Simultaneous version and tonic as first sign 1/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Simultaneous version and tonic as first sign · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Correct EZ lateralization among tonic-start/asymmetric-clonic sequences 3/4version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 3/4 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Correct EZ lateralization among tonic-start/asymmetric-clonic sequences · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • 100%version; versive head and eye movementsPercentage · Cited-study populations as summarized in the current paper; Not reported · neck extension and late ipsiversion after generalized tonic-clonic seizure · Version within 10 seconds before motor generalization; late ipsiversion after generalized tonic-clonic seizure in the cited conditionPDF p.7, Version definition and cited value; PDF p.13, discussion of version; PDF p.14, discussion of cited version conditions
  • above 90%version; versive head and eye movementsOther reported value · Cited-study populations as summarized in the current paper; Not reported · version within 10 seconds or less before motor generalization · Version within 10 seconds before motor generalization; late ipsiversion after generalized tonic-clonic seizure in the cited conditionPDF p.7, Version definition and cited value; PDF p.13, discussion of version; PDF p.14, discussion of cited version conditions
  • 4 temporal non-version-first seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · non-version first; temporal · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • 29 version-first seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · version first · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • 5 extra-temporal non-version-first seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · non-version first; extra-temporal · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • 38 sequence seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • p=0.693version as the initial sign versus non-version as the initial signP value · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • 14 extra-temporal version-first seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · version first; extra-temporal · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • 15 temporal version-first seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · version first; temporal · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
  • 9 non-version-first seizuresversion as the initial sign versus non-version as the initial signCount · 38 representative sequence seizures classified by temporal versus extra-temporal EZ origin · non-version first · initial sign of the pre-secondary-generalization motor sequencePDF p.10, Results; PDF p.11, Discussion; PDF p.19, Table 2
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • recurrent ictal speech utterances; oro-alimentary automatisms; right-sided versionIn the patient’s habitual partial seizures, an aura of nausea was followed by staring gaze, partial loss of consciousness, oro-alimentary automatisms, right-sided version, and postictal confusion; family reported recurrent stereotyped French or English sentence repetitions from age 18.PDF p.2, left column, paragraph beginning “Partial seizures began”; PDF p.2, right column, paragraph beginning “Five stereotyped and spontaneous electroclinical seizures”
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • versionTable 3 reports version in 6% of the temporo-polar synthesis (evidence grade Low).PDF p.5, Table 3
  • versionTable 3 reports a 0–100% range for version across the temporo-polar reports (evidence grade Low).PDF p.5, Table 3
Reported values
  • 6%versionPercentage · Temporo-polar semiology synthesis represented in Table 3 · later after propagation to symptomatogenic areasPDF p.5, Table 3
  • range 0–100%versionPercentage Range · Temporo-polar semiology synthesis represented in Table 3 · later after propagation to symptomatogenic areasPDF p.5, Table 3
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • versive seizuresThe review defines versive seizures as forced involuntary turning of the head and eyes in one direction with neck extension; the frontal eye fields are the symptomatogenic zone. Versive seizures appear earlier in frontal than temporal seizures and can be the first frontal-lobe sign; they have highly lateralizing value toward the contralateral hemisphere, especially within 10 seconds before secondary generalization. Reliability requires distinguishing epileptic versive seizures from non-versive natural head turning.PDF p.4, Versive seizures
Reported values
  • Within 10 seconds before secondary generalizationversive seizuresCount · Patients with frontal-lobe, temporal-lobe, or partial seizures; no cohort reported · Ictal; especially within 10 seconds before secondary generalizationPDF p.4, Versive seizures
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • atypical post-tapering seizures with contralateral versionTwo patients had one or two atypical post-tapering seizures with contralateral version; these were excluded from propagation-pattern classification because they deviated from habitual semiology and reflected inadequate contralateral electrode coverage.PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring
wyllie1986.pdfStructured design not resolved · 5 findings · 43 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.893
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • versive and nonversive head and eye movementsIn the 74 seizures from 37 patients, all 61 versive seizures were contralateral to the cerebral hemisphere of seizure onset and none was ipsilateral, whereas nonversive turning occurred on both sides and was judged nonlocalizing.PDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • versive head and eye movement together or separatelyThe head and eyes moved together in 40 of 61 versive seizures; the remaining 21 included 14 with head version but incomplete eye visibility and 7 with eye version without head movement, and isolated eye version occurred in 2 occipital-onset seizures from one patient and 5 frontal-onset seizures from another.PDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • smooth and jerking versive movementThe versive movement was smooth in 40 seizures (65%) and jerking in 21 (35%), independently of other ictal EEG and clinical features.PDF p.3, paragraph beginning “The clinical appearance of contraversion varied”
  • persistence of contraversion and ipsiversion after generalizationAmong versive seizures with secondary generalization, contraversive head and eye movement persisted through the generalized tonic-clonic phase in 8 seizures (30%) for 6-53 seconds (mean 24); in 4 seizures it waned and the head and eyes returned to midline before another 42-62 seconds (mean 55) of convulsion, while in 4 seizures it continued throughout the convulsion, and 12 (44%) generalized seizures ended with ipsiversion.PDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • quiet staring and staring with automatisms before contraversionQuiet staring preceded contraversion for 8 versive seizures for 2-31 seconds (mean 17), while staring with automatisms preceded contraversion for 18 seizures for 4-227 seconds (mean 34); all seizures with automatisms before contraversion originated in temporal lobes, whereas the quiet-staring subgroup arose from temporal (25%) and extratemporal (75%) locations.PDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
Reported values
  • Versive movements contralateral 61/61versive and nonversive head and eye movementsPercentage · n/N 61/61 · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Versive; contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Patients n=37versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Overall · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Occipital Versive contralateral n=2versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Versive; contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Frontal Nonversive contralateral n=2versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Frontal onset; Nonversive contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Temporal-onset seizures n=31versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Temporal onset · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Versive movements ipsilateral 0/61versive and nonversive head and eye movementsPercentage · n/N 0/61 · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Versive; ipsilateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Temporal Nonversive contralateral n=4versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Temporal onset; Nonversive contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Nonversive movements contralateral 6/13versive and nonversive head and eye movementsPercentage · n/N 6/13 · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Nonversive; contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Nonversive movements ipsilateral 7/13versive and nonversive head and eye movementsPercentage · n/N 7/13 · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Nonversive; ipsilateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Temporal Nonversive ipsilateral n=7versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Temporal onset; Nonversive ipsilateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Seizures with lateral head/eye movement n=74versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Overall · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Frontal-onset seizures n=39versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Frontal onset · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Temporal Versive contralateral n=20versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Versive; contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Parietal-onset seizures n=2versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Parietal onset · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Parietal Versive contralateral n=2versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Versive; contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Frontal Versive contralateral n=37versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Versive; contralateral · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • Occipital-onset seizures n=2versive and nonversive head and eye movementsCount · 37 patients; 74 seizures with lateral head and eye movement; onset regions frontal, temporal, parietal, and occipital · Occipital onset · ictal; first or observed lateral head and eye movementPDF p.1, Article abstract; PDF p.2, Table 1; PDF p.2, results paragraph
  • one patient with occipital-onset isolated eye versionversive head and eye movement together or separatelyCount · 27 patients; 61 versive seizures · occipital onset · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • head version with incomplete eye visibility 14 seizuresversive head and eye movement together or separatelyCount · 27 patients; 61 versive seizures · head version; eyes incompletely visible · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • eye version without head movement 7 seizuresversive head and eye movement together or separatelyCount · 27 patients; 61 versive seizures · eye version without head movement · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • one patient with frontal-onset isolated eye versionversive head and eye movement together or separatelyCount · 27 patients; 61 versive seizures · frontal onset · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • 2 occipital-onset seizuresversive head and eye movement together or separatelyCount · 27 patients; 61 versive seizures · occipital onset · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • 5 frontal-onset seizuresversive head and eye movement together or separatelyCount · 27 patients; 61 versive seizures · frontal onset · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • head and eyes together 40/61versive head and eye movement together or separatelyPercentage · n/N 40/61 · 27 patients; 61 versive seizures · head and eyes together · ictal versive movementPDF p.2, results paragraph describing visibility and isolated eye version; PDF p.2, paragraph stating contralaterality for head-and-eye or eye-only version
  • 21 (35%)smooth and jerking versive movementPercentage · n/N 21/61 · 61 versive seizures from 27 patients · jerking versive movement · Ictal contraversionPDF p.3, paragraph beginning “The clinical appearance of contraversion varied”
  • 40 (65%)smooth and jerking versive movementPercentage · n/N 40/61 · 61 versive seizures from 27 patients · smooth versive movement · Ictal contraversionPDF p.3, paragraph beginning “The clinical appearance of contraversion varied”
  • persistence duration 6–53 secondspersistence of contraversion and ipsiversion after generalizationRange · Versive seizures with secondary generalized tonic-clonic activity · persistent contraversion · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • another 42–62 seconds of convulsionpersistence of contraversion and ipsiversion after generalizationRange · Versive seizures with secondary generalized tonic-clonic activity · waning after return to midline · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • waning with return to midline in 4 seizurespersistence of contraversion and ipsiversion after generalizationCount · Versive seizures with secondary generalized tonic-clonic activity · waning · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • mean 55 seconds of convulsionpersistence of contraversion and ipsiversion after generalizationMean · Versive seizures with secondary generalized tonic-clonic activity · waning after return to midline · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • continued subset from 3 patientspersistence of contraversion and ipsiversion after generalizationCount · Versive seizures with secondary generalized tonic-clonic activity · continued throughout · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • continued throughout convulsion in 4 seizurespersistence of contraversion and ipsiversion after generalizationCount · Versive seizures with secondary generalized tonic-clonic activity · continued throughout · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • waning subset from 3 patientspersistence of contraversion and ipsiversion after generalizationCount · Versive seizures with secondary generalized tonic-clonic activity · waning · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • mean persistence duration 24 secondspersistence of contraversion and ipsiversion after generalizationMean · Versive seizures with secondary generalized tonic-clonic activity · persistent contraversion · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • 12/27 (44%) ended with ipsiversionpersistence of contraversion and ipsiversion after generalizationPercentage · n/N 12/27 · Versive seizures with secondary generalized tonic-clonic activity · end of generalized seizure · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • persistent contraversion 8/27 (30%)persistence of contraversion and ipsiversion after generalizationPercentage · n/N 8/27 · Versive seizures with secondary generalized tonic-clonic activity · persistent contraversion · Generalized tonic-clonic phase and end of seizure after secondary generalizationPDF p.3, paragraphs describing persistence through generalized tonic-clonic activity and ipsiversion at the end
  • Quiet staring before contraversion 8/61 (13%)quiet staring and staring with automatisms before contraversionPercentage · n/N 8/61 · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring-with-automatisms duration mean 34 seconds (range 4–227)quiet staring and staring with automatisms before contraversionMean · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring subgroup temporal origin 25%quiet staring and staring with automatisms before contraversionPercentage · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring; temporal origin · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring-with-automatisms subgroup temporal origin 18/18quiet staring and staring with automatisms before contraversionPercentage · n/N 18/18 · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring duration mean 17 seconds (range 2–31)quiet staring and staring with automatisms before contraversionMean · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring subgroup extratemporal origin 75%quiet staring and staring with automatisms before contraversionPercentage · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring; extratemporal origin · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring with automatisms before contraversion 18/61 (30%)quiet staring and staring with automatisms before contraversionPercentage · n/N 18/61 · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion

22 contributing manuscripts; source-reported values remain separate and are not pooled.

Auditory auraReported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: IpsilateralAlso reported: Right hemisphereNo single reliable side17 manuscripts · 41 findings · 47 reported values
Weighted evidence supportevidence weight 35.15 across 17 manuscripts · 4 independent primary study · 9 narrative, educational, or cited context · 3 systematic review or meta-analysis · 1 case report or observation

The review links early ictal dysphasia to dominant-hemisphere involvement and unilateral elementary auditory aura to contralateral seizure onset. The review restates that prior analyses associated auditory aura with the dominant hemisphere. The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. The review states that the perceived side of a simple auditory aura is not a reliable epilepsy-lateralizing sign. The cited 2018 auditory-seizure study was reported to have a dominant-hemisphere SOZ in 60%. Unilateral ear plugging was reported in three cases to indicate seizure onset in the contralateral temporal lobe auditory cortex. In the cited 18-patient auditory-aura series, bilateral sound perception predominated, with three contralateral-ear cases. Stimulation-evoked auditory sensations were perceived mostly in the ear contralateral to stimulation (57.6%), with bilateral perception in 36.4% and ipsilateral perception in 6%. This finding provides no lateralization information. The TL-versus-T+ auditory-aura comparison provides no lateralization information. The cited EZ-extent statement provides no lateralization information. The combined somatosensory and auditory aura observation reports no hemisphere direction. This finding provides no hemispheric lateralization information. No cerebral hemisphere or body-side direction is reported. No seizure lateralization is reported. The primary comparison reports no hemisphere-level lateralization; it compares M, ML, and L temporal-onset subtypes. No lateralization result is reported in this corpus-size finding. The educational definition of auditory aura supplies no lateralizing direction.

Source-defined result groups 25
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyauditory manifestation; operculoinsular SOZ · auditory versus visual manifestation and extrafrontal SOZ subgroup · patient as represented by Table 2 n; sign-specific denominator Not reported1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyauditory manifestation; temporal SOZ · auditory versus visual manifestation and extrafrontal SOZ subgroup · patient as represented by Table 2 n; sign-specific denominator Not reported1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyipsilateral · posterior/inferior versus other insular sites; simple versus complex auditory response; ear-laterality categories · evoked auditory response1 manuscript · 1 reported value · not pooled
Localization: ParietalObserved proportion 5.6%All reported · patients1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 8.0%auditory responses · posterior/inferior versus other insular sites; simple versus complex auditory response; ear-laterality categories · evoked auditory response1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelycontralateral · posterior/inferior versus other insular sites; simple versus complex auditory response; ear-laterality categories · evoked auditory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyvisual manifestation; posterior SOZ · auditory versus visual manifestation and extrafrontal SOZ subgroup · patient as represented by Table 2 n; sign-specific denominator Not reported1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 12.5%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Auditory aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Auditory aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separately2 diagnostic-accuracy studies comparing lateral and mesial TLE for Auditory aura · lateral TLE versus mesial TLE · random-effects diagnostic-accuracy estimate1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 33.3%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelybilateral · posterior/inferior versus other insular sites; simple versus complex auditory response; ear-laterality categories · evoked auditory response1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 84.6%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: orbitofrontal cortex-restricted epileptogenic-zone networkSource-defined values retained separatelyOFC-restricted EZN cases · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · posterior/inferior versus other insular sites; simple versus complex auditory response; ear-laterality categories · evoked auditory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separately2 diagnostic-accuracy studies comparing lateral and mesial TLE for Auditory aura · lateral TLE versus mesial TLE · random-effects diagnostic-accuracy estimate1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 17

Alphabetical by manuscript.

asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • auditory auraOne patient had an auditory aura.PDF p.2, Results
Reported values
  • 1/18 (5.5%) auditory auraauditory auraPercentage · n/N 1/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 6 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • auditory auraAuditory auras did not differ significantly overall or across the source's illusion and hallucination subcategories.PDF p.6, Table 2; PDF p.8, auditory aura discussion
  • auditory aura and extensive epileptogenic zoneThe source reports that prior findings suggested that, in TL epilepsy, patients with auditory auras may have an extensive epileptogenic zone extending beyond the temporal lobe.PDF p.8, auditory aura discussion
Reported values
  • T+ 4.3%auditory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2; PDF p.8, auditory aura discussion
  • T+ 8.7%auditory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2; PDF p.8, auditory aura discussion
  • TL 3.4%auditory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2; PDF p.8, auditory aura discussion
  • TL 3.4%auditory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2; PDF p.8, auditory aura discussion
  • T+ 8.7%auditory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2; PDF p.8, auditory aura discussion
  • TL 0%auditory auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2; PDF p.8, auditory aura discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Auditory features in ADPEAFIn autosomal dominant partial epilepsy with auditory features, the review describes simple unformed auditory symptoms such as humming, buzzing, or ringing as most common, with less frequent complex sounds or distortions; specific sounds may precipitate seizures, and olfactory, visceral, vertiginous, experiential, or autonomic auras may also occur.PDF p.3, ADPEAF paragraph
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • lateral/neocortical temporal seizure; auditory aura; ictal dysphasiaLateral or neocortical temporal seizures are described as having fewer auras and often auditory or vertiginous features; elementary sounds such as humming, ringing, and buzzing indicate primary auditory cortex, complex sounds indicate auditory association areas, elementary unilateral auditory aura indicates contralateral onset, and early ictal dysphasia may indicate dominant-hemisphere involvement.PDF p.6, Lateral/neocortical temporal lobe; PDF p.3, Figure 1
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 2 findings · 11 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • auditory seizures in a cited 2018 retrospective studyThe review attributes to a 2018 retrospective study that the SOZ was mainly in the dominant hemisphere (60%) and that 89% of AS had a temporal SOZ.PDF p.5, section 6.1; PDF p.7, section 6.2.1
  • auditory seizures (AS) and auditory phenomena (AP)The review analyzed 174 cases comprising 200 AS from 70 articles; Level A covered 115 cases/131 AS, Level B covered 59 cases/69 AS, and the SOZ-to-perceived-side lateralization analysis included 99 cases comprising 114 AS.PDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
Reported values
  • 60%auditory seizures in a cited 2018 retrospective studyPercentage · Cited 2018 retrospective AS study; endpoint sample sizes were not stated in this review · cited 2018 retrospective study · Ictal ASPDF p.5, section 6.1; PDF p.7, section 6.2.1
  • 89%auditory seizures in a cited 2018 retrospective studyPercentage · Cited 2018 retrospective AS study; endpoint sample sizes were not stated in this review · cited 2018 retrospective study · Ictal ASPDF p.5, section 6.1; PDF p.7, section 6.2.1
  • 70 articlesauditory seizures (AS) and auditory phenomena (AP)Count · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · overall review corpus · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 99 casesauditory seizures (AS) and auditory phenomena (AP)Count · n/N 99/174 cases · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · paired SOZ-to-perceived-side lateralization analysis · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 59 casesauditory seizures (AS) and auditory phenomena (AP)Count · n/N 59/174 cases · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level B · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 131 ASauditory seizures (AS) and auditory phenomena (AP)Count · n/N 131/200 AS · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level A · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 200 ASauditory seizures (AS) and auditory phenomena (AP)Count · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · overall review corpus · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 69 ASauditory seizures (AS) and auditory phenomena (AP)Count · n/N 69/200 AS · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level B · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 174 casesauditory seizures (AS) and auditory phenomena (AP)Count · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · overall review corpus · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 115 casesauditory seizures (AS) and auditory phenomena (AP)Count · n/N 115/174 cases · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level A · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 114 ASauditory seizures (AS) and auditory phenomena (AP)Count · n/N 114/200 AS · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · paired SOZ-to-perceived-side lateralization analysis · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.37 · 1 × 0.9 × 1.521
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • auditory sensationOne restricted-OFC case had an auditory sensation.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • somatosensory and auditory aura; frontal subgroupOne frontal-subgroup aura combined a nonpainful somatosensory aura with an auditory sensation.PDF p.3, Aura
Reported values
  • 1 patientauditory sensationCount · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 1 patientsomatosensory and auditory aura; frontal subgroupCount · n/N 1/11 · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 20 findings · 6 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • auditory aura; dominant hemisphereThe source cites prior analyses in which auditory auras were considered a predictor of epileptogenic-zone lateralization to the dominant hemisphere, while this review evaluates lateral versus mesial temporal localization instead.PDF p.8, Differentiating ictal semiologies
  • transverse gyrus of Heschl; auditory auraThe source states that intraoperative stimulation of the lateral temporal lobe, particularly the transverse gyrus of Heschl, can produce an auditory sensation, especially when an auditory aura is part of habitual seizures.PDF p.1, Introduction
  • auditory auraThe source concludes that auditory aura is the only specific semiology identified for lateral temporal lobe seizures, although it occurs in a minority of patients.PDF p.1, Abstract; PDF p.7, Discussion; PDF p.10, Conclusions
  • Auditory auraTable 3 reports 3 studies assessing Auditory aura.PDF p.6, Table 3
  • Auditory auraTable 3 reports 54 patients assessed for Auditory aura.PDF p.6, Table 3
  • Auditory auraTable 3 reports 5.9–9.1% as the percentage range or value for Auditory aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Auditory auraTable 4 reports overall odds of 0.08 for occurrence of Auditory aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Auditory auraTable 4 reports a 95% confidence interval of 0.03–0.23 for the overall odds of Auditory aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Auditory auraThe heterogeneity test for the Table 4 odds estimate for Auditory aura has p=0.9237.PDF p.7, Table 4
  • Auditory aura; lateral versus mesial comparisonTable 5 reports 2 studies comparing Auditory aura in lateral and mesial TLE.PDF p.9, Table 5
  • Auditory aura; lateral TLE patient denominatorTable 5 reports 32 lateral-TLE patients assessed for Auditory aura.PDF p.9, Table 5
  • Auditory aura; mesial TLE patient denominatorTable 5 reports 51 mesial-TLE patients assessed for Auditory aura.PDF p.9, Table 5
  • Auditory aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 5.9–6.7% for Auditory aura.PDF p.9, Table 5
  • Auditory aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–12.9% for Auditory aura.PDF p.9, Table 5
  • Auditory aura; diagnostic sensitivityTable 6 reports overall sensitivity 0.06 for Auditory aura in 2 studies comparing lateral with mesial TLE.PDF p.9, Table 6
  • Auditory aura; diagnostic sensitivity confidence intervalTable 6 reports a 95% confidence interval of 0.02–0.22 for sensitivity of Auditory aura.PDF p.9, Table 6
  • Auditory aura; sensitivity heterogeneityThe heterogeneity test for sensitivity of Auditory aura has p=0.9272.PDF p.9, Table 6
  • Auditory aura; diagnostic specificityTable 6 reports overall specificity 0.98 for Auditory aura in 2 studies comparing lateral with mesial TLE.PDF p.9, Table 6
  • Auditory aura; diagnostic specificity confidence intervalTable 6 reports a 95% confidence interval of 0.88–1.00 for specificity of Auditory aura.PDF p.9, Table 6
  • Auditory aura; specificity heterogeneityThe heterogeneity test for specificity of Auditory aura has p=0.8316.PDF p.9, Table 6
Reported values
  • 5.9–9.1%Auditory auraPercentage Range · Lateral temporal epilepsy patients assessed for Auditory aura · ictalPDF p.6, Table 3
  • odds 0.08odds of occurrence; Auditory auraOdds · Lateral temporal epilepsy patients assessed for Auditory aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 5.9–6.7%Auditory aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Auditory aura · Lateral TLE patients assessed for Auditory aura · ictalPDF p.9, Table 5
  • 0–12.9%Auditory aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Auditory aura · Mesial TLE patients assessed for Auditory aura · ictalPDF p.9, Table 5
  • sensitivity 0.06Auditory aura; diagnostic sensitivitySensitivity · 2 diagnostic-accuracy studies comparing lateral and mesial TLE for Auditory aura · 2 diagnostic-accuracy studies comparing lateral and mesial TLE for Auditory aura · ictal sign presencePDF p.9, Table 6
  • specificity 0.98Auditory aura; diagnostic specificitySpecificity · 2 diagnostic-accuracy studies comparing lateral and mesial TLE for Auditory aura · 2 diagnostic-accuracy studies comparing lateral and mesial TLE for Auditory aura · ictal sign presencePDF p.9, Table 6
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • auditory aurasSimple auditory auras such as ringing or buzzing are associated with the primary auditory cortex, while complex voices, music, hallucinations, or illusions are associated with auditory association areas in the temporo-occipital cortex. Although auditory information has bilateral innervation, the contralateral ear is better represented in auditory cortex.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 3 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • auditory and visual nonmotor manifestationsAuditory and visual manifestations were observed only in extrafrontal SHE; visual symptoms were associated with a posterior cortex SOZ, whereas auditory symptoms were associated with either a temporal or an operculoinsular SOZ.PDF p.5, section 3.3; PDF p.6, Table 2
Reported values
  • visual posterior 2auditory and visual nonmotor manifestationsCount · Extrafrontal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists auditory n=1 in temporal and n=1 in operculoinsular subgroups and visual n=2 in the posterior subgroup · visual manifestation; posterior SOZ · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, Table 2
  • auditory operculoinsular 1auditory and visual nonmotor manifestationsCount · Extrafrontal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists auditory n=1 in temporal and n=1 in operculoinsular subgroups and visual n=2 in the posterior subgroup · auditory manifestation; operculoinsular SOZ · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, Table 2
  • auditory temporal 1auditory and visual nonmotor manifestationsCount · Extrafrontal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists auditory n=1 in temporal and n=1 in operculoinsular subgroups and visual n=2 in the posterior subgroup · auditory manifestation; temporal SOZ · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • auditory auraAuditory auras are among the reported clinical manifestations of insular seizures.PDF p.2, Clinical Features
  • auditory sensation from very posteroinferior insulaAuditory sensations were evoked by stimulating the very posteroinferior part of the insula.PDF p.5, Other Insular Responses
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Auditory auraAuditory auras are reported across populations at variable frequency, and unilateral ear plugging is described as a sign that can lateralize seizure onset to the contralateral temporal lobe auditory cortex.PDF p.3, section 2.4 Auditory auras; PDF p.3, section 2.4.1 Mechanism
  • Auditory auraThe Cleveland Clinic series included 18 patients with auditory auras; 15 heard bilateral sounds and 3 localized the aura to the contralateral ear, with the epileptogenic zone determined by seizure freedom after surgery in 10 and presurgical evaluation in 8.PDF p.3, section 2.4 Auditory auras
Reported values
  • Frequency 2-16% of patients, depending on aura type and reviewed populationAuditory auraPercentage · Patients with focal epilepsy as summarized in a review and case series · Ictal auraPDF p.3, section 2.4 Auditory auras; PDF p.3, section 2.4.1 Mechanism
  • Bilateral sounds 15/18Auditory auraPercentage · n/N 15/18 · 18 patients with auditory auras in the Cleveland Clinic series · Bilateral sounds · Ictal auraPDF p.3, section 2.4 Auditory auras
  • Patients with auditory auras n=18Auditory auraCount · 18 patients with auditory auras in the Cleveland Clinic series · Ictal auraPDF p.3, section 2.4 Auditory auras
  • EZ determined by seizure freedom after surgery 10/18Auditory auraPercentage · n/N 10/18 · 18 patients with auditory auras in the Cleveland Clinic series · Postoperative seizure-freedom determination · Ictal auraPDF p.3, section 2.4 Auditory auras
  • Contralateral-ear aura 3/18Auditory auraPercentage · n/N 3/18 · 18 patients with auditory auras in the Cleveland Clinic series · Contralateral ear · Ictal auraPDF p.3, section 2.4 Auditory auras
  • EZ determined by presurgical evaluation 8/18Auditory auraPercentage · n/N 8/18 · 18 patients with auditory auras in the Cleveland Clinic series · Presurgical-evaluation determination · Ictal auraPDF p.3, section 2.4 Auditory auras
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Auditory auraIsolated auditory hallucinations or illusions are auditory auras; complex auditory phenomena with broader perceptual alterations are auditory only when clearly predominant, otherwise they are psychic auras.PDF p.3, Auras, subsection Auditory auras; PDF p.2, Table 1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • sensory hallucination or illusion (visual, auditory, vestibular)The combined category of visual, auditory, or vestibular sensory hallucination or illusion was more frequent in L than M or ML patients.PDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
Reported values
  • 6/18 (33.3%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 6/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
  • 3/24 (12.5%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
  • 11/13 (84.6%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 11/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 9 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • auditory sensationsAuditory sensations occurred in 44 responses (8%) from the very posterior and inferior insula; 69.7% were unpleasant and 30.3% neutral, 81.8% (n=36) were simple auditory hallucinations, 18.2% (n=8) were more complex with ear vibration/pressure/paresthesiae, and perception was contralateral in 57.6%, bilateral in 36.4%, and ipsilateral in 6%.PDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
Reported values
  • neutral 30.3%auditory sensationsPercentage · 44 auditory responses in the 550-response series · neutral · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • complex 18.2% (n=8)auditory sensationsPercentage · n/N 8/44 · 44 auditory responses in the 550-response series · complex ear vibration/pressure/paresthesiae · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • unpleasant 69.7%auditory sensationsPercentage · 44 auditory responses in the 550-response series · unpleasant · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • simple hallucination 81.8% (n=36)auditory sensationsPercentage · n/N 36/44 · 44 auditory responses in the 550-response series · simple auditory hallucination · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • bilateral 36.4%auditory sensationsPercentage · 44 auditory responses in the 550-response series · bilateral · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • 44 responses (8%)auditory sensationsPercentage · n/N 44/550 · 44 auditory responses in the 550-response series · auditory responses · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • contralateral 57.6%auditory sensationsPercentage · 44 auditory responses in the 550-response series · contralateral · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • OR=0.81 for y-coordinate locationauditory sensationsOdds ratio · 44 auditory responses in the 550-response series · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
  • ipsilateral 6%auditory sensationsPercentage · 44 auditory responses in the 550-response series · ipsilateral · stimulation-evoked auditory responsePDF p.3, Results; PDF p.5, Other Types of Evoked Sensations and Fig. 5C; PDF p.6, continuation
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • stimulation-evoked somatosensory, auditory, vestibular, olfactory, gustatory, and viscerosensory symptomsThe chapter reports that electrical stimulation studies evoked somatosensory symptoms, including pain, from the posterior two-thirds of the insula; auditory and vestibular symptoms from the posterior insula; and olfactory, gustatory, and viscerosensory symptoms, including laryngeal constriction, from the midinsula, whereas stimulation of the most anterior portion rarely evoked symptoms unless a larger network seizure was elicited.PDF p.3, insular functional differentiation and electrical cortical stimulation
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • auditory aurasThe review describes simple auditory auras such as a buzz or noise as arising from Heschl's gyrus in the superior temporal gyrus and states that perceived sound laterality is not reliable for lateralizing the epilepsy, even when the patient perceives the sound on one side.PDF p.2, Auditory auras

17 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal contralateral tonic eye deviationSource terms: Ictal eye deviation; Ictal tonic eye deviationReported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side17 manuscripts · 75 findings · 110 reported values
Weighted evidence supportevidence weight 34.78 across 17 manuscripts · 3 manuscript weight pending · 4 independent primary study · 3 structured design not resolved · 5 narrative, educational, or cited context · 2 systematic review or meta-analysis · 3 case report or observation

The cited discussion does not establish a reliable lateralizing direction for forceful head turning. ATLP was usually on the same side as version, with one complex two-direction version exception; the head was midline or returning to midline when ATLP appeared. The authors hypothesize that initial or primary MST involvement would produce initial ipsilateral conjugate eye deviation. Aggregate eye-deviation direction is not reported. Source reports contralateral limb posturing in a sequential occipital-onset phenotype. No lateralizing direction is reported for the visual-aura sequence. The source describes visual aura followed by head-eye deviation and contralateral tonic posturing as activity propagates through dorsal parietal nodes toward premotor areas. The seizure contains a leftward head/eye deviation, preserved as a body-side observation without cerebral lateralization inference. Table 2 records rightward head, eye, and body deviation in a case with source-reported right occipital onset. Eye deviation was contralateral in 13/20 eye-deviation seizures (65%) and ipsilateral in 7/20 (35%), but the directional difference was not statistically significant. Eye version direction was not reported, so the frontal cohort data cannot support a lateralizing direction. The review lists eye deviation as contralateral to the seizure focus and usually accompanied by forced head turning in the same direction. The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. No lateralization axis information is reported for the 41% head-and-eye-deviation frequency. This educational statement supplies no lateralizing direction. Both tables list forced eye version as contralateral. The adapted review table lists eye version as contralateral. The current paper restates that version has high positive predictive value for the side of ictal onset without specifying a left/right or ipsi/contra direction. Patient 9 had forced tonic head-and-eye deviation to the right, but the onset hemisphere is not supplied. The primary comparison reports no lateralization; head and/or eye deviation over the whole seizure course did not differ significantly across M, ML, and L temporal-onset groups. No head/eye direction relative to the seizure hemisphere is reported. The primary result reports no lateralization; late head and/or eye deviation did not differ significantly across M, ML, and L temporal-onset groups. The review states that forced sustained eye version before secondary generalization is reliably contralateral, whereas without generalization it may be ipsilateral or contralateral depending on the activated region. This finding provides no lateralization information. Frequency only; no lateralization is reported. No lateralization axis information is reported for the 0–50% head-eye-deviation range. No lateralization axis information is reported for the moderate head-eye-deviation association grade. No lateralization is reported. The source reports head and eye deviation in 14% of patients and describes it as contralateral to seizure onset. No seizure lateralization is reported. No directional head-eye side or hemisphere is reported. No lateralization axis information is reported for head-eye deviation versus affective/autonomic aura. No lateralization axis information is reported for head-eye deviation versus autonomic signs. This record provides no seizure lateralization. No hemisphere or body-side direction is reported. No lateralization evidence is reported. Figure 6 reports OR 7.7 for Affective/autonomic aura relative to Head-eye deviation, with no hemisphere or lateralization direction. Figure 6 reports OR 5.7 for Autonomic signs relative to Head-eye deviation, with no hemisphere or lateralization direction. No lateralizing direction is reported. No lateralizing semiology is reported for the tonic-clonic versus head-eye-deviation odds comparison. No lateralizing semiology is reported for the reciprocal head-eye-deviation versus tonic-clonic odds comparison. In Case 1, forced right eye deviation and right head turning were ipsilateral to the right temporo-occipital focus, while later left-leg tonic posturing and left version were contralateral during seizure progression. The Figure 5 caption reports absolute left eye version, but it does not state whether that direction is ipsilateral or contralateral to the seizure side and conflicts with the same case's rightward narrative description. In Case 2, initial forced right eye deviation was ipsilateral to the right temporal epileptogenic region, whereas later left-arm tonic posturing and left facial clonia were contralateral motor signs. In Case 2, the epileptogenic/ictal region was right-sided and the initial eye deviation was ipsilateral to it. The report restates cited direct-stimulation studies in which posterior inferior temporal sulcus stimulation induced constant ipsilateral eye deviation. The current report restates a cited right temporo-occipital case with forced ipsilateral eye deviation and homodromous head turning. No independent lateralization axis record is present; the card concerns the timing of contraversive movement relative to onset region. Cited reports found ipsiversion in 50% and 48% of seizures with head/eye turning and concluded that forced turning at onset had no localizing or lateralizing value. The cited study reports 4/16 ipsiversion in a selected series; no cerebral reference frame is resolved. The cited series reported ipsiversion incidence of 3% in a larger series and 4/16 (25%) in a selected series. No source lateralization is reported. The cited stereo-EEG series reported ocular deviation contralateral to the ictal discharge in all 16 patients. The cited series reports contraversive head and eye movements in 29% of 55 patients without a resolved cerebral reference frame. Both depth-studied patients had contralateral head and eye deviation. The review restates that late forced head and eye version can be ipsilateral when initial contraversion ends during generalization, but can remain contralateral when initial contraversion persists. In the cited Wyllie series, late deviation was contralateral when initial contraversion persisted and ipsilateral when initial contraversion ended. The cited series reports late ipsiversion after an initial contraversive movement in 6 of 38 selected patients, always ipsilateral to the epilepsy focus.

Source-defined result groups 30
Localization: TemporalObserved proportion 33.3%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: L onset subtype / M onset subtype / ML onset subtypeObserved proportion 22.2%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeObserved proportion 65.0%Contralateral to seizure focus · Ipsilateral to seizure focus · eye-deviation seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 37.5%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: OccipitalObserved proportion 100.0%All reported · seizure spread beyond occipital lobe · cases1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / IpsilateralSource-defined values retained separatelyAll reported · ATLP side versus version side and EEG laterality · instance1 manuscript · 1 reported value · not pooled
Localization: L onset subtype / M onset subtype / ML onset subtypeObserved proportion 12.5%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeObserved proportion 35.0%Ipsilateral to seizure focus · Contralateral to seizure focus · eye-deviation seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%initial semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Localization: Frontal / Occipital / Parietal / TemporalObserved proportion 86.5%frontal · onset regions and preceding ictal event categories · seizure; patient counts in parentheses in Table 21 manuscript · 1 reported value · not pooled
Localization: Frontal / Occipital / Parietal / TemporalObserved proportion 57.4%total · onset regions and preceding ictal event categories · seizure; patient counts in parentheses in Table 21 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyContralateral to seizure focus · Ipsilateral to seizure focus · all analyzed seizures1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / IpsilateralSource-defined values retained separatelyGroup II with ATLP and version · ATLP side versus version side and EEG laterality · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyIpsilateral to seizure focus · Contralateral to seizure focus · all analyzed seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 33.3%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · seizure/ictal SEEG recording1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 23.1%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: L onset subtype / M onset subtype / ML onset subtypeObserved proportion 23.1%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyDystonic posturing · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 6.6%combined set-of-semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 33.3%All reported · seizure1 manuscript · 2 reported values · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 50.0%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%All reported · seizure spread beyond occipital lobe · cases1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.5%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 17

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 9 forced right head/eye deviationHead and eyes forced tonic deviation to the right was listed for patient 9.PDF p.4, Figure 3
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Eye deviationEye deviation is listed as contralateral to the seizure focus and is usually associated with forced head turning in the same direction; version occurs in temporal and extratemporal onset seizures.PDF p.4, Table 2; PDF p.4, section 4 Lateralizing Features in Temporal Lobe Epilepsy
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 31 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • dystonic posturing; head-eye deviation; tonic-clonic manifestationsThe review links dystonic posturing, head/eye deviation, and tonic-clonic manifestations to propagation rather than the earliest seizure phase.PDF p.11, Anatomical and clinical correlations
  • head-eye deviationThe source reports a frequency of 14% for head-eye deviation.PDF p.13, Table 3
  • head-eye deviation; reported frequency rangeThe source reports a frequency range of 0–50% for head-eye deviation.PDF p.13, Table 3
  • head-eye deviation; ACC association gradeTable 3 assigns the source's Moderate overall association grade to head-eye deviation.PDF p.13, Table 3
  • head-eye deviation; Figure 4 rateFigure 4 displays a 14% rate for head-eye deviation.PDF p.10, Figure 4
  • head-eye deviation; contralateral to seizure onsetHead and eye deviation occurred in 14% of patients and was contralateral to seizure onset.PDF p.9, Objective symptomatology
  • pairwise OR: Head-eye deviation relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Autonomic signsFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Facial expression changeFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.3 for Head-eye deviation relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.4 for Head-eye deviation relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.6 for Head-eye deviation relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Dystonic posturingFigure 6 reports an odds ratio of 0.7 for Head-eye deviation relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Head-eye deviationFigure 6 reports an odds ratio of 9.6 for Vocalization/verbalization relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Head-eye deviationFigure 6 reports an odds ratio of 9.1 for Hypermotor-complex motor behavior relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Head-eye deviationFigure 6 reports an odds ratio of 7.7 for Affective/autonomic aura relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Head-eye deviationFigure 6 reports an odds ratio of 5.7 for Autonomic signs relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Head-eye deviationFigure 6 reports an odds ratio of 5.2 for Facial expression change relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Head-eye deviationFigure 6 reports an odds ratio of 4.6 for Motor (gestural) automatisms relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Head-eye deviationFigure 6 reports an odds ratio of 3.4 for Loss of consciousness relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Head-eye deviationFigure 6 reports an odds ratio of 2.7 for Post-ictal confusion/behavior change disinhibition relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Head-eye deviationFigure 6 reports an odds ratio of 1.6 for Chapeau de gendarme relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Head-eye deviationFigure 6 reports an odds ratio of 1.5 for Dystonic posturing relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Head-eye deviationFigure 6 reports an odds ratio of 0.9 for Laughter relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Head-eye deviationFigure 6 reports an odds ratio of 0.6 for Oro-alimentary automatisms relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Head-eye deviationFigure 6 reports an odds ratio of 0.6 for Tonic-clonic relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Head-eye deviationFigure 6 reports an odds ratio of 0.4 for F to BTC relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to LaughterFigure 6 reports an odds ratio of 1.5 for Head-eye deviation relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.7 for Head-eye deviation relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Tonic-clonicFigure 6 reports an odds ratio of 2.8 for Head-eye deviation relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to F to BTCFigure 6 reports an odds ratio of 2.8 for Head-eye deviation relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 14% (frequency range 0–50%)head-eye deviationPercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.13, Table 3
  • 14%head-eye deviation; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.10, Figure 4
  • 14%head-eye deviation; contralateral to seizure onsetPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • OR 0.1pairwise OR: Head-eye deviation relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Head-eye deviation relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Head-eye deviation relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Head-eye deviation relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Head-eye deviation relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Vocalization/verbalization relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.1pairwise OR: Hypermotor-complex motor behavior relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.7pairwise OR: Affective/autonomic aura relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.7pairwise OR: Autonomic signs relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.2pairwise OR: Facial expression change relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.6pairwise OR: Motor (gestural) automatisms relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.4pairwise OR: Loss of consciousness relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Chapeau de gendarme relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Dystonic posturing relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Laughter relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Oro-alimentary automatisms relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Tonic-clonic relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: F to BTC relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Head-eye deviation relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Head-eye deviation relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.8pairwise OR: Head-eye deviation relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.8pairwise OR: Head-eye deviation relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Forced eye versionBoth tables list Forced eye version as Contralateral.PDF p.2, Lateralizing signs/Localization table row "Forced eye version" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Forced eye version" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • eye versionEye version is a forced, sustained conjugate deviation that usually accompanies head version and reliably lateralizes to the contralateral hemisphere before secondary generalization. Without generalization it may be ipsilateral or contralateral to the epileptogenic lesion depending on whether occipital or frontal regions are activated.PDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Eye versionEye-version semiology was absent as initial semiology (0/61, 0%) and occurred in 4/61 individuals (7%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 0/61 (0%)Eye versionPercentage · n/N 0/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 4/61 (7%)Eye versionPercentage · n/N 4/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Eye versionTable 3 associates eye version with frontal eye fields (BA 8) and extra-striate cortex (BA 19) and lists contralateral lateralisation.PDF p.4, Table 3
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 2 findings · 2 reported values
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • ATLP following head and eye versionAt the time of ATLP, the head was midline or returning to midline from version in all instances, and ATLP was on the same side as version in all but one Group II patient; the exception had left version followed by right version, right ATLP, and generalized clonic movements, with EEG higher over the left hemisphere.PDF p.3, Other characteristics of ATLP—item 2
  • head/eye versionThe methods section characterizes version as a well-recognized lateralizing sign with good interobserver agreement and high positive predictive value for the side of ictal onset.PDF p.2, Methods—definition and comparison of version
Reported values
  • Head midline or returning to midline at ATLP in all instancesATLP following head and eye versionPercentage · Group II patients with ATLP and version; one symptomatic generalized epilepsy exception is described · ATLP after version and before generalized clonic movementsPDF p.3, Other characteristics of ATLP—item 2
  • ATLP on same side as version in all but one Group II patientATLP following head and eye versionPercentage · Group II patients with ATLP and version; one symptomatic generalized epilepsy exception is described · Group II with ATLP and version · ATLP after version and before generalized clonic movementsPDF p.3, Other characteristics of ATLP—item 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Late ipsiversionThe review identifies ipsilateral forced head and eye version at the end of a generalized tonic-clonic seizure as a distinct lateralizing sign, especially when an initial contraversion ends during the generalized phase; if initial contraversion persists, late version can remain contralateral.PDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversionIn Wyllie et al., a study of 61 seizures in 27 patients with version, 9 patients had a late versive movement; when initial contraversion persisted, late deviation was contralateral in 3 patients, and when initial contraversion ended, late version was ipsilateral in 6 patients.PDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversionChee et al. found late ipsiversion after an initial contraversive movement before generalization in 6 of 38 selected patients, always ipsilateral to the epilepsy focus as determined by ictal EEG.PDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
Reported values
  • 6 patients had ipsilateral late versionLate ipsiversionCount · 27 patients with 61 seizures and version; 9 patients with late versive movement · initial contraversion ended · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • 3 patients had contralateral late deviationLate ipsiversionCount · 27 patients with 61 seizures and version; 9 patients with late versive movement · initial contraversion persisted · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • 61 seizuresLate ipsiversionCount · 27 patients with 61 seizures and version; 9 patients with late versive movement · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • 9/27 patients had late movementLate ipsiversionPercentage · n/N 9/27 · 27 patients with 61 seizures and version; 9 patients with late versive movement · late versive movement · End of generalized tonic-clonic seizurePDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversion in 6/38 patientsLate ipsiversionPercentage · n/N 6/38 · 38 selected patients with frontal and temporal lobe epilepsy; 6 with late ipsiversion · Before or at the end of generalizationPDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
  • Late ipsiversion ipsilateral to epilepsy focus 6/6Late ipsiversionPercentage · n/N 6/6 · 38 selected patients with frontal and temporal lobe epilepsy; 6 with late ipsiversion · Patients with late ipsiversion · Before or at the end of generalizationPDF p.4, section 3.2 Late ipsiversion at the end of a generalized seizure
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 3 findings · 10 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • head and/or eyes deviationHead and/or eyes deviation over the whole seizure course did not differ significantly across M, ML, and L groups.PDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • early head and/or eyes deviationEarly head and/or eyes deviation did not differ significantly across M, ML, and L groups.PDF p.6, Table 4; PDF p.6, Early features
  • late head and/or eyes deviationLate head and/or eyes deviation did not differ significantly across M, ML, and L groups.PDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
Reported values
  • ML=9/18 (50%)head and/or eyes deviationPercentage · n/N 9/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • L=5/13 (38.5%)head and/or eyes deviationPercentage · n/N 5/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • M=9/24 (37.5%)head and/or eyes deviationPercentage · n/N 9/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • p=0.69head and/or eyes deviationP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • 4/18 (22.2%)early head and/or eyes deviationPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 3/24 (12.5%)early head and/or eyes deviationPercentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 3/13 (23.1%)early head and/or eyes deviationPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 6/18 (33.3%)late head and/or eyes deviationPercentage · n/N 6/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
  • 8/24 (33.3%)late head and/or eyes deviationPercentage · n/N 8/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
  • 3/13 (23.1%)late head and/or eyes deviationPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 2 findings · 4 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • severity of head turning and eye movementThe discussion reports that Ochs et al. (1984) and Robillard et al. (1983) found no localizing or lateralizing value for forceful head turning at clinical seizure onset, while Wyllie et al. (1986) found lateralizing significance only for very severe head and eye movements with marked sustained unnatural positioning.PDF p.5, Discussion; PDF p.6, Discussion
  • eye deviationEye deviation inclined toward the side contralateral to seizure origin, but the source states that this tendency was not statistically significant.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
Reported values
  • 7/20 ipsilateral eye-deviation seizures (35%)eye deviationPercentage · n/N 7/20 · 19 patients with unilateral TLE; 20 eye-deviation seizures · Ipsilateral to seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • Ipsilateral eye deviation in 6% of all 116 seizureseye deviationPercentage · 19 patients with unilateral TLE; 20 eye-deviation seizures · Ipsilateral to seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • Contralateral eye deviation in 12% of all 116 seizureseye deviationPercentage · 19 patients with unilateral TLE; 20 eye-deviation seizures · Contralateral to seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 13/20 contralateral eye-deviation seizures (65%)eye deviationPercentage · n/N 13/20 · 19 patients with unilateral TLE; 20 eye-deviation seizures · Contralateral to seizure focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfCase report or observation · 5 findings · 5 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • ocular deviation within first 10 secondsThe source reports a cited stereo-EEG series of 16 patients with ocular deviation within the first 10 seconds of seizure onset.PDF p.20, Discussion
  • tonic ocular deviation in cited stereo-EEG seriesOcular deviation was tonic in 14 of the 16 cited patients.PDF p.20, Discussion
  • contralateral ocular deviation in cited stereo-EEG seriesOcular deviation was contralateral to the ictal discharge in all 16 patients in the cited series.PDF p.20, Discussion
  • contraversive head and eye movement in Ludwig and Ajmone-MarsanThe source reports contraversive head and eye movements in 29% of 55 patients in the cited Ludwig and Ajmone-Marsan series.PDF p.20, Discussion
  • contralateral head and eye deviation with occipital-localized seizureTwo depth-studied patients had contralateral head and eye deviation while the seizure remained localized to the occipital lobe.PDF p.6, Results, Non-visual manifestations
Reported values
  • 16 patients with ocular deviation within 10 secondsocular deviation within first 10 secondsCount · cited stereo-EEG occipital seizure series · seizure onsetPDF p.20, Discussion
  • 14/16 patientstonic ocular deviation in cited stereo-EEG seriesProportion · n/N 14/16 · 16 cited patients with early ocular deviation · seizure onsetPDF p.20, Discussion
  • 16/16 patientscontralateral ocular deviation in cited stereo-EEG seriesProportion · n/N 16/16 · 16 cited patients with early ocular deviation · seizure onsetPDF p.20, Discussion
  • 29% of 55 patientscontraversive head and eye movement in Ludwig and Ajmone-MarsanPercentage · cited Ludwig and Ajmone-Marsan occipital epilepsy series · ictal manifestationPDF p.20, Discussion
  • 2 casescontralateral head and eye deviation with occipital-localized seizureCount · n/N 2/2 · two depth-studied cohort patients · ictal onset and early evolutionPDF p.6, Results, Non-visual manifestations
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 2 findings · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • head and eye deviationHead and eye deviation occurred in 41% of patients.PDF p.4, Results, Other seizure characteristics
  • adversive head and eye movement after parietal spreadThe source suggests that adversive head and eye movements may reflect spread from the superior parietal lobule to the frontal lobe.PDF p.10, Discussion
Reported values
  • 41%head and eye deviationPercentage · 82-patient parietal epilepsy series · ictal motor or oculomotor phasePDF p.4, Results, Other seizure characteristics
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 6 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • tonic eye deviationTonic eye deviation occurred in 11 of 19 patients (57.9%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • visual aura to head-eye deviation or pursuitIn Phenotype III, a visual aura rapidly progresses to head-eye deviation or eye pursuit.PDF p.9, Phenotype III; PDF p.13, Phenotype III discussion
  • dorsal parietal to premotor motor evolutionThe authors link rapid motor evolution after visual aura to propagation to dorsal parietal nodes and then premotor areas.PDF p.13, Phenotype III discussion
  • head and eye deviation to the leftTable 2 records head and eye deviation to the left in a seizure that followed left-upper-limb tonic posturing.PDF p.6, Table 2 Case 1 Sz1
  • head-eye-body deviation to the rightTable 2 records head, eye, and body deviation to the right in Case 5.PDF p.6, Table 2 Case 5
Reported values
  • 11/19 (57.9%) tonic eye deviationtonic eye deviationPercentage · n/N 11/19 · 19 patients monitored with SEEG · ictal oculomotor semiologyPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
wyllie1986.pdfStructured design not resolved · 4 findings · 45 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • ictal events preceding contraversive head and eye movementThirty-five of 61 versive seizures (57%) began with the versive movement; these were predominantly frontal-onset (91%) and none was temporal-onset, whereas the other versive seizures were preceded by quiet staring or staring with automatisms as detailed in Table 2.PDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • ipsiversion in Ochs and Robillard seriesThe current paper reports that Ochs et al. and Robillard et al. found ipsiversion in 50% and 48%, respectively, of seizures with head and eye turning and concluded that forced head turning at clinical seizure onset had no localizing or lateralizing value.PDF p.3, discussion paragraph comparing Ochs and Robillard; PDF p.5, references 31-32
  • ipsiversion in Ajmone Marsan and Abraham seriesThe current paper reports that Ajmone Marsan and Abraham found ipsiversion in 4 of 16 pentylenetetrazol-induced seizures with version and lateralized ictal EEG, but cautions that the seizures were selected to illustrate other electroclinical features and the 25% incidence may not have been representative.PDF p.4, paragraph beginning “Ajmone Marsan and Abraham”; PDF p.6, reference 39
  • ipsiversion in Ajmone Marsan and Ralston seriesThe current paper reports a 3% incidence of ipsiversion in a larger series of pentylenetetrazol-induced seizures by Ajmone Marsan and Ralston and suggests that this may have been a more accurate assessment than the 25% incidence in the selected Ajmone Marsan and Abraham series.PDF p.4, paragraph comparing the 3% and 25% incidences; PDF p.6, reference 38
Reported values
  • frontal all versive seizures: 37 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by staring with automatisms: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by staring with automatisms: 14 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal all versive seizures: 10 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by quiet staring: 5 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by quiet staring: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by quiet staring: 1 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by quiet staring: 2 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by quiet staring: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by staring with automatisms: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total all versive seizures: 27 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by staring with automatisms: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total all versive seizures: 61 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total version at onset 35/61 (57%)ictal events preceding contraversive head and eye movementPercentage · n/N 35/61 · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal no preceding ictal event; version at onset: 1 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal no preceding ictal event; version at onset: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total no preceding ictal event; version at onset: 12 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by quiet staring: 8 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by staring with automatisms: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by quiet staring: 8 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital preceded by quiet staring: 0 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by quiet staring: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal no preceding ictal event; version at onset: 10 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by quiet staring: 5 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital no preceding ictal event; version at onset: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal no preceding ictal event; version at onset: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • total preceded by staring with automatisms: 18 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · total · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal all versive seizures: 20 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal all versive seizures: 2 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal preceded by staring with automatisms: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital all versive seizures: 1 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital no preceding ictal event; version at onset: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • parietal all versive seizures: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · parietal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal all versive seizures: 14 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal version at onset 32/37 (91%)ictal events preceding contraversive head and eye movementPercentage · n/N 32/37 · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal no preceding ictal event; version at onset: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by staring with automatisms: 18 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • frontal preceded by staring with automatisms: 0 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · frontal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • temporal preceded by staring with automatisms: 14 patientsictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · temporal · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • occipital all versive seizures: 2 seizuresictal events preceding contraversive head and eye movementCount · 27 patients; 61 versive seizures categorized by frontal, temporal, parietal, or occipital onset · occipital · Pre-contraversion ictal phase and onset of versive movementPDF p.2, Table 2; PDF p.2, paragraph beginning “Thirty-five (57%)”; PDF p.5, conclusion
  • 50%ipsiversion in Ochs and Robillard seriesPercentage · Seizures with head and eye turning in the cited Ochs report; cohort details not reported here · Ochs et al. · Head turning at clinical seizure onsetPDF p.3, discussion paragraph comparing Ochs and Robillard; PDF p.5, references 31-32
  • 48%ipsiversion in Ochs and Robillard seriesPercentage · Seizures with head and eye turning in the cited Robillard report; cohort details not reported here · Robillard et al. · Head turning at clinical seizure onsetPDF p.3, discussion paragraph comparing Ochs and Robillard; PDF p.5, references 31-32
  • Ipsiversion 4 of 16 seizures (25%)ipsiversion in Ajmone Marsan and Abraham seriesPercentage · n/N 4/16 · Pentylenetetrazol-induced seizures selected to illustrate other electroclinical features in the cited series · Ictal head and eye turningPDF p.4, paragraph beginning “Ajmone Marsan and Abraham”; PDF p.6, reference 39
  • Ipsiversion incidence 3% in larger cited seriesipsiversion in Ajmone Marsan and Ralston seriesPercentage · Larger pentylenetetrazol-induced seizure series cited by the current paper · Larger Ajmone Marsan and Ralston series · Ictal head and eye turningPDF p.4, paragraph comparing the 3% and 25% incidences; PDF p.6, reference 38
  • Ipsiversion incidence 4/16 (25%) in selected cited seriesipsiversion in Ajmone Marsan and Ralston seriesPercentage · n/N 4/16 · Larger pentylenetetrazol-induced seizure series cited by the current paper · Selected Ajmone Marsan and Abraham series · Ictal head and eye turningPDF p.4, paragraph comparing the 3% and 25% incidences; PDF p.6, reference 38
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdfCase report or observation · 7 findings · 3 reported values
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
Case report or observation · Class III · Evidence weight 1.50 · 1 × 1.5 × 1
This is a two-case report with no control or comparator group. Case-1 was a 24-year-old right-handed man; 32 habitual seizures were recorded during 3 days of scalp video-EEG, with two followed by secondary GTCS, and two right-hemisphere SEEG implantations were performed 4 months apart. Case-2 was a 19-year-old right-handed man; three habitual seizures were captured on video-EEG and right temporal neocortical, temporal-pole, and medial-structure regions were explored with SEEG. The source describes scalp EEG, MRI, FDG-PET, SEEG onset and propagation, anatomical reconstruction, cortical resection, and seizure-free follow-up of 17 months for Case-1 and 25 months for Case-2. Case-1 MRI/FDG-PET was reported unremarkable for an evaluable lesion; Case-2 MRI and PET findings were reported in the right middle-posterior inferior temporal/fusiform and medial temporal regions. No cohort-wide denominator for ipsiversive eye deviation, no control comparison, and no population-level frequency or diagnostic statistic are reported.
Findings
  • Authors’ proposed MST/smooth-pursuit mechanism for ipsiversive deviationThe authors hypothesize that lateralization of eye deviation during temporo-occipital seizures depends on whether MST is involved initially or primarily; they state that seizures originating from or primarily involving posterior ITG or the anterior bank of AOS, identified as human MST, would probably induce initial ipsilateral conjugate eye deviation.PDF p.1, Abstract; PDF p.9, Discussion and Conclusion
  • Case-1 forced eye deviation and head turningIn the Case-1 habitual seizure chronology, forced eye deviation to the right was followed by right-sided head turning, left-leg tonic posturing, left version, and GTCS in the described sequence.PDF p.2, Case-1 case presentation; PDF p.2, Fig. 1 caption
  • Case-1 Fig. 5 initial eyes left versionThe Fig. 5 caption for a Case-1 first-implantation ictal SEEG trace states that seizure onset was on G’12-13 and L’12-13, exploring the posterior inferior temporal area, and that the initial eyes showed left version.PDF p.4, Fig. 5 caption
  • Case-2 forced right eye deviation with left motor signsIn Case-2, the reported habitual seizure chronology was eyes open and staring followed by forced deviation to the right, proximal left-arm tonic posturing with a clenched left fist, and left facial clonia in one seizure; the episodes included loss of consciousness.PDF p.5, Case-2 case presentation; PDF p.8-9, Discussion
  • Case-2 posterior inferior temporal/AOS ictal localization preceding ipsiversive eye deviationIn Case-2, the source states that ictal SEEG confirmed the putative lesion as epileptogenic and that the most posterior cortical part of the inferior temporal gyrus, occupying the anterior bank of AOS, was involved by ictal discharges within 5 s before the initial clinical sign, identified as the ipsilateral eye deviation.PDF p.5, Case-2 case presentation; PDF p.6, Case-2 SEEG results
  • Cited direct-stimulation association of posterior inferior temporal sulcus with ipsilateral eye deviationThe current report states that comparative studies found the vicinity of the posterior branch of the inferior temporal sulcus to be motion-sensitive and that direct stimulation of this area induces constant ipsilateral eye deviation.PDF p.2, Background
  • Cited Kaplan case with ipsiversive eye deviation and right temporo-occipital onsetThe authors state that the ipsiversive eye deviation with homodromous head turning in their cases is similar to the case reported by Kaplan and that the cited case’s epileptic seizure originated from the right temporo-occipital cortex.PDF p.9, Discussion
Reported values
  • left facial clonia occurred in 1 of 3 captured habitual seizuresCase-2 forced right eye deviation with left motor signsCount · n/N 1/3 · Case-2; three habitual seizures were captured on video-EEG, but the source does not state that every listed component occurred in all three · ictal onset and progressionPDF p.5, Case-2 case presentation; PDF p.8-9, Discussion
  • Qualitative semiologic sequenceCase-2 forced right eye deviation with left motor signsCount · n/N 1/3 · Case-2; three habitual seizures were captured on video-EEG, but the source does not state that every listed component occurred in all three · ictal onset and progressionPDF p.5, Case-2 case presentation; PDF p.8-9, Discussion
  • Ictal discharge involvement within 5 s before initial ipsilateral eye deviationCase-2 posterior inferior temporal/AOS ictal localization preceding ipsiversive eye deviationCount · Case-2 · ictal activity immediately before the initial clinical signPDF p.5, Case-2 case presentation; PDF p.6, Case-2 SEEG results

17 contributing manuscripts; source-reported values remain separate and are not pooled.

AuraReported: Left hemisphereAlso reported: Right hemisphereNo single reliable side16 manuscripts · 51 findings · 34 reported values
Weighted evidence supportevidence weight 34.55 across 16 manuscripts · 2 manuscript weight pending · 4 independent primary study · 2 systematic review or meta-analysis · 7 narrative, educational, or cited context · 2 structured design not resolved · 1 case report or observation

A right middle frontal gyrus lesion case had left-face/left-arm clonic spread and fencing posture, with semiology and ictal EEG interpreted as right frontocentral onset. The source explicitly reports a left temporal pole lesion; the right-ear siren is retained as an auditory-side description without a hemisphere inference. The source explicitly reports a left temporal-pole lesion for the patient with the the source's own stomach-turning aura description. The source explicitly reports a right temporal-pole lesion for the patient with the the source's own clicking-and-intense-fear aura description. The source explicitly reports a right temporal-pole lesion for the patient with the the source's own anxiety and deja-vu aura description. The source explicitly reports a right temporal-pole lesion for the patient with the the source's own tunnel-vision, nausea, and deja-vu aura description. The source explicitly reports a right temporal-pole lesion for the patient with the the source's own fear and indescribable-feeling aura description. The review describes selected auras as relatively specific for temporal-lobe epilepsy but generally lacking useful lateralizing value. The review reports that auras are more common with right temporal than bitemporal epilepsy and that viscerosensory or experiential auras trend toward right temporal association. The paper restates that auras, especially epigastric sensations, were more frequent before RTL than LTL seizures. The cited study reported no significant overall aura lateralization while experiential auras tended to occur more often in right temporal lobe seizures. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. The review says auras may provide lateralizing information but reports no specific lateralizing direction here. No side direction is reported for auras in aggregate. No seizure lateralization is reported. No lateralizing direction is reported for ability to warn at seizure onset. No source-supported hemispheric or body-side lateralization is reported. No lateralizing direction is reported for the aura comparison. No lateralizing direction is reported for the aura count. No cerebral hemisphere or body-side direction is reported. No source-supported lateralizing direction is reported for the frontal-subgroup auras. No lateralizing direction is reported.

Source-defined result groups 8
Localization: ParietalObserved proportion 72.2%All reported · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 41.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: anterior cingulate cortex/cingulate seizure casesSource-defined values retained separatelypatient-level frequency synthesized across eligible studies1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 66.7%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: OFC-involving epileptogenic zone / orbitofrontal cortex (OFC)Source-defined values retained separatelyEntire OFC-involving group · patients with aura1 manuscript · 1 reported value · not pooled
Localization: ParietalObserved proportion 93.9%All reported · no aura · patients1 manuscript · 1 reported value · not pooled
Localization: OFC-restricted epileptogenic zone / orbitofrontal cortex (OFC)Observed proportion 19.2%OFC-restricted EZN group · patients with aura1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 100.0%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 16

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 3 findings · 3 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.389
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior auraAuras were reported in three of six typical anterior cases.PDF p.3, Clinical Presentation
  • posterior cingulate auraAuras were reported in all four posterior cingulate patients.PDF p.5, Posterior Cingulate Epilepsy
  • posterior cingulate multiple aurasTwo posterior cingulate patients had multiple auras.PDF p.5, Clinical Presentation
Reported values
  • 3/6 (50%) with auratypical anterior auraPercentage · n/N 3/6 · 6 typical anterior cingulate cases · auraPDF p.3, Clinical Presentation
  • 4/4 (100%) with auraposterior cingulate auraPercentage · n/N 4/4 · 4 posterior cingulate cases · auraPDF p.5, Posterior Cingulate Epilepsy
  • 2/4 with multiple aurasposterior cingulate multiple aurasProportion · n/N 2/4 · 4 posterior cingulate cases · auraPDF p.5, Clinical Presentation
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 8 findings · 8 reported values
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • aurasThirteen of 18 patients described auras.PDF p.1, Abstract; PDF p.2, Results; PDF p.4, Discussion
  • Bartolomei et al. 2011 auraTable 1 reports 82% aura in the cited Bartolomei et al. 2011 cohort.PDF p.3, Table 1
  • Salanova et al. 1995a auraTable 1 reports 94% aura in the cited Salanova et al. 1995a cohort.PDF p.3, Table 1
  • Salanova et al. 1995b auraTable 1 reports 79% aura in the cited Salanova et al. 1995b cohort.PDF p.3, Table 1
  • Kim et al. 2004b auraTable 1 reports 67.5% aura in the cited Kim et al. 2004b cohort.PDF p.3, Table 1
  • Kim et al. 2004a auraTable 1 reports 78.9% aura in the cited Kim et al. 2004a cohort.PDF p.3, Table 1
  • Francione et al. 2015 auraTable 1 reports 80% aura in the cited Francione et al. 2015 cohort.PDF p.3, Table 1
  • Asadollahi et al. 2017 (this study) auraTable 1 reports 72% aura in the cited Asadollahi et al. 2017 (this study) cohort.PDF p.3, Table 1
Reported values
  • 13/18 (72%) patients with aurasaurasPercentage · n/N 13/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · preoperative ictal symptom historyPDF p.1, Abstract; PDF p.2, Results; PDF p.4, Discussion
  • 82% auraBartolomei et al. 2011 auraPercentage · Bartolomei et al. 2011 cohort · auraPDF p.3, Table 1
  • 94% auraSalanova et al. 1995a auraPercentage · Salanova et al. 1995a cohort · auraPDF p.3, Table 1
  • 79% auraSalanova et al. 1995b auraPercentage · Salanova et al. 1995b cohort · auraPDF p.3, Table 1
  • 67.5% auraKim et al. 2004b auraPercentage · Kim et al. 2004b cohort · auraPDF p.3, Table 1
  • 78.9% auraKim et al. 2004a auraPercentage · Kim et al. 2004a cohort · auraPDF p.3, Table 1
  • 80% auraFrancione et al. 2015 auraPercentage · Francione et al. 2015 cohort · auraPDF p.3, Table 1
  • 72% auraAsadollahi et al. 2017 (this study) auraPercentage · Asadollahi et al. 2017 (this study) cohort · auraPDF p.3, Table 1
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 4 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.86 · 2 × 1.5 × 1.952
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • auraAuras of varying types were reported in 71 of 80 analyzed seizures (88.7%).PDF p.5, Seizure clinical semiology
  • ability to warn at seizure onset auraThe ability to warn at seizure onset was more frequent in TL than T+ seizures.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Ability to warn at seizure onset
Reported values
  • 71/80 seizures (88.7%) with an auraauraPercentage · n/N 71/80 · 80 analyzed seizures, one typical seizure per patient · ictal onsetPDF p.5, Seizure clinical semiology
  • T+ 43.5%ability to warn at seizure onset auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Ability to warn at seizure onset
  • TL 78%ability to warn at seizure onset auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Ability to warn at seizure onset
  • P=0.003ability to warn at seizure onset auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Ability to warn at seizure onset
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 3 findings · 1 reported value
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Aura phenomena and localizing versus lateralizing valueThe review reports that rising epigastric sensation, fear, déjà vu, jamais vu, visceral or auditory illusions, complex auditory or visual hallucinations, gustatory or olfactory hallucinations, and elementary auditory hallucinations may correlate with temporal-lobe seizure onset or be relatively specific for TLE, while auras often have localizing value but usually lack lateralizing significance.PDF p.1, abstract; PDF p.2, section 2.2 Aura
  • Aura occurrence and durationAuras are described as simple partial seizures that can occur in isolation, occur in the majority of patients at the onset of a CPS, and can last from seconds to 1–2 minutes before consciousness is lost.PDF p.1, abstract; PDF p.2, section 2.2 Aura
  • Aura as spread pattern versus seizure-onset markerThe review states that reciprocal mesial and neocortical temporal connections may be activated to produce an aura and suggests that aura type may indicate the pattern of seizure spread more than the site of seizure onset.PDF p.3, final paragraph of section 3
Reported values
  • seconds to 1–2 minutesAura occurrence and durationRange · Patients with TLE or CPSs as discussed by the review; no single cohort reported. · Pre-consciousness ictal onsetPDF p.1, abstract; PDF p.2, section 2.2 Aura
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 4 findings · 2 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • auraThe source reports a frequency of 58% for aura.PDF p.13, Table 3
  • aura; reported frequency rangeThe source reports a frequency range of 0–96% for aura.PDF p.13, Table 3
  • aura; ACC association gradeTable 3 assigns the source's High overall association grade to aura.PDF p.13, Table 3
  • aura; Figure 4 rateFigure 4 displays a 58.1% rate for aura.PDF p.10, Figure 4
Reported values
  • 58% (frequency range 0–96%)auraPercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.13, Table 3
  • 58.1%aura; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.10, Figure 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfCase report or observation · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • aura; behavioural arrest; left-face clonic activity; fencing postureIn an illustrative 50-year-old man with a right middle frontal gyrus cystic lesion, a seizure evolved from an aura to behavioural arrest, left-face clonic movements spreading over the left arm, and left-arm extension in a fencing posture before secondary generalisation; the authors state that the semiology and ictal EEG supported right frontocentral onset.PDF p.3, Video case 1 and Figure 1; PDF p.3, Figure 2 caption
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 9 findings · 8 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.58 · 1 × 0.9 × 1.759
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • OFC + group (EZN extending beyond OFC); aura; oro-alimentary automatisms; gestural automatismsThe source characterizes EZN extending beyond the OFC as having richer semiological profiles, with temporal extension more often associated with aura, oro-alimentary automatisms, and sleep.PDF p.6, Semiological profile; PDF p.7, Conclusion
  • aura; OFC-extended EZNAuras were reported in 11 of 33 OFC-extended cases.PDF p.3, Aura
  • aura; OFC-restricted EZNAuras were reported in five of 26 OFC-restricted cases.PDF p.3, Aura
  • aura; entire OFC-involving groupAcross the entire 87-case group, aura was documented in 30% of cases.PDF p.3, Aura
  • aura; Chibane cited cohortChibane et al. were reported as having a 43.8% aura prevalence in their cohort.PDF p.3, Aura
  • aura; temporal OFC-extended subgroupAuras were reported in 58% of the temporal subgroup of OFC-extended cases.PDF p.3, Aura
  • aura; frontal OFC-extended subgroupAuras were reported in 18% of the frontal subgroup of OFC-extended cases.PDF p.3, Aura
  • aura; insular OFC-extended subgroupTwo patients in the insular subgroup had reported auras.PDF p.3, Aura
  • aura; frontal OFC-extended subgroupTwo patients in the frontal subgroup had reported auras.PDF p.3, Aura
Reported values
  • 11/33 (33%)aura; OFC-extended EZNPercentage · n/N 11/33 · OFC-extended EZN group · OFC-extended EZN group · ictal auraPDF p.3, Aura
  • 5/26 (19%)aura; OFC-restricted EZNPercentage · n/N 5/26 · OFC-restricted EZN group · OFC-restricted EZN group · ictal auraPDF p.3, Aura
  • 30%aura; entire OFC-involving groupPercentage · Entire OFC-involving group · Entire OFC-involving group · ictal auraPDF p.3, Aura
  • 43.8%aura; Chibane cited cohortPercentage · Chibane cited cohort · Chibane cited cohort · ictal auraPDF p.3, Aura
  • 58%aura; temporal OFC-extended subgroupPercentage · Temporal subgroup of OFC-extended EZN · Temporal subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
  • 18%aura; frontal OFC-extended subgroupPercentage · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
  • 2 patientsaura; insular OFC-extended subgroupCount · n/N 2/10 · Insular subgroup of OFC-extended EZN · Insular subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
  • 2 patientsaura; frontal OFC-extended subgroupCount · n/N 2/11 · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 2 findings
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Aura lateralization in cited studiesThe current paper states that its finding of more frequent auras, especially epigastric sensations, before RTL seizures concurred with Gupta et al. (1983) and Taylor and Lochery (1987).PDF p.5, Discussion, aura paragraph
  • Aura lateralization in a cited study with null resultThe current paper reports that Palmini and Gloor (1992) did not detect a statistically significant lateralizing value for auras, although experiential auras with complex visual and auditory hallucinations tended to originate more frequently in RTL.PDF p.5, Discussion, aura paragraph
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • aurasAs first ictal symptoms, auras provide important localizing and lateralizing information about the relationship between the symptomatogenic and epileptogenic zones. They are reported by most patients with temporal and parieto-occipital epilepsies, are associated with favorable outcome after temporal lobectomy, and were reported to localize the most likely lobe of origin as well as EEG and imaging.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • aura; unique type of sensationIn the included patients, auras were described as mostly a unique type of sensation rather than mixed symptoms.PDF p.6, Anatomical and clinical correlations
  • AuraTable 2 reports 14/21 (67%) for Aura; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • AuraTable 2 reports 5/12 patients with Aura in the prefrontal operculum group.PDF p.7, Table 2
  • AuraTable 2 reports 9/9 patients with Aura in the precentral Rolandic operculum group.PDF p.7, Table 2
  • AuraFisher's exact comparison of Aura between the prefrontal and precentral Rolandic operculum groups has p=0.007.PDF p.7, Table 2
Reported values
  • 14/21 (67%)AuraPercentage · n/N 14/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 5/12 patientsAuraProportion · n/N 5/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 9/9 patientsAuraProportion · n/N 9/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • auras not visible on videoMost auras in insular seizures cannot be appreciated on video.PDF p.3, Video EEG
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • AuraAuras consist exclusively of subjective ictal symptoms, usually occur at the beginning of a seizure, are generally brief, and may occur in isolation; their epileptic nature can be documented objectively when they consistently evolve into a dialeptic or motor seizure or when EEG monitoring shows an EEG seizure pattern during the aura.PDF p.2, Auras; PDF p.3, Auras
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • temporal aurasIn a selected group with proven mesial temporal origin, more than 90% of patients reported an aura; auras were more common with right than bitemporal epilepsy, epigastric aura was most common, and viscerosensory or experiential auras strongly supported temporal involvement with a trend toward right temporal association, whereas absent aura was more common with bitemporal epilepsy.PDF p.49
Reported values
  • >90% reported aura in the selected proven mesial temporal grouptemporal aurasPercentage · selected patients with proven mesial temporal origin and broader temporal lobe epilepsy teaching groups · preictal and early ictal auraPDF p.49
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • presence of auraeAurae were present in 77 of 82 patients.PDF p.3, Results, Aurae; PDF p.4, Table 1
Reported values
  • 77/82 (94%) patientspresence of auraePercentage · n/N 77/82 · 82 patients with nontumoural parietal lobe epilepsy treated surgically · aura or seizure onsetPDF p.3, Results, Aurae; PDF p.4, Table 1
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 8 findings · 2 reported values
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • patient 2 auraTable 1 reports patient 2 with the the source's own aura description: hears a siren in the right ear.PDF p.3, Table 1
  • patient 3 auraTable 1 reports patient 3 with the the source's own aura description: funny feeling in stomach, like stomach is turning in circles.PDF p.3, Table 1
  • patient 4 auraTable 1 reports patient 4 with the the source's own aura description: something clicks in mind and intense fear.PDF p.3, Table 1
  • patient 5 auraTable 1 reports patient 5 with the the source's own aura description: anxiety; deja-vu.PDF p.3, Table 1
  • patient 7 auraTable 1 reports patient 7 with the the source's own aura description: tunnel vision, nausea and deja vu.PDF p.3, Table 1
  • patient 8 auraTable 1 reports patient 8 with the the source's own aura description: fear; indescribable feeling (rare).PDF p.3, Table 1
  • auras in temporal pole lesion cohortSix of eight patients reported an aura before seizures.PDF p.2, Results
  • auras among hypermotor patientsTwo of four patients with hypermotor seizures reported auras.PDF p.4, Seizure semiology on video-EEG recording
Reported values
  • 6/8 patients with auraauras in temporal pole lesion cohortProportion · n/N 6/8 · 8-patient temporal pole lesion cohort · preoperative auraPDF p.2, Results
  • 2/4 hypermotor patients with auraauras among hypermotor patientsProportion · n/N 2/4 · 4 patients with hypermotor seizure semiology · auraPDF p.4, Seizure semiology on video-EEG recording
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • ictal aurasAuras occurred in 10 of 19 patients (52.6%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
Reported values
  • 10/19 (52.6%) aurasictal aurasPercentage · n/N 10/19 · 19 patients monitored with SEEG · aura/ictal semiologyPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

16 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal impaired awarenessReported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere14 manuscripts · 58 findings · 46 reported values
Weighted evidence supportevidence weight 34.12 across 14 manuscripts · 4 independent primary study · 6 narrative, educational, or cited context · 4 systematic review or meta-analysis

The cited study reports greater impairment with bitemporal or left-temporal seizures and more preserved consciousness with nondominant-temporal seizures. Whole-course loss of contact occurred in 74% of left and 62% of right temporal seizures, with no statistically significant side difference. Initial loss of contact occurred in 28% of left and 19% of right temporal seizures, without a statistically significant side difference. The narrative reports impaired consciousness during propagation without any left/right hemisphere direction. The 35% impaired-consciousness narrative reports no hemisphere or body-side direction. No hemisphere or body-side direction is reported. The temporal lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The frontal lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The occipital lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The parietal lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The cited network-coupling summary reports no hemisphere or body-side direction. The alternate-source summary reports no hemisphere or body-side association for impaired consciousness. The alternate-source synchrony summary provides no hemisphere or body-side direction. The cited study summary reports no side or hemisphere association. No hemisphere or body-side association is reported. Wake versus sleep/stupor at seizure onset provides no hemisphere or body-side direction.

Source-defined result groups 26
Localization: hypothalamusSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelybasal temporal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 53.8%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given LOA/dialeptic semiology · localizing data point1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: cingulateSource-defined values retained separatelycingulate localization · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 70.8%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyoccipital localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: OFC-restricted EZNObserved proportion 23.1%OFC-restricted EZN cases · patients1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft temporal lobe · right temporal lobe · seizure; exact denominator not reported1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 41.0%combined set-of-semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 69.2%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft temporal lobe · seizure; exact source unit not further specified1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyposterior temporal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 72.2%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyright temporal lobe · left temporal lobe · seizure; exact denominator not reported1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyright temporal lobe · seizure; exact source unit not further specified1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given LOA/dialeptic semiology · localizing data point1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 19.7%initial semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.9%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 14

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 29 findings · 15 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • dialeptic-LOA-LOCTable 1 defines or exemplifies the the source's own semiology category “dialeptic-LOA-LOC” as Blank stare, loss of awareness, loss of contact, psychomotor arrest, distant gaze, dreamy state, loss of consciousness excluding generalized seizures, or dyscognitive states.PDF p.7, Table 1 Semiology descriptions and frequencies
  • dialeptic-LOA-LOCDialeptic-LOA-LOC comprised 8.3% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • dialeptic/LOA; Figure 3 all-data subsetFigure 3 reports N = 753 for the all-data dialeptic/LOA panel.PDF p.9, Figure 3 and caption
  • dialeptic/LOA; Figure 3 non-topological subsetFigure 3 reports N = 291 for the non-topological dialeptic/LOA panel.PDF p.9, Figure 3 and caption
  • dialeptic/LOA; temporal lobeLoss-of-awareness/dialeptic semiology was temporal in origin in 42%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; temporal lobeThe 95% CI for dialeptic/LOA; temporal lobe was 36%–49%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; frontal lobeLoss-of-awareness/dialeptic semiology was frontal in origin in 28%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; frontal lobeThe 95% CI for dialeptic/LOA; frontal lobe was 23%–34%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; cingulatedialeptic/LOA semiology was cingulate in 3%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; cingulateThe 95% CI for dialeptic/LOA; cingulate was 1%–4%.PDF p.8, Seizure semiology localizing values
  • loss of awareness; occipital lobeLoss of awareness had an intrinsic localizing OR of 2.9 for occipital localization.PDF p.8, Relative localizing values of semiologies
  • loss of awareness; occipital lobeThe 95% CI for loss of awareness; occipital lobe was 1.8–4.6.PDF p.8, Relative localizing values of semiologies
  • loss of awareness; posterior temporalLoss of awareness had an intrinsic localizing OR of 2.0 for posterior temporal localization.PDF p.8, Relative localizing values of semiologies
  • loss of awareness; posterior temporalThe 95% CI for loss of awareness; posterior temporal was 1.0–3.6.PDF p.8, Relative localizing values of semiologies
  • loss of awareness; basal temporalLoss of awareness had an intrinsic localizing OR of 5.8 for basal temporal localization.PDF p.8, Relative localizing values of semiologies
  • loss of awareness; basal temporalThe 95% CI for loss of awareness; basal temporal was 2.4–14.3.PDF p.8, Relative localizing values of semiologies
  • dialeptic/LOA; occipital lobedialeptic/LOA localizing distribution included occipital lobe at 9%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; occipital lobeThe 95% CI for the occipital lobe dialeptic/LOA distribution was 6%–11%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; parietal lobedialeptic/LOA localizing distribution included parietal lobe at 8%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; parietal lobeThe 95% CI for the parietal lobe dialeptic/LOA distribution was 5%–11%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; hypothalamusdialeptic/LOA localizing distribution included hypothalamus at 8%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; hypothalamusThe 95% CI for the hypothalamus dialeptic/LOA distribution was 5%–10%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; cingulatedialeptic/LOA localizing distribution included cingulate at under 5%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; cingulateThe 95% CI for the cingulate dialeptic/LOA distribution was 1%–4%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; insuladialeptic/LOA localizing distribution included insula at under 5%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; insulaThe 95% CI for the insula dialeptic/LOA distribution was 1%–4%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; temporal cited resultA cited study is restated as reporting 35% of cases with dialeptic/altered-consciousness seizures involving the temporal region.PDF p.12, Localizing probabilities
  • dialeptic/LOA; frontal cited resultA cited study is restated as reporting 16% of cases with dialeptic/altered-consciousness seizures involving the frontal region.PDF p.12, Localizing probabilities
  • dialeptic/LOA; parieto-occipital cited resultA cited study is restated as reporting 5% of cases with dialeptic/altered-consciousness seizures involving the parieto-occipital region.PDF p.12, Localizing probabilities
Reported values
  • dialeptic-LOA-LOC 8.3%dialeptic-LOA-LOCPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • dialeptic/LOA; temporal lobe 42%dialeptic/LOA; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; frontal lobe 28%dialeptic/LOA; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; cingulate 3%dialeptic/LOA; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 2.9loss of awareness; occipital lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 2.0loss of awareness; posterior temporalOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 5.8loss of awareness; basal temporalOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • dialeptic/LOA; occipital lobe 9%dialeptic/LOA; occipital lobePercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; parietal lobe 8%dialeptic/LOA; parietal lobePercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; hypothalamus 8%dialeptic/LOA; hypothalamusPercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; cingulate under 5%dialeptic/LOA; cingulatePercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; insula under 5%dialeptic/LOA; insulaPercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • temporal localization 35%dialeptic/LOA; temporal cited resultPercentage · cited altered-consciousness seizure cohortPDF p.12, Localizing probabilities
  • frontal localization 16%dialeptic/LOA; frontal cited resultPercentage · cited altered-consciousness seizure cohortPDF p.12, Localizing probabilities
  • parieto-occipital localization 5%dialeptic/LOA; parieto-occipital cited resultPercentage · cited altered-consciousness seizure cohortPDF p.12, Localizing probabilities
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • loss of contact during temporal lobe seizuresThe source reports a previous suggestion that loss of contact in TL epilepsy is a consequence of discharge extending outside the temporal lobe.PDF p.8, Ability to warn at seizure onset
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Loss of awareness (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports loss of awareness in 27 cases (45%).PDF p.7, Table 4
Reported values
  • 27/60 (45%)Loss of awareness (Table 4)Percentage · n/N 27/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • impaired consciousness and long-distance synchronizationIn temporal seizures, impairment of consciousness is not constant and may appear at different times depending on spread; a cited quantification study found synchronization indices for extra-temporal interactions significantly increased in seizures with loss of consciousness compared with seizures without loss, only from the middle of the seizure to its end, involving posterior supra-sylvian areas and posterior thalamus (pulvinar).PDF p.6, section 7
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 3 findings · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • impairment of consciousnessIn the source's application of the proposed ILAE framework, impairment of consciousness is treated as a major criterion for classifying focal seizures.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • impairment of consciousness; focal seizure classificationSix restricted-OFC cases met the source's impairment-of-consciousness criterion.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • impairment of consciousness; unspecifiedFor 20 restricted-OFC cases, the authors did not specify whether the impairment-of-consciousness criterion was met.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 6/26 patientsimpairment of consciousness; focal seizure classificationCount · n/N 6/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 6 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • impaired consciousness during seizure propagationDuring seizure propagation, impaired consciousness was observed in three patients.PDF p.6, Anatomical and clinical correlations
  • impaired consciousness during seizure propagationDuring seizure propagation, the source reports impaired consciousness in 35% of patients.PDF p.6, Anatomical and clinical correlations
  • Impaired consciousnessTable 2 reports 8/21 (38%) for Impaired consciousness; timing is late, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Impaired consciousnessTable 2 reports 4/12 patients with Impaired consciousness in the prefrontal operculum group.PDF p.7, Table 2
  • Impaired consciousnessTable 2 reports 4/9 patients with Impaired consciousness in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Impaired consciousnessFisher's exact comparison of Impaired consciousness between the prefrontal and precentral Rolandic operculum groups has p=0.673.PDF p.7, Table 2
Reported values
  • 3 patients (35%)impaired consciousness during seizure propagationPercentage · Included fronto-opercular epilepsy patients with propagation data · Included fronto-opercular epilepsy patients with propagation data · ictal propagationPDF p.6, Anatomical and clinical correlations
  • 8/21 (38%)Impaired consciousnessPercentage · n/N 8/21 · 21 included fronto-opercular epilepsy patients · LatePDF p.7, Table 2
  • 4/12 patientsImpaired consciousnessProportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · LatePDF p.7, Table 2
  • 4/9 patientsImpaired consciousnessProportion · n/N 4/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · LatePDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • loss of awareness in MORTEMUS insular near-SUDEP casesBoth MORTEMUS insular near-SUDEP cases had loss of awareness during the associated seizures.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
Reported values
  • loss of awareness in both casesloss of awareness in MORTEMUS insular near-SUDEP casesProportion · n/N 2/2 · 2 MORTEMUS insular near-SUDEP cases · ictal/peri-ictal periodPDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Impaired awarenessImpaired awareness was the most common initial semiology, occurring in 12/61 individuals (20%), and occurred in 25/61 (41%) in the combined set-of-semiology.PDF p.3, Results; PDF p.5, Table 2
Reported values
  • Initial 12/61 (20%)Impaired awarenessPercentage · n/N 12/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
  • Combined 25/61 (41%)Impaired awarenessPercentage · n/N 25/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Impaired or spared consciousnessA further cited study found consciousness was most commonly impaired in bitemporal or left temporal seizures and more frequently spared in non-dominant temporal lobe seizures.PDF p.3, section 1.3
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 5 findings · 11 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • ictal loss of contact by temporal sideAcross the whole seizure course, loss of contact occurred in 74% of left and 62% of right temporal lobe seizures, without statistical significance.PDF p.6, General ictal characteristics
  • initial loss of contact by temporal sideInitial loss of contact occurred in 28% of left and 19% of right temporal seizures without a statistically significant side difference, regardless of seizure subtype.PDF p.6, Early features
  • initial or secondary loss of contactWhen loss of contact was counted regardless of timing, its frequency did not differ across M, ML, and L groups.PDF p.6, Table 3; PDF p.6, General ictal characteristics
  • initial loss of contactLoss of contact during the first 10 seconds was more frequent in L and ML than M patients, and the authors interpret initial loss of contact as reflecting early temporal-neocortical involvement in pure L or ML networks.PDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Initial loss of contact
  • late loss of contact in MTLSThe discussion reports that late loss of contact in medial temporal lobe seizures was frequent, had a mean delay of 43.9 seconds, and was temporally correlated with secondary propagation of the discharge to neocortex.PDF p.8, Initial loss of contact
Reported values
  • 62%ictal loss of contact by temporal sidePercentage · left and right temporal lobe seizures in the 55-patient cohort; denominators not reported · right temporal lobe · whole ictal course, regardless of timingPDF p.6, General ictal characteristics
  • 74%ictal loss of contact by temporal sidePercentage · left and right temporal lobe seizures in the 55-patient cohort; denominators not reported · left temporal lobe · whole ictal course, regardless of timingPDF p.6, General ictal characteristics
  • 28%initial loss of contact by temporal sidePercentage · left and right temporal seizures in the 55-patient cohort; denominators not reported · left temporal lobe · initial ictal phase, first 10 secondsPDF p.6, Early features
  • 19%initial loss of contact by temporal sidePercentage · left and right temporal seizures in the 55-patient cohort; denominators not reported · right temporal lobe · initial ictal phase, first 10 secondsPDF p.6, Early features
  • L 9/13 (69.2%)initial or secondary loss of contactPercentage · n/N 9/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · whole ictal course, regardless of timingPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • M 17/24 (70.8%)initial or secondary loss of contactPercentage · n/N 17/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · whole ictal course, regardless of timingPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • ML 13/18 (72.2%)initial or secondary loss of contactPercentage · n/N 13/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · whole ictal course, regardless of timingPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • M 0/24 (0%)initial loss of contactPercentage · n/N 0/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal phase, first 10 secondsPDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Initial loss of contact
  • L 7/13 (53.8%)initial loss of contactPercentage · n/N 7/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal phase, first 10 secondsPDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Initial loss of contact
  • ML 7/18 (38.9%)initial loss of contactPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal phase, first 10 secondsPDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Initial loss of contact
  • Mean delay 43.9 slate loss of contact in MTLSCount · medial temporal lobe seizures; denominator not reported · late ictal loss of contact after initial dischargePDF p.8, Initial loss of contact
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 6 findings · 7 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • impaired consciousnessThe review reports that Arthuis et al. (2009) found excessive synchrony, expressed as h2 functional coupling, between temporal and extra-temporal structures, notably parietal cortex and thalamus, in temporal-lobe seizures with marked alteration of consciousness.PDF p.4, Table 1, Impaired consciousness row, 2009
  • impaired consciousnessThe review reports that Lambert et al. (2012) found increased synchrony associated with progressively greater altered responsiveness in parietal-lobe seizures and a statistically significant nonlinear relationship between h2 values and degree of alteration of consciousness, suggesting a threshold effect.PDF p.4, Table 1, Impaired consciousness row, 2012
  • impaired consciousnessThe review reports that Bonini et al. (2016) found the highest synchrony in frontal-lobe seizures with marked altered consciousness and significant correlations between consciousness scores and h2 values in prefrontal and parietal regions but not the premotor cortex.PDF p.4, Table 1, Impaired consciousness row, 2016
  • impaired consciousnessIn the summarized Arthuis et al. study, temporal-lobe seizures with marked alteration of consciousness showed excessive synchrony or functional coupling between temporal and extra-temporal structures, notably parietal cortex and thalamus.PDF p.4, Table 1, Arthuis et al. 2009 row; PDF p.11, mechanism 2
  • impaired consciousnessIn the summarized Lambert et al. study of parietal seizures, increased synchrony was associated with progressively greater altered responsiveness and a statistically significant nonlinear relationship was found between h2 values and degree of alteration of consciousness, suggesting a threshold effect.PDF p.4, Table 1, Lambert et al. 2012 row
  • impaired consciousnessIn the summarized Bonini et al. study of frontal seizures, marked altered consciousness was associated with the highest synchrony, and consciousness scores correlated significantly with h2 values in prefrontal and parietal regions but not in the premotor cortex.PDF p.4, Table 1, Bonini et al. 2016 row; PDF p.11, mechanism 2
Reported values
  • n=12 subjectsimpaired consciousnessCount · 12 subjects with temporal-lobe epilepsy · Period of semiologic expressionPDF p.4, Table 1, Impaired consciousness row, 2009
  • increased synchrony and statistically significant nonlinear h2 relationship with alteration of consciousnessimpaired consciousnessCount · 10 subjects with parietal-lobe epilepsy · Period of semiologic expressionPDF p.4, Table 1, Impaired consciousness row, 2012
  • n=10 subjectsimpaired consciousnessCount · 10 subjects with parietal-lobe epilepsy · Period of semiologic expressionPDF p.4, Table 1, Impaired consciousness row, 2012
  • 24 subjectsimpaired consciousnessCount · 24 subjects with frontal-lobe epilepsy · frontal-lobe epilepsy study · Period of semiologic expressionPDF p.4, Table 1, Impaired consciousness row, 2016
  • 12 subjectsimpaired consciousnessCount · 12 subjects with temporal-lobe epilepsy; number of seizures Not reported · ictal, during altered consciousnessPDF p.4, Table 1, Arthuis et al. 2009 row; PDF p.11, mechanism 2
  • Subjects in 3-T fMRI humming study n=10impaired consciousnessCount · 10 subjects with parietal-lobe epilepsy; number of seizures Not reported · ictal, during altered responsivenessPDF p.4, Table 1, Lambert et al. 2012 row
  • 24 subjectsimpaired consciousnessCount · 24 subjects with frontal-lobe epilepsy; number of seizures Not reported · Bonini et al. frontal-lobe epilepsy study · ictal, during altered consciousnessPDF p.4, Table 1, Bonini et al. 2016 row; PDF p.11, mechanism 2
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 1 finding · 4 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 2.40 · 2 × 1.2 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • level of vigilance at seizure onsetPICA occurrence was not associated with wake versus sleep/stupor at seizure onset.PDF p.6, Table 2, Level of vigilance at seizure onset; PDF p.6, Awareness of Apnea in the Postictal Period
Reported values
  • ICA-only; sleep/stupor 25 (53%)level of vigilance at seizure onsetPercentage · Patients with seizure-related disordered breathing; Table 2 row labeled 69 seizures, comparing PICA with ICA-only seizures · ICA-only; sleep/stupor · seizure onset and postictal outcomePDF p.6, Table 2, Level of vigilance at seizure onset; PDF p.6, Awareness of Apnea in the Postictal Period
  • ICA-only; wake 22 (47%)level of vigilance at seizure onsetPercentage · Patients with seizure-related disordered breathing; Table 2 row labeled 69 seizures, comparing PICA with ICA-only seizures · ICA-only; wake · seizure onset and postictal outcomePDF p.6, Table 2, Level of vigilance at seizure onset; PDF p.6, Awareness of Apnea in the Postictal Period
  • PICA; sleep/stupor 10 (45%)level of vigilance at seizure onsetPercentage · Patients with seizure-related disordered breathing; Table 2 row labeled 69 seizures, comparing PICA with ICA-only seizures · PICA; sleep/stupor · seizure onset and postictal outcomePDF p.6, Table 2, Level of vigilance at seizure onset; PDF p.6, Awareness of Apnea in the Postictal Period
  • PICA; wake 12 (55%)level of vigilance at seizure onsetPercentage · Patients with seizure-related disordered breathing; Table 2 row labeled 69 seizures, comparing PICA with ICA-only seizures · PICA; wake · seizure onset and postictal outcomePDF p.6, Table 2, Level of vigilance at seizure onset; PDF p.6, Awareness of Apnea in the Postictal Period
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • initial loss of contactThe source states that initial loss of contact is shared with lateral temporal seizures.PDF p.5, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • TPOJ and PCC-PCu early synchronizationEarly engagement of TPOJ and PCC/PCu is described as driving widespread network synchronization, early impaired consciousness, and secondary generalization.PDF p.14, Key Hubs Act as Accelerators and Switches

14 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal aphasia / language disturbanceSource terms: Postictal aphasiaReported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side16 manuscripts · 27 findings · 34 reported values
Weighted evidence supportevidence weight 32.3 across 16 manuscripts · 2 manuscript weight pending · 4 independent primary study · 2 systematic review or meta-analysis · 7 narrative, educational, or cited context · 1 case report or observation · 2 structured design not resolved

The review states that anarthria alone is insufficient for hemispheric lateralization. The educational statement says dominant-hemisphere seizures can produce the same phonatory symptoms as non-dominant seizures, with dysphasia additionally possible in dominant-hemisphere seizures. The review is subtype-dependent: ictal speech arrest is not reliably lateralizing, whereas selected ictal language and postictal aphasia patterns are associated with dominant, usually right nondominant, or left dominant temporal language networks. The case observation records left parietotemporal EEG abnormalities with right facial twitching and is normalized by the card as bilateral laterality context. The review describes ictal or postictal dys/aphasia as having approximately 90% lateralisation value but gives no direction and says its localisation value is poor. Dysphasia was much more frequent in dominant-origin temporal-lobe seizures (27 seizures in 12 patients) than in nondominant-origin seizures (3 seizures in 2 patients), with all nondominant events being isolated paraphasias. The review distinguishes dominant-hemisphere dysphasia, nondominant ictal speech or preserved awareness, contralateral RINCH motions, and nonlateralizing speech arrest. The review links ictal or postictal dysphasia to the dominant hemisphere, formed nonsensical ictal speech to the nondominant hemisphere, and explicitly describes speech arrest as non-lateralising. The review describes postictal aphasia as a predominantly dominant-hemisphere lateralizing sign and reports 80–90% reliability. The review associates postictal aphasia with the dominant hemisphere in temporal-lobe seizures. Both handbook tables list postictal aphasia as indicating the dominant hemisphere. Prolonged postictal language delay was reported in dominant-hemisphere frontal seizures, especially when frontal onset spread to the dominant temporal lobe. The cited result reports prolonged postictal language delay with a structural lesion only in nondominant temporal complex partial seizures. The review states that postictal aphasia almost always indicates dominant-hemisphere involvement. The review states that language recovery is related to hemisphere of onset but does not specify a direction. The review states that postictal aphasia lateralizes to the language-dominant hemisphere and that delayed language recovery is particularly associated with left temporal epilepsy; ipsilateral temporal extension modifies the frontal comparison. Postictal dysphasia predominantly followed dominant-temporal seizures (12/13), with one nondominant exception. Postictal dysphasia strongly favored left-temporal seizures: 24 of 26 affected patients were left-sided, with two right-sided exceptions. Postictal aphasia occurred after 37 left-temporal seizures and no right-temporal seizures in this cohort. The current paper reports that several cited studies found postictal dysphasia to lateralize seizure origin to the dominant hemisphere. The review assigns postictal verbal-memory impairment and aphasia to dominant-hemisphere suggestion and visual-memory impairment to nondominant-hemisphere suggestion. The review reports that postictal aphasia or dysphasia points to the language-dominant hemisphere, with cited PPVs of 80-100%. The review restates that 92% of patients with postictal dysphasia had the presumed epileptogenic zone in the language-dominant hemisphere. The finding reports no cerebral lateralization. The M, ML, and L onset-subtype comparison does not report a lateralization direction.

Source-defined result groups 19
Lateralization: Dominant hemisphere / Left hemisphereObserved proportion 0.0%RTL; all analyzed seizures · LTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 23.1%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin; first patient · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 92.3%left temporal seizures · right temporal seizures · patient with postictal dysphasia1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin; second patient · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 2 reported values · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft temporal lobe · right temporal lobe · temporal seizure/patient; exact denominator not reported1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 50.0%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 61.1%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelydominant-origin · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 7.7%nondominant temporal-lobe origin · dominant origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Left hemisphereObserved proportion 50.7%LTL; all analyzed seizures · RTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Left hemisphereObserved proportion 59.3%LTL CPS · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Left hemisphereObserved proportion 26.3%LTL PE · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 92.3%dominant temporal-lobe origin · nondominant origin · patient1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelydominant-origin · dominant-origin versus nondominant-origin dysphasia observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyright temporal lobe · left temporal lobe · temporal seizure/patient; exact denominator not reported1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 16

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • post-ictal language deficitPost-ictal language deficit did not differ significantly between TL and T+ groups.PDF p.6, Table 2; PDF p.9, Post-ictal signs
Reported values
  • P=0.78post-ictal language deficitP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · post-ictalPDF p.6, Table 2; PDF p.9, Post-ictal signs
  • TL 42.4%post-ictal language deficitPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · post-ictalPDF p.6, Table 2; PDF p.9, Post-ictal signs
  • T+ 39.1%post-ictal language deficitPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · post-ictalPDF p.6, Table 2; PDF p.9, Post-ictal signs
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Postictal aphasiaThe review's differential table reports postictal aphasia as common in temporal seizures involving the dominant hemisphere and rare in frontal seizures unless they spread to the temporal lobe; the narrative later calls postictal aphasia a very reliable lateralizing sign with 80–90% reliability.PDF p.2, Table 1; PDF p.4, Table 2; PDF p.5, language paragraph
  • Postictal aphasia as a lateralizing signPostictal aphasia is described as a very reliable lateralizing sign with 80–90% reliability and as implying dominant-hemisphere temporal seizure origin.PDF p.2, Table 1; PDF p.4, Table 2; PDF p.5, language-disturbances paragraph
Reported values
  • 80–90% reliability reported in narrativePostictal aphasiaPercentage · Temporal versus frontal seizures; dominant-hemisphere temporal seizures; the cited reliability denominator is not reported. · PostictalPDF p.2, Table 1; PDF p.4, Table 2; PDF p.5, language paragraph
  • 80–90% reliabilityPostictal aphasia as a lateralizing signPercentage · Temporal lobe seizures evaluated with postictal language testing; denominator not reported. · PostictalPDF p.2, Table 1; PDF p.4, Table 2; PDF p.5, language-disturbances paragraph
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • ictal/postictal dysphasia; ictal speech; preserved awareness; RINCH motionsIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value and must be distinguished from non-lateralising speech arrest; formed nonsensical ictal speech and preserved awareness during ictal automatisms point to the nondominant hemisphere, while rhythmic ictal non-clonic hand motions may be contralateral in temporal lobe epilepsy and peri-ictal drinking, spitting, vomiting, or urge to urinate point to a nondominant focus.PDF p.10, Lateralising signs
  • ictal/postictal dysphasia; speech arrest; ictal speechIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value; speech arrest is described as non-lateralising, whereas ictal speech consisting of formed nonsensical phrases is a non-dominant sign.PDF p.10, Lateralising signs
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Postictal aphasiaBoth tables list Postictal aphasia as Dominant hemisphere.PDF p.2, Lateralizing signs/Localization table row "Postictal aphasia" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Postictal aphasia" (printed p.5)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 2 findings · 4 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Postictal aphasiaPostictal aphasia occurred only after LTL seizures and was statistically more common in LTL than RTL seizures; it was recorded after 32 LTL CPS and 5 LTL PE seizures.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • Postictal dysphasia and dominant hemisphere in cited studiesThe current paper states that several cited studies showed postictal dysphasia to lateralize seizure origin to the dominant hemisphere.PDF p.5, Discussion, postictal-aphasia paragraph
Reported values
  • RTL seizures with postictal aphasia 0/54Postictal aphasiaPercentage · n/N 0/54 · RTL seizure group, n=54, versus LTL seizure group, n=73; LTL subgroup includes 54 CPS and 19 PE seizures · RTL; all analyzed seizures · PostictalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • LTL PE seizures with postictal aphasia 5/19Postictal aphasiaPercentage · n/N 5/19 · RTL seizure group, n=54, versus LTL seizure group, n=73; LTL subgroup includes 54 CPS and 19 PE seizures · LTL PE · PostictalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • LTL CPS with postictal aphasia 32/54 (59%)Postictal aphasiaPercentage · n/N 32/54 · RTL seizure group, n=54, versus LTL seizure group, n=73; LTL subgroup includes 54 CPS and 19 PE seizures · LTL CPS · PostictalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • LTL seizures with postictal aphasia 37/73 (51%)Postictal aphasiaPercentage · n/N 37/73 · RTL seizure group, n=54, versus LTL seizure group, n=73; LTL subgroup includes 54 CPS and 19 PE seizures · LTL; all analyzed seizures · PostictalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal verbal and visual memory impairment and postictal aphasiaPostictal verbal memory impairment is suggestive of a dominant-hemisphere temporal focus, visual memory impairment of a nondominant-hemisphere focus, and postictal aphasia strongly suggests a dominant-hemisphere focus.PDF p.9, Postictal state
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 2 findings · 10 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • dysphasiasDysphasias occurred in 30 seizures in 14 patients: 27 seizures in 12 patients with dominant-origin seizures and 3 seizures in 2 patients with nondominant-origin seizures; all three nondominant dysphasias were isolated paraphasias, one patient had 2 ictal seizures, the second had 1 postictal seizure, and all other dysphasias were postictal and arose from the dominant hemisphere.PDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • postictal dysphasiaAmong 13 patients with postictal dysphasia, 12 (92%) had seizures originating from the dominant temporal lobe and 1 from the nondominant temporal lobe; the association was statistically significant.PDF p.1, abstract; PDF p.4, Table 6 and Results; PDF p.5, Discussion and conclusion
Reported values
  • 27 dominant-origin seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · dominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 2 ictal nondominant dysphasia seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin; first patient · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 14 patients with dysphasiadysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 3 nondominant-origin seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 2 nondominant-origin patientsdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 1 postictal nondominant dysphasia seizuredysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · nondominant-origin; second patient · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 12 dominant-origin patientsdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · dominant-origin · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 30 dysphasia seizuresdysphasiasCount · 14 patients and 30 dysphasia seizures within the 35-patient temporal-lobe epilepsy cohort · mixed; 2 ictal seizures in one patient and 1 postictal seizure in a second nondominant-origin patient, with all other dysphasias postictalPDF p.3, Table 3 and Results; PDF p.4, Table 5 and Results; PDF p.5, Discussion
  • 1/13postictal dysphasiaPercentage · n/N 1/13 · 13 patients with postictal dysphasia in the 35-patient temporal-lobe epilepsy cohort · nondominant temporal-lobe origin · postictalPDF p.1, abstract; PDF p.4, Table 6 and Results; PDF p.5, Discussion and conclusion
  • 12/13 (92%)postictal dysphasiaPercentage · n/N 12/13 · 13 patients with postictal dysphasia in the 35-patient temporal-lobe epilepsy cohort · dominant temporal-lobe origin · postictalPDF p.1, abstract; PDF p.4, Table 6 and Results; PDF p.5, Discussion and conclusion
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 2 findings
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • speech arrest; anarthria; dysarthria; dysphasiaThe source states that speech arrest, including anarthria or dysarthria, can be the first sign of seizures starting from the frontal operculum, while anarthria alone is not sufficient to assign hemispheric lateralization.PDF p.9, Discussion
  • dominant hemisphere; non-dominant hemisphere; dysphasia; postictal language disorderThe source states that seizures in dominant and non-dominant hemispheres can produce the same phonatory symptoms, while dominant-hemisphere seizures may additionally produce dysphasia that can persist postictally.PDF p.9, Discussion
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 3 findings · 2 reported values
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Ictal or postictal dys/aphasiaThe review describes ictal or postictal dys/aphasia as a valuable finding with approximately 90% lateralisation value, while stating that its localisation value is poor.PDF p.5, section 1.9
  • Postictal aphasia/dysphasiaThe review states that postictal aphasia almost always indicates dominant-hemisphere involvement, occurs in 12% of temporal-lobe epilepsy cases, and had no lobar preference in the cited series of postictal dysphasia.PDF p.5, section 1.9
  • Postictal dysphasia recoveryThe review states that the duration of postictal dysphasia is unclear from published cases, while language recovery is related to structural etiology and hemisphere of onset.PDF p.6, section 1.9
Reported values
  • Approximately 90% lateralisation valueIctal or postictal dys/aphasiaPercentage · Video-EEG seizure literature; exact population not reported · ictal or postictalPDF p.5, section 1.9
  • 12% of temporal-lobe epilepsy casesPostictal aphasia/dysphasiaPercentage · Temporal-lobe epilepsy cases and cited seizure series; exact denominators not reported · postictalPDF p.5, section 1.9
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal aphasia and dysphasiaPostictal aphasia or dysphasia lateralizes to the language-dominant hemisphere, and delayed language recovery may be predictive.PDF p.10, section 5.3
  • postictal dysphasiaGabr et al. found the presumed epileptogenic zone in the language-dominant hemisphere in 92% of patients with postictal dysphasia.PDF p.10, section 5.3
Reported values
  • positive predictive values reported between 80% and 100%postictal aphasia and dysphasiaPercentage · patients with postictal language dysfunction · postictalPDF p.10, section 5.3
  • 92%postictal dysphasiaPercentage · patients with postictal dysphasia, all tested for language dominance by Wada · postictalPDF p.10, section 5.3
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 6 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.12 · 2 × 1.5 × 1.707
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • postictal dysphasia and temporal sidePostictal dysphasia was more frequent in left than right temporal lobe seizures, and 24 of the 26 patients with postictal dysphasia had left temporal seizures.PDF p.7, Postictal behavior
  • postictal dysphasiaPostictal dysphasia did not differ significantly across M, ML, and L onset subtypes when grouped by electrophysiologic subtype.PDF p.6, Table 3; PDF p.7, Postictal behavior
Reported values
  • 12.5%postictal dysphasia and temporal sidePercentage · 26 patients with postictal dysphasia within the 55-patient cohort; side-specific comparison denominators not reported · right temporal lobe · postictalPDF p.7, Postictal behavior
  • 24/26 (92%)postictal dysphasia and temporal sidePercentage · n/N 24/26 · 26 patients with postictal dysphasia within the 55-patient cohort; side-specific comparison denominators not reported · left temporal seizures · postictalPDF p.7, Postictal behavior
  • 61.5%postictal dysphasia and temporal sidePercentage · 26 patients with postictal dysphasia within the 55-patient cohort; side-specific comparison denominators not reported · left temporal lobe · postictalPDF p.7, Postictal behavior
  • ML 11/18 (61.1%)postictal dysphasiaPercentage · n/N 11/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · postictalPDF p.6, Table 3; PDF p.7, Postictal behavior
  • M 12/24 (50%)postictal dysphasiaPercentage · n/N 12/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · postictalPDF p.6, Table 3; PDF p.7, Postictal behavior
  • L 3/13 (23.1%)postictal dysphasiaPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · postictalPDF p.6, Table 3; PDF p.7, Postictal behavior
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • ictal language and postictal aphasiaIctal speech arrest is not reliably lateralizing; focal aware speech arrest may represent dominant temporal aphasia, well-formed ictal language strongly suggests a nondominant, usually right, temporal lobe, ictal jargon is associated with dominant temporal involvement, and postictal aphasia strongly supports left dominant temporal localization.PDF p.50; PDF p.51; PDF p.52
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • post-ictal dysphasiaPost-ictal dysphasia occurred in six of 42 patients.PDF p.6, Results, Non-visual manifestations
Reported values
  • 6/42 (14%) patientspost-ictal dysphasiaPercentage · n/N 6/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · post-ictalPDF p.6, Results, Non-visual manifestations
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • post-ictal dysphasiaPost-ictal dysphasia occurred in 7% of patients.PDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
Reported values
  • 7%post-ictal dysphasiaPercentage · 82-patient parietal epilepsy series · post-ictalPDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • post-ictal aphasiaThe review states that postictal aphasia lateralizes temporal-lobe epilepsy to the language-dominant hemisphere and that language recovery after the ictal EEG stops is significantly more delayed in left temporal lobe epilepsy. Postictal language delay is described as less affected in frontal-lobe epilepsy unless seizure activity extends to the ipsilateral temporal lobe. The review requires a cooperative patient who tries to understand and speak, continuous testing, and slow progressive recovery over 10-20 minutes.PDF p.6, Post ictal aphasia
Reported values
  • Progressive language recovery over 10-20 minutes as a diagnostic contextpost-ictal aphasiaCount · Cooperative patients with temporal lobe epilepsy compared with frontal lobe epilepsy; no cohort reported · Postictal, after the ictal EEG pattern has stoppedPDF p.6, Post ictal aphasia
unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 3 findings · 2 reported values
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • aphasia with left parietotemporal periodic/rhythmic sharp wavesFigure 3 shows a 58-year-old male with an acute symptomatic focal to bilateral tonic-clonic seizure followed by Epilepsia partialis continua with aphasia and right facial twitching due to a left middle cerebral artery stroke; ongoing aphasia is shown with left parietotemporal periodic and rhythmic sharp waves, and an otherwise identical record without motor symptoms shows lateralized periodic discharges turning into ictal rhythmic discharges pronounced over C3.PDF p.4, Fig.3a–b caption and EEG rendering
  • prolonged postictal language delay after frontal CPSThe review reports prolonged postictal language delay in 7% of frontal complex partial seizures confined to the dominant frontal lobe compared with 91% of complex partial seizures that started as frontal and spread to the dominant temporal lobe.PDF p.5, §6
  • structural lesion and postictal language delay in temporal CPSThe review reports that the presence of a structural lesion significantly prolonged postictal language delay only in patients with non-dominant temporal complex partial seizures, supporting an interaction between seizure origin and patterns of seizure spread.PDF p.5, §6
Reported values
  • 91%prolonged postictal language delay after frontal CPSPercentage · Patients with frontal complex partial seizures · frontal-onset seizures spreading to the dominant temporal lobe · postictalPDF p.5, §6
  • 7%prolonged postictal language delay after frontal CPSPercentage · Patients with frontal complex partial seizures · seizures confined to the dominant frontal lobe · postictalPDF p.5, §6

16 contributing manuscripts; source-reported values remain separate and are not pooled.

Olfactory aura (uncinate fit)Source terms: Olfactory auraReported: Left hemisphereNo single reliable side15 manuscripts · 42 findings · 23 reported values
Weighted evidence supportevidence weight 31.35 across 15 manuscripts · 2 independent primary study · 8 narrative, educational, or cited context · 4 systematic review or meta-analysis · 1 case report or observation

Insular stimulation-evoked olfactory sensations were perceived in the nasal cavity and were not lateralized. Right-sided motor manifestations accompanied a case interpreted as left mesial temporal epilepsy. The cited table describes olfactory aura as non-lateralising. The review states that olfactory auras have no lateralizing value. Olfactory and gustatory auras are summarized as generally nonlateralizing. The TL-versus-T+ comparison provides no lateralizing direction. No lateralizing direction is reported. No hemispheric lateralization is reported. The cited stimulation prevalence provides no hemispheric direction. The mesial-versus-lateral temporal comparison provides no hemispheric direction. The study-count record provides no hemispheric direction. This lateral-versus-mesial temporal statistic provides no hemispheric lateralization. The lateral-temporal prevalence result provides no hemispheric direction. The occurrence odds provide no hemispheric direction. The lateral-TLE prevalence result provides no hemispheric direction. The mesial-TLE prevalence range provides no hemispheric direction. This record provides no seizure lateralization. This record provides no hemispheric lateralization. No seizure lateralization is reported.

Source-defined result groups 17
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyparietal localization given olfactory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Olfactory/gustatory aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ 4.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyinsular localization given olfactory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyunpleasant or indefinable odors · evoked olfactory response1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 1.1%olfactory responses · evoked olfactory response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft sphenoidal · left versus right temporal/sphenoidal recording maxima · source-defined interictal sharp-wave observations and single-case seizure observations1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyparietal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyright sphenoidal · left versus right temporal/sphenoidal recording maxima · source-defined interictal sharp-wave observations and single-case seizure observations1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft anterior temporal · left versus right temporal/sphenoidal recording maxima · source-defined interictal sharp-wave observations and single-case seizure observations1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyinsular localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given olfactory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Olfactory/gustatory aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given olfactory aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 1.7% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 15

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 15 findings · 7 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • olfactoryTable 1 defines or exemplifies the the source's own semiology category “olfactory” as Any kind of ictal smell, for example burning.PDF p.7, Table 1 Semiology descriptions and frequencies
  • olfactoryOlfactory semiology comprised 4.6% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • olfactory; Figure 3 all-data subsetFigure 3 reports N = 980 for the all-data olfactory panel.PDF p.9, Figure 3 and caption
  • olfactory; Figure 3 non-topological subsetFigure 3 reports N = 161 for the non-topological olfactory panel.PDF p.9, Figure 3 and caption
  • olfactory aura; frontal lobeOlfactory auras were frontal in 21% of the estimate.PDF p.8, Seizure semiology localizing values
  • olfactory aura; frontal lobeThe 95% CI for olfactory aura; frontal lobe was 15%–28%.PDF p.8, Seizure semiology localizing values
  • olfactory aura; parietal lobeOlfactory auras were parietal in 28% of the estimate.PDF p.8, Seizure semiology localizing values
  • olfactory aura; parietal lobeThe 95% CI for olfactory aura; parietal lobe was 20%–35%.PDF p.8, Seizure semiology localizing values
  • olfactory aura; temporal lobeOlfactory auras were temporal in 40% of the estimate.PDF p.8, Seizure semiology localizing values
  • olfactory aura; temporal lobeThe 95% CI for olfactory aura; temporal lobe was 31%–49%.PDF p.8, Seizure semiology localizing values
  • olfactory aura; insulaolfactory aura indicated insular localization in 44%.PDF p.8, Seizure semiology localizing values
  • olfactory aura; parietal lobeOlfactory auras had an intrinsic localizing OR of 4.6 for parietal localization.PDF p.8, Relative localizing values of semiologies
  • olfactory aura; parietal lobeThe 95% CI for olfactory aura; parietal lobe was 3.2–6.5.PDF p.8, Relative localizing values of semiologies
  • olfactory aura; insulaOlfactory auras had an intrinsic localizing OR of 3.8 for insular localization.PDF p.8, Relative localizing values of semiologies
  • olfactory aura; insulaThe 95% CI for olfactory aura; insula was 2.1–6.9.PDF p.8, Relative localizing values of semiologies
Reported values
  • olfactory 4.6%olfactoryPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • olfactory aura; frontal lobe 21%olfactory aura; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • olfactory aura; parietal lobe 28%olfactory aura; parietal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • olfactory aura; temporal lobe 40%olfactory aura; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • olfactory aura; insula 44%olfactory aura; insulaPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 4.6olfactory aura; parietal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 3.8olfactory aura; insulaOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • olfactory auraOne patient had an olfactory aura.PDF p.2, Results
Reported values
  • 1/18 (5.5%) olfactory auraolfactory auraPercentage · n/N 1/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • olfactory hallucinationOlfactory hallucinations did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 1.7%olfactory hallucinationPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • T+ 4.3%olfactory hallucinationPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • P=0.48olfactory hallucinationP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Olfactory (Table 3)Table 3 reports olfactory symptoms in 1 case (1%), more at seizure onset.PDF p.6, Table 3
  • Olfactory (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports olfactory symptoms in 1 case (2%).PDF p.7, Table 4
Reported values
  • 1 case (1%)Olfactory (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 1/60 (2%)Olfactory (Table 4)Percentage · n/N 1/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • gustatory; olfactory; vestibular; autonomic auraTable 3 maps gustatory aura to insula or mesiotemporal regions, olfactory aura to insula, mesiotemporal, or orbitofrontal regions, vestibular aura to posterior temporal or parietal regions, and autonomic aura to insula, amygdala, or cingulate regions.PDF p.10, Table 3; PDF p.3, Figure 1
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 12 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • epigastric aura; olfactory/gustatory auraThe source states that absence of epigastric or olfactory/gustatory auras may be more indicative of lateral than mesial temporal seizures, whereas their presence points toward mesial rather than lateral onset.PDF p.7, Discussion; PDF p.10, Conclusions
  • Olfactory/gustatory auraTable 3 reports 3 studies assessing Olfactory/gustatory aura.PDF p.6, Table 3
  • Olfactory/gustatory auraTable 3 reports 42 patients assessed for Olfactory/gustatory aura.PDF p.6, Table 3
  • Olfactory/gustatory auraTable 3 reports 0% as the percentage range or value for Olfactory/gustatory aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Olfactory/gustatory auraTable 4 reports overall odds of 0.04 for occurrence of Olfactory/gustatory aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Olfactory/gustatory auraTable 4 reports a 95% confidence interval of 0.01–0.19 for the overall odds of Olfactory/gustatory aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Olfactory/gustatory auraThe heterogeneity test for the Table 4 odds estimate for Olfactory/gustatory aura has p=0.9159.PDF p.7, Table 4
  • Olfactory/gustatory aura; lateral versus mesial comparisonTable 5 reports 3 studies comparing Olfactory/gustatory aura in lateral and mesial TLE.PDF p.9, Table 5
  • Olfactory/gustatory aura; lateral TLE patient denominatorTable 5 reports 42 lateral-TLE patients assessed for Olfactory/gustatory aura.PDF p.9, Table 5
  • Olfactory/gustatory aura; mesial TLE patient denominatorTable 5 reports 67 mesial-TLE patients assessed for Olfactory/gustatory aura.PDF p.9, Table 5
  • Olfactory/gustatory aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0% for Olfactory/gustatory aura.PDF p.9, Table 5
  • Olfactory/gustatory aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–18.8% for Olfactory/gustatory aura.PDF p.9, Table 5
Reported values
  • 0%Olfactory/gustatory auraPercentage · Lateral temporal epilepsy patients assessed for Olfactory/gustatory aura · ictalPDF p.6, Table 3
  • odds 0.04odds of occurrence; Olfactory/gustatory auraOdds · Lateral temporal epilepsy patients assessed for Olfactory/gustatory aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0%Olfactory/gustatory aura; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Olfactory/gustatory aura · Lateral TLE patients assessed for Olfactory/gustatory aura · ictalPDF p.9, Table 5
  • 0–18.8%Olfactory/gustatory aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Olfactory/gustatory aura · Mesial TLE patients assessed for Olfactory/gustatory aura · ictalPDF p.9, Table 5
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfCase report or observation · 1 finding · 3 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • Case Study 1 olfactory aura, dystonic posturing, and left temporal findingsIn Case Study 1, a right-handed woman had recurrent unusual-odor auras without initial loss of consciousness, later seizures with loss of awareness, oral/manual automatisms, unintelligible speech, left-hand automatisms, right-arm dystonic posturing, and head version to the right. Interictal sharp waves were maximal at the left sphenoidal electrode in 90% of the source-defined observations versus 5% at the left anterior temporal and 5% at the right sphenoidal electrode, and ictal rhythmic delta followed by repetitive spiking was maximal in the left temporal region; the chapter's discussion interpreted the combined history and testing as left mesial temporal lobe epilepsy.PDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
Reported values
  • 5% right sphenoidalCase Study 1 olfactory aura, dystonic posturing, and left temporal findingsPercentage · Single illustrative case, 31-year-old right-handed woman with poorly controlled seizures · right sphenoidal · aura, ictal, and interictalPDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
  • 90% left sphenoidalCase Study 1 olfactory aura, dystonic posturing, and left temporal findingsPercentage · Single illustrative case, 31-year-old right-handed woman with poorly controlled seizures · left sphenoidal · aura, ictal, and interictalPDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
  • 5% left anterior temporalCase Study 1 olfactory aura, dystonic posturing, and left temporal findingsPercentage · Single illustrative case, 31-year-old right-handed woman with poorly controlled seizures · left anterior temporal · aura, ictal, and interictalPDF p.12, Case Study 1, history and seizure description; PDF p.12, Case Study 1, interictal and ictal EEG paragraph; PDF p.12, Case Study 1, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • olfactory and gustatory aurasOlfactory auras are typically unpleasant and often associated with gustatory phenomena; stimulation of the amygdala, olfactory bulb, insula, or posterior orbitofrontal region can produce olfactory sensations or illusions. Gustatory auras can be difficult to distinguish from olfactory disturbances, and stimulation of the parietal operculum or mesiobasal temporal regions can produce gustatory hallucinations.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • olfactory and gustatory hallucinationsUnpleasant olfactory and gustatory hallucinations can result from seizures involving mesial temporal structures, particularly the amygdala, but are not pathognomonic because gustatory symptoms with hypersalivation and olfactory symptoms have also been reported with opercular and orbitofrontal seizures, respectively.PDF p.8, Focal sensory seizures; PDF p.10, Temporal plus epilepsy
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • olfactory auraOlfactory auras are among the reported clinical manifestations of insular seizures.PDF p.2, Clinical Features
  • olfactory stimulation responsesOlfactory sensations represented 1% of all responses in the cited insular stimulation series.PDF p.5, Other Insular Responses; PDF p.5, Figure 4 panel 5
Reported values
  • 1% olfactory responsesolfactory stimulation responsesPercentage · all responses in the cited insular stimulation series · stimulation-evoked semiologyPDF p.5, Other Insular Responses; PDF p.5, Figure 4 panel 5
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Olfactory auraTable 2 associates olfactory aura with orbitofrontal cortex, amygdala (uncinate), and insula and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Olfactory auraPerception of a smell as an epileptic phenomenon is an olfactory aura; when complex perceptual alterations coexist, the episode is psychic unless the olfactory aura is clearly predominant.PDF p.3, Auras, subsection Olfactory auras; PDF p.2, Table 1
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • olfactory sensationsSix olfactory responses (1%) were evoked from the insula; odors were unpleasant or indefinable in the remaining three cases described by the source, were located in the nasal cavity, and were not lateralized.PDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
Reported values
  • 6 olfactory responses (1%)olfactory sensationsPercentage · n/N 6/550 · 6 olfactory responses in the 550-response series · olfactory responses · stimulation-evoked olfactory sensationPDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
  • three other described casesolfactory sensationsCount · 6 olfactory responses in the 550-response series · unpleasant or indefinable odors · stimulation-evoked olfactory sensationPDF p.3, Results and Table 1; PDF p.5, Other Types of Evoked Sensations and Fig. 5A
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • stimulation-evoked somatosensory, auditory, vestibular, olfactory, gustatory, and viscerosensory symptomsThe chapter reports that electrical stimulation studies evoked somatosensory symptoms, including pain, from the posterior two-thirds of the insula; auditory and vestibular symptoms from the posterior insula; and olfactory, gustatory, and viscerosensory symptoms, including laryngeal constriction, from the midinsula, whereas stimulation of the most anterior portion rarely evoked symptoms unless a larger network seizure was elicited.PDF p.3, insular functional differentiation and electrical cortical stimulation
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • olfactory aurasThe review states that olfactory auras are usually unpleasant smells, have no lateralizing value, and are most frequently seen in mesial temporal lobe epilepsy; it also reports that a relatively high percentage of these patients have neoplasms involving the amygdala.PDF p.2, Olfactory auras

15 contributing manuscripts; source-reported values remain separate and are not pooled.

Visual auraReported: BilateralAlso reported: ContralateralNo single reliable side13 manuscripts · 35 findings · 30 reported values
Weighted evidence supportevidence weight 31.31 across 13 manuscripts · 5 independent primary study · 6 narrative, educational, or cited context · 2 systematic review or meta-analysis

Source reports contralateral limb posturing in a sequential occipital-onset phenotype. The source describes visual aura followed by head-eye deviation and contralateral tonic posturing as activity propagates through dorsal parietal nodes toward premotor areas. No cerebral hemisphere or body-side direction is reported in the cited restatement. Visual auras are commonly bilateral and nonlateralizing, with an occasional unilateral visual field contralateral to the symptomatogenic zone. The review restates contralateral visual-field relations for visual auras, with simple visual phenomena linked to areas 17–19 and complex phenomena to the temporo-parieto-occipital junction. No seizure lateralization is reported. No lateralizing direction is reported for the visual-aura-to-automatism phenotype. No lateralizing direction is reported for the visual-aura sequence. No source-supported lateralizing direction is reported for the visual aura. No source-supported hemispheric or body-side lateralization is reported. No cerebral hemisphere or body-side direction is reported. No lateralizing direction is reported for visual sensations. No lateralizing direction is reported for the visual symptom row. The primary comparison reports no hemisphere-level lateralization; it compares M, ML, and L temporal-onset subtypes. No lateralizing direction is reported for visual auras.

Source-defined result groups 17
Localization: TemporalSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyauditory manifestation; operculoinsular SOZ · auditory versus visual manifestation and extrafrontal SOZ subgroup · patient as represented by Table 2 n; sign-specific denominator Not reported1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyauditory manifestation; temporal SOZ · auditory versus visual manifestation and extrafrontal SOZ subgroup · patient as represented by Table 2 n; sign-specific denominator Not reported1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Visual aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyvisual manifestation; posterior SOZ · auditory versus visual manifestation and extrafrontal SOZ subgroup · patient as represented by Table 2 n; sign-specific denominator Not reported1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 12.5%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 33.3%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 84.6%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: OccipitalObserved proportion 73.8%All reported · no visual aura · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Visual aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 13

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 8 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • visual auraVisual auras did not differ significantly overall between TL and T+ groups, although the table reports a significant subcategory P value for visual illusions and not for visual hallucinations.PDF p.6, Table 2
Reported values
  • T+ 13%visual auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • TL visual illusions 5.1%visual auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
  • T+ visual illusions 13%visual auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • T+ visual hallucinations 4.3%visual auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • TL 6.8%visual auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
  • P=0.36visual auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
  • P=0.02visual auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
  • TL visual hallucinations 1.7%visual auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • visual sensationsVisual sensations accounted for 5% of the sensory manifestations in the narrative summary.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Visual (Table 3)Table 3 reports visual symptoms in 4 cases (5%), more at seizure onset.PDF p.6, Table 3
  • Visual (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports visual symptoms in 2 cases (3%).PDF p.7, Table 4
Reported values
  • 5% visual sensationsvisual sensationsPercentage · reviewed basal temporal seizure cases · ictal onset in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 4 cases (5%)Visual (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 2/60 (3%)Visual (Table 4)Percentage · n/N 2/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • occipital lobe seizure; visual auraOccipital lobe seizures are usually characterized by visual aura in 40%–75% of patients, with oculomotor features such as eye deviation, blinking, or nystagmus less commonly reported.PDF p.7, Occipital lobe seizures
Reported values
  • visual aura 40%–75%occipital lobe seizure; visual auraPercentage Range · patients with occipital lobe epilepsy · ictal aura/early manifestationPDF p.7, Occipital lobe seizures
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.35 · 1 × 0.9 × 1.5
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • visual aura; insular subgroupOne insular-subgroup patient had a visual aura.PDF p.3, Aura
Reported values
  • 1 patientvisual aura; insular subgroupCount · n/N 1/10 · Insular subgroup of OFC-extended EZN · Insular subgroup of OFC-extended EZN · ictal auraPDF p.3, Aura
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Visual auraTable 3 reports 3 studies assessing Visual aura.PDF p.6, Table 3
  • Visual auraTable 3 reports 54 patients assessed for Visual aura.PDF p.6, Table 3
  • Visual auraTable 3 reports 0–6.7% as the percentage range or value for Visual aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Visual auraTable 4 reports overall odds of 0.05 for occurrence of Visual aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Visual auraTable 4 reports a 95% confidence interval of 0.01–0.18 for the overall odds of Visual aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Visual auraThe heterogeneity test for the Table 4 odds estimate for Visual aura has p=0.8723.PDF p.7, Table 4
  • Visual aura; lateral versus mesial comparisonTable 5 reports 2 studies comparing Visual aura in lateral and mesial TLE.PDF p.9, Table 5
  • Visual aura; lateral TLE patient denominatorTable 5 reports 32 lateral-TLE patients assessed for Visual aura.PDF p.9, Table 5
  • Visual aura; mesial TLE patient denominatorTable 5 reports 51 mesial-TLE patients assessed for Visual aura.PDF p.9, Table 5
  • Visual aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0–6.7% for Visual aura.PDF p.9, Table 5
  • Visual aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–5% for Visual aura.PDF p.9, Table 5
Reported values
  • 0–6.7%Visual auraPercentage Range · Lateral temporal epilepsy patients assessed for Visual aura · ictalPDF p.6, Table 3
  • odds 0.05odds of occurrence; Visual auraOdds · Lateral temporal epilepsy patients assessed for Visual aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0–6.7%Visual aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Visual aura · Lateral TLE patients assessed for Visual aura · ictalPDF p.9, Table 5
  • 0–5%Visual aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Visual aura · Mesial TLE patients assessed for Visual aura · ictalPDF p.9, Table 5
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 3 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • auditory and visual nonmotor manifestationsAuditory and visual manifestations were observed only in extrafrontal SHE; visual symptoms were associated with a posterior cortex SOZ, whereas auditory symptoms were associated with either a temporal or an operculoinsular SOZ.PDF p.5, section 3.3; PDF p.6, Table 2
Reported values
  • visual posterior 2auditory and visual nonmotor manifestationsCount · Extrafrontal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists auditory n=1 in temporal and n=1 in operculoinsular subgroups and visual n=2 in the posterior subgroup · visual manifestation; posterior SOZ · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, Table 2
  • auditory operculoinsular 1auditory and visual nonmotor manifestationsCount · Extrafrontal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists auditory n=1 in temporal and n=1 in operculoinsular subgroups and visual n=2 in the posterior subgroup · auditory manifestation; operculoinsular SOZ · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, Table 2
  • auditory temporal 1auditory and visual nonmotor manifestationsCount · Extrafrontal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists auditory n=1 in temporal and n=1 in operculoinsular subgroups and visual n=2 in the posterior subgroup · auditory manifestation; temporal SOZ · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Visual aura prevalence in occipital lobe seizuresThe review reports that visual auras occur in approximately more than 70% of series reporting occipital-lobe seizures.PDF p.6, section 1.12
Reported values
  • Approximately >70% of occipital-lobe seizure seriesVisual aura prevalence in occipital lobe seizuresPercentage · Series reporting occipital-lobe seizures · ictalPDF p.6, section 1.12
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Visual aura and homonymous hemifield auraThe review states that homonymous hemifield defects and auras lateralize the seizure focus to the contralateral hemisphere; simple visual auras are linked to contralateral areas 17-19, while more complex visual auras may involve the temporo-parieto-occipital junction.PDF p.3, section 2.5 Visual auras; PDF p.3, section 2.5.1 Mechanism; PDF p.12, Table 1
Reported values
  • 28.6% of occipital-lobe epilepsy patientsVisual aura and homonymous hemifield auraPercentage · Patients with occipital or other focal epilepsy with visual manifestations · occipital-lobe epilepsy · Ictal auraPDF p.3, section 2.5 Visual auras; PDF p.3, section 2.5.1 Mechanism; PDF p.12, Table 1
  • 100% contralateralVisual aura and homonymous hemifield auraPercentage · Patients with occipital or other focal epilepsy with visual manifestations · patients with hemifield visual aura · Ictal auraPDF p.3, section 2.5 Visual auras; PDF p.3, section 2.5.1 Mechanism; PDF p.12, Table 1
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Visual auraIsolated visual hallucinations or illusions are visual auras; when visual phenomena occur with complex perceptual distortions they remain visual only if clearly predominant for a significant part of the aura, otherwise they are psychic auras, while poorly defined blurry vision is unclassifiable.PDF p.3, Auras, subsection Visual auras; PDF p.2, Table 1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • sensory hallucination or illusion (visual, auditory, vestibular)The combined category of visual, auditory, or vestibular sensory hallucination or illusion was more frequent in L than M or ML patients.PDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
Reported values
  • 6/18 (33.3%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 6/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
  • 3/24 (12.5%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
  • 11/13 (84.6%)sensory hallucination or illusion (visual, auditory, vestibular)Percentage · n/N 11/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2; PDF p.5, Semiologic analysis; PDF p.8, Sensory illusions and hallucinations
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 5 findings · 4 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • visual auras in Ludwig and Ajmone-MarsanThe source reports that visual auras occurred in 47% of Ludwig and Ajmone-Marsan’s patients.PDF p.20, Discussion
  • visual auras in Blume et al.The source reports that visual auras occurred in 68% of Blume et al.’s patients.PDF p.20, Discussion
  • Gowers ocular and visual warningsThe source recounts Gowers’ five the source's own categories of ocular and visual warnings: sensation in the eyeball, diplopia, apparent increase or diminution in object size, loss of sight, and distinct elementary visual sensations.PDF p.2, Introduction
  • visual sensations in focal epilepsyPenfield and Kristiansen reported visual sensations as the initial seizure manifestation in 11 of 222 surgically treated patients with focal epilepsy, with each seizure originating in the occipital lobe.PDF p.2, Introduction
  • visual auraVisual auras occurred in 31 of 42 patients.PDF p.4, Results, Visual auras
Reported values
  • 47%visual auras in Ludwig and Ajmone-MarsanPercentage · cited Ludwig and Ajmone-Marsan occipital epilepsy series · aura or seizure onsetPDF p.20, Discussion
  • 68%visual auras in Blume et al.Percentage · cited Blume et al. posterior-cortex surgery series · aura or seizure onsetPDF p.20, Discussion
  • 11/222 patients with visual sensations as initial manifestationvisual sensations in focal epilepsyProportion · n/N 11/222 · Penfield and Kristiansen cited surgical series · seizure onsetPDF p.2, Introduction
  • 31/42 (73%) patientsvisual auraPercentage · n/N 31/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · aura or seizure onsetPDF p.4, Results, Visual auras
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • visual aurasThe review states that visual auras are often perceived in front of both eyes without clear lateralization, but may occasionally be lateralized to one visual field contralateral to the symptomatogenic zone and may be localized to an upper or lower field; simple visual hallucinations are assigned to Brodmann areas 17 and 18, while complex hallucinations or illusions more likely involve parieto-temporal association cortex or adjacent lobes. During or after amaurosis, flashing lights may appear over the blind field.PDF p.2, Visual auras
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 7 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • dorsal parietal to premotor motor evolutionThe authors link rapid motor evolution after visual aura to propagation to dorsal parietal nodes and then premotor areas.PDF p.13, Phenotype III discussion
  • pure visual phenotypePhenotype I is defined by exclusive subjective visual auras, including elementary visual hallucinations, amaurosis, or visual obscuration, without objective motor or autonomic progression.PDF p.9, Phenotype I
  • visual aura to automatism phenotypePhenotype II is characterized primarily by oropharyngeal, limb, or verbal automatisms, with or without a preceding visual aura.PDF p.9, Phenotype II
  • Pattern I pure visual signsPattern I seizures presented pure visual auras without objective motor or autonomic symptoms.PDF p.9, Pattern I
  • absent or overshadowed visual aura in temporal-like semiologyOccipital seizure semiology may closely resemble temporal-lobe epilepsy when visual auras are absent, brief, or overshadowed.PDF p.13, Phenotype II discussion
  • visual aura to head-eye deviation or pursuitIn Phenotype III, a visual aura rapidly progresses to head-eye deviation or eye pursuit.PDF p.9, Phenotype III; PDF p.13, Phenotype III discussion

13 contributing manuscripts; source-reported values remain separate and are not pooled.

Tonic motor phenomenonReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphere15 manuscripts · 46 findings · 49 reported values
Weighted evidence supportevidence weight 31.3 across 15 manuscripts · 1 manuscript weight pending · 4 independent primary study · 1 structured design not resolved · 3 systematic review or meta-analysis · 6 narrative, educational, or cited context · 1 case report or observation

The source describes visual aura followed by head-eye deviation and contralateral tonic posturing as activity propagates through dorsal parietal nodes toward premotor areas. Ipsilateral tonic motor signs were associated with T+ seizures at P=0.05, but the side reference is not defined and the overall tonic-motor comparison did not differ significantly. In the unilateral TLE cohort, tonic posture occurred only contralateral to the EEG seizure-onset focus in 17 seizures from 12 patients. The review describes early upper-limb and orofacial elementary motor signs as mainly contralateral tonic, clonic, or dystonic manifestations. At onset, 8/21 fronto-opercular epilepsy patients had contralateral brachial tonic, clonic, or dystonic posturing. Four of 12 prefrontal-operculum patients had contralateral brachial tonic, clonic, or dystonic posturing at onset. Four of nine precentral Rolandic-operculum patients had contralateral brachial tonic, clonic, or dystonic posturing at onset. This row restates the Fisher exact test for the contralateral brachial combined-sign comparison. The cited table lists tonic semiology as contralateral if unilateral. The cited table associates tonic posturing with contralateral lateralisation. The review states that clearly unilateral tonic activity points toward the contralateral seizure-onset side, while bilateral/asymmetric patterns and cohort distributions remain context-dependent. The patient-level observation reports bilateral tonic activity with right arm extension. The review says tonic seizures often involve bilateral proximal contraction, while clearly unilateral tonic seizures strongly support contralateral seizure origin. Version-first and version-plus-tonic sequence counts are reported, with correct EZ lateralization in 3/4 tonic-start/asymmetric-clonic sequences and 1/1 M2e-to-clonic sequence, but no direction is stated. The review describes head/eye deviation as suggesting an ipsilateral focus and other listed unilateral motor signs as usually indicating a contralateral focus. No seizure-hemisphere lateralization is reported; bilateral refers to tonic body distribution. No lateralization relationship is reported. No lateralizing information is supplied. No lateralization information is reported. No lateralization is reported. No lateralizing direction is reported for the the source's own tonic category. No lateralizing semiology is reported; this row is a figure-panel sample-size label for tonic data. No lateralizing semiology is reported; this row is a figure-panel sample-size label for the non-topological tonic data. The tonic estimate reports localization only. No lateralizing direction is reported for the tonic cingulate estimate. No lateralizing direction is reported for the tonic-cingulate percentage. No lateralizing direction is reported for the tonic-seizure frontal-lobe association. No lateralizing direction is reported for the tonic-to-clonic propagation description.

Source-defined result groups 16
Lateralization: ContralateralSource-defined values retained separatelyipsilateral · ipsilateral versus contralateral to EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 75.0%Correct EZ lateralization among tonic-start/asymmetric-clonic sequences · Version-first versus non-version-first order; variable sequence patterns · representative seizure (source also uses patient labels)1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 100.0%Correct EZ lateralization in M2e-to-clonic sequence · Version-first versus non-version-first order; variable sequence patterns · representative seizure (source also uses patient labels)1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 44.4%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 14.7%contralateral · ipsilateral versus contralateral to EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: cingulateSource-defined values retained separatelycingulate localization · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 55.6%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelycontralateral · ipsilateral versus contralateral to EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: ParietalObserved proportion 60.9%All reported · tonic-posturing patients without superior parietal involvement · patients with tonic posturing1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 38.1%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 42.9%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 15

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 18 findings · 8 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • tonicTable 1 defines or exemplifies the the source's own semiology category “tonic” as Stiff posturing of one or more limbs or torso.PDF p.7, Table 1 Semiology descriptions and frequencies
  • tonicTonic semiology comprised 9.8% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • tonic; Figure 3 all-data subsetFigure 3 reports N = 971 for the all-data tonic panel.PDF p.9, Figure 3 and caption
  • tonic; Figure 3 non-topological subsetFigure 3 reports N = 345 for the non-topological tonic panel.PDF p.9, Figure 3 and caption
  • tonic; temporal lobe; all dataTonic semiology localized to the temporal lobe in 48% of all-data estimates.PDF p.7, Seizure semiology localizing values
  • tonic; temporal lobe; all dataThe 95% CI for the all-data temporal-lobe estimate for tonic semiology was 44%–53%.PDF p.7, Seizure semiology localizing values
  • tonic; temporal lobe; non-topologicalTonic semiology localized to the temporal lobe in 20% of the non-topological estimate.PDF p.7, Seizure semiology localizing values
  • tonic; temporal lobe; non-topologicalThe 95% CI for the non-topological temporal-lobe estimate for tonic semiology was 15%–24%.PDF p.7, Seizure semiology localizing values
  • tonic; frontal lobe; non-topologicalTonic semiology localized to the frontal lobe in 54% of the non-topological estimate.PDF p.8, Seizure semiology localizing values
  • tonic; frontal lobe; non-topologicalThe 95% CI for the non-topological frontal-lobe estimate for tonic semiology was 47%–61%.PDF p.8, Seizure semiology localizing values
  • tonic; frontal lobe; all dataTonic semiology localized to the frontal lobe in 29% of the all-data estimate.PDF p.8, Seizure semiology localizing values
  • tonic; frontal lobe; all dataThe 95% CI for the all-data frontal-lobe estimate for tonic semiology was 26%–32%.PDF p.8, Seizure semiology localizing values
  • tonic; frontal lobeTonic seizures originated mainly from the frontal lobe in 54%.PDF p.8, Seizure semiology localizing values
  • tonic; frontal lobeThe 95% CI for tonic; frontal lobe was 47%–61%.PDF p.8, Seizure semiology localizing values
  • tonic; cingulatetonic semiology was cingulate in 7%.PDF p.8, Seizure semiology localizing values
  • tonic; cingulateThe 95% CI for tonic; cingulate was 4%–9%.PDF p.8, Seizure semiology localizing values
  • tonic seizures; frontal lobeTonic seizures had an intrinsic localizing OR of 3.0 for frontal-lobe onset.PDF p.8, Relative localizing values of semiologies
  • tonic seizures; frontal lobeThe 95% CI for tonic seizures; frontal lobe was 2.4–3.7.PDF p.8, Relative localizing values of semiologies
Reported values
  • tonic 9.8%tonicPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • tonic; temporal lobe; all data 48%tonic; temporal lobe; all dataPercentage · non-topological localizing data points unless otherwise statedPDF p.7, Seizure semiology localizing values
  • tonic; temporal lobe; non-topological 20%tonic; temporal lobe; non-topologicalPercentage · non-topological localizing data points unless otherwise statedPDF p.7, Seizure semiology localizing values
  • tonic; frontal lobe; non-topological 54%tonic; frontal lobe; non-topologicalPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • tonic; frontal lobe; all data 29%tonic; frontal lobe; all dataPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • tonic; frontal lobe 54%tonic; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • tonic; cingulate 7%tonic; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 3.0tonic seizures; frontal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 2 bilateral tonic right-arm extensionBilateral tonic activity with right arm extension was listed for patient 2.PDF p.4, Figure 3
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 11 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • tonic motor signsTonic motor signs did not differ significantly overall between TL and T+ groups, but the ipsilateral tonic subtype was associated with T+ seizures.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • tonic motor signsSimple motor signs were common and most often consisted of tonic motor signs, reported in 48.7% of analyzed seizures.PDF p.5, Seizure clinical semiology
Reported values
  • TL ipsilateral 25.4%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • P=0.13tonic motor signsP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL bilateral 25.4%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL contralateral 37.3%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ ipsilateral 47.8%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ tonic motor 60.9%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL tonic motor 37.3%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ bilateral 39.1%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ contralateral 52.2%tonic motor signsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • P=0.05tonic motor signsP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Motor signs
  • tonic motor signs 48.7%tonic motor signsPercentage · 80 analyzed seizures, one typical seizure per patient · ictalPDF p.5, Seizure clinical semiology
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • tonic posturing; clonic jerksThe source describes clonic jerks following focal tonic manifestations as likely reflecting propagation from the SMA to the primary motor area.PDF p.7, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • tonic seizuresTonic seizures involve sustained contraction with posturing; although proximal muscles are often affected bilaterally, clearly unilateral tonic seizures strongly support seizure origin in the contralateral hemisphere.PDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
Reported values
  • Tonic contraction lasts at least 3 secondstonic seizuresCount · patients with focal epilepsy · ictal motorPDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • unilateral dystonic posturing, head/eye deviation, clonic or tonic movements, and hypokinesiaSecondary motor signs related to propagation outside the temporal lobe may lateralize the seizure-onset zone: unilateral dystonic posturing is usually contralateral to the focus, head or eye deviation suggests an ipsilateral focus, and other unilateral clonic or tonic movements or limb immobility usually indicate a contralateral focus.PDF p.8, Focal impaired awareness seizures
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 9 findings · 6 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; orofacial; brachial; tonic; clonic; dystonicElementary motor symptoms were described as early, mainly involving the orofacial regions and/or arms; arm manifestations were mainly contralateral tonic, clonic, or dystonic seizures or postures.PDF p.6, Anatomical and clinical correlations; PDF p.8, Discussion
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 8/21 (38%) for Brachial contralateral (tonic and/or clonic or dystonic posture); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Moderate.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 4/12 patients with Brachial contralateral (tonic and/or clonic or dystonic posture) in the prefrontal operculum group.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Table 2 reports 4/9 patients with Brachial contralateral (tonic and/or clonic or dystonic posture) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Brachial contralateral (tonic and/or clonic or dystonic posture)Fisher's exact comparison of Brachial contralateral (tonic and/or clonic or dystonic posture) between the prefrontal and precentral Rolandic operculum groups has p=0.673.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 9/21 (43%) for Elementary motor: orofacial (tonic and/or clonic, grimace); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 4/12 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the prefrontal operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 5/9 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Fisher's exact comparison of Elementary motor: orofacial (tonic and/or clonic, grimace) between the prefrontal and precentral Rolandic operculum groups has p=0.396.PDF p.7, Table 2
Reported values
  • 8/21 (38%)Brachial contralateral (tonic and/or clonic or dystonic posture)Percentage · n/N 8/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsBrachial contralateral (tonic and/or clonic or dystonic posture)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 4/9 patientsBrachial contralateral (tonic and/or clonic or dystonic posture)Proportion · n/N 4/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
  • 9/21 (43%)Elementary motor: orofacial (tonic and/or clonic, grimace)Percentage · n/N 9/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 5/9 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 5/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • tonic motor manifestationTonic motor manifestations are among the clinical manifestations reported with insular seizures.PDF p.2, Clinical Features
  • tonic motor sign frontal-like symptomFrontal-like insular seizures may include tonic motor signs.PDF p.2, Clinical Features
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Tonic seizure patternTable 2 associates tonic semiology with primary motor cortex and SSMA and lists contralateral lateralisation if unilateral.PDF p.3, Table 2
  • Tonic posturingTable 3 associates tonic posturing with SSMA, basal ganglia, cingulum, and primary motor cortex (M1) and contralateral lateralisation.PDF p.4, Table 3
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • tonic seizureThe source defines tonic seizures as sustained muscle contractions, usually lasting more than 3 seconds, that lead to positioning.PDF p.4, Simple motor seizures
  • Tonic seizureTonic seizures consist of sustained muscle contractions, usually lasting more than 3 seconds, that lead to positioning.PDF p.4, Simple motor seizures, Tonic seizures; PDF p.2, Table 1
Reported values
  • muscle-contraction duration usually >3 stonic seizureDuration Threshold · ictalPDF p.4, Simple motor seizures
  • Usually >3 s muscle-contraction durationTonic seizureCount · IctalPDF p.4, Simple motor seizures, Tonic seizures; PDF p.2, Table 1
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 1 finding · 13 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.12 · 2 × 1.15 × 1.79
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version-first ictal motor sequence; version plus tonic and/or M2e progressionAmong the 38 sequence seizures, version was the first motor sign in 29/38; among those 29 version-first seizures, M2e followed in 15/29 and tonic posturing in 7/29, which the authors combine as version followed by a tonic seizure in 22/29 because they treat M2e as a special tonic form. One seizure had simultaneous version and tonic posturing as the first sign followed by secondary generalization and asymmetric clonic ending; three of the remaining non-version-first seizures showed version plus tonic activity in a different order; in total 33/38 showed version plus tonic activity in variable order. Version was absent in 5/38, four seizures started with tonic activity and ended with asymmetric clonic ending, three of those lateralized the EZ correctly, and one M2e-to-clonic sequence lateralized the EZ correctly.PDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
Reported values
  • Correct EZ lateralization in M2e-to-clonic sequence 1/1version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/1 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Correct EZ lateralization in M2e-to-clonic sequence · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2e-to-clonic sequence 1/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · M2e-to-clonic sequence · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version absent 5/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 5/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version absent · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version as second sign in non-version-first seizures 4/9version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 4/9 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version as second sign in non-version-first seizures · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Non-version-first with version plus tonic in different order 3/9version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 3/9 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Non-version-first with version plus tonic in different order · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version plus tonic in variable order 33/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 33/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version plus tonic in variable order · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Tonic start with asymmetric clonic ending 4/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 4/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Tonic start with asymmetric clonic ending · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Tonic posturing second after version 7/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 7/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Tonic posturing second after version · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version followed by tonic including M2e 22/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 22/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version followed by tonic including M2e · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version first 29/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 29/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version first · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2e second after version 15/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 15/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · M2e second after version · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Simultaneous version and tonic as first sign 1/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Simultaneous version and tonic as first sign · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Correct EZ lateralization among tonic-start/asymmetric-clonic sequences 3/4version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 3/4 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Correct EZ lateralization among tonic-start/asymmetric-clonic sequences · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 1 finding · 3 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • tonic postureIn the unilateral TLE cohort, tonic posture occurred only on the side contralateral to the EEG seizure focus.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
Reported values
  • 12 patients with contralateral tonic posturetonic postureCount · 19 patients with unilateral TLE; tonic posture occurred in 12 patients · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 0 ipsilateral seizurestonic postureCount · 19 patients with unilateral TLE; tonic posture occurred in 12 patients · ipsilateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 17 contralateral seizures (15% of all 116 seizures)tonic posturePercentage · n/N 17/116 · 19 patients with unilateral TLE; tonic posture occurred in 12 patients · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 2 findings · 2 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • tonic posturing of extremitiesTonic posturing of the extremities occurred in 28% of patients.PDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
  • superior parietal epileptogenic zone with tonic posturingFourteen of 23 patients with tonic posturing had epileptogenic zones including the superior parietal lobule.PDF p.4, Results, Other seizure characteristics; PDF p.6, Discussion
Reported values
  • 28%tonic posturing of extremitiesPercentage · 82-patient parietal epilepsy series · ictal motor phasePDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
  • 14/23 (61%) patientssuperior parietal epileptogenic zone with tonic posturingPercentage · n/N 14/23 · 23 patients with tonic posturing · ictal motor phase and seizure-onset localizationPDF p.4, Results, Other seizure characteristics; PDF p.6, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 2 findings · 3 reported values
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • tonic seizures in focal epilepsyThe review states that focal tonic seizures preferentially affect proximal muscle groups, may be unilateral or bilateral, and tend to be asymmetric; consciousness is often preserved at onset. Preserved consciousness during bilateral motor activity can localize a focus to the supplementary motor area. Tonic seizures are reported in 62.2% of frontal-lobe epilepsy and 1.7% of temporal-lobe epilepsy; temporal-lobe tonic seizures were unilateral, whereas 32% of frontal-lobe tonic seizures were bilateral. A clearly unilateral tonic seizure has high lateralizing significance toward the contralateral seizure onset.PDF p.3, Tonic seizures
  • tonic seizures originating from SSMAThe review states that tonic seizures originating from the SSMA may appear bilateral from onset, but careful analysis can show initiation in one body part followed by rapid movement to other limbs; less often the posture is unilateral or restricted to one limb, while proximal-limb and axial involvement remains prominent.PDF p.3, Tonic seizures; PDF p.4, Tonic seizures (continued)
Reported values
  • tonic seizures 62.2% in frontal-lobe epilepsytonic seizures in focal epilepsyPercentage · Patients with focal epilepsy, compared between frontal-lobe and temporal-lobe epilepsy; cohort denominators not reported · frontal-lobe epilepsy · Ictal tonic seizure, especially onsetPDF p.3, Tonic seizures
  • 32% of frontal-lobe tonic seizures were bilateraltonic seizures in focal epilepsyPercentage · Patients with focal epilepsy, compared between frontal-lobe and temporal-lobe epilepsy; cohort denominators not reported · frontal-lobe tonic seizures · Ictal tonic seizure, especially onsetPDF p.3, Tonic seizures
  • tonic seizures 1.7% in temporal-lobe epilepsytonic seizures in focal epilepsyPercentage · Patients with focal epilepsy, compared between frontal-lobe and temporal-lobe epilepsy; cohort denominators not reported · temporal-lobe epilepsy · Ictal tonic seizure, especially onsetPDF p.3, Tonic seizures
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • dorsal parietal to premotor motor evolutionThe authors link rapid motor evolution after visual aura to propagation to dorsal parietal nodes and then premotor areas.PDF p.13, Phenotype III discussion

15 contributing manuscripts; source-reported values remain separate and are not pooled.

AutomatismsReported: ContralateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere16 manuscripts · 33 findings · 32 reported values
Weighted evidence supportevidence weight 30.6 across 16 manuscripts · 2 manuscript weight pending · 3 independent primary study · 6 narrative, educational, or cited context · 4 systematic review or meta-analysis · 2 structured design not resolved · 1 case report or observation

The review associates mesial-temporal automatisms with hand or mouth movements, ictal speech with nondominant seizures, and unilateral dystonic posturing with a contralateral seizure-onset relation. Automatisms with preserved responsiveness were reported as lateralizing to the non-dominant hemisphere, right in the described right-handed subgroup, with one left-language-dominant left temporal exception. The cited series includes delayed motor signs, including source-described contralateral dystonia, without a reported onset-side direction. The review describes automatisms with dystonia as a strong but direction-unspecified lateralisation clue and preserves the ictal/postictal distinction. The cited study is restated as associating dominant-hemisphere focal-onset seizures with automatisms with loss of awareness and nondominant seizures with retained awareness. The cited study attributes preserved responsiveness during oral or manual automatisms to nondominant temporal onset. Automatisms were more frequent in the RTL group than the LTL group: 52/54 (96%) versus 55/73 (75%), with source-reported p=0.003. The review states that automatisms with preserved responsiveness generally lateralize temporal seizures to the nondominant hemisphere, with one reported exception. The cited study restatement reports preserved-responsiveness automatisms exclusively in right nondominant temporal seizures and not in left temporal seizures. The additional case of automatisms with preserved consciousness was reported in right temporal lobe epilepsy. A case was reported with left hemispheric epilepsy and right-sided language dominance. The case reports a right temporal seizure focus with right-sided language dominance, a dominant-temporal exception to the usual nondominant pattern. The source reports no lateralizing direction for the network-propagation account of occipital-onset seizures. No lateralizing direction is reported. The review classification of ictal feature categories reports no lateralizing direction. No lateralization information is reported. No lateralizing direction is reported for the whole-group prevalence of automatisms. No lateralizing direction is reported for the whole-group automatisms cluster coefficient. No lateralizing direction is reported for the fronto-temporal subgroup automatisms coefficient. No lateralizing direction is reported for the oral or gestural automatism cohort. No hemisphere or body-side direction is reported. No source-supported lateralizing direction is reported for the cited occipital-plus organization summary. The pooled automatisms prevalence is 25%; no hemisphere or body-side direction is reported. I2 heterogeneity was 14.19% with source-reported p=0.28; no hemisphere direction is reported.

Source-defined result groups 10
Lateralization: Right hemisphereObserved proportion 75.3%LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphereObserved proportion 100.0%All reported · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Right hemisphereObserved proportion 100.0%All reported · usual nondominant-hemisphere association · patient1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 96.3%RTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Non-dominant hemisphere / Right hemisphereSource-defined values retained separatelyAll reported · Lobar subgroup comparison within the surgical cohort. · Seizure and patient counts for sign occurrence; narrative subgroup includes seizures and patients.1 manuscript · 1 reported value · not pooled
Localization: Parietal / TemporalObserved proportion 78.6%All reported · automatisms without the listed extension · patients with oral or gestural automatisms1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · usual nondominant-hemisphere association · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · patient1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 100.0%All reported · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Non-dominant hemisphere / Right hemisphereObserved proportion range 75.0–80.0% (median 77.5%)narrative right-handed subgroup · Lobar subgroup comparison within the surgical cohort. · Seizure and patient counts for sign occurrence; narrative subgroup includes seizures and patients.1 manuscript · 2 reported values · not pooled
Evidence by contributing manuscript 16

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • ictal vocalization with automatismsA cited study of 102 patients reported 91% sensitivity for detecting temporal-lobe seizures when ictal vocalizations co-occurred with automatisms.PDF p.12, Localizing probabilities
  • ictal vocalization with automatismsThe same cited study reported 70% specificity for detecting temporal-lobe seizures when ictal vocalizations co-occurred with automatisms.PDF p.12, Localizing probabilities
Reported values
  • sensitivity 91%ictal vocalization with automatismsSensitivity · 102 patients with ictal vocalizationPDF p.12, Localizing probabilities
  • specificity 70%ictal vocalization with automatismsSpecificity · 102 patients with ictal vocalizationPDF p.12, Localizing probabilities
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 2 findings · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • atypical anterior automatismsAutomatisms were observed in one atypical anterior patient without the violent component seen in the typical group.PDF p.5, Clinical Presentation
  • posterior cingulate staring and automatisms cited caseThe discussion cites a lesional posterior cingulate case with seizures characterized by staring and automatisms.PDF p.7, Discussion
Reported values
  • 1/4 automatisms without violent componentatypical anterior automatismsProportion · n/N 1/4 · 4 atypical anterior cingulate cases · ictal semiologyPDF p.5, Clinical Presentation
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • delayed motor signs (Duchowny study)The cited Duchowny series is described as having behavioral arrest and delayed motor signs including version, contralateral dystonia, clonic jerks, and automatisms.PDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Automatisms in temporal-versus-frontal differentialTable 1 reports automatisms as common and longer in temporal lobe seizures and less common in frontal lobe seizures.PDF p.2, Table 1
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 5 findings · 2 reported values
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • automatismsThe discussion identifies automatisms as a possible early localizing sign in SMA epilepsy because they were mostly reported at seizure onset.PDF p.8, Discussion
  • automatismsTable 3 lists 11 patients for the the source's own ictal symptom “automatisms”; its table phase label is onset.PDF p.6, Table 3
  • automatismsTable 3 reports a pooled prevalence of 25% for the the source's own ictal symptom “automatisms”; its table phase label is onset.PDF p.6, Table 3
  • automatisms; between-study heterogeneityThe source reports I2 heterogeneity of 14.19% for pooled automatisms prevalence.PDF p.5, Results
  • automatisms; heterogeneity testThe source reports p = 0.28 for the between-study heterogeneity test of pooled automatisms prevalence.PDF p.5, Results
Reported values
  • 25% pooled prevalenceautomatismsPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
  • I2 = 14.19%automatisms; between-study heterogeneityHeterogeneity I2 · Patients with SMA or pre-SMA epilepsy in the selected studies · ictal symptom prevalence analysisPDF p.5, Results
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • mesial temporal automatisms; ictal speech; unilateral dystonic posturingMesial temporal automatisms often involve the hands or mouth; less common vocalisations and ictal speech are associated with non-dominant seizures; unilateral dystonic posturing can occur and is described as a contralateral sign.PDF p.5, Mesial temporal lobe including hippocampus
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 8 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 4.36 · 2 × 1.5 × 1.452
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Automatisms with preserved responsivenessAutomatisms with preserved responsiveness were reported as lateralizing to the non-dominant hemisphere with 62% PPV and inter-observer kappa of 0.89, with a right-hemisphere pattern in the described right-handed subgroup and one left-language-dominant exception.PDF p.3, Table 1; PDF p.3, §5.1
Reported values
  • frontal PPV 0%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 4/5 patientsAutomatisms with preserved responsivenessPercentage · n/N 4/5 · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · narrative right-handed subgroup · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 6/8 seizuresAutomatisms with preserved responsivenessPercentage · n/N 6/8 · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · narrative right-handed subgroup · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • overall PPV 62%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • occipital PPV 100%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • temporal PPV 60%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • inter-observer kappa 0.89Automatisms with preserved responsivenessKappa · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • parietal PPV 100%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Automatisms overallAutomatisms overall were more frequent in RTL than in LTL seizures.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
Reported values
  • 55/73 (75%)Automatisms overallPercentage · n/N 55/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • 52/54 (96%)Automatisms overallPercentage · n/N 52/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • automatisms with preserved responsivenessOral or manual automatisms with preserved responsiveness reliably localize seizure onset to the nondominant temporal lobe because seizure propagation does not reach the language-dominant temporal lobe or extratemporal structures.PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Automatisms with dystoniaThe review states that automatisms may be ictal or postictal and provide strong lateralisation clues when associated with dystonia; manipulative automatisms may be more common postictally, and EEG can help distinguish ictal from postictal automatisms.PDF p.4, section 1.6
  • Automatisms with awarenessThe review reports that dominant-hemisphere focal-onset seizures with automatisms were associated with loss of awareness, while non-dominant seizures were associated with retained awareness.PDF p.3, section 1.3
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfCase report or observation · 5 findings · 9 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • automatisms with preserved responsivenessAutomatisms with preserved responsiveness generally lateralize temporal lobe seizures to the nondominant hemisphere, with one reported exception.PDF p.6, section 3.10; PDF p.7, section 3.10 continuation; PDF p.12, Table 1
  • automatisms with preserved responsivenessEbner et al. observed automatisms with preserved responsiveness exclusively in right nondominant temporal seizures and not in left temporal seizures.PDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • automatisms with preserved consciousnessAn additional case of automatisms with preserved consciousness was reported in right temporal lobe epilepsy.PDF p.7, section 3.10
  • automatisms with preserved responsivenessA case was reported with left hemispheric epilepsy and right-sided language dominance.PDF p.7, section 3.10
  • automatisms with preserved responsiveness and ictal dysphasiaJanszky et al. reported a dominant-temporal exception to the usual nondominant lateralization of preserved-responsive automatisms.PDF p.7, section 3.10; PDF p.12, Table 1
Reported values
  • 100% nondominantautomatisms with preserved responsivenessPercentage · patients with temporal lobe epilepsy · TLE with preserved-responsive automatisms · ictalPDF p.12, Table 1
  • 5.7%automatisms with preserved responsivenessPercentage · patients with temporal lobe epilepsy · temporal lobe epilepsy · ictalPDF p.12, Table 1
  • one exceptionautomatisms with preserved responsivenessCount · patients with temporal lobe epilepsy · reported exception · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation; PDF p.12, Table 1
  • none observed in left temporal seizuresautomatisms with preserved responsivenessCount · 123 patients with temporal lobe epilepsy diagnosed by video/EEG and MRI · left temporal seizures · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • 7/123 (5.7%) overallautomatisms with preserved responsivenessPercentage · n/N 7/123 · 123 patients with temporal lobe epilepsy diagnosed by video/EEG and MRI · all TLE patients · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • 10% of right nondominant TLE patientsautomatisms with preserved responsivenessPercentage · 123 patients with temporal lobe epilepsy diagnosed by video/EEG and MRI · right nondominant TLE · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • 1 caseautomatisms with preserved consciousnessCount · n/N 1/1 · one patient with right temporal lobe epilepsy · ictalPDF p.7, section 3.10
  • 1 caseautomatisms with preserved responsivenessCount · n/N 1/1 · one patient with left hemispheric epilepsy · ictalPDF p.7, section 3.10
  • 1 caseautomatisms with preserved responsiveness and ictal dysphasiaCount · n/N 1/1 · one 25-year-old woman with right temporal lobe epilepsy · ictalPDF p.7, section 3.10; PDF p.12, Table 1
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • altered conscious level; automatic motor behavior; verbal automatismsThe review reports that Marchi et al. (2016) found widespread epileptogenic-zone organization typical of occipital-plus epilepsy, with temporal and/or parietal cortex commonly involved; altered conscious level was more common with widespread posterior neocortical onset, while automatic motor behavior and/or verbal automatisms were more often seen with occipitotemporal organization.PDF p.6, Table 2, Occipital lobe row
Reported values
  • 29 subjectsaltered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy and 194 seizures · occipital-lobe epilepsy study · Seizure onset and semiologic expressionPDF p.6, Table 2, Occipital lobe row
  • 194 seizuresaltered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy and 194 seizures · occipital-lobe epilepsy study · Seizure onset and semiologic expressionPDF p.6, Table 2, Occipital lobe row
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 7 findings · 5 reported values
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • automatisms; elementary motor; hyperkinetic; autonomic; emotional; grimace; cognitive; other subjectiveThe source classifies ictal features into automatisms, elementary motor, hyperkinetic, autonomic, emotional, grimace, cognitive, and other subjective categories for the cluster and prevalence analyses.PDF p.4, Statistical analysis
  • emotional; autonomic; automatisms; hyperkinetic behavior; grimaceAcross groups, the source places autonomic and emotional features at seizure onset, while automatisms, hyperkinetic behavior, and grimace are associated with propagation.PDF p.2, Key points; PDF p.9, Seizure semiology
  • automatisms; whole groupAutomatisms were reported in 80 of 109 patients (73%) in the whole group.PDF p.5, All group
  • automatisms; fronto-temporal subgroupAutomatisms was reported in 88% of the fronto-temporal subgroup (33 patients).PDF p.5, Fronto-temporal subgroup
  • automatisms; temporo-frontal subgroupAutomatisms was reported in 67% of the temporo-frontal subgroup (76 patients).PDF p.5, Temporo-frontal subgroup
  • association coefficient; automatisms as isolated clusterThe source reports an association coefficient of >0.3 for automatisms as isolated cluster in the whole group.PDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient; automatisms as isolated clusterThe source reports an association coefficient of >0.2 for automatisms as isolated cluster in the fronto-temporal subgroup.PDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
Reported values
  • 80/109 (73%)automatisms; whole groupPercentage · n/N 80/109 · 109 review patients, whole group · ictal propagationPDF p.5, All group
  • 88%automatisms; fronto-temporal subgroupPercentage · 33 patients, fronto-temporal subgroup · ictal propagationPDF p.5, Fronto-temporal subgroup
  • 67%automatisms; temporo-frontal subgroupPercentage · 76 patients, temporo-frontal subgroup · ictal propagationPDF p.5, Temporo-frontal subgroup
  • association coefficient >0.3association coefficient; automatisms as isolated clusterAssociation Coefficient · 109 review patients · ictal symptom co-occurrencePDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient >0.2association coefficient; automatisms as isolated clusterAssociation Coefficient · 33 fronto-temporal subgroup patients · ictal symptom co-occurrencePDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 4.25 · 2 × 1.35 × 1.573
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • inferior parietal or opercular extension with automatismsEleven of 14 patients with oral or gestural automatisms had epileptogenic zones extending into the inferior parietal lobule, parietal operculum, or superior-posterior temporal region.PDF p.4, Results, Other seizure characteristics; PDF p.6, Discussion
Reported values
  • 11/14 (79%) patientsinferior parietal or opercular extension with automatismsPercentage · n/N 11/14 · 14 patients with oral or gestural automatisms · ictal propagation and seizure-onset localizationPDF p.4, Results, Other seizure characteristics; PDF p.6, Discussion
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • timing of automatisms; medio-lateral rapid-propagation groupThe source states that the only significant difference reported by Maillard was earlier timing of automatisms in the medio-lateral rapid-propagation group.PDF p.7, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • occipital onset with temporal-like automatism and motor expressionThe source concludes that occipital-onset seizures can produce temporal-like automatisms and frontal- or parietal-like motor symptoms through network propagation.PDF p.12, Key Findings and Phenotype-Propagation Pattern Correspondences; PDF p.14, Clinical Translation

16 contributing manuscripts; source-reported values remain separate and are not pooled.

Fear auraSource terms: Ictal fearReported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side17 manuscripts · 34 findings · 24 reported values
Weighted evidence supportevidence weight 30.37 across 17 manuscripts · 2 manuscript weight pending · 9 narrative, educational, or cited context · 2 structured design not resolved · 4 systematic review or meta-analysis · 2 independent primary study

The stimulation-site count contains no lateralization information. The cited stimulation response provides no hemispheric direction. This finding provides no lateralization information. The single-patient aura occurrence provides no hemispheric direction. This lateral-versus-mesial temporal statistic provides no hemispheric lateralization. The lateral-temporal prevalence range provides no hemispheric direction. The occurrence odds provide no hemispheric direction. The lateral-TLE prevalence range provides no hemispheric direction. The mesial-TLE prevalence range provides no hemispheric direction. No hemisphere or body-side direction is reported. This record provides no hemispheric lateralization. The cited prefrontal prevalence series provides no lateralizing direction. The cited fear/anxiety network account provides no lateralizing direction. The stimulation responses contain no lateralization information. This record provides no seizure lateralization. The cited table describes fear aura as non-lateralising. No lateralizing direction is reported. The cited emotional-expression statement reports no hemisphere or lateralization direction. The temporal-subtype result provides no hemispheric direction. The review table labels both fear and déjà vu/jamais vu as nonlateralizing, while noting an often-nondominant tendency only for déjà vu/jamais vu. The review places fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo between lateral and medial temporal patterns. Ictal fear has been associated with possible right-hemispheric lateralization.

Source-defined result groups 13
Localization: TemporalObserved proportion 22.2%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 37.5%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 17.1%Visceral responses · viscero-psychic symptom presentations · evoked visceral response1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Table 3 point estimate 13% · Table 3 between-report frequency range1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 50.0%Viscero-psychic responses · viscero-psychic symptom presentations · evoked viscero-psychic response1 manuscript · 1 reported value · not pooled
Localization: orbitofrontal cortex-restricted epileptogenic-zone networkObserved proportion 3.8%OFC-restricted EZN cases · patients with affective phenomena1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Fear aura/psychic aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other Table 3 temporo-polar sign estimates · Table 3 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Fear aura/psychic aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 50.0%Viscero-psychic responses · viscero-psychic symptom presentations · evoked viscero-psychic response1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 17

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 3 findings · 2 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.5
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical group fear/laughter/personality patternThe abstract characterizes the typical anterior group by hypermotor seizures, infrequent generalization, and fear, laughter, or severe interictal personality changes.PDF p.1, Abstract
  • typical anterior fear auraFear was present in all three typical anterior cases with aura.PDF p.3, Clinical Presentation
  • anterior cingulate fear aura aggregateFear was seen as an aura in three anterior cingulate cases.PDF p.6, Discussion
Reported values
  • 3/3 fear aura among aura-positive casestypical anterior fear auraProportion · n/N 3/3 · 3 typical anterior aura-positive cases · auraPDF p.3, Clinical Presentation
  • 3/10 fear auraanterior cingulate fear aura aggregateProportion · n/N 3/10 · 10 anterior cingulate cases · auraPDF p.6, Discussion
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Fear (Table 3)Table 3 reports fear in 1 case (1%), more at seizure onset.PDF p.6, Table 3
  • Fear (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports fear in 4 cases (7%).PDF p.7, Table 4
Reported values
  • 1 case (1%)Fear (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 4/60 (7%)Fear (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • affective phenomena; fearOne restricted-OFC case described affective phenomena, specifically fear.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 1/26 (3.8%)affective phenomena; fearPercentage · n/N 1/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Fear aura/psychic auraTable 3 reports 5 studies assessing Fear aura/psychic aura.PDF p.6, Table 3
  • Fear aura/psychic auraTable 3 reports 81 patients assessed for Fear aura/psychic aura.PDF p.6, Table 3
  • Fear aura/psychic auraTable 3 reports 0–40% as the percentage range or value for Fear aura/psychic aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Fear aura/psychic auraTable 4 reports overall odds of 0.10 for occurrence of Fear aura/psychic aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Fear aura/psychic auraTable 4 reports a 95% confidence interval of 0.02–0.45 for the overall odds of Fear aura/psychic aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Fear aura/psychic auraThe heterogeneity test for the Table 4 odds estimate for Fear aura/psychic aura has p=0.0243.PDF p.7, Table 4
  • Fear aura/psychic aura; lateral versus mesial comparisonTable 5 reports 4 studies comparing Fear aura/psychic aura in lateral and mesial TLE.PDF p.9, Table 5
  • Fear aura/psychic aura; lateral TLE patient denominatorTable 5 reports 58 lateral-TLE patients assessed for Fear aura/psychic aura.PDF p.9, Table 5
  • Fear aura/psychic aura; mesial TLE patient denominatorTable 5 reports 87 mesial-TLE patients assessed for Fear aura/psychic aura.PDF p.9, Table 5
  • Fear aura/psychic aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0–40% for Fear aura/psychic aura.PDF p.9, Table 5
  • Fear aura/psychic aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 18.8–35.5% for Fear aura/psychic aura.PDF p.9, Table 5
Reported values
  • 0–40%Fear aura/psychic auraPercentage Range · Lateral temporal epilepsy patients assessed for Fear aura/psychic aura · ictalPDF p.6, Table 3
  • odds 0.10odds of occurrence; Fear aura/psychic auraOdds · Lateral temporal epilepsy patients assessed for Fear aura/psychic aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0–40%Fear aura/psychic aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Fear aura/psychic aura · Lateral TLE patients assessed for Fear aura/psychic aura · ictalPDF p.9, Table 5
  • 18.8–35.5%Fear aura/psychic aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Fear aura/psychic aura · Mesial TLE patients assessed for Fear aura/psychic aura · ictalPDF p.9, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • fear and déjà vu or jamais vu auras in Table 1Table 1 lists fear as arising from the amygdala, hippocampus, and mesial frontal lobe and as nonlateralizing; it lists déjà vu or jamais vu as arising from the uncus, entorhinal cortex, and temporal neocortex and as nonlateralizing, often nondominant.PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal fear or anxietySudden ictal fear or anxiety resembling a panic attack may highlight an amygdala seizure onset; dysphoric, euphoric, and ultimately ecstatic feelings are also described in the mesial temporal semiology spectrum.PDF p.8, Focal emotional seizures
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 1 reported value
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • inner sensation of fear before hypermotor semiologyAn inner sensation of fear before the start of hypermotor semiology evolved into SP4 or SP3 in most SHE cases, reported as 86%.PDF p.8, section 4.3
Reported values
  • Percentage evolving to SP4 or SP3, 86%inner sensation of fear before hypermotor semiologyPercentage · SHE cases with an inner sensation of fear before hypermotor behavior · pre-hypermotor nonmotor symptom -> ictal SP3/SP4PDF p.8, section 4.3
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • viscero-psychic responsesViscero-psychic symptoms were elicited at 14 insular stimulation sites.PDF p.5, Visceral Symptoms
  • fear associated with viscero-psychic symptomsThoracic or abdominal heaviness was associated with a feeling of fear in viscero-psychic responses.PDF p.5, Visceral Symptoms
Reported values
  • 14 stimulation sites with viscero-psychic symptomsviscero-psychic responsesCount · visceral responses in the cited insular stimulation series · stimulation-evoked autonomic/affective semiologyPDF p.5, Visceral Symptoms
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Fear auraTable 2 associates fear aura with amygdala, hippocampus, and mesial frontal lobe (anterior cingulate) and describes it as non-lateralising.PDF p.3, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal fearIctal fear has been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 4 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • fearInitial fear was more frequent in M and ML than L patients and was absent in the L group.PDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Fear or anxiety
Reported values
  • ML=4/18 (22.2%)fearPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Fear or anxiety
  • p=0.026fearP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Fear or anxiety
  • M=9/24 (37.5%)fearPercentage · n/N 9/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Fear or anxiety
  • L=0/13 (0%)fearPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.7, Fear or anxiety
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.76 · 1 × 0.9 × 1.957
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • viscero-psychic symptomsThe 14 viscero-psychic responses combined a visceral sensation with anxiety or fear; thoracic or abdominal constriction/heaviness accompanied anxiety in 7 of 14, and anxiety ranged from mild to panic and could be isolated in 7 of 14 cases.PDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
Reported values
  • Isolated anxiety 7/14viscero-psychic symptomsCount · n/N 7/14 · 14 viscero-psychic responses within the 82 visceral responses · Viscero-psychic responses · stimulation-evoked visceral and affective sensationPDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
  • 14 viscero-psychic responses within 82 visceral responsesviscero-psychic symptomsCount · n/N 14/82 · 14 viscero-psychic responses within the 82 visceral responses · Visceral responses · stimulation-evoked visceral and affective sensationPDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
  • Thoracic/abdominal constriction or heaviness with anxiety 7/14viscero-psychic symptomsCount · n/N 7/14 · 14 viscero-psychic responses within the 82 visceral responses · Viscero-psychic responses · stimulation-evoked visceral and affective sensationPDF p.3, Results and Table 1; PDF p.5, Visceral Sensations and Fig. 4C
mcgonigal-frontal-lobe-seizures-overview-update-2022.pdfNarrative, educational, or cited context · 2 findings · 3 reported values
mcgonigal-frontal-lobe-seizures-overview-update-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This document is a review/Neurological Update and reports or synthesizes observations from multiple SEEG, intracerebral-recording, and other cited series rather than a single study population. It specifically describes a cited SEEG series of 54 patients with FLE and a cited series of 42 patients with prefrontal seizures for emotional prevalence; other cited cohort sizes, ascertainment details, reference standards, and region-specific denominators are not reported in the document. The review frames its electroclinical correlations as group-level aids for presurgical sublobar hypotheses. It states that both seizure onset and propagation contribute to semiological expression and distinguishes elementary motor signs from complex motor behavior.
Findings
  • fear/threat-response emotional spectrum in a 42-patient prefrontal SEEG seriesThe review reports, from a 42-patient prefrontal SEEG series attributed to Singh et al. (in preparation), that around 40% had fear at seizure onset as an aura, around 20% had an anxious or fearful facial expression, and around 10% had full-blown threat-response behavior; it describes a spectrum from fearful face with or without freezing, through defense gestures, to explosive hyperkinetic escape or fight behavior.PDF p.5, Emotional semiology
  • fear/anxiety localizationFor prefrontal seizures with apparent fear or anxiety, the review reports a main role for ventromesial prefrontal cortex and especially posterior orbitofrontal cortex, with co-involvement of mesial temporal structures including amygdala with or without temporal pole; the described pattern includes fear feeling, fearful/anxious face, and upper-limb defense posture.PDF p.5, Emotional semiology
Reported values
  • around 10%fear/threat-response emotional spectrum in a 42-patient prefrontal SEEG seriesPercentage · 42 patients with prefrontal seizures explored with SEEG · full-blown threat-response behavior · Ictal onset for fear aura; ictal for objective facial expression and threat-response behaviorPDF p.5, Emotional semiology
  • around 40%fear/threat-response emotional spectrum in a 42-patient prefrontal SEEG seriesPercentage · 42 patients with prefrontal seizures explored with SEEG · fear at seizure onset as an aura · Ictal onset for fear aura; ictal for objective facial expression and threat-response behaviorPDF p.5, Emotional semiology
  • around 20%fear/threat-response emotional spectrum in a 42-patient prefrontal SEEG seriesPercentage · 42 patients with prefrontal seizures explored with SEEG · anxious or fearful facial expression · Ictal onset for fear aura; ictal for objective facial expression and threat-response behaviorPDF p.5, Emotional semiology
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • affective ACC expressionStronger emotional expressions such as fear or menace, with open eyes, hypermotor, and autonomic features, were linked to the rostroventral “affective” ACC.PDF p.8, Discussion
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • fear; anxiety; facial expression of fear/horror; orbitofrontal cortex; amygdalaThe source states that hyperkinetic behavior following intense fear or anxiety with facial fear/horror expression has been related to limbic imbalance, particularly decoupling between orbitofrontal cortex and amygdala.PDF p.12, Discussion
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 2 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • fear; auditory hallucinations; gustatory hallucinations; sensory hallucinations; vertigoThe source describes fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo as intermediate features between lateral and medial temporal patterns.PDF p.5, Discussion
  • aura of fearTable 3 reports aura of fear in 13% of the temporo-polar synthesis (evidence grade Low).PDF p.5, Table 3
  • aura of fearTable 3 reports a 0–100% range for aura of fear across the temporo-polar reports (evidence grade Low).PDF p.5, Table 3
Reported values
  • 13%aura of fearPercentage · Temporo-polar semiology synthesis represented in Table 3 · clinical onsetPDF p.5, Table 3
  • range 0–100%aura of fearPercentage Range · Temporo-polar semiology synthesis represented in Table 3 · clinical onsetPDF p.5, Table 3
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 1 finding · 1 reported value
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • fear and indescribable feeling aura in hypermotor seizureOne hypermotor patient reported fear and an indescribable feeling as an aura.PDF p.4, Seizure semiology on video-EEG recording; PDF p.3, Table 1
Reported values
  • 1/4 hypermotor patients with fear/indescribable-feeling aurafear and indescribable feeling aura in hypermotor seizureProportion · n/N 1/4 · 4 hypermotor patients · auraPDF p.4, Seizure semiology on video-EEG recording; PDF p.3, Table 1

17 contributing manuscripts; source-reported values remain separate and are not pooled.

Gelastic seizures (ictal mirthless laughter - pathognomonic for hypothalamic hamartoma)Source terms: Gelastic seizuresReported: BilateralAlso reported: Right hemisphere15 manuscripts · 69 findings · 56 reported values
Weighted evidence supportevidence weight 28.6 across 15 manuscripts · 2 independent primary study · 5 systematic review or meta-analysis · 7 narrative, educational, or cited context · 1 case report or observation

The cited table describes gelastic semiology as non-lateralising. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. No lateralizing direction is reported for the two discussed laughter cases. The source text reports an internal laughter-count discrepancy but no hemisphere direction, while the prefilled lateralization value says right. The review reports 6 gelastic-behavior cases; the bilateral qualifier concerns spasms, not cerebral hemisphere direction. Laughing or crying did not differ significantly between TL and T+ groups; no hemisphere or body-side direction is reported. No seizure lateralization is reported. No lateralizing direction is reported. The review associations contain no lateralization information. No lateralization information is reported for the gelastic-seizure context comparison. No lateralization information is reported. No source-supported hemispheric or body-side lateralization is reported. No lateralizing direction is reported for the other-automatisms subset. No lateralizing direction is reported for the review-table gelastic behavior result. No lateralizing direction is reported for the restricted high/very-high-confidence subset. No hemisphere or body-side direction is reported for the initial clinical semiology. The cited gelastic-seizure localization summary reports no lateralizing direction. The cited gelastic-seizure series reports no hemisphere direction. No lateralizing direction is reported for the illustrative gelastic-seizure case. Laughter frequency was reported as 10% with a source-reported 0–50% across-study range; no hemisphere direction is reported. No lateralizing direction is reported for the laughter frequency range. Laughter was reported at 9.7%; no hemisphere direction is reported. Nine patients represented 10% of reviewed cases; the denominator is not printed and the 93-patient cohort total is not substituted. Three of nine laughter-positive patients had laughter at onset or as a defining seizure feature; no hemisphere direction is reported. Six of nine laughter-positive patients had inconstant laughter or laughter at seizure end; no hemisphere direction is reported. The source reports OR <0.1 for laughter relative to vocalization/verbalization; no hemisphere direction is reported. No lateralization axis information is reported for laughter versus affective/autonomic aura. The claim states OR 0.2 for laughter relative to autonomic signs, while the supplied statistic record states OR 0.1; no hemisphere direction is reported. The claim states OR 0.2 for laughter relative to facial expression change, while the supplied statistic record states OR 0.1; no hemisphere direction is reported. No hemisphere or body-side direction is reported. This finding provides no lateralization information. Figure 6 reports OR 11.7 for Affective/autonomic aura relative to Laughter, with no hemisphere or lateralization direction. No lateralizing direction is reported for the Figure 6 laughter-versus-F-to-BTC comparison. No lateralization information is reported for the gelastic-seizure definition.

Source-defined result groups 9
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 11.1%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 16.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 14.3%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 15

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • other automatisms; gelastic and dacrystic seizuresAmong the 108 cases categorized as other automatisms, 62 were gelastic or dacrystic seizures.PDF p.8, Seizure semiology localizing values
  • other automatisms; gelastic and dacrystic seizuresThe denominator for the reported gelastic/dacrystic subset was 108 other-automatisms cases.PDF p.8, Seizure semiology localizing values
Reported values
  • 62/108 other-automatisms casesother automatisms; gelastic and dacrystic seizuresProportion · n/N 62/108 · other automatisms category · gelastic or dacrystic seizuresPDF p.8, Seizure semiology localizing values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical group fear/laughter/personality patternThe abstract characterizes the typical anterior group by hypermotor seizures, infrequent generalization, and fear, laughter, or severe interictal personality changes.PDF p.1, Abstract
  • gelastic seizures in cingulate literatureThe discussion reports that gelastic seizures were reported in six of 16 anterior cingulate cases in the reviewed literature.PDF p.6, Discussion
Reported values
  • 6/16 gelastic seizuresgelastic seizures in cingulate literatureProportion · n/N 6/16 · reviewed anterior cingulate epilepsy cases · ictal semiologyPDF p.6, Discussion
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • laughing or cryingLaughing or crying did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 8.5%laughing or cryingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 4.3%laughing or cryingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 4 findings · 4 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • gelastic behaviorThe review reports gelastic behavior in six cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Gelastic Behavior (Table 3)Table 3 reports gelastic behavior in 6 cases (7%), more during propagation.PDF p.6, Table 3
  • Gelastic Behavior (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports gelastic behavior in 5 cases (8%).PDF p.7, Table 4
  • hyperkinetic/agitation plus gelastic behaviorThe co-occurrence analysis identified hyperkinetic/agitation with gelastic behavior in 22% of the 18-patient detailed-data set.PDF p.7, Figure 2 discussion
Reported values
  • 6 cases with gelastic behaviorgelastic behaviorCount · basal temporal seizure cases; three-patient DNET subset for spasms · ictal; propagation for gelastic behavior in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 6 cases (7%)Gelastic Behavior (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 5/60 (8%)Gelastic Behavior (Table 4)Percentage · n/N 5/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
  • 22% co-occurrencehyperkinetic/agitation plus gelastic behaviorPercentage · 18 patients with detailed semiology data · ictal; timing not otherwise reportedPDF p.7, Figure 2 discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Gelastic seizuresGelastic seizures are listed as localizing to temporal, hypothalamic, or frontal cingulate regions.PDF p.4, Table 2; PDF p.3, section 2.5 Automatisms
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 35 findings · 33 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • laughterThe source reports a frequency of 10% for laughter.PDF p.13, Table 3
  • laughter; reported frequency rangeThe source reports a frequency range of 0–50% for laughter.PDF p.13, Table 3
  • laughter; ACC association gradeTable 3 assigns the source's High overall association grade to laughter.PDF p.13, Table 3
  • laughter; Figure 4 rateFigure 4 displays a 9.7% rate for laughter.PDF p.10, Figure 4
  • laughterLaughter was reported in nine patients and represented 10% of the reviewed cases.PDF p.7, Objective symptomatology
  • laughter at onset or defining featureThree of the nine laughter cases had laughter at seizure onset or as a defining seizure feature.PDF p.7, Objective symptomatology
  • laughter late or inconstantSix of the nine laughter cases were inconstant or occurred at seizure end.PDF p.7, Objective symptomatology
  • pairwise OR: Laughter relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Laughter relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.1 for Laughter relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.1 for Laughter relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Autonomic signsFigure 6 reports an odds ratio of 0.2 for Laughter relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Facial expression changeFigure 6 reports an odds ratio of 0.2 for Laughter relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.2 for Laughter relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.3 for Laughter relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.3 for Laughter relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.4 for Laughter relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Dystonic posturingFigure 6 reports an odds ratio of 0.6 for Laughter relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Head-eye deviationFigure 6 reports an odds ratio of 0.9 for Laughter relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to LaughterFigure 6 reports an odds ratio of 14.5 for Vocalization/verbalization relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to LaughterFigure 6 reports an odds ratio of 13.7 for Hypermotor-complex motor behavior relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to LaughterFigure 6 reports an odds ratio of 11.7 for Affective/autonomic aura relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to LaughterFigure 6 reports an odds ratio of 8.6 for Autonomic signs relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to LaughterFigure 6 reports an odds ratio of 7.9 for Facial expression change relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to LaughterFigure 6 reports an odds ratio of 7 for Motor (gestural) automatisms relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to LaughterFigure 6 reports an odds ratio of 5.1 for Loss of consciousness relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to LaughterFigure 6 reports an odds ratio of 4.1 for Post-ictal confusion/behavior change disinhibition relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to LaughterFigure 6 reports an odds ratio of 2.4 for Chapeau de gendarme relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to LaughterFigure 6 reports an odds ratio of 2.2 for Dystonic posturing relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to LaughterFigure 6 reports an odds ratio of 1.5 for Head-eye deviation relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to LaughterFigure 6 reports an odds ratio of 0.9 for Oro-alimentary automatisms relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to LaughterFigure 6 reports an odds ratio of 0.9 for Tonic-clonic relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to LaughterFigure 6 reports an odds ratio of 0.5 for F to BTC relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.1 for Laughter relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Tonic-clonicFigure 6 reports an odds ratio of 2.6 for Laughter relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to F to BTCFigure 6 reports an odds ratio of 2.6 for Laughter relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 10% (frequency range 0–50%)laughterPercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.13, Table 3
  • 9.7%laughter; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.10, Figure 4
  • 9 patients (10%)laughterPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.7, Objective symptomatology
  • 3/9 laughter-positive patientslaughter at onset or defining featureProportion · n/N 3/9 · Reviewed ACC seizure cases with reported semiology · laughter-positive cases · Laughter-positive ACC casesPDF p.7, Objective symptomatology
  • 6/9 laughter-positive patientslaughter late or inconstantProportion · n/N 6/9 · Reviewed ACC seizure cases with reported semiology · laughter-positive cases · Laughter-positive ACC casesPDF p.7, Objective symptomatology
  • OR <0.1pairwise OR: Laughter relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Laughter relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Laughter relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Laughter relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Laughter relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Laughter relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Laughter relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Laughter relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Laughter relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Laughter relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Laughter relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 14.5pairwise OR: Vocalization/verbalization relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.7pairwise OR: Hypermotor-complex motor behavior relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 11.7pairwise OR: Affective/autonomic aura relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 8.6pairwise OR: Autonomic signs relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.9pairwise OR: Facial expression change relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7pairwise OR: Motor (gestural) automatisms relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.1pairwise OR: Loss of consciousness relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.1pairwise OR: Post-ictal confusion/behavior change disinhibition relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.4pairwise OR: Chapeau de gendarme relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.2pairwise OR: Dystonic posturing relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Head-eye deviation relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Oro-alimentary automatisms relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Tonic-clonic relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: F to BTC relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Laughter relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.9pairwise OR: Laughter relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.9pairwise OR: Laughter relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 7 findings · 6 reported values
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • focal atonic seizure; gelastic seizure; ictal poutingFocal atonic seizures may indicate involvement of negative motor areas or the supplementary motor area; gelastic seizures and ictal pouting may occur in mesiofrontal and anterior cingulate frontal seizures and are discussed as separate semiologies.PDF p.4, Other frontal regions; PDF p.3, Figure 1
  • gelastic seizure; hypothalamic hamartomaIn the cited case series from the authors’ centre, one third of gelastic seizure cases had hypothalamic hamartomas.PDF p.9, Gelastic seizures
  • gelastic seizure; temporal lobe sourceIn the same cited gelastic-seizure case series, one third of seizures were temporal.PDF p.9, Gelastic seizures
  • gelastic seizure; frontal sourceIn the same cited gelastic-seizure case series, one third of seizures were frontal.PDF p.9, Gelastic seizures
  • gelastic seizureGelastic seizures from hypothalamic hamartomas are described as usually beginning in early childhood, brief, stereotyped, and very frequent, with usually mirthless laughter without impaired consciousness, commonly accompanied by facial flushing or pupillary dilation and sometimes a dacrystic component; gelastic seizures from other brain structures usually present in adulthood, while temporal cases commonly include automotor features and loss of consciousness.PDF p.9, Gelastic seizures; PDF p.3, Figure 1
  • gelastic seizuresGelastic seizures typically arise from hypothalamic hamartomas, but the review states that a cited case series found one third of cases with hypothalamic hamartomas, one third temporal, and one third frontal; hypothalamic-hamartoma seizures usually begin in early childhood, are brief, stereotyped, and very frequent with mirthless laughter and common autonomic signs, whereas non-hypothalamic and especially temporal gelastic seizures usually present in adulthood as more complex automotor seizures with loss of consciousness.PDF p.9, Gelastic seizures
  • gelastic seizure with hypothalamic hamartomaIn video case 5, an 18-year-old right-handed man had gelastic seizures beginning at age 2, imaging-confirmed hypothalamic hamartoma, typical gelastic seizures without mirth, and loss of awareness in some seizures.PDF p.9, Video case 5 and Figure 6
Reported values
  • hypothalamic hamartoma in one third of casesgelastic seizure; hypothalamic hamartomaProportion · gelastic seizure case series from the authors’ centre · ictalPDF p.9, Gelastic seizures
  • temporal source in one third of seizuresgelastic seizure; temporal lobe sourceProportion · gelastic seizure case series from the authors’ centre · ictalPDF p.9, Gelastic seizures
  • frontal source in one third of seizuresgelastic seizure; frontal sourceProportion · gelastic seizure case series from the authors’ centre · ictalPDF p.9, Gelastic seizures
  • one thirdgelastic seizuresOther reported value · Cases in the cited gelastic-seizure series; exact denominator Not reported · hypothalamic hamartoma · Ictal onset and evolutionPDF p.9, Gelastic seizures
  • one thirdgelastic seizuresOther reported value · Cases in the cited gelastic-seizure series; exact denominator Not reported · temporal · Ictal onset and evolutionPDF p.9, Gelastic seizures
  • one thirdgelastic seizuresOther reported value · Cases in the cited gelastic-seizure series; exact denominator Not reported · frontal · Ictal onset and evolutionPDF p.9, Gelastic seizures
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • ictal laughter; gelastic automatismsThe source states that ictal laughter was relatively common in the reviewed cases but had limited localizing value.PDF p.4, Complex motor phenomena—automatisms
  • laughter and crying; mimic automatismsOne restricted-OFC case with mimic automatisms displayed a combination of laughter and crying.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 1 patientlaughter and crying; mimic automatismsCount · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • gelastic seizuresBrief laughter or grimacing with or without subjective mirth strongly suggests a hypothalamic hamartoma, although intracranial EEG and electrical-stimulation studies have identified the symptomatogenic zone in anteromesial frontal and basal temporal regions in isolated cases.PDF p.4, section 3.3 Complex motor seizures; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 7 findings · 5 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • laughter; mirthless laughterThe discussion states that two patients in the review were described as presenting with laughter or a sudden outburst of mirthless laughter.PDF p.9, Discussion
  • laughter; Table 2 versus discussion countThe source contains a direct internal discrepancy for laughter: the Table 2 result is 3/21 (14%), whereas the discussion states that two patients presented with laughter or mirthless laughter.PDF p.7, Table 2; PDF p.9, Discussion
  • Laughter (mirthless)Table 2 reports 3/21 (14%) for Laughter (mirthless); timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Laughter (mirthless)Table 2 reports 2/12 patients with Laughter (mirthless) in the prefrontal operculum group.PDF p.7, Table 2
  • Laughter (mirthless)Table 2 reports 1/9 patients with Laughter (mirthless) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Laughter (mirthless)Fisher's exact comparison of Laughter (mirthless) between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • two patientslaughter; mirthless laughterCount · Included fronto-opercular epilepsy patients described in the discussion · Included fronto-opercular epilepsy patients described in the discussion · ictalPDF p.9, Discussion
  • 3/21 (14%)Laughter (mirthless)Percentage · n/N 3/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 2/12 patientsLaughter (mirthless)Proportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 1/9 patientsLaughter (mirthless)Proportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
  • p=1Laughter (mirthless)P value · 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients · BothPDF p.7, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Gelastic seizureTable 2 associates gelastic semiology with hypothalamus, anteromesial frontal region, and basal temporal area and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 2 findings
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • gelastic seizureGelastic seizure is reserved for seizures in which laughing is the main ictal motor manifestation; the source classifies it separately because it is common in patients with hypothalamic hamartoma.PDF p.5, Complex motor seizures
  • Gelastic seizureGelastic seizures are seizures whose main motor manifestation is laughing; they may be preceded or followed by other seizure types and are classified separately because the source states that they are common in patients with hypothalamic hamartoma.PDF p.5, Complex motor seizures, Gelastic seizures; PDF p.2, Table 1
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 2 findings · 2 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 1 gelastic, singing, whistling, and verbal-automatism semiologyCase 1 was a 27-year-old right-handed woman whose seizures began at age 9 with uncontrollable laughter without associated emotion, sometimes singing or whistling, and sometimes repeated vocalizations such as “it doesn’t matter” or “no, no”; she could have a nonspecific “lucidity” warning, was usually aware with possible cognitive slowing, had nocturnal predominance without postictal deficit, and had 10–25-second seizures occurring 1–4 times per day.PDF p.8, Case 1; PDF p.8, Video-EEG data
  • gelastic seizureFor gelastic seizures without a hypothalamic hamartoma, the chapter reports seizure-onset zones in medial, inferior, or posterior temporal regions, superior or median frontal gyrus, anterior cingulate, orbitofrontal cortex, frontal operculum extending to anterior insula, and parietal lobe; temporo-basal onset is associated with subjective mirth, whereas frontal-lobe gelastic seizures lack that finding.PDF p.8, What localizations are suggested by the seizure semiology?
Reported values
  • Seizure duration 10–25 secondsCase 1 gelastic, singing, whistling, and verbal-automatism semiologyRange · Individual Case 1; 27-year-old right-handed woman, seizure onset age 9 · Ictal; aura/warning and postictal observationPDF p.8, Case 1; PDF p.8, Video-EEG data
  • Seizure frequency 1–4 per dayCase 1 gelastic, singing, whistling, and verbal-automatism semiologyRange · Individual Case 1; 27-year-old right-handed woman, seizure onset age 9 · Ictal; aura/warning and postictal observationPDF p.8, Case 1; PDF p.8, Video-EEG data
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • ictal laughterIctal laughter was reported among other non-visual symptoms in the cohort.PDF p.6, Results, Non-visual manifestations
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • gelastic seizuresThe review states that approximately 50% of cases with gelastic seizures have a hypothalamic hamartoma detectable by MRI, while extra-hypothalamic epilepsies have also been described in the anterior cingulate region and frontal, parietal, and temporal lobes.PDF p.5, Gelastic seizures
Reported values
  • Approximately 50% with MRI-detected hypothalamic hamartomagelastic seizuresPercentage · Patients with gelastic seizures; percentage denominator not reported · IctalPDF p.5, Gelastic seizures

15 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal cry / tonic vocalization (non-linguistic)Source terms: Ictal nonlinguistic vocalization; Ictal cry / tonic vocalizationReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side17 manuscripts · 45 findings · 41 reported values
Weighted evidence supportevidence weight 27.07 across 17 manuscripts · 4 manuscript weight pending · 3 independent primary study · 3 systematic review or meta-analysis · 4 structured design not resolved · 7 narrative, educational, or cited context

Non-speech vocalization occurred equally in RTL and LTL seizures, 31% versus 31%, and did not significantly lateralize temporal-lobe onset. No sign-specific lateralizing direction is reported. No lateralizing information is present. Ictal whistling is restated as non-lateralizing. The handbook lists ictal vocalization as a dominant-hemisphere sign, with a source reliability warning on one rendering. The cited review associates temporal verbal automatisms with the non-dominant language hemisphere and describes speech arrest/vocalization in cortical language areas. Cited-study restatement combines right-frontal/mesial-temporal ictal singing with nondominant-temporal ictal whistling. Comprehensible stereotyped ictal speech is described as suggesting a nondominant focus, while dominant-hemisphere lateralization of vocalizations remains controversial. The review states that pure ictal vocalizations may lateralize frontal lobe epilepsy to the left hemisphere. The cited Janszky series is restated as 9/11 pure ictal vocalizations in left frontal lobe epilepsy. No source-supported hemispheric or body-side lateralization is reported. No cerebral hemisphere or body-side direction is reported. The category definition contains no lateralizing evidence. No lateralizing direction is reported. No hemisphere or body-side direction is reported. The review reports no cerebral hemisphere or body-side direction for humming. No lateralizing direction is reported for ictal humming. No lateralizing direction is reported for humming in temporal-lobe seizures. No dominant/nondominant or sign-side lateralizing breakdown is reported for this subset. No lateralizing direction is reported for late vocalization. No lateralizing direction is reported for early automatisms or early vocalization.

Source-defined result groups 16
Localization: FrontalObserved proportion 9.5%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 29.6%RTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ 26.1% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 12.5%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelylateral temporal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given vocalization · localizing data point1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 16.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 16.9% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.9%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 7.7%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 23.3%LTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Localization: cingulateSource-defined values retained separatelycingulate localization · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given vocalization · localizing data point1 manuscript · 1 reported value · not pooled
Localization: fronto-opercular epilepsy cohortSource-defined values retained separatelyIncluded fronto-opercular epilepsy patients with propagation data · patients with propagation data1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 17

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 14 findings · 8 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • vocalization—unintelligible noisesTable 1 defines or exemplifies the the source's own semiology category “vocalization—unintelligible noises” as Grunting, mumbling, or humming, distinguished from ictal speech and dysphasia.PDF p.7, Table 1 Semiology descriptions and frequencies
  • vocalization—unintelligible noisesUnintelligible vocalization comprised 5.5% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • unintelligible vocalization; frontal lobeNon-sensical ictal vocalization was frontal in origin in 44%.PDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; frontal lobeThe 95% CI for unintelligible vocalization; frontal lobe was 35%–53%.PDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; temporal lobeNon-sensical ictal vocalization was temporal in origin in 36%.PDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; temporal lobeThe 95% CI for unintelligible vocalization; temporal lobe was 28%–45%.PDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; cingulateunintelligible vocalization semiology was cingulate in 9%.PDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; cingulateThe 95% CI for unintelligible vocalization; cingulate was 6%–13%.PDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; frontal lobeUnintelligible vocalizations had an intrinsic localizing OR of 1.5 for the frontal lobe.PDF p.8, Relative localizing values of semiologies
  • unintelligible vocalization; frontal lobeThe 95% CI for unintelligible vocalization; frontal lobe was 1.2–2.0.PDF p.8, Relative localizing values of semiologies
  • unintelligible vocalization; lateral temporalUnintelligible vocalizations had an intrinsic localizing OR of 2.8 for lateral temporal subregions.PDF p.8, Relative localizing values of semiologies
  • unintelligible vocalization; lateral temporalThe 95% CI for unintelligible vocalization; lateral temporal was 1.8–4.5.PDF p.8, Relative localizing values of semiologies
  • ictal vocalization with automatismsA cited study of 102 patients reported 91% sensitivity for detecting temporal-lobe seizures when ictal vocalizations co-occurred with automatisms.PDF p.12, Localizing probabilities
  • ictal vocalization with automatismsThe same cited study reported 70% specificity for detecting temporal-lobe seizures when ictal vocalizations co-occurred with automatisms.PDF p.12, Localizing probabilities
Reported values
  • vocalization—unintelligible noises 5.5%vocalization—unintelligible noisesPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • unintelligible vocalization; frontal lobe 44%unintelligible vocalization; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; temporal lobe 36%unintelligible vocalization; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • unintelligible vocalization; cingulate 9%unintelligible vocalization; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 1.5unintelligible vocalization; frontal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 2.8unintelligible vocalization; lateral temporalOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • sensitivity 91%ictal vocalization with automatismsSensitivity · 102 patients with ictal vocalizationPDF p.12, Localizing probabilities
  • specificity 70%ictal vocalization with automatismsSpecificity · 102 patients with ictal vocalizationPDF p.12, Localizing probabilities
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 3 findings · 3 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.5
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior early loud vocalizationEarly loud vocalization was seen in four of six typical anterior patients.PDF p.5, Clinical Presentation
  • atypical anterior early loud vocalizationEarly loud vocalization was seen in two of four atypical anterior patients.PDF p.5, Clinical Presentation
  • anterior cingulate early loud vocalization aggregateEarly loud vocalization was seen in six of 10 anterior cingulate cases.PDF p.6, Discussion
Reported values
  • 4/6 (67%) early loud vocalizationtypical anterior early loud vocalizationPercentage · n/N 4/6 · 6 typical anterior cingulate cases · ictal semiologyPDF p.5, Clinical Presentation
  • 2/4 (50%) early loud vocalizationatypical anterior early loud vocalizationPercentage · n/N 2/4 · 4 atypical anterior cingulate cases · ictal semiologyPDF p.5, Clinical Presentation
  • 6/10 early loud vocalizationanterior cingulate early loud vocalization aggregateProportion · n/N 6/10 · 10 anterior cingulate cases · ictal semiologyPDF p.6, Discussion
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • moaningMoaning did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 16.9%moaningPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 26.1%moaningPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • P=0.35moaningP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal whistlingIctal whistling is described as a rare automatism during temporal-lobe seizures that localizes to temporal-lobe origin but is not lateralizing.PDF p.3, section 2.5 Automatisms; PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 2 findings
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • ictal speech arrest, vocalization, and verbal automatismsThe review states that most seizures involving cortical language areas reduce to speech arrest or vocalization depending on the involved area and its distance from ventral central regions; verbal automatisms occur in temporal seizures and are associated with the non-dominant language hemisphere, while aphasia-like abnormal production is less frequent.PDF p.7, section 8
  • ictal hummingA low, steady, continuous tone with closed lips may occur in temporal seizures and is generally delayed after onset; cited SEEG processing associated humming with increased coherence among superior temporal gyrus, planum temporale, and inferior frontal gyrus areas 44/45, while another cited series found simultaneous ictal SPECT hyperperfusion in the same three areas.PDF p.6, section 7
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Ictal vocalization (p.2 rendered "ictal vocalization*"; p.3 rendered "Ictal vocalization")Both tables list Ictal vocalization as Dominant hemisphere; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table entry "ictal vocalization*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Ictal vocalization" (printed p.5)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Vocalization other than speechVocalization other than speech did not differ significantly between RTL and LTL seizures.PDF p.4, Table 5; PDF p.2, feature definitions
Reported values
  • RTL 16 (31%)Vocalization other than speechPercentage · n/N 16/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.4, Table 5; PDF p.2, feature definitions
  • LTL 17 (31%)Vocalization other than speechPercentage · n/N 17/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.4, Table 5; PDF p.2, feature definitions
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal speech, verbal automatisms, and ictal vocalizationsIctal vocalizations and ictal speech are reported in TLE but are not exclusive to it; comprehensible stereotyped speech, including rare second-language automatisms, suggests a nondominant-hemisphere focus, whereas the lateralizing value of vocalizations toward the dominant hemisphere remains controversial.PDF p.8, Focal impaired awareness seizures
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 4 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.778
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • vocalization in secondarily generalized seizuresFifteen of 36 vocalization seizures (40%) were secondarily generalized and vocalization was the only speech manifestation in all 15; among all 20 secondarily generalized seizures, 15 (75%) had vocalization as the only speech manifestation, while the remaining 5 had either ictal identifiable speech (2) or no speech manifestations (3).PDF p.3, Results
Reported values
  • 15/20 secondarily generalized seizures (75%) had vocalization onlyvocalization in secondarily generalized seizuresPercentage · n/N 15/20 · 36 vocalization seizures and 20 secondarily generalized seizures within the 100-seizure cohort · secondarily generalized seizures · ictal vocalization and ictal identifiable speech; no phase-specific speech manifestation was reported for the three no-speech seizuresPDF p.3, Results
  • 15/36 vocalization seizures (40%) were secondarily generalizedvocalization in secondarily generalized seizuresPercentage · n/N 15/36 · 36 vocalization seizures and 20 secondarily generalized seizures within the 100-seizure cohort · vocalization seizures · ictal vocalization and ictal identifiable speech; no phase-specific speech manifestation was reported for the three no-speech seizuresPDF p.3, Results
  • 2 secondarily generalized seizures had ictal identifiable speechvocalization in secondarily generalized seizuresCount · 36 vocalization seizures and 20 secondarily generalized seizures within the 100-seizure cohort · ictal identifiable speech · ictal vocalization and ictal identifiable speech; no phase-specific speech manifestation was reported for the three no-speech seizuresPDF p.3, Results
  • 3 secondarily generalized seizures had no speech manifestationsvocalization in secondarily generalized seizuresCount · 36 vocalization seizures and 20 secondarily generalized seizures within the 100-seizure cohort · no speech manifestations · ictal vocalization and ictal identifiable speech; no phase-specific speech manifestation was reported for the three no-speech seizuresPDF p.3, Results
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 6 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • vocalization (grunts) during seizure propagationDuring seizure propagation, vocalization in the form of grunts was observed in two patients.PDF p.6, Anatomical and clinical correlations
  • vocalization (grunts) during seizure propagationDuring seizure propagation, the source reports vocalization (grunts) in 12% of patients.PDF p.6, Anatomical and clinical correlations
  • Vocalization (grunts)Table 2 reports 2/21 (10%) for Vocalization (grunts); timing is late, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Vocalization (grunts)Table 2 reports 2/12 patients with Vocalization (grunts) in the prefrontal operculum group.PDF p.7, Table 2
  • Vocalization (grunts)Table 2 reports 0/9 patients with Vocalization (grunts) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Vocalization (grunts)Fisher's exact comparison of Vocalization (grunts) between the prefrontal and precentral Rolandic operculum groups has p=0.486.PDF p.7, Table 2
Reported values
  • 2 patients (12%)vocalization (grunts) during seizure propagationPercentage · Included fronto-opercular epilepsy patients with propagation data · Included fronto-opercular epilepsy patients with propagation data · ictal propagationPDF p.6, Anatomical and clinical correlations
  • 2/21 (10%)Vocalization (grunts)Percentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · LatePDF p.7, Table 2
  • 2/12 patientsVocalization (grunts)Proportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · LatePDF p.7, Table 2
  • 0/9 patientsVocalization (grunts)Proportion · n/N 0/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · LatePDF p.7, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • pure ictal vocalizationsPure ictal vocalizations may lateralize frontal lobe epilepsy to the left hemisphere.PDF p.9, section 4.3; PDF p.10, section 4.3 continuation
  • pure ictal vocalizationsJanszky et al. found left frontal lobe epilepsy in 9 of 11 patients with pure ictal vocalizations.PDF p.9, section 4.3; PDF p.10, section 4.3 continuation
Reported values
  • 9/11 had left frontal-lobe epilepsypure ictal vocalizationsPercentage · n/N 9/11 · 27 frontal lobe epilepsy patients seizure free after surgery · frontal-lobe epilepsy cohort · ictalPDF p.9, section 4.3; PDF p.10, section 4.3 continuation
  • 11/27 had pure ictal vocalizationspure ictal vocalizationsPercentage · n/N 11/27 · 27 frontal lobe epilepsy patients seizure free after surgery · frontal-lobe epilepsy cohort · ictalPDF p.9, section 4.3; PDF p.10, section 4.3 continuation
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 3 findings · 6 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • early vocalizationsEarly vocalizations, defined here as groaning, howling, moaning, or humming during the first half of the seizure, were more frequent in ML than M or L patients.PDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Vocal verbal and nonverbal automatisms
  • late vocalizationLate vocalization showed no statistically significant difference across M, ML, and L groups.PDF p.7, Table 5; PDF p.7, Later features
  • ictal humming and limbic-neocortical involvementThe discussion restates that a prior study of ictal humming found these automatisms when the ictal discharge involved both limbic and neocortical superior and middle temporal gyri.PDF p.8, Vocal verbal and nonverbal automatisms
Reported values
  • M 3/24 (12.5%)early vocalizationsPercentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Vocal verbal and nonverbal automatisms
  • L 1/13 (7.7%)early vocalizationsPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Vocal verbal and nonverbal automatisms
  • ML 7/18 (38.9%)early vocalizationsPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features; PDF p.8, Vocal verbal and nonverbal automatisms
  • 2/13 (15.4%)late vocalizationPercentage · n/N 2/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
  • 5/24 (20.8%)late vocalizationPercentage · n/N 5/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
  • 0/18 (0%)late vocalizationPercentage · n/N 0/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 5 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • hummingThe review reports that Bartolomei et al. (2002) studied humming in temporal-lobe seizures and found rhythmic discharge over the superior temporal gyrus at 6 or 15 Hz with increased coherence between the superior temporal gyrus and prefrontal cortex.PDF p.4, Table 1, Humming row
  • hummingIn the summarized Bartolomei et al. study, humming in temporal-lobe seizures was associated during semiologic expression with rhythmic 6-Hz or 15-Hz discharge over the superior temporal gyrus and increased coherence between the superior temporal gyrus and prefrontal cortex.PDF p.4, Table 1, Bartolomei et al. 2002 row; PDF p.11, mechanism 1
Reported values
  • rhythmic discharge at 6 or 15 HzhummingCount · 3 subjects with temporal-lobe epilepsy · Period of semiologic expressionPDF p.4, Table 1, Humming row
  • n=3 subjectshummingCount · 3 subjects with temporal-lobe epilepsy · Period of semiologic expressionPDF p.4, Table 1, Humming row
  • Auditory steady-state stimulation 6 HzhummingFrequency · 3 subjects with temporal-lobe epilepsy; number of seizures Not reported · 6-Hz condition · ictal, during semiologic expressionPDF p.4, Table 1, Bartolomei et al. 2002 row; PDF p.11, mechanism 1
  • Auditory steady-state stimulation 15 HzhummingFrequency · 3 subjects with temporal-lobe epilepsy; number of seizures Not reported · 15-Hz condition · ictal, during semiologic expressionPDF p.4, Table 1, Bartolomei et al. 2002 row; PDF p.11, mechanism 1
  • Subjects with humming paradigm n=3hummingCount · 3 subjects with temporal-lobe epilepsy; number of seizures Not reported · ictal, during semiologic expressionPDF p.4, Table 1, Bartolomei et al. 2002 row; PDF p.11, mechanism 1
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • ictal singing and ictal whistlingThe chapter reports ictal singing from the right frontal lobe, particularly prefrontal cortex and mesial temporal regions, and describes ictal whistling as a nonverbal vocalization often reported in nondominant temporal lobe epilepsy.PDF p.8, What localizations are suggested by the seizure semiology?
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • early automatisms; early vocalization; rapid medial/lateral involvementThe source reports that early automatisms and vocalization may be more frequent when medial and lateral temporal regions are involved rapidly.PDF p.5, Discussion
  • early vocalizationTable 6 reports early vocalization in 14% of the medio-lateral synthesis (evidence grade Moderate).PDF p.6, Table 6
  • early vocalizationTable 6 reports a 0–38% range for early vocalization across the medio-lateral reports (evidence grade Moderate).PDF p.6, Table 6
  • early vocalization; Maillard cohortThe review states that early vocalization occurred in 28% of Maillard's patients.PDF p.7, Discussion
Reported values
  • 14%early vocalizationPercentage · Medio-lateral temporal seizure semiology synthesis represented in Table 6 · at onsetPDF p.6, Table 6
  • range 0–38%early vocalizationPercentage Range · Medio-lateral temporal seizure semiology synthesis represented in Table 6 · at onsetPDF p.6, Table 6
  • 28%early vocalization; Maillard cohortPercentage · Maillard cohort as restated in the review · early ictal phasePDF p.7, Discussion
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 1 finding · 1 reported value
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • quick-onset vocal soundsAmong the four hypermotor patients, the source reports 2 patients with quick onset and moaning, barking, or squealing vocal sound.PDF p.4, Seizure semiology on video-EEG recording
Reported values
  • 2/4 quick-onset vocal soundsquick-onset vocal soundsProportion · n/N 2/4 · 4 patients with hypermotor seizure semiology · ictal semiologyPDF p.4, Seizure semiology on video-EEG recording
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • vocalizationTable 2 records vocalization in a seizure sequence with asymmetric tonic posturing and eye blinking.PDF p.6, Table 2 Case 2

17 contributing manuscripts; source-reported values remain separate and are not pooled.

Unilateral manual automatisms (ipsilateral fumbling, picking, patting)Source terms: Unilateral manual automatismsReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphereNo single reliable side14 manuscripts · 57 findings · 40 reported values
Weighted evidence supportevidence weight 26.69 across 14 manuscripts · 1 manuscript weight pending · 2 independent primary study · 5 narrative, educational, or cited context · 3 systematic review or meta-analysis · 3 case report or observation · 1 structured design not resolved

This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. In Case 5, right-hand automatisms were ipsilateral to the right occipital onset. A cited report states that early unilateral motor automatisms without dystonia may point contralateral to neocortical temporal onset. The review associates unilateral limb or upper-limb automatisms with an ipsilateral focus or onset, while retaining cited reports that isolated upper-limb automatisms have no lateralizing value. The handbook labels ictal unilateral automatisms as ipsilateral, with a reliability caveat in one table. Limb automatisms showed no significant lateralizing difference: bilateral and ipsilateral forms were more common than contralateral forms at onset, and after excluding automatisms constrained by contralateral posturing, ipsilateral and contralateral onset frequencies were approximately equal. The cited review describes unilateral limb automatisms as lateralizing only in relation to the opposite limb's tonic or dystonic posturing. The cited Dupont series is restated as predominantly ipsilateral automatisms in mesial TLE, exclusively contralateral automatisms in neocortical TLE, and contralateral dystonia plus ipsilateral automatisms only in mesial TLE. Case 5 had source-described right occipital onset and later bilateral hand automatisms. This record provides no seizure lateralization. No lateralizing direction is reported for the visual-aura-to-automatism phenotype. Left hand is a the source's own symptomatic body-side modifier; no cerebral hemisphere relation is supplied. Right upper limb is a the source's own symptomatic body-side modifier; no cerebral hemisphere relation is supplied. No hemisphere direction is asserted. No hemisphere or body-side direction is reported. No source-supported hemispheric lateralization is reported. No hemisphere or body-side result is reported. The semiology category definition contains no lateralization evidence. The row reports an all-data panel sample size, not lateralization evidence. The row reports a non-topological panel sample size, not lateralization evidence. No lateralizing direction is reported. No lateralization axis information is reported for oral and manual automatisms in the cingulate context. Left-hand automatisms and right version are the source's own sequence directions; no cerebral hemisphere relation is supplied. No source lateralization is reported. No cerebral side or body-side result is reported. Extremity automatisms did not differ significantly between right and left TLE (RTL 37 [71%] versus LTL 47 [85%], NS). The case reports bilateral hand fumbling/picking without cerebral-side information.

Source-defined result groups 31
Localization: TemporalSource-defined values retained separately4 diagnostic-accuracy studies comparing lateral and mesial TLE for Manual automatisms · lateral TLE versus mesial TLE · random-effects diagnostic-accuracy estimate1 manuscript · 1 reported value · not pooled
Localization: lateral temporal onset (L) / medial temporal onset (M) / medial-lateral temporal onset (ML)Observed proportion 38.9%ML; Table 4 · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLTL; bilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.9%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLTL; contralateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLTL; ipsilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyRTL; contralateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: lateral temporal onset (L) / medial temporal onset (M) / medial-lateral temporal onset (ML)Observed proportion 7.7%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyRTL; contralateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 68.5%RTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separately4 diagnostic-accuracy studies comparing lateral and mesial TLE for Manual automatisms · lateral TLE versus mesial TLE · random-effects diagnostic-accuracy estimate1 manuscript · 1 reported value · not pooled
Localization: lateral temporal onset (L) / medial temporal onset (M) / medial-lateral temporal onset (ML)Observed proportion 33.3%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Manual automatisms · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 66.7%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLTL; ipsilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 15.4%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Manual automatisms · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyRTL; bilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyRTL; ipsilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLTL; bilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Localization: lateral temporal onset (L) / medial temporal onset (M) / medial-lateral temporal onset (ML)Observed proportion 38.9%ML; prose · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 23.1%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyRTL; bilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyRTL; ipsilateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 55.6%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 64.4%LTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyLTL; contralateral · RTL versus LTL and within-group laterality patterns · seizure with extremity automatism1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 58.3%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyanterior temporal localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 14

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 12 findings · 5 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • oral and manual automatismsTable 1 defines or exemplifies the the source's own semiology category “oral and manual automatisms” as Upper-limb automatisms, automotor stereotyped distal limb movements, fiddling, pedal automatisms, lip smacking, chewing, oro-alimentary/orofacial automatisms, ictal drinking, or ictal swallowing.PDF p.7, Table 1 Semiology descriptions and frequencies
  • oral and manual automatismsOral and manual automatisms comprised 9.7% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • oral and manual automatisms; Figure 3 all-data subsetFigure 3 reports N = 2298 for the all-data oral and manual automatisms panel.PDF p.9, Figure 3 and caption
  • oral and manual automatisms; Figure 3 non-topological subsetFigure 3 reports N = 342 for the non-topological oral and manual automatisms panel.PDF p.9, Figure 3 and caption
  • oral and manual automatisms; temporal lobeOral and manual automatisms were temporal in origin in 47%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; temporal lobeThe 95% CI for oral and manual automatisms; temporal lobe was 40%–53%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; frontal lobeOral and manual automatisms were frontal in origin in 31%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; frontal lobeThe 95% CI for oral and manual automatisms; frontal lobe was 25%–36%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; cingulateoral and manual automatisms semiology was cingulate in 10%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; cingulateThe 95% CI for oral and manual automatisms; cingulate was 7%–13%.PDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; anterior temporalOral and manual automatisms had an intrinsic OR of 2.4 for the anterior temporal subregion.PDF p.8, Relative localizing values of semiologies
  • oral and manual automatisms; anterior temporalThe 95% CI for oral and manual automatisms; anterior temporal was 1.7–3.3.PDF p.8, Relative localizing values of semiologies
Reported values
  • oral and manual automatisms 9.7%oral and manual automatismsPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • oral and manual automatisms; temporal lobe 47%oral and manual automatisms; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; frontal lobe 31%oral and manual automatisms; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • oral and manual automatisms; cingulate 10%oral and manual automatisms; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 2.4oral and manual automatisms; anterior temporalOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 10 left-hand automatismsLeft-hand automatisms followed by right version were listed for patient 10.PDF p.4, Figure 3
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 3 findings
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Early unilateral motor automatisms without dystonic posturing in neocortical TLESome authors reported that early-onset unilateral motor automatisms without dystonic posturing can localize seizure origin to the contralateral temporal-lobe neocortex.PDF p.3, neocortical TLE paragraph; PDF p.4, section 4 Lateralizing Features in Temporal Lobe Epilepsy
  • Unilateral upper-limb automatismThe review table and narrative associate unilateral limb or upper-limb automatisms with an ipsilateral seizure focus or onset, but also report that some authors found no lateralizing value for upper-limb automatisms in isolation.PDF p.4, Table 2; PDF p.4, section 4 Lateralizing Features in Temporal Lobe Epilepsy
  • Hand and mouth automatisms in mesial temporal onsetAutomatisms occur in almost two thirds of CPSs of mesial temporal lobe onset and often involve the hands, including fumbling, picking, or fidgeting, or the mouth, including chewing, lip smacking, or swallowing.PDF p.3, section 2.5 Automatisms
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • behavioural arrest; manual and oral automatismsTemporal lobe seizures are described as typically comprising behavioural arrest and manual and oral automatisms in two thirds of cases, with variable loss of awareness and postictal confusion.PDF p.4, Temporal lobe seizures
Reported values
  • behavioural arrest and manual/oral automatisms in two thirdsbehavioural arrest; manual and oral automatismsProportion · temporal lobe seizure literature · ictal and postictalPDF p.4, Temporal lobe seizures
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 20 findings · 7 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • oral automatisms; manual automatisms; behavioral arrestThe source identifies oral automatisms, manual automatisms, and behavioral arrests as the most common semiologies in lateral temporal epilepsy, while noting that they likely emerge during propagation rather than at seizure onset.PDF p.1, Abstract; PDF p.4, Anatomo-clinical correlations; PDF p.8, Discussion
  • Manual automatismTable 3 reports 5 studies assessing Manual automatism.PDF p.6, Table 3
  • Manual automatismTable 3 reports 86 patients assessed for Manual automatism.PDF p.6, Table 3
  • Manual automatismTable 3 reports 15.4–80% as the percentage range or value for Manual automatism; the overall association grade is Low.PDF p.6, Table 3
  • Manual automatismTable 3 reports 1 study with onset timing for Manual automatism.PDF p.6, Table 3
  • Manual automatismTable 3 reports an onset latency of 14 s for Manual automatism.PDF p.6, Table 3
  • odds of occurrence; Manual automatismsTable 4 reports overall odds of 0.97 for occurrence of Manual automatisms in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Manual automatismsTable 4 reports a 95% confidence interval of 0.42–2.26 for the overall odds of Manual automatisms.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Manual automatismsThe heterogeneity test for the Table 4 odds estimate for Manual automatisms has p=0.0142.PDF p.7, Table 4
  • Manual automatisms; lateral versus mesial comparisonTable 5 reports 4 studies comparing Manual automatisms in lateral and mesial TLE.PDF p.9, Table 5
  • Manual automatisms; lateral TLE patient denominatorTable 5 reports 64 lateral-TLE patients assessed for Manual automatisms.PDF p.9, Table 5
  • Manual automatisms; mesial TLE patient denominatorTable 5 reports 112 mesial-TLE patients assessed for Manual automatisms.PDF p.9, Table 5
  • Manual automatisms; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 15.4–80% for Manual automatisms.PDF p.9, Table 5
  • Manual automatisms; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 25–83.9% for Manual automatisms.PDF p.9, Table 5
  • Manual automatisms; diagnostic sensitivityTable 6 reports overall sensitivity 0.45 for Manual automatisms in 4 studies comparing lateral with mesial TLE.PDF p.9, Table 6
  • Manual automatisms; diagnostic sensitivity confidence intervalTable 6 reports a 95% confidence interval of 0.22–0.70 for sensitivity of Manual automatisms.PDF p.9, Table 6
  • Manual automatisms; sensitivity heterogeneityThe heterogeneity test for sensitivity of Manual automatisms has p=0.0154.PDF p.9, Table 6
  • Manual automatisms; diagnostic specificityTable 6 reports overall specificity 0.35 for Manual automatisms in 4 studies comparing lateral with mesial TLE.PDF p.9, Table 6
  • Manual automatisms; diagnostic specificity confidence intervalTable 6 reports a 95% confidence interval of 0.17–0.60 for specificity of Manual automatisms.PDF p.9, Table 6
  • Manual automatisms; specificity heterogeneityThe heterogeneity test for specificity of Manual automatisms has p=0.0022.PDF p.9, Table 6
Reported values
  • 15.4–80%Manual automatismPercentage Range · Lateral temporal epilepsy patients assessed for Manual automatism · ictalPDF p.6, Table 3
  • median onset latency 14 sManual automatismMedian · Lateral temporal epilepsy study reporting onset timing for Manual automatism · ictal onsetPDF p.6, Table 3
  • odds 0.97odds of occurrence; Manual automatismsOdds · Lateral temporal epilepsy patients assessed for Manual automatisms · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 15.4–80%Manual automatisms; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Manual automatisms · Lateral TLE patients assessed for Manual automatisms · ictalPDF p.9, Table 5
  • 25–83.9%Manual automatisms; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Manual automatisms · Mesial TLE patients assessed for Manual automatisms · ictalPDF p.9, Table 5
  • sensitivity 0.45Manual automatisms; diagnostic sensitivitySensitivity · 4 diagnostic-accuracy studies comparing lateral and mesial TLE for Manual automatisms · 4 diagnostic-accuracy studies comparing lateral and mesial TLE for Manual automatisms · ictal sign presencePDF p.9, Table 6
  • specificity 0.35Manual automatisms; diagnostic specificitySpecificity · 4 diagnostic-accuracy studies comparing lateral and mesial TLE for Manual automatisms · 4 diagnostic-accuracy studies comparing lateral and mesial TLE for Manual automatisms · ictal sign presencePDF p.9, Table 6
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Ictal unilateral automatismsBoth tables list Ictal unilateral automatisms as Ipsilateral; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Ictal unilateral automatisms*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Ictal unilateral automatisms" (printed p.5)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 3 findings · 14 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Limb automatisms: onset and late lateralityNo significant differences in lateralization of limb automatisms at onset or late in the seizure were identified; at onset, limb automatisms were more common bilaterally and ipsilaterally than contralaterally in both groups, and after excluding ipsilateral automatisms associated with contralateral posturing, contralateral and ipsilateral automatisms were approximately equal at onset.PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • Unilateral limb automatisms in cited studiesThe current paper reports that Wada (1982) considered unilateral automatisms to have lateralizing value, whereas Kotagal et al. (1989) considered them valuable only when accompanied by tonic or dystonic posturing in the opposite limb.PDF p.5, Discussion, limb-automatisms paragraph; PDF p.6, Discussion
  • Extremity automatismsExtremity automatisms did not differ significantly between RTL and LTL seizures.PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
Reported values
  • LTL bilateral onset 20 (43%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · LTL; bilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL ipsilateral late 11 (30%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · RTL; ipsilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL ipsilateral late 18 (38%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · LTL; ipsilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL bilateral late 22 (47%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · LTL; bilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL ipsilateral onset 13 (35%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · RTL; ipsilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL contralateral onset 7 (19%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · RTL; contralateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL ipsilateral onset 19 (40%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · LTL; ipsilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL contralateral late 7 (15%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · LTL; contralateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • LTL contralateral onset 8 (17%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · LTL; contralateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL contralateral late 12 (32%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · RTL; contralateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL bilateral late 14 (58%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · RTL; bilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL bilateral onset 17 (46%)Limb automatisms: onset and late lateralityPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; limb-automatisms subset · RTL; bilateral · Ictal onset and late ictal phasePDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.6, Discussion
  • RTL 37 (71%)Extremity automatismsPercentage · n/N 37/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • LTL 47 (85%)Extremity automatismsPercentage · n/N 47/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.4, numbered clinical-feature results; PDF p.4, Table 5
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • manual automatismsTemporal-like insular seizures may include manual automatisms.PDF p.2, Clinical Features
  • hand movement to throatHand movement to the throat is among the observed signs that suggest an insular focus.PDF p.3, Video EEG
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral motor automatisms with dystonic posturingDupont et al. reported predominantly ipsilateral automatisms in mesial TLE, exclusively contralateral automatisms in neocortical TLE, and the combination of contralateral dystonia with ipsilateral automatisms only in mesial TLE.PDF p.6, section 3.9
Reported values
  • 26/60 had unilateral motor automatismsunilateral motor automatisms with dystonic posturingCount · n/N 26/60 · 60 patients with temporal lobe epilepsy, including 26 with unilateral motor automatisms · ictalPDF p.6, section 3.9
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 3 findings · 11 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • upper-limb elementary automatismsUpper-limb elementary automatisms over the whole seizure course were more frequent in M and ML than L patients.PDF p.6, Table 3; PDF p.6, General ictal characteristics
  • early upper-limb elementary automatismsEarly upper-limb elementary automatisms were reported in M and ML more often than L numerically, but the comparison was not statistically significant; the ML percentage differs between the table and prose.PDF p.6, Table 4; PDF p.6, Early features
  • late upper-limb elementary automatismsLate upper-limb elementary automatisms were more frequent in M than ML or L patients.PDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Upper-limb automatisms
Reported values
  • L 3/13 (23.1%)upper-limb elementary automatismsPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • ML 10/18 (55.6%)upper-limb elementary automatismsPercentage · n/N 10/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • M 16/24 (66.7%)upper-limb elementary automatismsPercentage · n/N 16/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • prose ML=36.9%early upper-limb elementary automatismsPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML; prose · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • p=0.13early upper-limb elementary automatismsP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • Table 4 ML=7/18 (38.9%)early upper-limb elementary automatismsPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML; Table 4 · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • M=8/24 (33.3%)early upper-limb elementary automatismsPercentage · n/N 8/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • L=1/13 (7.7%)early upper-limb elementary automatismsPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • L 2/13 (15.4%)late upper-limb elementary automatismsPercentage · n/N 2/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Upper-limb automatisms
  • M 14/24 (58.3%)late upper-limb elementary automatismsPercentage · n/N 14/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Upper-limb automatisms
  • ML 7/18 (38.9%)late upper-limb elementary automatismsPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.8, Upper-limb automatisms
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfCase report or observation · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • hand-to-eye movementA hand-to-eye movement followed the non-painful eye sensation in the Figure 2 case.PDF p.7, Figure 2
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfCase report or observation · 1 finding
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • fumbling and picking at bed clothes in Fig. 2The Figure 2 tracing labels fumbling and picking at bed clothes with both hands during seizure evolution.PDF p.14, Fig. 2
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfNarrative, educational, or cited context · 1 finding
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • psychomotor semiology: limb automatismsTypical temporal psychomotor semiology included limb automatisms.PDF p.4, Seizure semiology on video-EEG recording
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 7 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • right-hand automatismsTable 2 records right-hand automatisms in Case 5 after tachycardia and behavioral pause.PDF p.6, Table 2 Case 5
  • bilateral hand automatismsTable 2 records progression to bilateral hand automatisms in Case 5.PDF p.6, Table 2 Case 5
  • orolingual and hand automatismsOrolingual/hand automatisms occurred in 10 of 19 patients (52.6%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
  • visual aura to automatism phenotypePhenotype II is characterized primarily by oropharyngeal, limb, or verbal automatisms, with or without a preceding visual aura.PDF p.9, Phenotype II
  • left-hand automatismsTable 2 records left-hand automatisms after the Case 6 Sz1 visual aura and rightward pursuit.PDF p.6, Table 2 Case 6 Sz1
  • right-upper-limb automatismsTable 2 records right-upper-limb automatisms in Case 11 after chewing/swallowing automatisms.PDF p.7, Table 2 Case 11
Reported values
  • 10/19 (52.6%) orolingual/hand automatismsorolingual and hand automatismsPercentage · n/N 10/19 · 19 patients monitored with SEEG · ictal automatismsPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

14 contributing manuscripts; source-reported values remain separate and are not pooled.

Bilateral asymmetric tonic posturing (fencing posture / BATS)Source terms: Bilateral asymmetric tonic posturingReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side16 manuscripts · 55 findings · 75 reported values
Weighted evidence supportevidence weight 25.91 across 16 manuscripts · 2 manuscript weight pending · 2 independent primary study · 3 systematic review or meta-analysis · 2 structured design not resolved · 8 narrative, educational, or cited context · 1 case report or observation

Source reports contralateral limb posturing in a sequential occipital-onset phenotype. This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. Phenotype III occipital seizures included progression to contralateral limb tonic posturing or asymmetric tonic posturing. Bilateral asymmetric tonic posture occurred in 5/21 (24%) of the included fronto-opercular epilepsy patients. Bilateral asymmetric tonic posture occurred in 2/12 patients in the prefrontal operculum group; the source reports p=0.611 for the subgroup comparison. Bilateral asymmetric tonic posture occurred in 3/9 patients in the precentral Rolandic operculum group. Two of seven PCE patients had bilateral asymmetric tonic seizures. The review describes the common SMA seizure pattern as tonic asymmetric posturing with variable head deviation and arm flexion generally contralateral to ictal discharge. The review describes unilateral/bilateral asymmetric tonic posturing as a possible early localizing sign in SMA epilepsy because it is mostly reported at seizure onset. The review restates contralateral frontal-eye-field involvement for versive seizures and possible SMA involvement for asymmetric tonic posturing. The cited table associates asymmetric tonic limb posturing during secondary generalized tonic-clonic seizures with contralateral direction. The extended elbow was contralateral to the source-reported ictal-onset side in 35 of 39 patients with ATLP. In Group I, the extended arm was contralateral to the seizure focus in 10/12 TLE patients and 7/8 XTLE patients with ATLP. ATLP was contralateral to the source-reported side of ictal EEG onset in 17/18 Group II patients (94.4%). Group I ATLP ratings had overall kappa 0.71, TLE kappa 0.68, and XTLE kappa 0.71, with overall p<0.01 for agreement. Group II ATLP had overall kappa 0.711 with p<0.001 for interobserver agreement. ATLP was usually on the same side as version, with one complex two-direction version exception; the head was midline or returning to midline when ATLP appeared. The lower extremity was generally extended ipsilateral to the extended upper limb, except in two seizures from two patients. In two Group II patients, initial ATLP was contralateral to ictal onset, followed by bilateral upper-limb extension/clonic movements; later apparent ATLP side could change during evolution. The case depicts right occipital onset, left head-eye version and left arm extension, right-arm flexion, and later bilateral extension and clonic jerking. The single case combines a nonlateralized visual aura with right-arm extension/right head deviation, left-arm flexion, and a left occipital focal pattern during the aura. ATLP was contralateral to ictal onset in both the patient's left- and right-temporal seizure types. The cited one-arm-flexed/one-arm-extended phenomenon was reported in 9% of metrazol-induced seizures and was considered non-lateralizing. SMA seizures are restated with bilateral tonic posturing, contralateral extension/head-eye deviation, and ipsilateral flexion. The review defines the initial figure-of-4 posture as extension of the limb contralateral to the epileptogenic hemisphere with flexion of the ipsilateral limb and reports 90% correct lateralization. The cited rule lateralizes seizure onset contralateral to the initially extended tonic arm in the figure-of-4 sign. The review describes the extended limb in the figure-of-four posture as contralateral to the seizure focus. The review reports that the extended elbow in asymmetric tonic limb posturing is predominantly contralateral to seizure onset, with ipsilateral and bilateral exceptions. The cited series predominantly associated the extended elbow component with the hemisphere contralateral to seizure onset. The cited study reported asymmetric tonic limb posturing as contralateral in 70%, ipsilateral in 17%, and bilateral in 13% of affected patients. The cited study restates asymmetric tonic arm extension with opposite-arm flexion as contralateral to seizure onset in 94% of temporal-lobe-epilepsy patients. The bilateral asymmetric-tonic-posture comparison reports no cerebral-side direction. No cerebral lateralization is reported for bilateral asymmetric tonic posture. The review describes the last clonic jerk at an asymmetric generalized-seizure ending as usually ipsilateral to the seizure-onset hemisphere. No hemisphere or body-side direction is reported. No lateralizing direction is reported for asymmetric tonic posturing. No lateralizing direction is reported for asymmetric tonic posturing heterogeneity. The cited anterior-versus-posterior insular comparison provides no lateralizing information. The ventral-versus-dorsal insular focus record provides no lateralizing information. The review describes brief bilateral asymmetric motor posturing with retained awareness and no postictal confusion; no hemisphere direction is reported. No lateralizing direction is reported for ATLP occurrence. ATLP occurred in 18/26 patients; no hemisphere or body-side direction is reported. ATLP occurred in 22/64 analyzed seizures; no hemisphere or body-side direction is reported. No lateralizing direction is reported for version or ATLP. No source-supported hemispheric or body-side lateralization is reported. No lateralizing direction is reported for ATLP onset time. No lateralizing direction is reported for ATLP duration. ATLP without prior version occurred in 9/23 patients; the card calls it the only observed lateralizing sign but gives no side direction. No seizure lateralization is reported. Patient 7 had right arm and leg extension followed by right arm clonic activity.

Source-defined result groups 18
Localization: TemporalObserved proportion 100.0%Temporal-lobe seizures with secondary generalization · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 94.4%All reported · ictal EEG onset side · patient1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 83.3%TLE with ATLP · XTLE · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / IpsilateralSource-defined values retained separatelyAll reported · ATLP side versus version side and EEG laterality · instance1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 87.5%XTLE with ATLP · TLE · patient1 manuscript · 1 reported value · not pooled
Lateralization: BilateralObserved proportion 28.6%All reported · hypermotor, dialeptic, and automotor seizures · patients1 manuscript · 1 reported value · not pooled
Lateralization: ATLP interobserver agreementSource-defined values retained separatelyOverall · TLE and XTLE subgroup agreement · observer rating1 manuscript · 1 reported value · not pooled
Lateralization: BilateralObserved proportion 16.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: BilateralObserved proportion 33.3%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Lateralization: ATLP interobserver agreementSource-defined values retained separatelyAll reported · observer ratings1 manuscript · 1 reported value · not pooled
Lateralization: ATLP interobserver agreementSource-defined values retained separatelyTLE · TLE and XTLE subgroup agreement · observer rating1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / ContralateralSource-defined values retained separatelyAll reported · Initial ATLP side versus later clonic/postural asymmetry · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / IpsilateralSource-defined values retained separatelyGroup II with ATLP and version · ATLP side versus version side and EEG laterality · patient1 manuscript · 1 reported value · not pooled
Lateralization: ATLP interobserver agreementSource-defined values retained separatelyXTLE · TLE and XTLE subgroup agreement · observer rating1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 89.7%All reported · ictal-onset side · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 89.7%asymmetric tonic limb posturing · non-contralateral · case1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%Primary GTC seizures · seizure1 manuscript · 1 reported value · not pooled
Lateralization: BilateralObserved proportion 23.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 16

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 7 asymmetric right tonicAsymmetric tonic right arm and leg extension followed by right arm clonic activity was listed for patient 7.PDF p.4, Figure 3
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 5 findings · 2 reported values
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • asymmetric tonic posturingThe discussion identifies asymmetric tonic posturing as a possible early localizing sign in SMA epilepsy because it is mostly reported at seizure onset.PDF p.8, Discussion
  • asymmetric tonic posturingTable 3 lists 17 patients for the the source's own ictal symptom “asymmetric tonic posturing”; its table phase label is onset.PDF p.6, Table 3
  • asymmetric tonic posturingTable 3 reports a pooled prevalence of 47% for the the source's own ictal symptom “asymmetric tonic posturing”; its table phase label is onset.PDF p.6, Table 3
  • asymmetric tonic posturing; between-study heterogeneityThe source reports I2 heterogeneity of 33.49% for pooled asymmetric tonic posturing prevalence.PDF p.4, Results
  • asymmetric tonic posturing; heterogeneity testThe source reports p = 0.07 for the between-study heterogeneity test of pooled asymmetric tonic posturing prevalence.PDF p.4, Results
Reported values
  • 47% pooled prevalenceasymmetric tonic posturingPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
  • I2 = 33.49%asymmetric tonic posturing; between-study heterogeneityHeterogeneity I2 · Patients with SMA or pre-SMA epilepsy in the selected studies · ictal symptom prevalence analysisPDF p.4, Results
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • supplementary motor area tonic asymmetric posturingThe review describes the common SMA seizure pattern as tonic asymmetric posturing with variable head deviation and arm flexion generally contralateral to ictal discharge; arm-raising and fencing postures are described as rare.PDF p.3, section 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • supplementary motor area seizure; fencing postureSupplementary motor area seizures are characterized by asymmetric bilateral tonic posturing, with or without impaired awareness, sometimes with contralateral upper-limb extension and ipsilateral upper-limb flexion in a fencing posture plus contralateral head and eye deviation; sensory tingling or tightness may precede the motor signs.PDF p.3, Supplementary motor area; PDF p.4, Supplementary motor area
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdfStructured design not resolved · 1 finding · 1 reported value
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.423
The study enrolled seven consecutive PCE patients; six had SEEG-identified posterior cingulate ictal onset and one had an MRI-identified postcingulate tumour. Four patients underwent CCEP. SEEG and scalp EEG were retrospectively analyzed with video-documented ictal semiology; the source used the Lüders seizure-classification scheme. The posterior cingulate was operationally defined caudal to the vertical posterior commissure line.
Findings
  • bilateral asymmetric tonic seizures in PCETwo of seven PCE patients had bilateral asymmetric tonic seizures.PDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
Reported values
  • 2/7 bilateral asymmetric tonic seizuresbilateral asymmetric tonic seizures in PCEProportion · n/N 2/7 · 7 PCE patients · ictal semiologyPDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • asymmetric tonic limb posturing or figure-4 signAsymmetric tonic limb posturing is a figure-4 posture in which the elbow contralateral to the epileptogenic hemisphere is extended and the ipsilateral limb flexes over the chest during the tonic phase of an SGTCS. The sign provides correct lateralization in 90% of cases, is most common in temporal-lobe seizures, and can change sides, so only its initial appearance should be used for lateralization.PDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
Reported values
  • Correct lateralization in 90% of casesasymmetric tonic limb posturing or figure-4 signPercentage · patients with secondarily generalized tonic-clonic seizures · initial tonic phase of SGTCSPDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • asymmetric tonic limb posturing (“figure-of-4” sign)During the tonic phase of a focal to bilateral tonic-clonic seizure, asymmetric tonic limb posturing, also called the “figure-of-4” sign, is described as contralateral to the seizure focus.PDF p.9, Focal to bilateral tonic-clonic seizures
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Bilateral asymmetric tonic postureTable 2 reports 5/21 (24%) for Bilateral asymmetric tonic posture; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Bilateral asymmetric tonic postureTable 2 reports 2/12 patients with Bilateral asymmetric tonic posture in the prefrontal operculum group.PDF p.7, Table 2
  • Bilateral asymmetric tonic postureTable 2 reports 3/9 patients with Bilateral asymmetric tonic posture in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Bilateral asymmetric tonic postureFisher's exact comparison of Bilateral asymmetric tonic posture between the prefrontal and precentral Rolandic operculum groups has p=0.611.PDF p.7, Table 2
Reported values
  • 5/21 (24%)Bilateral asymmetric tonic posturePercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 2/12 patientsBilateral asymmetric tonic postureProportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 3/9 patientsBilateral asymmetric tonic postureProportion · n/N 3/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 3 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Versive seizures and asymmetric tonic posturingThe review states that electrical stimulation of M1 and SMA produces myoclonic, tonic, clonic, tonic-clonic, or version responses; versive seizures indicate contralateral frontal eye field involvement, and asymmetric tonic posturing can indicate SMA involvement.PDF p.4, section 1.6
  • Asymmetric tonic limb posturingTable 3 associates asymmetric tonic limb posturing during secondary generalized tonic-clonic seizures with SSMA and precentral area and lists contralateral lateralisation.PDF p.4, Table 3
  • Brief bilateral asymmetric motor posturing with retained awarenessThe review states that seizures with brief bilateral asymmetric motor posturing, retained awareness, and no postictal confusion may indicate SMA semiology and may lack clear surface EEG manifestations.PDF p.7, section 1.18
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 25 findings · 49 reported values
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.903
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • asymmetric tonic limb posturing (ATLP) / “Figure 4 Sign”The article summary reports that the extended elbow was contralateral to the side of ictal onset in 35 of 39 patients who had ATLP during their seizures.PDF p.1, Summary—Results
  • extended arm in ATLPIn Group I, the extended arm was contralateral to the seizure focus in 10 of 12 TLE patients (83.3%) and 7 of 8 XTLE patients (87.5%) with ATLP.PDF p.3, Table 1—Patients with ATLP contralateral to focus; PDF p.3, Results—Group I; PDF p.6, Conclusion
  • ATLPIn Group II, ATLP was contralateral to the side of ictal EEG onset in 17 of 18 patients (94.4%) with ATLP.PDF p.3, Table 1—Patients with ATLP contralateral to focus; PDF p.3, Results—Group II; PDF p.6, Conclusion
  • ATLP interobserver agreementGroup I ATLP ratings had an overall kappa of 0.71, with kappa 0.68 in TLE and 0.71 in XTLE; the overall result was reported as p<0.01.PDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group I
  • ATLP interobserver agreementGroup II ATLP had a kappa score of 0.711 overall, reported as p<0.001.PDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group II
  • ATLP following head and eye versionAt the time of ATLP, the head was midline or returning to midline from version in all instances, and ATLP was on the same side as version in all but one Group II patient; the exception had left version followed by right version, right ATLP, and generalized clonic movements, with EEG higher over the left hemisphere.PDF p.3, Other characteristics of ATLP—item 2
  • ATLP limb configurationThe extended arm was usually in front of the trunk and occasionally raised; the flexed arm could be in front of or behind it; the lower extremity on the same side as the extended arm was also extended except in two seizures from two patients.PDF p.3, Other characteristics of ATLP—item 3; PDF p.4, Other characteristics of ATLP—item 4
  • ATLP changing sides during seizure evolutionIn two Group II patients, initial ATLP was contralateral to ictal onset, followed by bilateral upper-limb extension and clonic movements more prominent on the initial-ATLP side; the source states that initial ATLP was contralateral and that each patient showed the same ATLP side in all seizures with the phenomenon.PDF p.4, Other characteristics of ATLP—item 6; PDF p.5, Fig. 3 caption and images
  • ATLP in Figure 1Figure 1 depicts a secondarily generalized GTC seizure beginning in the right occipital region; after head/eye version to the left and return to midline, the left arm was tonically extended and the right arm flexed, followed by bilateral extension and clonic jerking.PDF p.2, Fig. 1 image and caption
  • ATLP in Figure 2Figure 2 depicts right-arm tonic extension with left-arm flexion in a patient whose seizures had a nonlateralized visual aura followed by right head deviation and secondary generalization; a focal seizure pattern was seen in the left occipital region during the aura.PDF p.2, Fig. 2 image and caption
  • ATLP with independent temporal onsetsIn an anecdotal patient with independent seizure onsets from the left and right temporal lobes, ATLP was contralateral to the side of ictal onset in both seizure types.PDF p.4, Anecdotal information
  • “asymmetrical generalized seizure” / asymmetric arm posturingThe article reports that Ajmone-Marsan and Ralston described one arm flexed and the other extended at the elbow in metrazol-induced seizures; it was seen in 9% and was thought not to have lateralizing significance.PDF p.5, Discussion
  • ATLPIn Group I seizures progressing to secondary generalization, ATLP occurred in 12 of 16 TLE patients (75%) and 8 of 15 XTLE patients (53.3%).PDF p.2, Results—Group I; PDF p.3, Table 1—Number of patients with ATLP in GTC seizures
  • ATLPIn Group I, ATLP appeared in 19 of 27 analyzed GTC seizures from TLE patients (70.3%) and 10 of 32 from XTLE patients (31.2%).PDF p.3, Table 1—Number of seizures showing ATLP
  • ATLPIn Group II, ATLP occurred in 18 of 26 patients (69.2%).PDF p.3, Results—Group II; PDF p.5, Discussion
  • ATLPIn Group II, 22 of 64 analyzed GTC or generalized clonic seizures showed ATLP (34.3%).PDF p.3, Table 1—Number of seizures showing ATLP
  • ATLP and versionTable 1 reports patient-level joint version/ATLP categories as TLE: version+ATLP 8/16, version without ATLP 1/16, ATLP without version 4/16, neither 3/16; XTLE: 4/15, 4/15, 4/15, 3/15; Group II: 10/26, 12/26, 9/26, 0, respectively.PDF p.3, Table 1—Version and ATLP
  • ATLP in every GTC seizureTable 1 reports ATLP in every GTC seizure for 10/12 TLE patients (83.3%), 6/8 XTLE patients (75%), and 2/26 Group II patients (7.6%).PDF p.3, Table 1—Patients who had ATLP in every GTC seizure
  • ATLP onset timeATLP appeared at a median of 23.5 seconds from clinical onset (range 4-108); onset was 28.5 seconds in TLE (range 11-108) versus 22.5 seconds in XTLE (range 4-52), without a statistically significant difference.PDF p.3, Results—ATLP timing
  • ATLP durationMedian ATLP duration was 10 seconds in XTLE patients (range 2-20) versus 4.5 seconds in temporal patients (range 2-20), without a statistically significant difference.PDF p.3, Results—ATLP duration; PDF p.6, Discussion
  • ATLP without prior versionIn Group II patients with partial-onset seizures evolving to GTC seizures, ATLP occurred without prior version in 9 of 23 patients (39.1%) and was the only observed lateralizing sign in those cases.PDF p.4, Other characteristics of ATLP—item 5; PDF p.5, Discussion; PDF p.1, Summary—Conclusions
  • ATLP in temporal epilepsy versus primary GTC in JMEIn an anecdotal patient with both JME and temporal lobe epilepsy, ATLP occurred in four temporal-lobe complex-partial seizures with secondary generalization but not in two primary GTC seizures.PDF p.4, Anecdotal information; PDF p.5, Discussion
  • ATLP in prior partial-onset seizure studyThe authors state that a previous study had noticed ATLP during partial-onset seizures progressing to secondary generalized tonic-clonic seizures.PDF p.1, Introduction
  • asymmetric tonic limb posturing and supplementary motor area seizuresThe article states that asymmetric tonic posturing of the limbs is typically observed in supplementary motor area seizures.PDF p.6, Discussion
  • asymmetric tonic posturing and SMA stimulationThe article states that asymmetric tonic posturing of the limbs can be reproduced with electrical stimulation of the supplementary motor area.PDF p.6, Discussion
Reported values
  • 35 of 39 patientsasymmetric tonic limb posturing (ATLP) / “Figure 4 Sign”Count · n/N 35/39 · Patients with ATLP across the two analyzed groups; aggregate construction Not reported · Tonic phase of a secondarily generalized GTC seizurePDF p.1, Summary—Results
  • 10/12 (83.3%)extended arm in ATLPPercentage · n/N 10/12 · Group I patients with ATLP; TLE and XTLE subgroups · TLE with ATLP · Tonic phase of secondarily generalized GTC seizuresPDF p.3, Table 1—Patients with ATLP contralateral to focus; PDF p.3, Results—Group I; PDF p.6, Conclusion
  • 7/8 (87.5%)extended arm in ATLPPercentage · n/N 7/8 · Group I patients with ATLP; TLE and XTLE subgroups · XTLE with ATLP · Tonic phase of secondarily generalized GTC seizuresPDF p.3, Table 1—Patients with ATLP contralateral to focus; PDF p.3, Results—Group I; PDF p.6, Conclusion
  • 17/18 patients (94.4%)ATLPPercentage · n/N 17/18 · Group II patients with ATLP · Tonic phase of GTC seizuresPDF p.3, Table 1—Patients with ATLP contralateral to focus; PDF p.3, Results—Group II; PDF p.6, Conclusion
  • TLE ATLP kappa 0.68ATLP interobserver agreementKappa · Group I observer ratings of ATLP presence/absence and side; TLE and XTLE subgroups · TLEPDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group I
  • XTLE ATLP kappa 0.71ATLP interobserver agreementKappa · Group I observer ratings of ATLP presence/absence and side; TLE and XTLE subgroups · XTLEPDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group I
  • Overall ATLP kappa 0.71ATLP interobserver agreementKappa · Group I observer ratings of ATLP presence/absence and side; TLE and XTLE subgroups · OverallPDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group I
  • p<0.001ATLP interobserver agreementP value · Group II observer ratings of ATLP presence/absence and sidePDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group II
  • kappa 0.711ATLP interobserver agreementKappa · Group II observer ratings of ATLP presence/absence and sidePDF p.3, Table 1—Kappa index for ATLP; PDF p.3, Results—Group II
  • Head midline or returning to midline at ATLP in all instancesATLP following head and eye versionPercentage · Group II patients with ATLP and version; one symptomatic generalized epilepsy exception is described · ATLP after version and before generalized clonic movementsPDF p.3, Other characteristics of ATLP—item 2
  • ATLP on same side as version in all but one Group II patientATLP following head and eye versionPercentage · Group II patients with ATLP and version; one symptomatic generalized epilepsy exception is described · Group II with ATLP and version · ATLP after version and before generalized clonic movementsPDF p.3, Other characteristics of ATLP—item 2
  • two seizuresATLP limb configurationCount · ATLP observations; exact subgroup Not reported · exceptions to same-side lower-extremity extension · Tonic phase of ATLPPDF p.3, Other characteristics of ATLP—item 3; PDF p.4, Other characteristics of ATLP—item 4
  • two patientsATLP limb configurationCount · ATLP observations; exact subgroup Not reported · patients contributing lower-extremity exceptions · Tonic phase of ATLPPDF p.3, Other characteristics of ATLP—item 3; PDF p.4, Other characteristics of ATLP—item 4
  • 2 patientsATLP changing sides during seizure evolutionCount · Two Group II patients with ATLP that changed side during seizure evolution · Initial ATLP followed by bilateral tonic extension and clonic phasePDF p.4, Other characteristics of ATLP—item 6; PDF p.5, Fig. 3 caption and images
  • within-patient side consistency stated qualitativelyATLP changing sides during seizure evolutionCount · Two Group II patients with ATLP that changed side during seizure evolution · Initial ATLP followed by bilateral tonic extension and clonic phasePDF p.4, Other characteristics of ATLP—item 6; PDF p.5, Fig. 3 caption and images
  • 9% of metrazol-induced seizures“asymmetrical generalized seizure” / asymmetric arm posturingPercentage · Metrazol-induced seizures in the cited reportPDF p.5, Discussion
  • XTLE patients with ATLP 8/15 (53.3%)ATLPPercentage · n/N 8/15 · Group I surgical patients with seizures progressing to secondary generalization; TLE and XTLE subgroups · XTLE · Tonic phase of secondarily generalized GTC seizuresPDF p.2, Results—Group I; PDF p.3, Table 1—Number of patients with ATLP in GTC seizures
  • TLE patients with ATLP 12/16 (75%)ATLPPercentage · n/N 12/16 · Group I surgical patients with seizures progressing to secondary generalization; TLE and XTLE subgroups · TLE · Tonic phase of secondarily generalized GTC seizuresPDF p.2, Results—Group I; PDF p.3, Table 1—Number of patients with ATLP in GTC seizures
  • 19/27 (70.3%)ATLPPercentage · n/N 19/27 · Group I analyzed secondarily generalized GTC seizures; TLE and XTLE subgroups · TLE · Tonic phase of secondarily generalized GTC seizuresPDF p.3, Table 1—Number of seizures showing ATLP
  • 10/32 (31.2%)ATLPPercentage · n/N 10/32 · Group I analyzed secondarily generalized GTC seizures; TLE and XTLE subgroups · XTLE · Tonic phase of secondarily generalized GTC seizuresPDF p.3, Table 1—Number of seizures showing ATLP
  • 18/26 patients (69.2%)ATLPPercentage · n/N 18/26 · Group II prospectively collected patients with GTC or generalized clonic seizures · Tonic phase of GTC seizuresPDF p.3, Results—Group II; PDF p.5, Discussion
  • 22/64 seizures (34.3%)ATLPPercentage · n/N 22/64 · Group II analyzed seizures · Tonic phase of GTC or generalized clonic seizuresPDF p.3, Table 1—Number of seizures showing ATLP
  • XTLE Version + ATLP 4/15ATLP and versionPercentage · n/N 4/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; Version + ATLPPDF p.3, Table 1—Version and ATLP
  • Group II Version + ATLP 10/26ATLP and versionPercentage · n/N 10/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; Version + ATLPPDF p.3, Table 1—Version and ATLP
  • XTLE ATLP without version 4/15ATLP and versionPercentage · n/N 4/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; ATLP without versionPDF p.3, Table 1—Version and ATLP
  • TLE ATLP without version 4/16ATLP and versionPercentage · n/N 4/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; ATLP without versionPDF p.3, Table 1—Version and ATLP
  • XTLE Neither 3/15ATLP and versionPercentage · n/N 3/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; NeitherPDF p.3, Table 1—Version and ATLP
  • TLE Neither 3/16ATLP and versionPercentage · n/N 3/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; NeitherPDF p.3, Table 1—Version and ATLP
  • TLE Version + ATLP 8/16ATLP and versionPercentage · n/N 8/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; Version + ATLPPDF p.3, Table 1—Version and ATLP
  • Group II Version without ATLP 12/26ATLP and versionPercentage · n/N 12/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; Version without ATLPPDF p.3, Table 1—Version and ATLP
  • TLE Version without ATLP 1/16ATLP and versionPercentage · n/N 1/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; Version without ATLPPDF p.3, Table 1—Version and ATLP
  • Group II Neither 0/26ATLP and versionPercentage · n/N 0/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; NeitherPDF p.3, Table 1—Version and ATLP
  • XTLE Version without ATLP 4/15ATLP and versionPercentage · n/N 4/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; Version without ATLPPDF p.3, Table 1—Version and ATLP
  • Group II ATLP without version 9/26ATLP and versionPercentage · n/N 9/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; ATLP without versionPDF p.3, Table 1—Version and ATLP
  • 2/26 (7.6%)ATLP in every GTC seizurePercentage · n/N 2/26 · Patients with Group I TLE, Group I XTLE, or Group II GTC seizures as represented in Table 1 · Group II · Tonic phase of GTC seizuresPDF p.3, Table 1—Patients who had ATLP in every GTC seizure
  • 6/8 (75%)ATLP in every GTC seizurePercentage · n/N 6/8 · Patients with Group I TLE, Group I XTLE, or Group II GTC seizures as represented in Table 1 · Group I XTLE · Tonic phase of GTC seizuresPDF p.3, Table 1—Patients who had ATLP in every GTC seizure
  • 10/12 (83.3%)ATLP in every GTC seizurePercentage · n/N 10/12 · Patients with Group I TLE, Group I XTLE, or Group II GTC seizures as represented in Table 1 · Group I TLE · Tonic phase of GTC seizuresPDF p.3, Table 1—Patients who had ATLP in every GTC seizure
  • XTLE range 4–52 sATLP onset timeRange · Patients/seizures with ATLP; TLE and XTLE comparison · XTLE · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • TLE median 28.5 sATLP onset timeMedian · Patients/seizures with ATLP; TLE and XTLE comparison · TLE · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • TLE range 11–108 sATLP onset timeRange · Patients/seizures with ATLP; TLE and XTLE comparison · TLE · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • Wilcoxon rank-sum p=0.46ATLP onset timeP value · Patients/seizures with ATLP; TLE and XTLE comparison · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • XTLE median 22.5 sATLP onset timeMedian · Patients/seizures with ATLP; TLE and XTLE comparison · XTLE · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • overall median 23.5 sATLP onset timeMedian · Patients/seizures with ATLP; TLE and XTLE comparison · overall · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • overall range 4–108 sATLP onset timeRange · Patients/seizures with ATLP; TLE and XTLE comparison · overall · Onset of ATLP during a secondarily generalized GTC seizurePDF p.3, Results—ATLP timing
  • XTLE median ATLP duration 10 seconds (range 2–20)ATLP durationMedian · Patients/seizures with ATLP; XTLE and temporal comparison · XTLE · ATLP during secondarily generalized GTC seizurePDF p.3, Results—ATLP duration; PDF p.6, Discussion
  • TLE median ATLP duration 4.5 seconds (range 2–20)ATLP durationMedian · Patients/seizures with ATLP; XTLE and temporal comparison · TLE · ATLP during secondarily generalized GTC seizurePDF p.3, Results—ATLP duration; PDF p.6, Discussion
  • 9/23 patients (39.1%)ATLP without prior versionPercentage · n/N 9/23 · Group II patients with partial-onset seizures evolving to GTC seizures · ATLP during evolution to secondary generalizationPDF p.4, Other characteristics of ATLP—item 5; PDF p.5, Discussion; PDF p.1, Summary—Conclusions
  • ATLP in temporal-lobe seizures with secondary generalization 4/4ATLP in temporal epilepsy versus primary GTC in JMEPercentage · n/N 4/4 · One anecdotal patient with JME and temporal lobe epilepsy, excluded from Groups I and II · Temporal-lobe seizures with secondary generalization · Secondary generalization versus primary GTC seizurePDF p.4, Anecdotal information; PDF p.5, Discussion
  • ATLP in primary GTC seizures 0/2ATLP in temporal epilepsy versus primary GTC in JMEPercentage · n/N 0/2 · One anecdotal patient with JME and temporal lobe epilepsy, excluded from Groups I and II · Primary GTC seizures · Secondary generalization versus primary GTC seizurePDF p.4, Anecdotal information; PDF p.5, Discussion
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 5 findings · 15 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Asymmetric tonic limb posturing (figure-of-4 sign)The review describes asymmetric tonic limb posturing before bilateral tonic arm posturing as a lateralizing sign in which the extended elbow is usually contralateral to seizure onset; Table 1 summarizes 17.7% in temporal and 15% in extratemporal lobe epilepsy and 89% contralateral.PDF p.5, section 3.6 Asymmetric tonic limb posturing; PDF p.5, section 3.6.1 Mechanism; PDF p.12, Table 1
  • Asymmetric tonic limb posturing (figure-of-4 sign)Kotagal et al. retrospectively reviewed 59 secondary generalized tonic-clonic seizures in 31 patients seizure free after surgery and prospectively analyzed 64 seizures in 26 patients; the extended elbow was contralateral to seizure onset in 35 of 39 cases.PDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Asymmetric tonic limb posturingTrinka et al. noted asymmetric tonic limb posturing in 23 of 57 retrospectively and prospectively reviewed patients; it was contralateral in 70%, ipsilateral in 17%, and bilateral in 13%, with P < 0.001.PDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Asymmetric tonic arm extension with opposite arm flexionJobst et al. described asymmetric tonic arm extension with opposite arm flexion and found it contralateral in 94% of patients with temporal lobe epilepsy and documented seizure freedom 12 months after surgery.PDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Last clonic jerk and asymmetric endingThe review describes asymmetric ending of a generalized tonic-clonic seizure, particularly a last clonic jerk ipsilateral to the hemisphere of seizure onset, as a lateralizing sign with high reported observer agreement in the cited series.PDF p.5, section 3.4 Significance of last clonic jerk
Reported values
  • 15%Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · extratemporal lobe epilepsy · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.12, Table 1
  • 17.7%Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · temporal lobe epilepsy · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.12, Table 1
  • 35 of 39 (89%)Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · n/N 35/39 · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · asymmetric tonic limb posturing · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing; PDF p.5, section 3.6.1 Mechanism; PDF p.12, Table 1
  • 26 prospective patientsAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · prospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 64 prospective seizuresAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · prospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • extended elbow contralateral in 35/39 casesAsymmetric tonic limb posturing (figure-of-4 sign)Percentage · n/N 35/39 · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 59 retrospective seizuresAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · retrospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 31 retrospective patientsAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · retrospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • ATLP bilateral 13% of affected patientsAsymmetric tonic limb posturingPercentage · 57 patients with temporal lobe epilepsy · Bilateral · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • ATLP ipsilateral 17% of affected patientsAsymmetric tonic limb posturingPercentage · 57 patients with temporal lobe epilepsy · Ipsilateral · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • ATLP contralateral 70% of affected patientsAsymmetric tonic limb posturingPercentage · 57 patients with temporal lobe epilepsy · Contralateral · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Patients with ATLP 23/57Asymmetric tonic limb posturingPercentage · n/N 23/57 · 57 patients with temporal lobe epilepsy · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 94% contralateralAsymmetric tonic arm extension with opposite arm flexionPercentage · Patients with temporal lobe epilepsy and documented seizure freedom 12 months after surgery · Early tonic phase of secondary generalized seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Table 1 does not list this signLast clonic jerk and asymmetric endingCount · n/N 25/30 · Patients with mesial or temporal lobe epilepsy and generalized tonic-clonic seizures · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • specific series are reported in F012 and F013Last clonic jerk and asymmetric endingCount · n/N 25/30 · Patients with mesial or temporal lobe epilepsy and generalized tonic-clonic seizures · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • figure of 4 sign; asymmetric tonic limb posturingThe current paper reports that figure of 4 has been described as having approximately 90% contralateral lateralizing value and attributes to the original Kotagal report the rule that the initial tonic arm extension is the component to use because a later figure of 4 may appear on the opposite side.PDF p.7, figure of 4 definition and cited value; PDF p.8, cited initial-component rule; PDF p.12, discussion of the source definition
Reported values
  • Approximately 90% contralateral lateralizing valuefigure of 4 sign; asymmetric tonic limb posturingPercentage · Cited source population as summarized in the current paper; Not reported · Beginning of the tonic phase of a secondary generalized tonic-clonic seizurePDF p.7, figure of 4 definition and cited value; PDF p.8, cited initial-component rule; PDF p.12, discussion of the source definition
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • focal nonmotor unaware seizures; hyperkinetic features; asymmetric tonic posturing; elementary facial contractionsThe source relates more ventrally located insular foci to focal nonmotor unaware seizures and more dorsally located foci to motor manifestations caused by propagation toward frontal areas, including often sleep-related hyperkinetic features, asymmetric tonic posturing, or elementary facial contractions; patients are frequently unaware of these manifestations.PDF p.5, Ictal Semiology; PDF p.16, Summary
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 1 reported value
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • bilateral asymmetric tonic postureBilateral asymmetric tonic posture occurred in two patients.PDF p.4, Results—Seizure semiology; PDF p.10, Discussion
Reported values
  • 2/22 (9%)bilateral asymmetric tonic posturePercentage · n/N 2/22 · 22 patients with insulo-opercular epilepsy · ictal complex motor behaviorPDF p.4, Results—Seizure semiology; PDF p.10, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 3 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • asymmetric tonic posturingPhenotype III includes progression to asymmetric tonic posturing.PDF p.9, Phenotype III

16 contributing manuscripts; source-reported values remain separate and are not pooled.

Motionless stare / ictal behavioral arrest (hypomotor onset)Source terms: Motionless stare / behavioral arrest; Motionless stare / ictal behavioral arrestReported: Dominant hemisphereAlso reported: Right hemisphere14 manuscripts · 26 findings · 19 reported values
Weighted evidence supportevidence weight 25.55 across 14 manuscripts · 1 manuscript weight pending · 2 independent primary study · 7 narrative, educational, or cited context · 3 systematic review or meta-analysis · 1 structured design not resolved · 1 case report or observation

A right middle frontal gyrus lesion case had left-face/left-arm clonic spread and fencing posture, with semiology and ictal EEG interpreted as right frontocentral onset. The supplied evidence identifies the subsequent contraversion as directed contralateral to the hemisphere of seizure onset. No lateralization is reported for the behavioral-arrest phenotype. The study-specific ≥3-second definition reports no hemisphere or body-side direction. This finding provides no lateralization information. The TL-versus-T+ comparison provides no lateralization information. No hemisphere direction is asserted. This finding provides no hemispheric lateralization information. No source-supported hemispheric or body-side lateralization is reported. The educational duration description provides no lateralizing direction. The co-occurrence analysis provides no lateralization information. No lateralizing direction is reported for motionless staring. No cerebral hemisphere or body-side direction is reported. The PNES differential-diagnosis statement supplies no lateralizing direction. No lateralizing direction is reported. No lateralizing direction is reported for the staring observation.

Source-defined result groups 5
Localization: TemporalObserved proportion 100.0%Staring with automatisms · quiet staring versus staring with automatisms before contraversion · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 32.2% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyQuiet staring; extratemporal origin · Temporal origin · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyQuiet staring; temporal origin · Extratemporal origin · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ 43.5% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 14

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfNarrative, educational, or cited context · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • posterior cingulate staring and automatisms cited caseThe discussion cites a lesional posterior cingulate case with seizures characterized by staring and automatisms.PDF p.7, Discussion
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • staringStaring did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • T+ 43.5%staringPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • P=0.34staringP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • TL 32.2%staringPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 7 findings · 6 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • staring or behavioral arrestStaring or behavioral arrest was reported in 42% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Staring/Behavioral Arrest (Table 3)Table 3 reports staring or behavioral arrest in 35 cases (42%), more during propagation.PDF p.6, Table 3
  • Staring/Behavioral Arrest (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports staring or behavioral arrest in 17 cases (28%).PDF p.7, Table 4
  • staring/behavioral arrest plus pleasant sensationThe co-occurrence analysis identified staring/behavioral arrest with pleasant sensation in 22% of the 18-patient detailed-data set.PDF p.7, Figure 2 discussion
  • motionless staring in HS (Mirandola study)Motionless staring occurred in 20 HS patients (81%) in the cited comparison.PDF p.7, cited-study discussion
  • motionless staring in basal temporal/PIT group (Mirandola study)Motionless staring occurred in 6 PIT patients (43%) in the cited comparison.PDF p.7, cited-study discussion
  • motionless staring group comparison (Mirandola study)The cited comparison of motionless staring between HS and PIT groups is reported as statistically significant at p<.05.PDF p.7, cited-study discussion
Reported values
  • 42% staring/behavioral arreststaring or behavioral arrestPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 35 cases (42%)Staring/Behavioral Arrest (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 17/60 (28%)Staring/Behavioral Arrest (Table 4)Percentage · n/N 17/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
  • 22% co-occurrencestaring/behavioral arrest plus pleasant sensationPercentage · 18 patients with detailed semiology data · ictal; timing not otherwise reportedPDF p.7, Figure 2 discussion
  • 81% (n = 20)motionless staring in HS (Mirandola study)Percentage · source-reported HS group; the preceding sentence describes 36 HS patients, which is not used as this statistic's denominator · ictalPDF p.7, cited-study discussion
  • 6/14 patients (43%)motionless staring in basal temporal/PIT group (Mirandola study)Percentage · n/N 6/14 · 14 PIT-lesion patients in the cited Mirandola comparison · ictalPDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Initial motionless stareTable 1 reports an initial motionless stare as common in temporal lobe seizures and less common in frontal lobe seizures.PDF p.2, Table 1
  • Behavioural arrest and staring with altered consciousnessCPSs are described as associated with altered consciousness and amnesia, typically with behavioural arrest and staring lasting 30 seconds to 1–2 minutes.PDF p.2, section 2.3 Altered Consciousness
Reported values
  • 30 seconds to 1–2 minutesBehavioural arrest and staring with altered consciousnessCount · Patients with CPSs as described in the review; no single cohort reported. · IctalPDF p.2, section 2.3 Altered Consciousness
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • aura; behavioural arrest; left-face clonic activity; fencing postureIn an illustrative 50-year-old man with a right middle frontal gyrus cystic lesion, a seizure evolved from an aura to behavioural arrest, left-face clonic movements spreading over the left arm, and left-arm extension in a fencing posture before secondary generalisation; the authors state that the semiology and ictal EEG supported right frontocentral onset.PDF p.3, Video case 1 and Figure 1; PDF p.3, Figure 2 caption
  • behavioural arrest; manual and oral automatismsTemporal lobe seizures are described as typically comprising behavioural arrest and manual and oral automatisms in two thirds of cases, with variable loss of awareness and postictal confusion.PDF p.4, Temporal lobe seizures
Reported values
  • behavioural arrest and manual/oral automatisms in two thirdsbehavioural arrest; manual and oral automatismsProportion · temporal lobe seizure literature · ictal and postictalPDF p.4, Temporal lobe seizures
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 1 finding
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • oral automatisms; manual automatisms; behavioral arrestThe source identifies oral automatisms, manual automatisms, and behavioral arrests as the most common semiologies in lateral temporal epilepsy, while noting that they likely emerge during propagation rather than at seizure onset.PDF p.1, Abstract; PDF p.4, Anatomo-clinical correlations; PDF p.8, Discussion
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Behavioural arrest with preserved posterior dominant alphaThe review states that behavioural arrest with preserved posterior dominant alpha rhythm and no other EEG abnormality is virtually always indicative of PNES, while behavioural arrest spells may otherwise show subtle midline rhythmic EEG slowing.PDF p.7, section 1.18
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Hypomotor seizureHypomotor seizures are defined by decreased or absent motor activity without new motor manifestations and are used exclusively when consciousness cannot be tested during or after the seizure, including in newborns, infants, and severely mentally retarded patients; the source states that consciousness is probably altered in many such patients but may be preserved in a few.PDF p.5, Special seizures, Hypomotor seizures; PDF p.2, Table 1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfNarrative, educational, or cited context · 1 finding
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • staring or behavioral arrest in neocortical temporal lobe seizuresThe discussion restates that staring or behavioral arrest had been reported as the most common manifestation of neocortical temporal lobe seizures, but not as a discriminating feature between medial and lateral temporal lobe seizures.PDF p.8, Initial loss of contact
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfCase report or observation · 1 finding
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • eyes staring in Fig. 2The Figure 2 tracing labels eyes staring during the illustrated depth-recorded seizure.PDF p.14, Fig. 2
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • hypomotor seizuresThe review limits the term hypomotor seizures to patients in whom consciousness cannot be tested during or after the seizure and states that, in focal epilepsy, these seizures occur most frequently in temporal and parietal lobe epilepsy.PDF p.5, Hypomotor seizures
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfNarrative, educational, or cited context · 1 finding
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • psychomotor semiology: staringTypical temporal psychomotor semiology included staring.PDF p.4, Seizure semiology on video-EEG recording
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 5 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • behavioral-arrest onset phenotypePhenotype V begins with behavioral arrest and progresses to oculomotor or motor signs, including limb tonic or hypermotor activity, with a tendency to evolve into GTCS.PDF p.9, Phenotype V
  • behavioral arrest operational definitionThe source operationalizes behavioral arrest as sustained cessation of ongoing voluntary behavior, including speech and limb movement, with reduced responsiveness lasting at least three seconds on synchronized video-EEG/SEEG review.PDF p.9, Phenotype V
  • behavioral arrest from posterior midline involvementThe authors associate early PCu/PCC involvement with initial behavioral arrest in Phenotype V.PDF p.14, Phenotype V discussion
  • motor arrest and staringTable 2 records motor arrest or staring as an early seizure sign in multiple cases.PDF p.6, Table 2 cases 1, 4, and 5
  • staring with unresponsivenessTable 2 records staring with unresponsiveness after oropharyngeal automatisms and eye blinking.PDF p.6, Table 2 Case 1 Sz2
Reported values
  • reduced responsiveness lasting ≥3 secondsbehavioral arrest operational definitionThreshold · Phenotype V seizure classification · early ictal semiologyPDF p.9, Phenotype V
wyllie1986.pdfStructured design not resolved · 1 finding · 7 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.893
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • quiet staring and staring with automatisms before contraversionQuiet staring preceded contraversion for 8 versive seizures for 2-31 seconds (mean 17), while staring with automatisms preceded contraversion for 18 seizures for 4-227 seconds (mean 34); all seizures with automatisms before contraversion originated in temporal lobes, whereas the quiet-staring subgroup arose from temporal (25%) and extratemporal (75%) locations.PDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
Reported values
  • Quiet staring before contraversion 8/61 (13%)quiet staring and staring with automatisms before contraversionPercentage · n/N 8/61 · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring-with-automatisms duration mean 34 seconds (range 4–227)quiet staring and staring with automatisms before contraversionMean · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring subgroup temporal origin 25%quiet staring and staring with automatisms before contraversionPercentage · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring; temporal origin · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring-with-automatisms subgroup temporal origin 18/18quiet staring and staring with automatisms before contraversionPercentage · n/N 18/18 · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring duration mean 17 seconds (range 2–31)quiet staring and staring with automatisms before contraversionMean · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring subgroup extratemporal origin 75%quiet staring and staring with automatisms before contraversionPercentage · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring; extratemporal origin · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring with automatisms before contraversion 18/61 (30%)quiet staring and staring with automatisms before contraversionPercentage · n/N 18/61 · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion

14 contributing manuscripts; source-reported values remain separate and are not pooled.

Sensory auraReported: Contralateral10 manuscripts · 26 findings · 17 reported values
Weighted evidence supportevidence weight 24.06 across 10 manuscripts · 1 manuscript weight pending · 3 narrative, educational, or cited context · 4 systematic review or meta-analysis · 2 independent primary study · 1 structured design not resolved

Seven of 18 patients had sensory auras contralateral to the resected side. The educational statement gives no hemisphere or body-side direction for focal aware or focal sensory auras. No hemisphere or body-side relationship is reported. The study and patient counts report no hemisphere direction. The study or patient count reports no hemisphere direction. The sensory-aura prevalence supplies no hemisphere direction. The lateral-TLE sensory-aura prevalence supplies no hemisphere direction. The mesial-TLE sensory-aura prevalence supplies no hemisphere direction. The basal-temporal sensory-sensation prevalence reports no hemisphere direction. The Table 3 sensory prevalence reports no hemisphere direction. The restricted basal-temporal subset prevalence reports no hemisphere direction. No hemisphere-direction relationship is reported. No body-side, hemisphere, or dominance direction is reported. No hemisphere or body-side relationship is assigned. The heterogeneity-test p value has no lateralization content. The multimodal aura clue reports no hemisphere direction. No seizure lateralization is reported. The review places fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo between lateral and medial temporal patterns. The term medio-lateral describes temporal network organization, not hemisphere laterality. The term medio-lateral describes a temporal network, not hemisphere laterality.

Source-defined result groups 11
Localization: SMA / pre-SMASource-defined values retained separatelyAll reported · patients with the ictal symptom1 manuscript · 1 reported value · not pooled
Localization: medio-lateral temporal network / temporo-lateral region / temporo-mesial regionSource-defined values retained separatelyAll reported · Table 6 point estimate 33% · Table 6 between-report frequency range1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 38.9%All reported · ipsilateral resected side · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalSource-defined values retained separatelyExtrafrontal SHE · Frontal SHE · patient1 manuscript · 1 reported value · not pooled
Localization: orbitofrontal cortex-restricted EZNObserved proportion 11.5%OFC-restricted EZN cases · patients with sensory phenomena1 manuscript · 1 reported value · not pooled
Localization: ParietalObserved proportion 38.9%All reported · ipsilateral resected side · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalSource-defined values retained separatelyExtrafrontal SHE · Operculoinsular SOZ · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalSource-defined values retained separatelyFrontal SHE · Extrafrontal SHE · patient1 manuscript · 1 reported value · not pooled
Localization: medio-lateral temporal network / temporo-lateral region / temporo-mesial regionSource-defined values retained separatelyAll reported · other Table 6 medio-lateral sign frequencies · Table 6 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalObserved proportion 75.0%Frontal SHE · frontal versus extrafrontal focal sensory onset · sensory manifestation1 manuscript · 1 reported value · not pooled
Localization: Frontal / ParietalSource-defined values retained separatelyExtrafrontal SHE · Parietal SOZ near postcentral gyrus · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 10

Alphabetical by manuscript.

asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • sensory auras contralateral to resected sideSeven patients had sensory auras contralateral to the resected side.PDF p.2, Results
Reported values
  • 7/18 (38.8%) contralateral sensory aurassensory auras contralateral to resected sidePercentage · n/N 7/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • sensory sensationsSensory sensations were reported in 27% of patients.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Sensory (Table 3)Table 3 reports sensory symptoms in 22 cases (27%), with timing marked onset/propagation uncertain.PDF p.6, Table 3
  • Sensory (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports sensory symptoms in 15 cases (25%).PDF p.7, Table 4
  • sensory symptomsThe review characterizes sensory symptoms as rare and visual symptoms as infrequently observed in basal temporal seizures.PDF p.8, Discussion
Reported values
  • 27% sensory sensationssensory sensationsPercentage · reviewed basal temporal seizure patients · ictal onset/propagation uncertain in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 22 cases (27%)Sensory (Table 3)Percentage · Table 3 basal temporal seizure cases · onset/propagation?PDF p.6, Table 3
  • 15/60 (25%)Sensory (Table 4)Percentage · n/N 15/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 5 findings · 2 reported values
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • sensory phenomena; sensory aura; paresthesiaSensory phenomena associated with SMA epilepsy may be diffuse and poorly localized, including nonspecific cephalic sensations, paresthesia, or a sense of impending movement.PDF p.7, Discussion
  • sensory phenomenaTable 3 lists 8 patients for the the source's own ictal symptom “sensory phenomena”; its table phase label is onset.PDF p.6, Table 3
  • sensory phenomenaTable 3 reports a pooled prevalence of 11% for the the source's own ictal symptom “sensory phenomena”; its table phase label is onset.PDF p.6, Table 3
  • sensory phenomena; between-study heterogeneityThe source reports I2 heterogeneity of 0.00% for pooled sensory phenomena prevalence.PDF p.5, Results
  • sensory phenomena; heterogeneity testThe source reports p = 0.59 for the between-study heterogeneity test of pooled sensory phenomena prevalence.PDF p.5, Results
Reported values
  • 11% pooled prevalencesensory phenomenaPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
  • I2 = 0.00%sensory phenomena; between-study heterogeneityHeterogeneity I2 · Patients with SMA or pre-SMA epilepsy in the selected studies · ictal symptom prevalence analysisPDF p.5, Results
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • sensory phenomenaSensory phenomena were reported in three of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 3/26 (11.6%)sensory phenomenaPercentage · n/N 3/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 8 findings · 3 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Sensory auraTable 3 reports 1 studies assessing Sensory aura.PDF p.6, Table 3
  • Sensory auraTable 3 reports 15 patients assessed for Sensory aura.PDF p.6, Table 3
  • Sensory auraTable 3 reports 6.7% as the percentage range or value for Sensory aura; the overall association grade is Low.PDF p.6, Table 3
  • Sensory aura; lateral versus mesial comparisonTable 5 reports 1 studies comparing Sensory aura in lateral and mesial TLE.PDF p.9, Table 5
  • Sensory aura; lateral TLE patient denominatorTable 5 reports 15 lateral-TLE patients assessed for Sensory aura.PDF p.9, Table 5
  • Sensory aura; mesial TLE patient denominatorTable 5 reports 31 mesial-TLE patients assessed for Sensory aura.PDF p.9, Table 5
  • Sensory aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 6.7% for Sensory aura.PDF p.9, Table 5
  • Sensory aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 16.1% for Sensory aura.PDF p.9, Table 5
Reported values
  • 6.7%Sensory auraPercentage · Lateral temporal epilepsy patients assessed for Sensory aura · ictalPDF p.6, Table 3
  • 6.7%Sensory aura; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Sensory aura · Lateral TLE patients assessed for Sensory aura · ictalPDF p.9, Table 5
  • 16.1%Sensory aura; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Sensory aura · Mesial TLE patients assessed for Sensory aura · ictalPDF p.9, Table 5
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 5 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 4.62 · 2 × 1.5 × 1.54
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • focal sensory onsetFocal sensory onset occurred in 14% of frontal SHE and 39% of extrafrontal SHE. In frontal SHE, 9/12 sensory manifestations were associated with a small lesion in the precentral gyrus or supplementary motor area (SMA). In extrafrontal SHE, sensory onset was associated with a parietal SOZ near the postcentral gyrus (n=5) or an operculoinsular SOZ (n=12).PDF p.5, section 3.3; PDF p.6, section 3.3
Reported values
  • Frontal focal sensory onset 14%focal sensory onsetPercentage · Frontal and extrafrontal SHE patients in the 115-patient SOZ-defined semiology cohort · Frontal SHE · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, section 3.3
  • Extrafrontal sensory onset with parietal SOZ near postcentral gyrus n=5focal sensory onsetCount · Frontal and extrafrontal SHE patients in the 115-patient SOZ-defined semiology cohort · Extrafrontal SHE · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, section 3.3
  • Frontal sensory manifestations associated with precentral gyrus or SMA lesion 9/12focal sensory onsetPercentage · n/N 9/12 · Frontal and extrafrontal SHE patients in the 115-patient SOZ-defined semiology cohort · Frontal SHE · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, section 3.3
  • Extrafrontal sensory onset with operculoinsular SOZ n=12focal sensory onsetCount · Frontal and extrafrontal SHE patients in the 115-patient SOZ-defined semiology cohort · Extrafrontal SHE · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, section 3.3
  • Extrafrontal focal sensory onset 39%focal sensory onsetPercentage · Frontal and extrafrontal SHE patients in the 115-patient SOZ-defined semiology cohort · Extrafrontal SHE · early nonmotor seizure onsetPDF p.5, section 3.3; PDF p.6, section 3.3
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfNarrative, educational, or cited context · 1 finding
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • focal aware and focal sensory auras across regionsThe authors state that auras classified in the latest ILAE seizure classification as focal aware or focal sensory seizures can be seen in seizures arising from both temporal and extratemporal regions.PDF p.5, Discussion
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfStructured design not resolved · 1 finding
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • pure sensory hallucinations and dreamy stateThe authors distinguish pure sensory illusions or hallucinations from complex or mnemonic experiential phenomena, interpreting pure sensory hallucinations as related to a neocortical epileptogenic network and dreamy state as tending to a network including temporolimbic structures.PDF p.9, Trends toward other electroclinical correlations, Dreamy state
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • co-occurring sensory aurasCo-occurrence of somatosensory, auditory, gustatory, and/or olfactory auras is presented as a clue to ictal insular involvement because the insula is described as an important multimodal integrative sensory area.PDF p.5, Ictal Semiology; PDF p.13, What localizations are suggested by the seizure semiology?
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 2 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • fear; auditory hallucinations; gustatory hallucinations; sensory hallucinations; vertigoThe source describes fear, auditory or gustatory hallucinations, sensory hallucinations, and vertigo as intermediate features between lateral and medial temporal patterns.PDF p.5, Discussion
  • sensory hallucinationsTable 6 reports sensory hallucinations in 33% of the medio-lateral synthesis (evidence grade Low).PDF p.6, Table 6
  • sensory hallucinationsTable 6 reports a 33–33% range for sensory hallucinations across the medio-lateral reports (evidence grade Low).PDF p.6, Table 6
Reported values
  • 33%sensory hallucinationsPercentage · Medio-lateral temporal seizure semiology synthesis represented in Table 6 · earlyPDF p.6, Table 6
  • range 33–33%sensory hallucinationsPercentage Range · Medio-lateral temporal seizure semiology synthesis represented in Table 6 · earlyPDF p.6, Table 6

10 contributing manuscripts; source-reported values remain separate and are not pooled.

Unilateral tonic posturingReported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphere10 manuscripts · 14 findings · 57 reported values
Weighted evidence supportevidence weight 22.82 across 10 manuscripts · 3 narrative, educational, or cited context · 3 independent primary study · 3 systematic review or meta-analysis · 1 case report or observation

The cited synthesis reports rare ipsilateral tonic motor signs during frontal-lobe seizures and relates them to frontal stimulation findings. Cerebral lateralization: these signs are contralateral to seizure onset; target lobe is not differentiated by these signs alone. Unilateral tonic posturing is reported as contralateral to the epileptogenic zone, with lobar-subgroup variation. The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. Patient 8 had sudden stiffening of the left arm with oral automatisms. The review restates contralateral unilateral tonic posturing with different ranges in TLE and EXTLE cohorts. The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. The review restates a generally contralateral but cohort-variable lateralization pattern for unilateral tonic activity. The cited frontal-lobe series is summarized as contralateral unilateral tonic posturing in 89% of cases. No source lateralization is reported. The source reports a unilateral body-side modifier but no body-side distribution and no cerebral hemisphere.

Source-defined result groups 16
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyEXTLE · TLE · patient1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyfrontal · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelytemporal · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · case1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyTLE · EXTLE · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyoccipital · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyoverall · incorrect direction · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyparietal · other lobar subgroups · sign-positive occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 10

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 8 left-arm stiffening and oral automatismsSudden stiffening of the left arm and oral automatisms were listed for patient 8.PDF p.4, Figure 3
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • ipsilateral tonic motor signThe source states that ipsilateral tonic motor signs have been reported during frontal lobe seizures and that this is consistent with frontal-lobe electrical stimulation results.PDF p.8, Motor signs
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • unilateral tonic changesUnilateral tonic changes were reported in 25% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Unilateral tonic (Table 3)Table 3 reports unilateral tonic signs in 21 cases (25%), more during propagation.PDF p.6, Table 3
  • Unilateral tonic (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports unilateral tonic signs in 9 cases (15%).PDF p.7, Table 4
Reported values
  • 25% unilateral tonic changesunilateral tonic changesPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 21 cases (25%)Unilateral tonic (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 9/60 (15%)Unilateral tonic (Table 4)Percentage · n/N 9/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionThe review describes unilateral clonic movements, unilateral tonic or dystonic posturing, and early forced head version as robust lateralising motor signs with positive predictive value greater than 80%, and states that these signs are contralateral to the side of seizure onset.PDF p.10, Lateralising signs
Reported values
  • positive predictive value >80%unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionPositive predictive value · focal seizure literature · ictal onset/early ictalPDF p.10, Lateralising signs
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 16 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Unilateral tonicUnilateral tonic posturing had moderate inter-observer agreement and a 77% contralateral PPV overall, with a lower PPV in frontal than temporal, parietal, or occipital epilepsy.PDF p.3, Table 1; PDF p.3, §5.1
Reported values
  • 3 patientsUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · frontal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 patientsUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · parietal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 33% PPVUnilateral tonicPositive predictive value · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · frontal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 3 seizuresUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · parietal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • kappa 0.56Unilateral tonicKappa · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · overall · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 100% PPVUnilateral tonicPositive predictive value · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · parietal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 11 seizuresUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · temporal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 100% PPVUnilateral tonicPositive predictive value · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · occipital · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 14 patientsUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · overall sign-positive occurrences · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 6 seizuresUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · frontal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 77% overall PPVUnilateral tonicPositive predictive value · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · overall · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 2 seizuresUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · occipital · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 91% PPVUnilateral tonicPositive predictive value · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · temporal · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 1 patientsUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · occipital · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 22 seizuresUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · overall sign-positive occurrences · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 8 patientsUnilateral tonicCount · Sign-positive occurrences included 22 seizures in 14 patients overall; temporal 11 seizures/8 patients, frontal 6/3, parietal 3/2, and occipital 2/1. · temporal · IctalPDF p.3, Table 1; PDF p.3, §5.1
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • unilateral tonic posturingUnilateral tonic posturing occurred in 17% of TLE cases and 15% of EXTLE cases; it was contralateral to the epileptogenic zone in 40–86% of TLE patients and 67–89% of EXTLE patients.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • Contralateral to EZ in TLE patients 40%–86%unilateral tonic posturingRange · TLE and EXTLE cases or patients, with the source using both terms · TLE · ictal motorPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • Unilateral tonic posturing in TLE cases 17%unilateral tonic posturingPercentage · TLE and EXTLE cases or patients, with the source using both terms · TLE · ictal motorPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • Contralateral to EZ in EXTLE patients 67%–89%unilateral tonic posturingRange · TLE and EXTLE cases or patients, with the source using both terms · EXTLE · ictal motorPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • Unilateral tonic posturing in EXTLE cases 15%unilateral tonic posturingPercentage · TLE and EXTLE cases or patients, with the source using both terms · EXTLE · ictal motorPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal motor (unilateral tonic)Focal motor (unilateral tonic) semiology was absent as initial semiology (0/61, 0%) and occurred in 11/61 individuals (18%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • 11/61 (18%) combinedFocal motor (unilateral tonic)Percentage · n/N 11/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • 0/61 (0%) initialFocal motor (unilateral tonic)Percentage · n/N 0/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 7 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Unilateral tonic activityThe review describes unilateral tonic activity as potentially lateralizing but not uniformly predictive across studies; its table summarizes 48.1% in frontal lobe epilepsy and 89% contralateral, with the supplementary motor area and other motor structures proposed as symptomatogenic regions.PDF p.5, section 3.5 Unilateral tonic activity; PDF p.5, section 3.5.1 Mechanism; PDF p.12, Table 1
  • Unilateral tonic posturingIn a series of patients with frontal lobe epilepsy, Janszky et al. found unilateral tonic posturing contralateral to the seizure focus in 89% of cases.PDF p.5, section 3.5 Unilateral tonic activity; PDF p.12, Table 1
  • Unilateral tonic seizureWerhahn et al. selected 123 patients with 170 tonic seizures from 481 consecutive patients with focal epilepsy; among 24 patients with a known epileptogenic zone and unilateral tonic seizures, a blinded observer always classified the epileptogenic zone correctly.PDF p.5, section 3.5 Unilateral tonic activity
Reported values
  • Unilateral tonic activity in 48.1% of frontal-lobe epilepsy patientsUnilateral tonic activityPercentage · Patients with focal, temporal, extratemporal, or frontal lobe epilepsy · Frontal lobe epilepsy · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity; PDF p.5, section 3.5.1 Mechanism; PDF p.12, Table 1
  • 89% contralateralUnilateral tonic posturingPercentage · Patients with frontal lobe epilepsy · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity; PDF p.12, Table 1
  • 170 tonic seizuresUnilateral tonic seizureCount · 123 patients with 170 tonic seizures selected from 481 consecutive patients with focal epilepsy; 24 with known zone and unilateral tonic seizures · selected 123 patients · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • 24 patientsUnilateral tonic seizureCount · n/N 24/123 · 123 patients with 170 tonic seizures selected from 481 consecutive patients with focal epilepsy; 24 with known zone and unilateral tonic seizures · known epileptogenic zone and unilateral tonic seizures · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • always classified correctlyUnilateral tonic seizureOther reported value · 123 patients with 170 tonic seizures selected from 481 consecutive patients with focal epilepsy; 24 with known zone and unilateral tonic seizures · known-zone unilateral-tonic subgroup · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • 123 patientsUnilateral tonic seizureCount · n/N 123/481 · 123 patients with 170 tonic seizures selected from 481 consecutive patients with focal epilepsy; 24 with known zone and unilateral tonic seizures · selected 123 patients · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • 481 consecutive patientsUnilateral tonic seizureCount · 123 patients with 170 tonic seizures selected from 481 consecutive patients with focal epilepsy; 24 with known zone and unilateral tonic seizures · source focal-epilepsy population · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 1 finding · 24 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction

10 contributing manuscripts; source-reported values remain separate and are not pooled.

Speech automatismsReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere12 manuscripts · 28 findings · 56 reported values
Weighted evidence supportevidence weight 22.82 across 12 manuscripts · 5 independent primary study · 2 case report or observation · 4 narrative, educational, or cited context · 1 systematic review or meta-analysis

The case observation records right-sided version during habitual partial seizures. Coprolalia and related verbal automatisms have limited lateralizing value toward the nondominant hemisphere and can arise from either hemisphere. The cited Hadidane-series restatement reports verbal automatisms in 54% of right-sided basal temporal seizures versus 11% of left-sided seizures, with p=0.001. Among 100 patients, dysphasia was reported with 30 left-sided versus 4 right-sided resections, speech automatisms with 16 left-sided versus 22 right-sided resections, and no speech disturbance with 14 left-sided versus 19 right-sided resections. Among 23 patients with speech automatisms, 13 were associated with the presumed recessive temporal lobe and 10 with the dominant temporal lobe; selected utterance types showed 11 recessive-side versus 4 dominant-side instances. Among 23 speech-automatism patients, 7 had exclusive-right, 14 bilateral, 1 exclusive-left, and 1 normal interictal EEG; bilateral discharges were right-predominant in 6 and left-predominant in 8. Postoperative speech automatisms persisted in 3/6 patients with continued seizures after dominant temporal-lobe removal and in none of 9 after right-sided resection; the continuing cases had recessive-temporal spike foci. The primary study reports relatively frequent slight left hemicranial diminution in paroxysmal dysphasia and speculates about left posterior temporal speech mechanisms; hemicranial-side context for speech automatisms remained mixed. The cited Bingley restatement reports speech automatism in 6/24 unilateral dominant-focus patients versus 10/17 unilateral recessive-focus patients, with 25% versus 56% when emphasized bilateral foci are included and significance reported at 0.01; 29/74 cases were reported overall. The case had a consistently right sphenoidal EEG focus during recurrent psychomotor seizures; the later left-arm abduction is retained as a separate event feature. The cited Serafetinides and Falconer study restatement reports 7 exclusive-right, 14 bilateral, 1 exclusive-left, and 1 normal EEG among 23 speech-automatism patients. Verbal automatisms were more frequent in the medial-lateral temporal subgroup than in medial or lateral subgroups, with an unquantified nonsignificant trend toward right temporal lateralization. The primary result reports a nonsignificant trend toward right temporal lateralization of verbal automatisms: 31.3% right temporal versus 15.4% left temporal. Speech automatism occurred more often with right- than left-hemisphere EEG-defined foci, 10 cases versus 3, with P<0.05. A cited case restatement describes speech automatism reproduced by right-amygdalar stimulation with right temporal sharp activity. The review preserves conflicting cited left- and right-hemisphere dominance associations while reporting that the current study favored right-hemisphere foci. The review proposes that speech automatism may involve non-temporal or occasionally leftward regions distant from the temporal lobe, without a settled hemispheric direction. No lateralizing direction is reported for the visual-aura-to-automatism phenotype. No hemisphere or body-side direction is reported. The primary TL-versus-T+ verbal-automatism comparison provides no lateralization information. The OFC-restricted EZN review statement reports no hemisphere or lateralization direction. This finding provides no lateralization information. No lateralization axis information is reported for speech automatisms during atypical absence seizures. The review's reactive-automatism classification provides no side or lateralization direction. The primary result distinguishes paroxysmal dysphasia from ictal speech automatism without reporting a hemisphere or lateralization direction. No lateralization axis information is reported for the occipital-plus organization summary. No lateralization axis information is reported for the cited paroxysmal dysphasia and ictal speech-automatism frequency.

Source-defined result groups 12
Localization: TemporalSource-defined values retained separatelyright temporal · right versus left temporal lobe1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Right hemisphereObserved proportion 4.3%exclusive left-sided · Exclusive right-sided versus bilateral versus exclusive left-sided interictal discharges; normal EEG · patient/case as source labels1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Right hemisphereObserved proportion 60.9%bilateral · Exclusive right-sided versus bilateral versus exclusive left-sided interictal discharges; normal EEG · patient/case as source labels1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphere / Right hemisphereObserved proportion 0.0%continued seizures after right-sided resection · dominant temporal-lobe removal · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Right hemisphereSource-defined values retained separatelyleft-predominant bilateral · Exclusive right-sided versus bilateral versus exclusive left-sided interictal discharges; normal EEG · patient/case as source labels1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyleft temporal · right versus left temporal lobe1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft temporal · right versus left temporal lobe1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Right hemisphereSource-defined values retained separatelyright-predominant bilateral · Exclusive right-sided versus bilateral versus exclusive left-sided interictal discharges; normal EEG · patient/case as source labels1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphere / Right hemisphereObserved proportion 50.0%continued seizures after dominant temporal-lobe removal · right-sided resection · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyright temporal · right versus left temporal lobe1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Right hemisphereObserved proportion 30.4%exclusive right-sided · Exclusive right-sided versus bilateral versus exclusive left-sided interictal discharges; normal EEG · patient/case as source labels1 manuscript · 1 reported value · not pooled
Localization: OFC-involving seizure casesSource-defined values retained separatelyAll reported · patients with coprolalia1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 12

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • verbal automatismsVerbal automatisms did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 20.3%verbal automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • P=0.4verbal automatismsP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • T+ 13%verbal automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • verbal automatisms (Hadidane study)The review reports verbal automatisms in 54% of right-sided basal temporal seizures in the cited Hadidane series.PDF p.7, cited-study discussion; PDF p.9, Discussion
Reported values
  • 54% right-sided basal temporal seizuresverbal automatisms (Hadidane study)Percentage · right-sided basal temporal seizures in the cited Hadidane series · right-sided seizures · ictalPDF p.7, cited-study discussion; PDF p.9, Discussion
  • 11% left-sided basal temporal seizuresverbal automatisms (Hadidane study)Percentage · left-sided basal temporal seizures in the cited Hadidane series · left-sided seizures · ictalPDF p.7, cited-study discussion; PDF p.9, Discussion
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • OFC group (EZN restricted to OFC); hyperkinetic behavior; verbal automatisms; sleep-related seizuresThe source characterizes seizures with an EZN restricted to the OFC as having a relatively sparse semiological profile, mainly hyperkinetic behavior and verbal automatisms, often associated with sleep.PDF p.5, Semiological profiles; PDF p.7, Conclusion
  • coprolalia; verbal automatismsCoprolalia was documented in one patient in the reviewed OFC-involving literature.PDF p.5, Vocal automatisms
Reported values
  • 1 patientcoprolalia; verbal automatismsCount · OFC-involving seizure cases · ictalPDF p.5, Vocal automatisms
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfNarrative, educational, or cited context · 2 findings · 5 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • speech automatismsThe source reports that Serafetinides and Falconer studied 23 patients with speech automatisms: 7 had exclusively right-sided discharges, 14 bilateral discharges, 1 exclusively left-sided discharge, and 1 a normal EEG.PDF p.5, Discussion
  • paroxysmal dysphasia and ictal speech automatismsThe source reports that, after excluding speech arrest and vocalization, Serafetinides and Falconer found paroxysmal dysphasia and ictal speech automatisms in 67% of their patients.PDF p.5, Discussion
Reported values
  • 1 exclusively left-sidedspeech automatismsCount · 23 patients with speech automatisms in the cited Serafetinides and Falconer series · exclusively left-sided · ictal/automatisms; exact phase not otherwise reported in this restatementPDF p.5, Discussion
  • 7 exclusively right-sidedspeech automatismsCount · 23 patients with speech automatisms in the cited Serafetinides and Falconer series · exclusively right-sided · ictal/automatisms; exact phase not otherwise reported in this restatementPDF p.5, Discussion
  • 1 normal EEGspeech automatismsCount · 23 patients with speech automatisms in the cited Serafetinides and Falconer series · normal EEG · ictal/automatisms; exact phase not otherwise reported in this restatementPDF p.5, Discussion
  • 14 bilateralspeech automatismsCount · 23 patients with speech automatisms in the cited Serafetinides and Falconer series · bilateral · ictal/automatisms; exact phase not otherwise reported in this restatementPDF p.5, Discussion
  • 67% of patients with paroxysmal dysphasia and/or ictal speech automatismsparoxysmal dysphasia and ictal speech automatismsPercentage · Patients in the cited Serafetinides and Falconer series; exact denominator not reported in this passage · paroxysmal/ictal according to the cited phenomenon namesPDF p.5, Discussion
ictal-speech-disturbance-cerebral-dominance.pdfIndependent primary study · 4 findings · 10 reported values
ictal-speech-disturbance-cerebral-dominance.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
The authors collected about 43 cases with ictal speech disturbances over 8 years. Interictal EEG was examined at least twice per case; laterality was defined by a spike or sharp-wave focus, unilateral dominant spike or sharp wave, or unilateral slow wave corresponding to same-region brain damage or tumor. Laterality was confirmed in 36 cases; 7 cases with independent foci, no laterality, or normal findings were excluded. The statistical report concerns 34 right-handed epileptics because 2 left-handed patients could not be tested statistically. A control pool comprised 243 right-handed patients with unilateral abnormal EEG findings, 136 left and 117 right, and was assessed by t test.
Findings
  • speech automatismSpeech automatism occurred significantly more often with right-hemisphere than left-hemisphere EEG-defined foci in the reported right-handed epileptic cases, 10 cases versus 3, with P<0.05.PDF p.3, Results, Table I; PDF p.5, Discussion and Summary item 2
  • speech automatismThe current article reports a cited case in which speech automatism was reproduced by electrical stimulation of the right amygdalar area after cortical exposure, with right temporal sharp activity also recognized; the patient had one attack.PDF p.5, Discussion paragraph beginning “Driver and his coworkers”
  • speech automatism and cerebral dominanceThe authors summarize conflicting prior reports: two cited reports associate speech automatism with left-hemisphere dominance, while two others suggest right-hemisphere dominance is necessary; the present study found significantly more right-hemisphere foci.PDF p.5, Discussion opening paragraph; PDF p.5, Summary item 2
  • speech automatismThe authors propose that speech automatism may occur when pathological excitation does not spread to speech areas during a confusional state, and that it may arise from regions other than the temporal lobe, including occasionally leftward regions distant from the temporal lobe.PDF p.5, Discussion paragraphs beginning “Speech automatism seem” and “The question of why”
Reported values
  • P<0.05speech automatismP value · 34 right-handed epileptics in the report; 13 speech-automatism cases in the Table II summation · ictalPDF p.3, Results, Table I; PDF p.5, Discussion and Summary item 2
  • left 3 casesspeech automatismCount · 34 right-handed epileptics in the report; 13 speech-automatism cases in the Table II summation · left-hemisphere EEG focus · ictalPDF p.3, Results, Table I; PDF p.5, Discussion and Summary item 2
  • right 10 casesspeech automatismCount · 34 right-handed epileptics in the report; 13 speech-automatism cases in the Table II summation · right-hemisphere EEG focus · ictalPDF p.3, Results, Table I; PDF p.5, Discussion and Summary item 2
  • one attackspeech automatismCount · One cited patient with temporal-lobe epilepsy · cited patient · ictalPDF p.5, Discussion paragraph beginning “Driver and his coworkers”
  • one patientspeech automatismCount · One cited patient with temporal-lobe epilepsy · cited temporal-lobe epilepsy case · ictalPDF p.5, Discussion paragraph beginning “Driver and his coworkers”
  • two cited reports associate speech automatism with left-hemisphere dominancespeech automatism and cerebral dominanceCount · Prior reports plus the current right-handed study population · leftward cited reports · ictalPDF p.5, Discussion opening paragraph; PDF p.5, Summary item 2
  • two cited reports suggest right-hemisphere dominancespeech automatism and cerebral dominanceCount · Prior reports plus the current right-handed study population · rightward cited reports · ictalPDF p.5, Discussion opening paragraph; PDF p.5, Summary item 2
  • current study right 10 casesspeech automatism and cerebral dominanceCount · Prior reports plus the current right-handed study population · right-hemisphere focus · ictalPDF p.5, Discussion opening paragraph; PDF p.5, Summary item 2
  • current study P<0.05speech automatism and cerebral dominanceP value · Prior reports plus the current right-handed study population · ictalPDF p.5, Discussion opening paragraph; PDF p.5, Summary item 2
  • current study left 3 casesspeech automatism and cerebral dominanceCount · Prior reports plus the current right-handed study population · left-hemisphere focus · ictalPDF p.5, Discussion opening paragraph; PDF p.5, Summary item 2
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 5 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • verbal automatismsVerbal automatisms over the whole seizure course were more frequent in ML than M or L patients.PDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
  • verbal automatisms and right temporal lateralizationThe authors noted a nonsignificant trend toward right temporal lateralization of verbal automatisms, regardless of delay and seizure subtype.PDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
Reported values
  • 7/18 (38.9%)verbal automatismsPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
  • 4/24 (16.7%)verbal automatismsPercentage · n/N 4/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
  • 0/13 (0%)verbal automatismsPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
  • 31.3% right temporalverbal automatisms and right temporal lateralizationPercentage · patients with verbal automatisms in the 55-patient cohort; denominators and counts not reported · right temporal · ictal course, timing not restrictedPDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
  • 15.4% left temporalverbal automatisms and right temporal lateralizationPercentage · patients with verbal automatisms in the 55-patient cohort; denominators and counts not reported · left temporal · ictal course, timing not restrictedPDF p.6, General ictal characteristics; PDF p.8, Vocal verbal and nonverbal automatisms
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • occipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsIn the summarized Marchi et al. study, widespread organization of the epileptogenic zone was typical in occipital or “occipital-plus” epilepsy, with temporal and/or parietal cortex commonly involved; altered conscious level was more common with widespread posterior neocortical onset, while automatic motor behavior and/or verbal automatisms were more often seen with occipitotemporal organization.PDF p.6, Table 2, Marchi et al. 2016 row
Reported values
  • 194 seizuresoccipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy; 194 seizures · Marchi et al. study · ictal onset and evolutionPDF p.6, Table 2, Marchi et al. 2016 row
  • 29 subjectsoccipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy; 194 seizures · Marchi et al. occipital-lobe epilepsy study · ictal onset and evolutionPDF p.6, Table 2, Marchi et al. 2016 row
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • recurrent ictal speech utterances; oro-alimentary automatisms; right-sided versionIn the patient’s habitual partial seizures, an aura of nausea was followed by staring gaze, partial loss of consciousness, oro-alimentary automatisms, right-sided version, and postictal confusion; family reported recurrent stereotyped French or English sentence repetitions from age 18.PDF p.2, left column, paragraph beginning “Partial seizures began”; PDF p.2, right column, paragraph beginning “Five stereotyped and spontaneous electroclinical seizures”
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • verbal automatisms; coprolaliaThe source states that verbal automatisms, particularly coprolalia, occur in temporal or orbitofrontal epilepsy, have limited lateralizing value toward the non-dominant hemisphere, and can be triggered by seizures from either hemisphere.PDF p.12, Discussion
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfIndependent primary study · 9 findings · 27 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Independent primary study · Class II · Evidence weight 3.22 · 2 × 0.9 × 1.79
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • pre-operative speech disturbance; dysphasia; speech automatismsAmong all 100 patients, a pre-operative speech abnormality connected with at least some seizures was recorded in 67 patients; dysphasia was recorded in 34 patients and speech automatisms in 38 patients, while 33 had no recorded speech disturbance.PDF p.4, Table I and immediately adjacent discussion; PDF p.12, Summary
  • speech automatismsWithin Group A, 23 patients with speech automatisms were associated with epilepsy in the recessive temporal lobe in 13 and the dominant temporal lobe in 10; after excluding warning and perplexity utterances considered probably not truly ictal, the source reports 11 recessive-side versus 4 dominant-side instances for recurrent, irrelevant, and emotional utterances.PDF p.5, Table II; PDF p.7, discussion of speech automatism laterality
  • speech automatisms; pre-operative interictal spike dischargesAmong 23 Group A patients with speech automatisms, pre-operative interictal EEG showed 7 exclusively right-sided temporal discharges, 14 bilateral discharges, 1 exclusively left-sided discharge, and 1 normal EEG; the bilateral discharges were right-predominant in 6 and left-predominant in 8.PDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • post-operative ictal speech automatismOf the 38 patients with pre-operative ictal speech automatisms, all but 3 had lost them post-operatively, including the 15 Group B patients with persisting fits; among 6 Group B patients with continued seizures after dominant temporal-lobe removal, 3 continued to show automatisms, whereas none of 9 patients with right-sided resections did.PDF p.9, discussion point (3); PDF p.11, prognostic discussion
  • paroxysmal dysphasia; ictal speech automatism; hemicranial diminutionPre-operative radiology showed a relatively high incidence of slight diminution of left hemicranial size among patients with paroxysmal dysphasia compared with the remainder, whereas similar diminution of either hemicranium was uncommon in patients with ictal speech automatisms; the authors speculated that dysphasia might involve wider-ranging discharges reaching vulnerable left posterior temporal speech mechanisms.PDF p.11, discussion of radiological studies
  • speech automatismThe current article reports that Bingley observed speech automatism in 29/74 temporal-lobe epilepsy cases of non-tumorous origin; it was present in 6/24 patients with a unilateral dominant-lobe EEG focus versus 10/17 with a unilateral recessive-lobe focus, and when emphasized bilateral foci were included it occurred in 25% of dominant-focus patients versus 56% of recessive-focus patients, a difference reported significant at the 0.01 level.PDF p.10, discussion of prior speech-automatism reports
  • recurrent speech automatism in an acquired languageIn an addendum case, a 38-year-old Polish patient with fluent Russian and English had psychomotor seizures that nearly always began with the recurrent English utterance “I beg your pardon” despite speaking Polish at home; the EEG focus was consistently right sphenoidal, and an induced metrazol seizure produced the utterance eight times at its commencement.PDF p.13, Addendum; PDF p.14, Addendum
  • paroxysmal dysphasia versus ictal speech automatismThe authors treated paroxysmal dysphasia and ictal speech automatism as different aspects of ictal speech disorder: in the few patients with both phenomena they occurred at separate times and never together in the same seizure.PDF p.9, discussion points (1); PDF p.12, Summary
  • paroxysmal dysphasia; ictal speech automatism; grand mal attacksThe authors report that more than three-quarters of the 34 patients with paroxysmal dysphasia also had grand mal attacks, whereas slightly less than half of the patients with ictal speech automatism had these major seizures.PDF p.11, discussion of seizure severity
Reported values
  • no speech disturbance 33/100pre-operative speech disturbance; dysphasia; speech automatismsPercentage · n/N 33/100 · All 100 consecutive temporal lobe epilepsy patients submitted to anterior temporal lobectomy · no recorded speech disturbance · Pre-operative; connected with at least some seizuresPDF p.4, Table I and immediately adjacent discussion; PDF p.12, Summary
  • any speech abnormality 67/100pre-operative speech disturbance; dysphasia; speech automatismsPercentage · n/N 67/100 · All 100 consecutive temporal lobe epilepsy patients submitted to anterior temporal lobectomy · any speech abnormality · Pre-operative; connected with at least some seizuresPDF p.4, Table I and immediately adjacent discussion; PDF p.12, Summary
  • speech automatisms 38/100pre-operative speech disturbance; dysphasia; speech automatismsPercentage · n/N 38/100 · All 100 consecutive temporal lobe epilepsy patients submitted to anterior temporal lobectomy · speech automatisms · Pre-operative; connected with at least some seizuresPDF p.4, Table I and immediately adjacent discussion; PDF p.12, Summary
  • dysphasia 34/100pre-operative speech disturbance; dysphasia; speech automatismsPercentage · n/N 34/100 · All 100 consecutive temporal lobe epilepsy patients submitted to anterior temporal lobectomy · dysphasia · Pre-operative; connected with at least some seizuresPDF p.4, Table I and immediately adjacent discussion; PDF p.12, Summary
  • 4 dominant-side instancesspeech automatismsCount · Group A; 23 patients with pre-operative speech automatisms · dominant temporal lobe · Pre-operative; warning, recurrent, irrelevant, emotional, or perplexity utterances at seizure onset, during seizure, or just afterPDF p.5, Table II; PDF p.7, discussion of speech automatism laterality
  • 13/23 recessive-associatedspeech automatismsPercentage · n/N 13/23 · Group A; 23 patients with pre-operative speech automatisms · recessive temporal lobe · Pre-operative; warning, recurrent, irrelevant, emotional, or perplexity utterances at seizure onset, during seizure, or just afterPDF p.5, Table II; PDF p.7, discussion of speech automatism laterality
  • 10/23 dominant-associatedspeech automatismsPercentage · n/N 10/23 · Group A; 23 patients with pre-operative speech automatisms · dominant temporal lobe · Pre-operative; warning, recurrent, irrelevant, emotional, or perplexity utterances at seizure onset, during seizure, or just afterPDF p.5, Table II; PDF p.7, discussion of speech automatism laterality
  • 11 recessive-side instancesspeech automatismsCount · Group A; 23 patients with pre-operative speech automatisms · recessive temporal lobe · Pre-operative; warning, recurrent, irrelevant, emotional, or perplexity utterances at seizure onset, during seizure, or just afterPDF p.5, Table II; PDF p.7, discussion of speech automatism laterality
  • normal EEG 1/23speech automatisms; pre-operative interictal spike dischargesCount · n/N 1/23 · Group A; 23 patients with speech automatisms · normal EEG · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • exclusive right 7/23speech automatisms; pre-operative interictal spike dischargesCount · n/N 7/23 · Group A; 23 patients with speech automatisms · exclusive right-sided · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • bilateral 14/23speech automatisms; pre-operative interictal spike dischargesCount · n/N 14/23 · Group A; 23 patients with speech automatisms · bilateral · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • 6 right-predominant bilateralspeech automatisms; pre-operative interictal spike dischargesCount · Group A; 23 patients with speech automatisms · right-predominant bilateral · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • 8 left-predominant bilateralspeech automatisms; pre-operative interictal spike dischargesCount · Group A; 23 patients with speech automatisms · left-predominant bilateral · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • exclusive left 1/23speech automatisms; pre-operative interictal spike dischargesCount · n/N 1/23 · Group A; 23 patients with speech automatisms · exclusive left-sided · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A speech automatism row
  • 3/6post-operative ictal speech automatismPercentage · n/N 3/6 · All 38 speech-automatism patients; Group B subgroup with 15 patients with persisting fits; comparison of 6 dominant-resection and 9 right-resection patients with continued seizures · continued seizures after dominant temporal-lobe removal · Post-operative follow-up during persistent or recurrent seizuresPDF p.9, discussion point (3); PDF p.11, prognostic discussion
  • 3/38post-operative ictal speech automatismPercentage · n/N 3/38 · All 38 speech-automatism patients; Group B subgroup with 15 patients with persisting fits; comparison of 6 dominant-resection and 9 right-resection patients with continued seizures · all pre-operative ictal speech-automatism patients · Post-operative follow-up during persistent or recurrent seizuresPDF p.9, discussion point (3); PDF p.11, prognostic discussion
  • none of 9post-operative ictal speech automatismPercentage · n/N 0/9 · All 38 speech-automatism patients; Group B subgroup with 15 patients with persisting fits; comparison of 6 dominant-resection and 9 right-resection patients with continued seizures · continued seizures after right-sided resection · Post-operative follow-up during persistent or recurrent seizuresPDF p.9, discussion point (3); PDF p.11, prognostic discussion
  • 15 Group B patients with persisting fitspost-operative ictal speech automatismCount · All 38 speech-automatism patients; Group B subgroup with 15 patients with persisting fits; comparison of 6 dominant-resection and 9 right-resection patients with continued seizures · Group B with persisting fits · Post-operative follow-up during persistent or recurrent seizuresPDF p.9, discussion point (3); PDF p.11, prognostic discussion
  • 35/38post-operative ictal speech automatismPercentage · n/N 35/38 · All 38 speech-automatism patients; Group B subgroup with 15 patients with persisting fits; comparison of 6 dominant-resection and 9 right-resection patients with continued seizures · all pre-operative ictal speech-automatism patients · Post-operative follow-up during persistent or recurrent seizuresPDF p.9, discussion point (3); PDF p.11, prognostic discussion
  • 56% with recessive focus when emphasized bilateral foci includedspeech automatismPercentage · Bingley’s cited 74 patients with non-tumorous temporal-lobe epilepsy; unilateral EEG-focus subgroups and bilateral-focus cases with side emphasis · Recessive focus including emphasized bilateral foci · Speech automatism during seizuresPDF p.10, discussion of prior speech-automatism reports
  • Speech automatism in 10/17 unilateral recessive-focus patientsspeech automatismCount · n/N 10/17 · Bingley’s cited 74 patients with non-tumorous temporal-lobe epilepsy; unilateral EEG-focus subgroups and bilateral-focus cases with side emphasis · Unilateral recessive-lobe EEG focus · Speech automatism during seizuresPDF p.10, discussion of prior speech-automatism reports
  • 25% with dominant focus when emphasized bilateral foci includedspeech automatismPercentage · Bingley’s cited 74 patients with non-tumorous temporal-lobe epilepsy; unilateral EEG-focus subgroups and bilateral-focus cases with side emphasis · Dominant focus including emphasized bilateral foci · Speech automatism during seizuresPDF p.10, discussion of prior speech-automatism reports
  • Speech automatism in 6/24 unilateral dominant-focus patientsspeech automatismCount · n/N 6/24 · Bingley’s cited 74 patients with non-tumorous temporal-lobe epilepsy; unilateral EEG-focus subgroups and bilateral-focus cases with side emphasis · Unilateral dominant-lobe EEG focus · Speech automatism during seizuresPDF p.10, discussion of prior speech-automatism reports
  • Speech automatism in 29/74 cases overallspeech automatismCount · n/N 29/74 · Bingley’s cited 74 patients with non-tumorous temporal-lobe epilepsy; unilateral EEG-focus subgroups and bilateral-focus cases with side emphasis · Non-tumorous temporal-lobe epilepsy · Speech automatism during seizuresPDF p.10, discussion of prior speech-automatism reports
  • eight repetitions at the commencement of the induced metrazol seizurerecurrent speech automatism in an acquired languageCount · One 38-year-old bilingual patient described in the addendum; Polish home language and acquired English · Addendum case · Seizure onset and early ictal period; induced metrazol seizure commencementPDF p.13, Addendum; PDF p.14, Addendum
  • slightly less than half of 38 speech-automatism patientsparoxysmal dysphasia; ictal speech automatism; grand mal attacksPercentage · Patients with pre-operative paroxysmal dysphasia and patients with pre-operative ictal speech automatisms · ictal speech automatism · Pre-operative seizure historyPDF p.11, discussion of seizure severity
  • more than three-quarters of 34 dysphasia patientsparoxysmal dysphasia; ictal speech automatism; grand mal attacksPercentage · Patients with pre-operative paroxysmal dysphasia and patients with pre-operative ictal speech automatisms · paroxysmal dysphasia · Pre-operative seizure historyPDF p.11, discussion of seizure severity
unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 2 findings · 1 reported value
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • speech automatisms during atypical absence seizuresSpeech automatisms during atypical absence seizures are described as phenomenologically overlapping with those in focal seizures of temporal lobe origin and as occurring in 12–39% of patients with temporal lobe epilepsies.PDF p.2, §2 paragraph beginning “Speech automatisms may be divided”
  • reactive speech automatismsThe review classifies complex automatic speech behavior such as swearing, verbal help seeking, and coprolalia as assumed reactive automatisms and states that they are not indicative of the seizure-onset zone.PDF p.2, §2 paragraph beginning “Complex automatic speech behavior”
Reported values
  • 12–39% of patients with temporal lobe epilepsiesspeech automatisms during atypical absence seizuresPercentage · Patients with temporal lobe epilepsies; atypical absence seizure context · ictalPDF p.2, §2 paragraph beginning “Speech automatisms may be divided”
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to automatism phenotypePhenotype II is characterized primarily by oropharyngeal, limb, or verbal automatisms, with or without a preceding visual aura.PDF p.9, Phenotype II
  • verbal automatismsTable 2 records vocalization/verbal automatisms in Case 11 after orolimentary and right-upper-limb automatisms.PDF p.7, Table 2 Case 11

12 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal pain (painful somatosensory seizure)Source terms: Ictal painReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere12 manuscripts · 48 findings · 44 reported values
Weighted evidence supportevidence weight 22.07 across 12 manuscripts · 1 manuscript weight pending · 2 case report or observation · 6 narrative, educational, or cited context · 2 independent primary study · 1 systematic review or meta-analysis · 1 structured design not resolved

In the illustrated case, painful tingling in the left hand was contralateral to right-insular seizure onset. The chapter restates that painful sensation has been described more frequently in the nondominant hemisphere. The case shows pain or pulling in the right face spreading to the right arm and leg. One patient had an aura of a tearing feeling in the left arm. Right facial pain, right-ear ringing, right hemibody and foot manifestations predominated in the early sequence, while left-sided stiffening occurred in half of seizures. Somatosensory auras are described as usually contralateral to the focus; right hemibody pain in the illustrative case suggested a left focus. Unilateral painful aura was usually contralateral to the symptomatogenic zone in perirolandic/parietal epilepsy, with an ipsilateral exception described in temporal lobe epilepsy. The review describes unilateral painful aura as contralateral to the suspected postcentral/parietal symptomatogenic zone. All three presumed perirolandic unilateral painful auras were contralateral, while one of two temporal cases was ipsilateral. Painful somatosensory seizures usually involve a specific body part contralateral to the cortical focus, but can be ipsilateral or bilateral. This finding provides no lateralization information. No lateralization information is reported. The case reports right-sided symptoms but no relation to a seizure-onset hemisphere. No hemisphere or body-side direction is reported. The cited anterior-versus-posterior insular comparison provides no lateralizing information. Ictal pain may present with unilateral truncal or peripheral distribution, but no seizure-relative direction is supplied. The case reports specify chest, genital, facial, pharyngeal, and lingual pain but no lateralizing direction. No hemisphere or body-side relationship is reported. No lateralizing direction is reported for painful somatosensory aura. No lateralizing direction is reported.

Source-defined result groups 13
Localization: Insular / ParietalObserved proportion 100.0%pain at seizure onset · other SOZ · patient1 manuscript · 1 reported value · not pooled
Localization: ParietalObserved proportion 2.5%All reported · other stimulation responses · patients with cortical stimulation1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · face versus upper-limb versus lower-limb representation · painful response restricted to one somatotopic body region1 manuscript · 2 reported values · not pooled
Localization: Insular / ParietalObserved proportion 100.0%choking sensation · other SOZ · patient1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 90.0%stimulation-evoked pain · patient-reported painful sensation1 manuscript · 1 reported value · not pooled
Localization: cingulate gyrusObserved proportion 0.0%All reported · painful aura · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyOFC-restricted EZN cases · patients1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphereObserved proportion 100.0%All reported · right-arm or nonlateralized aura · operative-map case1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · other evoked-sensation categories and insular locations · painful stimulation response; source also uses patient-level wording for behavioral observation1 manuscript · 1 reported value · not pooled
Localization: InsularObserved proportion 70.0%stimulation-evoked pain · patient-reported painful sensation1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyAll reported · face versus upper-limb versus lower-limb representation · painful response restricted to one somatotopic body region1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft-sided stiffening · Early diurnal versus later nocturnal/postoperative semiology · seizure1 manuscript · 1 reported value · not pooled
Localization: Insular / ParietalObserved proportion 100.0%vertigo or falling sensation · other SOZ · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 12

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 1 finding · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.573
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • absence of painful auraNone of the patients in the series reported painful auras despite preservation of awareness.PDF p.7, Discussion
Reported values
  • 0/14 painful aurasabsence of painful auraProportion · n/N 0/14 · 14 lesional cingulate epilepsy cases · auraPDF p.7, Discussion
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • pain; warmth auraTable 3 lists pain or warmth aura as localising to secondary somatosensory cortex or insula.PDF p.10, Table 3
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • somatosensory painTwo restricted-OFC cases had somatosensory pain involving the head and full body.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 2 patientssomatosensory painCount · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 3 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.90 · 2 × 1.5 × 1.301
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • pain, choking sensation, vertigo, and falling sensationAll four patients with pain at seizure onset and all three patients with a choking sensation had an insular SOZ, while all three patients with either vertigo or a falling sensation had a parietal SOZ.PDF p.6, section 3.3
Reported values
  • all four patientspain, choking sensation, vertigo, and falling sensationPercentage · n/N 4/4 · SHE patients with the specified sensory manifestations; source reports four pain cases, three choking cases, and three vertigo/falling cases · pain at seizure onset · at the beginning of the seizure/early sensory onsetPDF p.6, section 3.3
  • all three patientspain, choking sensation, vertigo, and falling sensationPercentage · n/N 3/3 · SHE patients with the specified sensory manifestations; source reports four pain cases, three choking cases, and three vertigo/falling cases · vertigo or falling sensation · at the beginning of the seizure/early sensory onsetPDF p.6, section 3.3
  • all three patientspain, choking sensation, vertigo, and falling sensationPercentage · n/N 3/3 · SHE patients with the specified sensory manifestations; source reports four pain cases, three choking cases, and three vertigo/falling cases · choking sensation · at the beginning of the seizure/early sensory onsetPDF p.6, section 3.3
hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 12 findings · 9 reported values
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • PSS sensory quality and body-side relationshipPSS may feel burning, stabbing, knife-like, prickling, throbbing, or muscle-tearing and can be intense enough to cause grimacing, screaming, or crying; sensations usually involve a specific body part such as a limb or a segmental distribution and usually occur contralateral to the cortical seizure focus, but may be ipsilateral or bilateral.PDF p.2, Table 1; PDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • epileptic ictal painThe review characterizes epileptic ictal pain as a rare phenomenon classically presenting as cephalic, abdominal, or unilateral truncal/peripheral pain and occurring mostly with focal-onset seizures.PDF p.1, Introduction; PDF p.2, Table 1
  • ictal pain frequencyThe review reports that ictal pain of any type occurs in 0.2% to 2.8% of patients with epilepsy overall, with rates approaching 4.1% in patients with focal epilepsy syndromes.PDF p.1, Introduction
  • ictal-pain diagnostic cluesThe review identifies brief, abrupt, stereotyped paroxysmal occurrence as a clue to ictal pain, with confusion or loss of awareness, clonic activity, and EEG abnormalities as possible accompanying indicators; empiric anti-epileptic drug response may help but is not specific, and pain may occur alone with little or no electrographic correlate.PDF p.1, Introduction
  • painful somatosensory seizures (PSS) frequencyThe review estimates PSS occurrence at about 0.2% to 0.6% of patients evaluated in an EMU and 1.5% of epilepsy cases specifically involving somatosensory seizures.PDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • epileptic ictal somatosensory pain in EMUThe review reports that a large retrospective review of 5,133 patients investigated in an EMU found documentation of epileptic ictal somatosensory pain in 10 patients.PDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • peripherally localized ictal painThe review reports that a retrospective review of 4,736 patients with epilepsy identified 4 patients with primarily peripherally localized ictal pain.PDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • unusual PSS topographiesThe review notes EEG-validated PSS cases presenting as ictal chest, genital, facial, pharyngeal, and lingual pain.PDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • PSS accompanying symptoms and tonic-pain distinctionPSS may accompany paraesthesias, thermal sensations, perceptual body distortion, or motor manifestations; pain caused by focal tonic muscle contraction and severe spasm should be distinguished from somatosensory-origin pain.PDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • painful somatosensory aura in focal epilepsyThe review reports that a case review of 604 consecutive focal-epilepsy cases found 6 patients with painful somatosensory auras, considered to arise from parietal or temporal regions by scalp EEG and neuroimaging; the review notes that some may have had operculo-insular onset or spread and that temporal-onset pain was postulated to reflect spread to SII.PDF p.4, Somatosensory Pain as a Symptom of Seizures, Localization; PDF p.5, Localization (continued)
  • cortical electrical stimulation and pain responsesThe review reports that an extensive study of 4,160 cortical electrical stimulations elicited pain in 60 of 558 triggered responses (11%) when stimulation involved SII and insular areas, with no pain or unpleasant sensations in any other reported regions.PDF p.5, Somatosensory Pain as a Symptom of Seizures, Localization
  • PSS propagation and symptom-localization interpretationThe review concludes that somatosensory pain perceptions are more likely related to ictal involvement of the insula and SII parietal operculum than to the parietal region alone, but stresses that this does not necessarily indicate seizure origin or a direct lesion there because seizures may spread into the pain network from other locations.PDF p.5, Somatosensory Pain as a Symptom of Seizures, Localization
Reported values
  • Ictal pain frequency 0.2%–2.8% in epilepsy overallictal pain frequencyRange · Patients with epilepsy overall versus patients with focal epilepsy syndromes · Epilepsy overall · ictalPDF p.1, Introduction
  • Ictal pain frequency approaching 4.1% in focal epilepsyictal pain frequencyPercentage · Patients with epilepsy overall versus patients with focal epilepsy syndromes · Focal epilepsy syndromes · ictalPDF p.1, Introduction
  • 1.5% of epilepsy cases involving somatosensory seizurespainful somatosensory seizures (PSS) frequencyPercentage · Patients with intractable focal epilepsy evaluated in an EMU versus epilepsy cases involving somatosensory seizures · epilepsy cases involving somatosensory seizures · IctalPDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • about 0.2%–0.6% of EMU-evaluated patientspainful somatosensory seizures (PSS) frequencyRange · Patients with intractable focal epilepsy evaluated in an EMU versus epilepsy cases involving somatosensory seizures · EMU-evaluated patients · IctalPDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • 10/5,133 patientsepileptic ictal somatosensory pain in EMUCount · n/N 10/5133 · 5,133 patients investigated in an EMU · IctalPDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • 4/4,736 patientsperipherally localized ictal painCount · n/N 4/4736 · 4,736 patients with epilepsy in a retrospective review · IctalPDF p.4, Somatosensory Pain as a Symptom of Seizures, Description
  • 6/604 casespainful somatosensory aura in focal epilepsyCount · n/N 6/604 · 604 consecutive cases of focal epilepsy · Somatosensory aura/ictalPDF p.4, Somatosensory Pain as a Symptom of Seizures, Localization; PDF p.5, Localization (continued)
  • Pain in 60/558 triggered responses (11%)cortical electrical stimulation and pain responsesPercentage · n/N 60/558 · Cortical electrical stimulation study summarized by the review · Responses elicited by stimulation involving SII and insular areas · Electrical stimulation; not an ictal phasePDF p.5, Somatosensory Pain as a Symptom of Seizures, Localization
  • 4,160 cortical electrical stimulationscortical electrical stimulation and pain responsesCount · Cortical electrical stimulation study summarized by the review · Electrical stimulation; not an ictal phasePDF p.5, Somatosensory Pain as a Symptom of Seizures, Localization
jobst-insula-and-its-epilepsies-2019.pdfCase report or observation · 16 findings · 4 reported values
jobst-insula-and-its-epilepsies-2019.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • Figure 3 painful tingling in left handThe patient in Figure 3 described a painful tingling sensation in the left hand after right-insular onset.PDF p.4, Figure 3B
  • posterior insular stimulation painful sensationsStimulation of the posterior insula typically produces painful sensations.PDF p.1, Abstract; PDF p.5, Somatosensory Sensations
  • painful sensations as suggestive insular featurePainful sensations are described as highly suggestive of insular or insulo-opercular seizures.PDF p.2, Clinical Features
  • expression of pain on video EEGExpression of pain is among the observed clinical signs that suggest an insular focus.PDF p.3, Video EEG
  • posterior-third painful sensationsPainful sensations were elicited mostly from the posterior third of the insula.PDF p.5, Somatosensory Sensations
  • burning painful sensationBurning was one the source's own description of painful sensations elicited from the posterior insula.PDF p.5, Somatosensory Sensations
  • electric-shock painful sensationElectric shock was one the source's own description of painful sensations elicited from the posterior insula.PDF p.5, Somatosensory Sensations
  • painful pins sensationPainful pins was one the source's own description of painful sensations elicited from the posterior insula.PDF p.5, Somatosensory Sensations
  • cramp painful sensationCramps were one the source's own description of painful sensations elicited from the posterior insula.PDF p.5, Somatosensory Sensations
  • rare painful responses to stimulationPainful responses were rare, occurring in 60 of more than 4000 stimulations.PDF p.5, Somatosensory Sensations
  • painful responses from insular and SII stimulationIn the cited stimulation study, painful responses were elicited only by insular and secondary somatosensory cortex stimulation.PDF p.5, Somatosensory Sensations
  • absence of painful responses from SI stimulationPainful responses were never observed when stimulating primary somatosensory cortex (SI) in the cited study.PDF p.5, Somatosensory Sensations
  • absence of painful responses from other cortical areasPainful responses were never observed when stimulating cortical areas other than the insula and SII in the cited study.PDF p.5, Somatosensory Sensations
  • insula or SII involved at onset of painful seizuresIn the cited SEEG study, the insula or SII was systematically involved at seizure onset in all five patients with painful seizures.PDF p.5, Somatosensory Sensations
  • ictal pain reproduced by insula or SII stimulationIctal pain was reproduced by stimulation of the insula or SII in the cited five-patient study.PDF p.5, Somatosensory Sensations
  • nociceptive symptoms suggest insular originNociceptive symptoms are described as highly suggestive of an insular-lobe origin.PDF p.5, Other Insular Responses
Reported values
  • 60/>4000 painful responsesrare painful responses to stimulationProportion · cited cortical stimulation series · stimulation-evoked painful symptomPDF p.5, Somatosensory Sensations
  • no painful responses observed with SI stimulationabsence of painful responses from SI stimulationCount · cited cortical stimulation series · stimulation-evoked painful symptomPDF p.5, Somatosensory Sensations
  • no painful responses observed in other cortical areasabsence of painful responses from other cortical areasCount · cited cortical stimulation series · stimulation-evoked painful symptomPDF p.5, Somatosensory Sensations
  • 5/5 insula or SII involved at onsetinsula or SII involved at onset of painful seizuresProportion · n/N 5/5 · 5 patients with painful seizures · ictal onsetPDF p.5, Somatosensory Sensations
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 7 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Painful auraThe review associates unilateral painful auras with a contralateral postcentral or parietal symptomatogenic zone in perirolandic or parietal epilepsy, while noting that temporal lobe epilepsy can produce an ipsilateral representation.PDF p.2, section 2.2 Painful auras; PDF p.2, section 2.2.1 Mechanism
  • Painful auraYoung and Blume found 24 patients with painful auras among 856 patients with epilepsy, including 10 with unilateral pain; the review reports unilateral pain as 1.2% and describes the suspected symptomatogenic zone as contralateral postcentral gyrus or parietal lobe.PDF p.2, section 2.2 Painful auras
  • Painful auraNair et al. reviewed 604 consecutive cases and found 25 patients with painful auras, including 5 with unilateral painful auras; the unilateral auras were contralateral in 3 patients with presumed perirolandic epilepsy, while 1 of 2 patients with unilateral pain and temporal lobe epilepsy had ipsilateral representation.PDF p.2, section 2.2 Painful auras
Reported values
  • 10 with unilateral painPainful auraCount · 24 patients with painful auras among 856 patients with epilepsy; 10 had unilateral pain · unilateral pain · Ictal auraPDF p.2, section 2.2 Painful auras
  • unilateral pain 1.2%Painful auraPercentage · n/N 10/856 · 24 patients with painful auras among 856 patients with epilepsy; 10 had unilateral pain · unilateral pain · Ictal auraPDF p.2, section 2.2 Painful auras
  • 24 patients with painful auras among 856Painful auraPercentage · n/N 24/856 · 24 patients with painful auras among 856 patients with epilepsy; 10 had unilateral pain · painful aura · Ictal auraPDF p.2, section 2.2 Painful auras
  • Unilateral painful auras 5/25Painful auraPercentage · n/N 5/25 · 604 consecutive cases; 25 patients with painful auras; 5 with unilateral painful auras · Painful-aura patients · Ictal auraPDF p.2, section 2.2 Painful auras
  • Presumed perirolandic unilateral painful auras contralateral 3/3Painful auraPercentage · n/N 3/3 · 604 consecutive cases; 25 patients with painful auras; 5 with unilateral painful auras · Presumed perirolandic epilepsy · Ictal auraPDF p.2, section 2.2 Painful auras
  • Temporal-lobe unilateral pain ipsilateral 1/2Painful auraPercentage · n/N 1/2 · 604 consecutive cases; 25 patients with painful auras; 5 with unilateral painful auras · Temporal lobe epilepsy · Ictal auraPDF p.2, section 2.2 Painful auras
  • Painful auras 25/604Painful auraPercentage · n/N 25/604 · 604 consecutive cases; 25 patients with painful auras; 5 with unilateral painful auras · Ictal auraPDF p.2, section 2.2 Painful auras
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 4 findings · 7 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 3.00 · 1 × 1.5 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • painful sensationsPainful sensations numbered 57 (10.4%) and were evoked in the posterior two thirds of the insula, mostly postero-superiorly where pain-response threshold was lowest; every patient reported by the source as having a painful sensation also showed spontaneous behavioral manifestations of pain.PDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3C
  • painful sensation descriptions and intensityPatients used burning, electric-shock, stinging, painful pins-and-needles, or crushing/cramp descriptions for stimulation-evoked pain, which had a mean visual analog scale score of 6.7/10 with a range of 4-9/10.PDF p.4, Somato-sensory Responses
  • somatotopic organization of painful responsesWhen pain was restricted to a single somatotopic region, a somatotopic organization was found in the caudal insula; the face representation was rostral to the upper-limb representation, which was above the lower-limb representation.PDF p.4, Somato-sensory Responses
  • ictal pain and insular/SII seizure-onset involvementRestating a cited SEEG study, the source reports that ictal pain in patients with painful seizures could be reproduced by insular or SII stimulation and that both the insula and SII were systematically involved at seizure onset.PDF p.7, Somato-sensory Responses
Reported values
  • behavioral pain manifestation reported for all source-described painful-sensation patientspainful sensationsCount · n/N 57/550 · 57 painful responses in the 550-response series; source describes patients reporting pain · stimulation-evoked painful sensationPDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3C
  • 57 painful responses (10.4% of 550 clinically eloquent responses)painful sensationsPercentage · 57 painful responses in the 550-response series; source describes patients reporting pain · stimulation-evoked painful sensationPDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3C
  • 6.7/10painful sensation descriptions and intensityMean · n/N 7/10 · Source-described patients reporting painful sensations after insular stimulation · stimulation-evoked pain · stimulation-evoked painful sensationPDF p.4, Somato-sensory Responses
  • 4–9/10painful sensation descriptions and intensityRange · n/N 9/10 · Source-described patients reporting painful sensations after insular stimulation · stimulation-evoked pain · stimulation-evoked painful sensationPDF p.4, Somato-sensory Responses
  • face rostral to upper limbsomatotopic organization of painful responsesCount · Painful responses restricted to a single somatotopic region: face, upper limb, or lower limb · stimulation-evoked painful sensationPDF p.4, Somato-sensory Responses
  • upper limb above lower limbsomatotopic organization of painful responsesCount · Painful responses restricted to a single somatotopic region: face, upper limb, or lower limb · stimulation-evoked painful sensationPDF p.4, Somato-sensory Responses
  • single-region painful responses 51% (n=29)somatotopic organization of painful responsesPercentage · Painful responses restricted to a single somatotopic region: face, upper limb, or lower limb · stimulation-evoked painful sensationPDF p.4, Somato-sensory Responses
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 2 findings · 5 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyCase 2 was a 46-year-old right-handed man whose seizures began with lancinating right facial pain followed within 2 seconds by high-pitched right-ear ringing descending along the right hemibody to the foot, sometimes with right-foot tremor, witnessed erratic right-sided and truncal movements, and left-sided stiffening in half the seizures; he was usually conscious without postictal paresis, had 10–15-second events up to 100 times per day triggered by sounds, and could develop hypersalivation, speech difficulty, later nocturnal hypermotor seizures, and urinary incontinence.PDF p.11, Case 2; PDF p.13, continuation of Case 2
  • painful somatosensory seizure and contralateral auraIn the Case 2 discussion, the source states that somatosensory auras are usually localized to primary sensory cortex, secondary somatosensory cortex in the parietal operculum, or the posterior third of the insular cortex; painful seizures likely arise in the same regions, although supplementary motor, inferior parietal, and cingulate localizations have been proposed, and somatosensory auras are usually contralateral to the epileptic focus even when the insula is involved.PDF p.13, What localizations are suggested by the seizure semiology?
Reported values
  • within 2 secondsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyDuration · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · early sensory sequence · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 10–15-second eventsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · habitual events · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 2–3 per monthCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · youth · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • in half the seizuresCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyOther reported value · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · left-sided stiffening · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • up to 100 times per dayCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyFrequency · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · later high-frequency period · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 5 findings · 5 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.27 · 2 × 1.35 × 1.952
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • pain or pulling in right face spreading to right arm and legFigure 3 shows an aura of pain or a sensation of pulling in the right face spreading to the right arm and leg.PDF p.8, Fig. 3
  • tearing feeling in left armFigure 4 shows an aura of a tearing feeling in the left arm.PDF p.9, Fig. 4
  • painful somatosensory auraPainful sensations were reported in 13 patients.PDF p.3, Results, Aurae; PDF p.8, Discussion
  • painful sensation after superior parietal area 5a stimulationTwo patients reported a painful sensation after stimulation of the superior parietal lobe behind the post-central gyrus at source-labeled area 5a.PDF p.5, Electrical cortical stimulation
  • right-fingertip tingling and pain in Fig. 1Figure 1 shows an aura of tingling and pain in the fingertips of the right hand followed by rightward head deviation and right-arm tonic posturing.PDF p.4, Fig. 1
Reported values
  • 1 casepain or pulling in right face spreading to right arm and legCount · n/N 1/1 · patient 36 (C.J.) · aura sequencePDF p.8, Fig. 3
  • 1 casetearing feeling in left armCount · n/N 1/1 · patient 34 (E.H.) · aura or seizure onsetPDF p.9, Fig. 4
  • 13 patientspainful somatosensory auraCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae; PDF p.8, Discussion
  • 2 patientspainful sensation after superior parietal area 5a stimulationCount · n/N 2/80 · 80 stimulated patients · stimulation responsePDF p.5, Electrical cortical stimulation
  • 1 caseright-fingertip tingling and pain in Fig. 1Count · n/N 1/1 · patient 7 (M.B.) · aura and ictal evolutionPDF p.4, Fig. 1
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • anesthesia; paresthesia; thermic dispersion; painful sensationThe source reports anesthesia, paresthesia, or thermic dispersion mainly with parietal stimulation, with the main effect in postcentral gyrus but additional involvement of precuneus and posterior cingulum; insular stimulation induced paresthesias and localized warmth, and painful sensations were preferentially associated with the posterior two thirds of the insula and were more frequently described in the nondominant hemisphere.PDF p.14, Somato-sensory sensations and pain

12 contributing manuscripts; source-reported values remain separate and are not pooled.

Goal-directed automatisms (reaching, searching, grabbing - quasi-purposeful)Source terms: Goal-directed automatismsReported: Right hemisphere9 manuscripts · 59 findings · 53 reported values
Weighted evidence supportevidence weight 21.82 across 9 manuscripts · 2 independent primary study · 4 narrative, educational, or cited context · 3 systematic review or meta-analysis

The review lists ictal spitting or drinking as localizing to a right temporal-lobe focus. No lateralizing axis is reported for the 67.5% gestural-automatism summary. The TL-versus-T+ comparison of looking around reports no lateralizing axis. No seizure lateralization is reported. The frontal motor hierarchy provides no lateralizing direction. The EZN-extension association provides no lateralizing information. No lateralizing direction is reported. No lateralization information is reported. No lateralization information is reported for grasping or clutching. The cited frontal rostrocaudal gradient is not lateralizing. No lateralizing direction is reported for the review-table gestural-automatism result. No lateralizing direction is reported for the restricted high/very-high-confidence subset. The rostrocaudal cluster gradient is not lateralizing. This record provides no seizure lateralization. No lateralization axis information is reported for motor gestural/oro-alimentary automatisms. No hemisphere or body-side direction is reported. The row reports an overall association grade, not lateralization evidence. Motor gestural automatisms were reported at 43%; no hemisphere direction is reported. No lateralization axis information is reported for motor gestural/oral automatisms. The source reports OR 0.5 for motor gestural automatisms relative to vocalization/verbalization; no hemisphere direction is reported. No lateralization axis information is reported for the motor-gestural versus affective/autonomic comparison. The source reports OR 0.8 for motor gestural automatisms relative to autonomic signs; no hemisphere direction is reported. The source reports OR 0.9 for motor gestural automatisms relative to facial expression change; no hemisphere direction is reported. No lateralization axis information is reported for affective/autonomic aura versus motor-gestural automatisms. No lateralization evidence is reported. This finding provides no lateralization information.

Source-defined result groups 10
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyTonic-clonic · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyF to BTC · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 3 findings · 4 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • gestural automatismsComplex behaviours were common and included gestural automatisms, reported in 67.5% of analyzed seizures.PDF p.5, Seizure clinical semiology
  • looking aroundLooking around did not differ significantly between TL and T+ groups.PDF p.6, Table 2
  • gestural automatisms and mesio-temporal structuresThe source states that gestural automatisms have been reported more often during mesio-temporal seizures than during neocortical or mesio-lateral temporal seizures and at a particularly high rate in TL seizures with mesio-temporal lesions.PDF p.8, Motor signs
Reported values
  • gestural automatisms 67.5%gestural automatismsPercentage · 80 analyzed seizures, one typical seizure per patient · ictalPDF p.5, Seizure clinical semiology
  • TL 32.2%looking aroundPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
  • P=0.5looking aroundP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • T+ 39.1%looking aroundPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • gestural automatismsGestural automatisms were reported in 25% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Gestural automatisms (Table 3)Table 3 reports gestural automatisms in 21 cases (25%), more during propagation.PDF p.6, Table 3
  • Gestural automatisms (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports gestural automatisms in 26 cases (43%).PDF p.7, Table 4
Reported values
  • 25% gestural automatismsgestural automatismsPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 21 cases (25%)Gestural automatisms (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 26/60 (43%)Gestural automatisms (Table 4)Percentage · n/N 26/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal spitting or drinkingIctal spitting or drinking is listed as localizing to a right temporal-lobe focus.PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfNarrative, educational, or cited context · 1 finding
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Consecutive presurgical SEEG series from Timone Hospital, Marseille, February 2000-November 2010: 54 patients in whom SEEG-defined EZ was within the frontal lobe, selected from 180 SEEG explorations; patients with inconclusive intracranial recording (n=1) or a nonpredominantly frontal EZ were excluded. All patients had noninvasive presurgical assessment and video-SEEG after complete or partial antiepileptic-drug withdrawal; 374 seizures were recorded and analyzed. The cohort included 22 male and 32 female patients, mean age 24.9 +/- 9.5 years, mean epilepsy duration 16.9 +/- 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed VEEG and electrical data; 31 ictal signs and 24 brain-area variables were scored 0-1-2 per patient, with rank-based PCA, hierarchical clustering, correlation matrices, and Kendall tests at p < 0.05. The source describes sampling 20 cortical regions in one methods passage and distinguishes the SEEG-defined EZ from the source-defined early spread network.
Findings
  • Ictal grasping or clutchingThe Discussion states that grasping or clutching occurs more frequently in seizures arising from frontal than extrafrontal regions, citing Gardella et al., 2006 and Leiguarda et al., 2008.PDF p.10, Electroclinical subgroups; PDF p.11, discussion of Group 3 behavior
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 31 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • motor gestural/oro-alimentary automatismsThe source reports a frequency of 43% for motor gestural/oro-alimentary automatisms.PDF p.13, Table 3
  • motor gestural/oro-alimentary automatisms; reported frequency rangeThe source reports a frequency range of 0–91% for motor gestural/oro-alimentary automatisms.PDF p.13, Table 3
  • motor gestural/oro-alimentary automatisms; ACC association gradeTable 3 assigns the source's High overall association grade to motor gestural/oro-alimentary automatisms.PDF p.13, Table 3
  • motor gestural automatisms; Figure 4 rateFigure 4 displays a 43% rate for motor gestural automatisms.PDF p.10, Figure 4
  • motor gestural/oral automatismsMotor gestural/oral automatisms were reported in 43% of patients.PDF p.9, Objective symptomatology
  • motor gestural automatisms typicalityMotor gestural automatisms met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • pairwise OR: Motor (gestural) automatisms relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.5 for Motor (gestural) automatisms relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.5 for Motor (gestural) automatisms relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.6 for Motor (gestural) automatisms relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Autonomic signsFigure 6 reports an odds ratio of 0.8 for Motor (gestural) automatisms relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Facial expression changeFigure 6 reports an odds ratio of 0.9 for Motor (gestural) automatisms relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 2.1 for Vocalization/verbalization relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 2 for Hypermotor-complex motor behavior relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 1.7 for Affective/autonomic aura relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 1.2 for Autonomic signs relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 1.1 for Facial expression change relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.7 for Loss of consciousness relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.6 for Post-ictal confusion/behavior change disinhibition relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.3 for Chapeau de gendarme relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.3 for Dystonic posturing relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.2 for Laughter relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.1 for Oro-alimentary automatisms relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.1 for Tonic-clonic relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Loss of consciousnessFigure 6 reports an odds ratio of 1.4 for Motor (gestural) automatisms relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 1.7 for Motor (gestural) automatisms relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 2.9 for Motor (gestural) automatisms relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Dystonic posturingFigure 6 reports an odds ratio of 3.1 for Motor (gestural) automatisms relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Head-eye deviationFigure 6 reports an odds ratio of 4.6 for Motor (gestural) automatisms relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to LaughterFigure 6 reports an odds ratio of 7 for Motor (gestural) automatisms relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 7.9 for Motor (gestural) automatisms relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Tonic-clonicFigure 6 reports an odds ratio of 13.1 for Motor (gestural) automatisms relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to F to BTCFigure 6 reports an odds ratio of 13.1 for Motor (gestural) automatisms relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 43% (frequency range 0–91%)motor gestural/oro-alimentary automatismsPercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.13, Table 3
  • 43%motor gestural automatisms; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.10, Figure 4
  • 43%motor gestural/oral automatismsPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • OR 0.5pairwise OR: Motor (gestural) automatisms relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Motor (gestural) automatisms relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Motor (gestural) automatisms relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Motor (gestural) automatisms relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Motor (gestural) automatisms relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Vocalization/verbalization relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2pairwise OR: Hypermotor-complex motor behavior relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Affective/autonomic aura relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Autonomic signs relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Facial expression change relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Loss of consciousness relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Chapeau de gendarme relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Dystonic posturing relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Laughter relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Oro-alimentary automatisms relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.4pairwise OR: Motor (gestural) automatisms relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Motor (gestural) automatisms relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Motor (gestural) automatisms relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.1pairwise OR: Motor (gestural) automatisms relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.6pairwise OR: Motor (gestural) automatisms relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7pairwise OR: Motor (gestural) automatisms relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.9pairwise OR: Motor (gestural) automatisms relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.1pairwise OR: Motor (gestural) automatisms relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.1pairwise OR: Motor (gestural) automatisms relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • elementary motor sign; complex motor sign; gestural behaviourIntracranial stereo-EEG literature is summarized as placing elementary clonic, tonic, and versive signs in precentral and premotor regions; less-natural proximal stereotypies such as rocking and turning in premotor/posterior prefrontal regions; and more integrated natural gestural behaviour with distal stereotypies such as manual automatisms in more anterior prefrontal regions including orbitofrontal cortex, frontal pole, and anterior cingulate.PDF p.2, Frontal lobe seizures; PDF p.3, Figure 1
  • elementary motor signs; complex motor signs; gestural behaviourThe review reports that intracranial stereo-EEG studies associate elementary clonic, tonic, and versive signs with precentral and premotor regions; more complex motor signs with more rostral frontal regions; non-integrated proximal stereotypies such as rocking and turning with premotor and posterior prefrontal regions; and integrated distal stereotypies such as manual automatisms with anterior prefrontal regions including orbitofrontal cortex, frontal pole, and anterior cingulate.PDF p.2, Frontal lobe seizures
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 12 findings · 9 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • OFC + group (EZN extending beyond OFC); aura; oro-alimentary automatisms; gestural automatismsThe source characterizes EZN extending beyond the OFC as having richer semiological profiles, with temporal extension more often associated with aura, oro-alimentary automatisms, and sleep.PDF p.6, Semiological profile; PDF p.7, Conclusion
  • frontal and insular EZN extension; hyperkinetic behavior; mimic automatisms; gestural automatismsFrontal and insular extensions are described as more likely to show hyperkinetic behavior, mimic automatisms, and gestural automatisms.PDF p.7, Conclusion
  • gestural automatismsThe source interprets gestural automatisms as potentially indicating an EZN extending beyond the OFC, particularly into the temporal lobe.PDF p.3, Complex motor phenomena—automatisms
  • gestural automatismsGestural automatisms were reported in five of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • gestural automatisms; HkB subgroupNo HkB case had gestural automatisms.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • gestural automatisms; non-HkB subgroupFive of the non-HkB cases had gestural automatisms.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • gestural automatisms; entire groupThe source reports 28% for gestural automatisms in the entire ofc-involving group.PDF p.3, Complex motor phenomena—automatisms
  • gestural automatisms; OFC-restricted EZNThe source reports 19% for gestural automatisms in the ofc-restricted ezn group.PDF p.3, Complex motor phenomena—automatisms
  • gestural automatisms; OFC-extended EZNThe source reports 36% for gestural automatisms in the ofc-extended ezn group.PDF p.3, Complex motor phenomena—automatisms
  • gestural automatisms; temporal subgroupThe source reports 50% for gestural automatisms in the temporal subgroup of ofc-extended ezn.PDF p.3, Complex motor phenomena—automatisms
  • gestural automatisms; frontal subgroupThe source reports 27% for gestural automatisms in the frontal subgroup of ofc-extended ezn.PDF p.3, Complex motor phenomena—automatisms
  • gestural automatisms; insular subgroupThe source reports 30% for gestural automatisms in the insular subgroup of ofc-extended ezn.PDF p.3, Complex motor phenomena—automatisms
Reported values
  • 5/26 (19.2%)gestural automatismsPercentage · n/N 5/26 · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 0/14 patientsgestural automatisms; HkB subgroupCount · n/N 0/14 · HkB subgroup within OFC-restricted EZN · HkB subgroup within OFC-restricted EZN · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 5/12 (41.6%)gestural automatisms; non-HkB subgroupPercentage · n/N 5/12 · Non-HkB subgroup within OFC-restricted EZN · Non-HkB subgroup within OFC-restricted EZN · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 28%gestural automatisms; entire groupPercentage · Entire OFC-involving group · Entire OFC-involving group · ictalPDF p.3, Complex motor phenomena—automatisms
  • 19%gestural automatisms; OFC-restricted EZNPercentage · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.3, Complex motor phenomena—automatisms
  • 36%gestural automatisms; OFC-extended EZNPercentage · OFC-extended EZN group · OFC-extended EZN group · ictalPDF p.3, Complex motor phenomena—automatisms
  • 50%gestural automatisms; temporal subgroupPercentage · Temporal subgroup of OFC-extended EZN · Temporal subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—automatisms
  • 27%gestural automatisms; frontal subgroupPercentage · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—automatisms
  • 30%gestural automatisms; insular subgroupPercentage · Insular subgroup of OFC-extended EZN · Insular subgroup of OFC-extended EZN · ictalPDF p.3, Complex motor phenomena—automatisms
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 5 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • elementary motor signs; gestural motor behavior; emotional expressionThe review reports that Bonini, McGonigal et al. (2014) identified four frontal-lobe semiologic groups along a rostro-caudal gradient: Group 1 had elementary motor signs without gestural motor behavior; Group 2 combined elementary and gestural motor signs, often with mainly proximal tonic signs and facial contraction; Group 3 had no elementary motor signs and often distal, integrated gestural behavior; and Group 4 had no elementary motor signs with integrated gestural behavior in an emotional, usually fearful, context.PDF p.6, Table 2, Frontal lobe row
  • elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresIn the summarized Bonini, McGonigal et al. study, automated clustering of clinical signs and brain areas involved in seizure onset and early propagation found a rostrocaudal frontal gradient with four groups: elementary motor signs without gestural behavior; elementary plus gestural signs with mainly proximal tonic signs and facial contraction; gestural behavior without elementary signs and often distal or integrated; and gestural behavior in an emotional, often fearful, context with an integrated appearance.PDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
Reported values
  • 374 seizureselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • 54 subjectselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • Semiology clusters n=4elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Patients in semiology series n=54elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Seizures in semiology series n=374elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • oral and gestural automatismsOral and gestural automatisms occurred in 17% of patients.PDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
Reported values
  • 17%oral and gestural automatismsPercentage · 82-patient parietal epilepsy series · ictal propagation or later ictal phasePDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Todd postictal paralysis (contralateral hemiparesis/hemiplegia)Source terms: Todd postictal paralysis; Todd paralysisReported: ContralateralAlso reported: Ipsilateral8 manuscripts · 12 findings · 33 reported values
Weighted evidence supportevidence weight 21.4 across 8 manuscripts · 4 narrative, educational, or cited context · 3 independent primary study · 1 systematic review or meta-analysis

The review restates an ipsilateral last clonic jerk and contralateral postictal Todd's paresis as lateralizing signs. The review lists postictal Todd's paresis as contralateral to the seizure focus. Ictal and postictal paresis are difficult to distinguish but are said to convey the same unspecified lateralization. The review restates Todd’s paresis as rare in LTM series and contralateral to the onset hemisphere in 93% of patients who experienced it. The review describes robust motor signs as predominantly contralateral to onset, with the last clonic jerk as an ipsilateral sign. The review states that postictal limb paresis or paralysis occurred in 0.5–13% of focal seizures and was always contralateral to the seizure-origin hemisphere. The current paper restates prior reports of almost 100% or 100% PPV for Todd’s paralysis lateralizing the EZ contralateral to the paralyzed side. The educational review calls Todd's paralysis non-localizing but highly lateralizing and describes preceding ipsilateral motor activity. The cited review describes unilateral ictal or postictal limb immobility as contralateral to the epileptogenic zone in almost all cases. The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. No lateralizing direction is reported for Todd’s paralysis in aggregate. Todd's paralysis occurred in 4/42 patients; no hemisphere or body-side direction is reported.

Source-defined result groups 8
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Postictal Todd’s paresisPostictal Todd’s paresis is listed as contralateral to the seizure focus.PDF p.4, Table 2
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • asymmetric clonic ending; postictal Todd’s paresisThe source states that an asymmetric clonic ending of the generalised phase, with the last clonic jerk ipsilateral to seizure onset, and postictal Todd’s paresis contralateral to seizure onset are lateralising signs; these signs do not distinguish frontal from extrafrontal onset.PDF p.10, Lateralising signs
  • robust lateralising motor signs; figure-of-4 sign; Todd’s paresisThe review describes unilateral clonic movements, unilateral tonic or dystonic posturing, and early head version as robust lateralising motor signs with positive predictive value greater than 80%, all contralateral to onset; it also states that before secondary generalization the extended arm in a figure-of-4 sign is contralateral, the last clonic jerk is ipsilateral, and postictal Todd’s paresis is contralateral to seizure onset.PDF p.10, Lateralising signs
Reported values
  • Positive predictive value >80% for the listed robust motor signsrobust lateralising motor signs; figure-of-4 sign; Todd’s paresisPercentage · Patients with focal seizures in the cited motor-sequence literature; exact cohort Not reported · Ictal onset, pre-generalization, generalized phase ending, and postictal periodPDF p.10, Lateralising signs
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • postictal limb paresis or Todd's paresisPostictal limb paresis or paralysis was found in 0.5–13% of focal seizures and was always contralateral to the hemisphere of seizure origin.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures
  • unilateral ictal or postictal immobile limbA sudden loss of tone in one upper limb while the opposite side expresses automatisms was observed in 5–28% of focal seizures, usually with temporal-lobe origin, and was contralateral to the epileptogenic zone in almost all cases.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • Present in 0.5–13% of focal seizurespostictal limb paresis or Todd's paresisPercentage · patients with focal seizures · postictalPDF p.4, section 4 Lateralizing motor signs in complex motor seizures
  • Observed in 5–28% of focal seizuresunilateral ictal or postictal immobile limbPercentage · patients with focal seizures · ictal or postictalPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Ictal and postictal paresisThe review states that ictal and postictal paresis are difficult to distinguish but provide the same lateralisation information.PDF p.4, section 1.6
  • Todd’s paresisThe review reports that Todd’s paresis occurs in less than 1% of LTM series and indicates onset in the contralateral hemisphere in 93% of patients who experience it.PDF p.4, section 1.6
Reported values
  • <1% of LTM seriesTodd’s paresisPercentage · LTM series; patients who experience Todd’s paresis · LTM series · postictalPDF p.4, section 1.6
  • 93% contralateral-onset proportionTodd’s paresisPercentage · LTM series; patients who experience Todd’s paresis · patients with Todd’s paresis · postictalPDF p.4, section 1.6
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 2 findings · 26 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • Todd's paralysisThe current paper reports that previous studies found Todd's paralysis to have an almost 100% or 100% positive predictive value for lateralizing the EZ to the contralateral hemisphere.PDF p.8, Todd's paralysis definition and cited value; PDF p.11, discussion of prior 100% PPV; PDF p.12, limitations of retrospective detection in the current cohort
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
Reported values
  • Todd's paralysis PPV almost 100%Todd's paralysisPositive predictive value · Cited-study populations as summarized in the current paper; Not reported · Cited estimate reported as almost 100% · PostictalPDF p.8, Todd's paralysis definition and cited value; PDF p.11, discussion of prior 100% PPV; PDF p.12, limitations of retrospective detection in the current cohort
  • Todd's paralysis PPV 100%Todd's paralysisPositive predictive value · Cited-study populations as summarized in the current paper; Not reported · Cited estimate reported as 100% · PostictalPDF p.8, Todd's paralysis definition and cited value; PDF p.11, discussion of prior 100% PPV; PDF p.12, limitations of retrospective detection in the current cohort
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • Todd’s paralysisTodd’s paralysis occurred in four of 42 patients.PDF p.6, Results, Non-visual manifestations
Reported values
  • 4/42 (10%) patientsTodd’s paralysisPercentage · n/N 4/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · post-ictalPDF p.6, Results, Non-visual manifestations
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • Todd's paralysisTodd’s paralysis occurred in 22% of patients.PDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
Reported values
  • 22%Todd's paralysisPercentage · 82-patient parietal epilepsy series · post-ictalPDF p.4, Results, Other seizure characteristics; PDF p.5, Table 2
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • Todd's paralysisThe review describes Todd's paralysis as a non-localizing but highly lateralizing sign and states that it is always preceded by prominent ipsilateral motor activity of the affected limb.PDF p.6, Todd's paralysis

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal confusionReported: IpsilateralAlso reported: Right hemisphere7 manuscripts · 37 findings · 43 reported values
Weighted evidence supportevidence weight 20.07 across 7 manuscripts · 3 independent primary study · 3 narrative, educational, or cited context · 1 systematic review or meta-analysis

No hemisphere or body-side direction is reported. The frontal-versus-temporal statement contains no lateralization information. The review table reports no hemisphere or body-side association for postictal confusion. No hemisphere or body-side direction is reported for postictal confusion. No lateralization axis information is reported for post-ictal confusion/behavior change disinhibition versus affective/autonomic aura. Figure 6 reports OR 2.9 for Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibition, with no hemisphere or lateralization direction. No lateralization evidence is reported.

Source-defined result groups 11
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 7.7%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / TemporalObserved proportion 19.4%Frontal SHE · Other SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 25.0%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / TemporalObserved proportion 13.3%Operculoinsular SHE · Other SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / TemporalObserved proportion 28.6%Posterior SHE · Other SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.9%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: ACC seizure casesSource-defined values retained separatelypatient1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / TemporalObserved proportion 66.7%Temporal SHE · Other SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • post-ictal confusionPost-ictal confusion was common, reported in 45% of analyzed seizures.PDF p.5, Seizure clinical semiology
  • post-ictal confusionPost-ictal confusion did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • post-ictal confusion 45%post-ictal confusionPercentage · 80 analyzed seizures, one typical seizure per patient · post-ictalPDF p.5, Seizure clinical semiology
  • TL 40.7%post-ictal confusionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · post-ictalPDF p.6, Table 2
  • T+ 52.2%post-ictal confusionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · post-ictalPDF p.6, Table 2
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Postictal confusionTable 1 reports postictal confusion as more prominent and longer after temporal lobe seizures than after frontal lobe seizures, where it is less prominent and short.PDF p.2, Table 1
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 30 findings · 29 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • postictal confusionPostictal confusion was reported in 36 patients across 18 studies, with 31% experiencing confusion.PDF p.9, Objective symptomatology
  • postictal confusion; reporting studiesPostictal confusion was reported in 18 studies.PDF p.9, Objective symptomatology
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Autonomic signsFigure 6 reports an odds ratio of 0.5 for Post-ictal confusion/behavior change disinhibition relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Facial expression changeFigure 6 reports an odds ratio of 0.5 for Post-ictal confusion/behavior change disinhibition relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.6 for Post-ictal confusion/behavior change disinhibition relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.8 for Post-ictal confusion/behavior change disinhibition relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 3.6 for Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 3.4 for Hypermotor-complex motor behavior relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 2.9 for Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 2.1 for Autonomic signs relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 1.9 for Facial expression change relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 1.7 for Motor (gestural) automatisms relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 1.2 for Loss of consciousness relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.6 for Chapeau de gendarme relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.5 for Dystonic posturing relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.4 for Head-eye deviation relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.3 for Laughter relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.2 for Oro-alimentary automatisms relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.2 for Tonic-clonic relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.1 for F to BTC relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 1.7 for Post-ictal confusion/behavior change disinhibition relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Dystonic posturingFigure 6 reports an odds ratio of 1.8 for Post-ictal confusion/behavior change disinhibition relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Head-eye deviationFigure 6 reports an odds ratio of 2.7 for Post-ictal confusion/behavior change disinhibition relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to LaughterFigure 6 reports an odds ratio of 4.1 for Post-ictal confusion/behavior change disinhibition relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 4.6 for Post-ictal confusion/behavior change disinhibition relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Tonic-clonicFigure 6 reports an odds ratio of 7.6 for Post-ictal confusion/behavior change disinhibition relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to F to BTCFigure 6 reports an odds ratio of 7.6 for Post-ictal confusion/behavior change disinhibition relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 31% of 36 included patientspostictal confusionPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure cases with postictal dataPDF p.9, Objective symptomatology
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.4pairwise OR: Hypermotor-complex motor behavior relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Autonomic signs relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.9pairwise OR: Facial expression change relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Motor (gestural) automatisms relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Loss of consciousness relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Chapeau de gendarme relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Dystonic posturing relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Head-eye deviation relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Laughter relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Oro-alimentary automatisms relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Tonic-clonic relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: F to BTC relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.8pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.1pairwise OR: Post-ictal confusion/behavior change disinhibition relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 7 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 6.00 · 2 × 1.5 × 2
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • postictal confusionPostictal confusion was assessed in 101/115 patients (88%) and occurred in 25. The temporal subgroup had 8/12 patients with postictal confusion (67%, P=0.001), compared with frontal 13/67 (19%), operculoinsular 2/15 (13%), and posterior 2/7 (28%). The discussion additionally reports that 48% of postictal confusion was associated with SP4.PDF p.7, section 3.5; PDF p.9, section 4.4
Reported values
  • Postictal confusion occurred in 25/101 assessed patientspostictal confusionCount · n/N 25/101 · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
  • Posterior SHE postictal confusion 2/7 (28%)postictal confusionPercentage · n/N 2/7 · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · Posterior SHE · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
  • Temporal SHE postictal confusion 8/12 (67%)postictal confusionPercentage · n/N 8/12 · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · Temporal SHE · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
  • Postictal confusion associated with SP4 48%postictal confusionPercentage · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · Postictal-confusion cases · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
  • Frontal SHE postictal confusion 13/67 (19%)postictal confusionPercentage · n/N 13/67 · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · Frontal SHE · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
  • Operculoinsular SHE postictal confusion 2/15 (13%)postictal confusionPercentage · n/N 2/15 · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · Operculoinsular SHE · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
  • Postictal confusion assessed 101/115 (88%)postictal confusionPercentage · n/N 101/115 · 101 SHE patients with assessable postictal status; SOZ subgroups with denominators as reported · postictalPDF p.7, section 3.5; PDF p.9, section 4.4
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfNarrative, educational, or cited context · 1 finding
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • fencing posture and postictal confusionThe source states that adopting a fencing posture and the duration of postictal confusion have been demonstrated to distinguish frontal-lobe from temporal-lobe epilepsy.PDF p.4, Discussion
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Deep confusion and stertorous breathingThe review states that postictal confusion can appear similar in PNES and epileptic seizures, but deep confusion and stertorous breathing favour epilepsy.PDF p.7, section 1.18
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 4 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • postictal confusionPostictal confusion did not differ significantly across M, ML, and L groups.PDF p.6, Table 3
Reported values
  • ML=7/18 (38.9%)postictal confusionPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · postictalPDF p.6, Table 3
  • p=0.14postictal confusionP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · postictalPDF p.6, Table 3
  • L=1/13 (7.7%)postictal confusionPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · postictalPDF p.6, Table 3
  • M=6/24 (25%)postictal confusionPercentage · n/N 6/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · postictalPDF p.6, Table 3

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal eye blinkingReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphere6 manuscripts · 9 findings · 8 reported values
Weighted evidence supportevidence weight 19.72 across 6 manuscripts · 3 independent primary study · 1 case report or observation · 1 systematic review or meta-analysis · 1 narrative, educational, or cited context

This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. A single case caption reports left temporal rhythmic 4–6/sec EEG activity during a focal seizure with restlessness, aphasia, and eye blinking. The review states that the fast phase of epileptic nystagmus is typically contralateral and the slow component ipsilateral to the seizure-onset hemisphere. The review gives contralateral direction for hemifield visual aura, simple unilateral auditory aura, and the fast nystagmus component, but ipsilateral direction for unilateral eye blinking. Seven patients had bilateral or lateralized eye blinking, but no side-specific direction or reference side was reported. The review states that unilateral ictal eye blinking generally lateralizes ipsilateral to the epileptogenic zone, with 83% ipsilateral in the reported subgroup. The aggregate eye-blinking prevalence reports no side direction. The cited onset prevalence reports no side direction for eye blinking. Blinking frequency in the occipital cohort reports no direction.

Evidence by contributing manuscript 6

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 3 findings · 2 reported values
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • eye blinking; epileptic nystagmusIn a cited large series, 20% of patients had eye blinking at seizure onset; the review also states that eye version can occur with occipital-localized ictal discharges and that epileptic nystagmus typically has its fast phase contralateral and slow component ipsilateral to the seizure-onset hemisphere.PDF p.8, Parieto-occipital junction
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmus; unilateral auditory auraA hemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; the fast component of epileptic nystagmus is contralateral to seizure onset; and a simple unilateral auditory aura, which the review notes is rare, is contralateral.PDF p.6, Lateral/neocortical temporal lobe; PDF p.8, Parieto-occipital junction; PDF p.10, Lateralising signs
  • eye blinking at seizure onsetIn a cited large series of occipital seizures, 20% of patients had eye blinking at seizure onset.PDF p.8, Parieto-occipital junction
Reported values
  • Eye blinking at onset in 20% of the cited serieseye blinking; epileptic nystagmusPercentage · Patients in the cited occipital epilepsy series and reported nystagmus cases; exact cohorts Not reported · Ictal onset and ictal evolutionPDF p.8, Parieto-occipital junction
  • eye blinking at seizure onset 20%eye blinking at seizure onsetPercentage · patients in a large occipital seizure series · seizure onsetPDF p.8, Parieto-occipital junction
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral ictal eye blinkingUnilateral ictal eye blinking generally lateralizes ipsilateral to the epileptogenic zone.PDF p.8, section 3.14; PDF p.12, Table 1
Reported values
  • Unilateral ictal eye blinking ipsilateral in 83%unilateral ictal eye blinkingPercentage · epilepsy monitoring unit patients with unilateral blinking unassociated with facial clonus · Patients with unilateral blinking · ictalPDF p.8, section 3.14; PDF p.12, Table 1
  • Unilateral ictal eye blinking in 1.5% of EMU patientsunilateral ictal eye blinkingPercentage · epilepsy monitoring unit patients with unilateral blinking unassociated with facial clonus · Epilepsy monitoring unit · ictalPDF p.8, section 3.14; PDF p.12, Table 1
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • blinkingBlinking occurred in eight of 42 patients.PDF p.6, Results, Non-visual manifestations
Reported values
  • 8/42 (19%) patientsblinkingPercentage · n/N 8/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.6, Results, Non-visual manifestations
unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 1 finding · 1 reported value
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • focal seizure with restlessness, aphasia, and eye blinkingFigure 2 depicts a 59-year-old female with a focal seizure involving restlessness, aphasia, and eye blinking, with a seizure pattern showing left temporal rhythmic 4–6/sec activity.PDF p.3, Fig.2 caption and EEG rendering
Reported values
  • Rhythmic 4–6/sec EEG activityfocal seizure with restlessness, aphasia, and eye blinkingCount · Female, 59 years; focal seizure · ictalPDF p.3, Fig.2 caption and EEG rendering
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 1 reported value
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • bilateral or lateralized eye blinkingBilateral or lateralized eye blinking occurred in seven patients.PDF p.3, Results—Seizure semiology; PDF p.9, Discussion
Reported values
  • 7/22 (32%)bilateral or lateralized eye blinkingPercentage · n/N 7/22 · 22 patients with insulo-opercular epilepsy · ictal/early motor semiologyPDF p.3, Results—Seizure semiology; PDF p.9, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • eye blinkingEye blinking occurred in 12 of 19 patients (63.2%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
Reported values
  • 12/19 (63.2%) eye blinkingeye blinkingPercentage · n/N 12/19 · 19 patients monitored with SEEG · ictal oculomotor semiologyPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Speech/language disturbance (unspecified subtype or phase)Reported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere9 manuscripts · 27 findings · 39 reported values
Weighted evidence supportevidence weight 19.02 across 9 manuscripts · 1 manuscript weight pending · 4 systematic review or meta-analysis · 3 narrative, educational, or cited context · 1 independent primary study · 1 structured design not resolved

The educational opercular-seizure description associates oral symptoms and speech difficulty with focal clonic movements of the contralateral face. The cited study restatement reports speech responses evoked in both nondominant and dominant language hemispheres. The review synthesis associates early aphasic features in basal temporal seizures with dominant-hemisphere onset. Interictal EEG side distributions differed by speech phenotype: dysphasia had 15 exclusive-left, 18 bilateral, and 1 exclusive-right discharge, while speech automatisms had 4 exclusive-left, 20 bilateral, 13 exclusive-right, and 1 normal EEG. Speech-disturbance responses occurred in both nondominant and dominant language hemispheres, 51.8% versus 48.2%, without a strong side preference. Speech manifestations occurred in at least one seizure in 34 of 35 patients, including 16/16 dominant-origin and 18/19 nondominant-origin patients. Speech manifestations occurred in 79/100 seizures, in 45/48 dominant-origin and 34/52 nondominant-origin seizures. Abnormal speech occurred in 41 seizures from 18 patients, with 34 seizures in 13 dominant-origin patients and 7 seizures in 5 nondominant-origin patients. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. No hemisphere or body-side direction is reported. The primary speech-dysfunction comparison reports no hemisphere or lateralizing direction. No lateralization axis information is reported for the historical lateral-temporal symptom description. The row reports the number of speech-disturbance studies, not lateralization evidence. The row reports a sample size, not lateralization evidence. No lateralization axis information is reported for the speech-disturbance odds confidence interval. No lateralization axis information is reported for the speech-disturbance heterogeneity test. No lateralization axis information is reported for the speech-disturbance study comparison. No lateralization axis information is reported for the 51 lateral-TLE patients assessed for speech disturbance. No lateralization axis information is reported for the 67 mesial-TLE patients assessed for speech disturbance. The review lists speech-status categories and gives no hemisphere or lateralizing direction.

Source-defined result groups 23
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyAll reported · dominant-origin versus nondominant-origin abnormal-speech observations · patient and seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Speech disturbance · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 52.6%Speech automatism · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 2.9%Dysphasia · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelydominant-origin · dominant-origin versus nondominant-origin abnormal-speech observations · patient and seizure1 manuscript · 2 reported values · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 2.6%Speech automatism · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 79.0%Overall · dominant-origin versus nondominant-origin seizures · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelynondominant-origin · dominant-origin versus nondominant-origin abnormal-speech observations · patient and seizure1 manuscript · 2 reported values · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 93.8%Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 52.9%Dysphasia · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 94.7%nondominant-origin · dominant-origin versus nondominant-origin patient groups · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 34.2%Speech automatism · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 44.1%Dysphasia · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 51.4%All reported · dominant-origin versus nondominant-origin abnormal-speech observations · patient and seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 97.1%all patients · dominant-origin versus nondominant-origin patient groups · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 10.5%Speech automatism · Dysphasia versus speech automatism across exclusive left, bilateral, exclusive right, and normal EEG categories · patient/case1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyDominant language hemisphere · evoked speech-disturbance response1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 100.0%dominant-origin · dominant-origin versus nondominant-origin patient groups · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 65.4%Nondominant-origin · Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Speech disturbance · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyNondominant language hemisphere · Dominant language hemisphere · evoked speech-disturbance response1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • language and verbal componentsThe review states that language and verbal components are emphasized in basal temporal seizures, with aphasic features frequently emerging early when seizures originate from the dominant hemisphere.PDF p.8, Discussion
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 12 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • auditory hallucinations; dreamy states; visual misperceptions; language disorders; focal impaired consciousness seizuresThe source's historical lateral-temporal description includes auditory hallucinations, dreamy states, visual misperceptions, language disorders, and progression to focal impaired consciousness seizures.PDF p.1, Introduction
  • Speech disturbanceTable 3 reports 3 studies assessing Speech disturbance.PDF p.6, Table 3
  • Speech disturbanceTable 3 reports 51 patients assessed for Speech disturbance.PDF p.6, Table 3
  • Speech disturbanceTable 3 reports 5.3–20% as the percentage range or value for Speech disturbance; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Speech disturbanceTable 4 reports overall odds of 0.13 for occurrence of Speech disturbance in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Speech disturbanceTable 4 reports a 95% confidence interval of 0.05–0.35 for the overall odds of Speech disturbance.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Speech disturbanceThe heterogeneity test for the Table 4 odds estimate for Speech disturbance has p=0.3305.PDF p.7, Table 4
  • Speech disturbance; lateral versus mesial comparisonTable 5 reports 3 studies comparing Speech disturbance in lateral and mesial TLE.PDF p.9, Table 5
  • Speech disturbance; lateral TLE patient denominatorTable 5 reports 51 lateral-TLE patients assessed for Speech disturbance.PDF p.9, Table 5
  • Speech disturbance; mesial TLE patient denominatorTable 5 reports 67 mesial-TLE patients assessed for Speech disturbance.PDF p.9, Table 5
  • Speech disturbance; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 5.3–20% for Speech disturbance.PDF p.9, Table 5
  • Speech disturbance; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 15–22.5% for Speech disturbance.PDF p.9, Table 5
Reported values
  • 5.3–20%Speech disturbancePercentage Range · Lateral temporal epilepsy patients assessed for Speech disturbance · ictalPDF p.6, Table 3
  • odds 0.13odds of occurrence; Speech disturbanceOdds · Lateral temporal epilepsy patients assessed for Speech disturbance · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 5.3–20%Speech disturbance; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Speech disturbance · Lateral TLE patients assessed for Speech disturbance · ictalPDF p.9, Table 5
  • 15–22.5%Speech disturbance; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Speech disturbance · Mesial TLE patients assessed for Speech disturbance · ictalPDF p.9, Table 5
e236615-full.pdfSystematic review or meta-analysis · 1 finding · 4 reported values
e236615-full.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • speech deficitsAmong cases in which speech deficits or their absence was reported, six had no speech deficits, six had receptive aphasia including the index case, one was globally aphasic, and one had non-specific speech abnormalities.PDF p.3, Discussion
Reported values
  • no speech deficit 6 casesspeech deficitsCount · Review cases with speech status reported · no speech deficitPDF p.3, Discussion
  • receptive aphasia 6 casesspeech deficitsCount · Review cases with speech status reported · receptive aphasiaPDF p.3, Discussion
  • global aphasia 1 casesspeech deficitsCount · Review cases with speech status reported · global aphasiaPDF p.3, Discussion
  • non-specific abnormality 1 casesspeech deficitsCount · Review cases with speech status reported · non-specific abnormalityPDF p.3, Discussion
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 3 findings · 12 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • speech manifestationsSpeech manifestations occurred in at least one seizure in 34 of 35 patients (97%); this included 16 of 16 dominant-origin patients and 18 of 19 nondominant-origin patients.PDF p.1, abstract; PDF p.2, Table 1 and Results
  • speech manifestationsSpeech manifestations were observed in 79 of 100 seizures (79%); 45 of 48 dominant-origin seizures (94%) and 34 of 52 nondominant-origin seizures (65%) had speech manifestations.PDF p.1, abstract; PDF p.2, Table 1 and Results; PDF p.5, Discussion
  • abnormal speechAbnormal speech occurred in 41 seizures from 18 patients (51.4% of patients); 34 seizures in 13 patients arose from the dominant side and 7 seizures in 5 patients from the nondominant side.PDF p.1, abstract; PDF p.3, Tables 2-3 and Results
Reported values
  • 34/35 patients (97%)speech manifestationsPercentage · n/N 34/35 · 35 patients with intractable temporal-lobe epilepsy undergoing temporal-lobectomy evaluation; patient-level analysis · all patients · ictal and/or postictal manifestationsPDF p.1, abstract; PDF p.2, Table 1 and Results
  • 18/19 nondominant-origin patientsspeech manifestationsPercentage · n/N 18/19 · 35 patients with intractable temporal-lobe epilepsy undergoing temporal-lobectomy evaluation; patient-level analysis · nondominant-origin · ictal and/or postictal manifestationsPDF p.1, abstract; PDF p.2, Table 1 and Results
  • 16/16 dominant-origin patientsspeech manifestationsPercentage · n/N 16/16 · 35 patients with intractable temporal-lobe epilepsy undergoing temporal-lobectomy evaluation; patient-level analysis · dominant-origin · ictal and/or postictal manifestationsPDF p.1, abstract; PDF p.2, Table 1 and Results
  • Nondominant-origin seizures with speech manifestations 34/52 (65%)speech manifestationsPercentage · n/N 34/52 · 100 seizures from 35 patients with intractable temporal-lobe epilepsy; seizure-level analysis · Nondominant-origin · ictal and/or postictal manifestationsPDF p.1, abstract; PDF p.2, Table 1 and Results; PDF p.5, Discussion
  • Speech manifestations 79/100 seizures (79%)speech manifestationsPercentage · n/N 79/100 · 100 seizures from 35 patients with intractable temporal-lobe epilepsy; seizure-level analysis · Overall · ictal and/or postictal manifestationsPDF p.1, abstract; PDF p.2, Table 1 and Results; PDF p.5, Discussion
  • Dominant-origin seizures with speech manifestations 45/48 (94%)speech manifestationsPercentage · n/N 45/48 · 100 seizures from 35 patients with intractable temporal-lobe epilepsy; seizure-level analysis · Dominant-origin · ictal and/or postictal manifestationsPDF p.1, abstract; PDF p.2, Table 1 and Results; PDF p.5, Discussion
  • 7 nondominant-origin seizuresabnormal speechCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · nondominant-origin · ictal or postictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results
  • 13 dominant-origin patientsabnormal speechCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · dominant-origin · ictal or postictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results
  • 5 nondominant-origin patientsabnormal speechCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · nondominant-origin · ictal or postictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results
  • 34 dominant-origin seizuresabnormal speechCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · dominant-origin · ictal or postictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results
  • 41 seizures with abnormal speechabnormal speechCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · ictal or postictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results
  • 18 patients (51.4%)abnormal speechPercentage · n/N 18/35 · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · ictal or postictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 6 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • oral symptoms; sialorrhea; speech difficulties; focal clonic movements of the contralateral faceThe source's introductory clinical description associates opercular seizures with oral symptoms such as sialorrhea and speech difficulties, together with focal clonic movements of the contralateral face.PDF p.2, Introduction
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • Speech dysfunctionTable 2 reports 6/21 (29%) for Speech dysfunction; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Moderate.PDF p.7, Table 2
  • Speech dysfunctionTable 2 reports 2/12 patients with Speech dysfunction in the prefrontal operculum group.PDF p.7, Table 2
  • Speech dysfunctionTable 2 reports 4/9 patients with Speech dysfunction in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Speech dysfunctionFisher's exact comparison of Speech dysfunction between the prefrontal and precentral Rolandic operculum groups has p=0.331.PDF p.7, Table 2
Reported values
  • 6/21 (29%)Speech dysfunctionPercentage · n/N 6/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 2/12 patientsSpeech dysfunctionProportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 4/9 patientsSpeech dysfunctionProportion · n/N 4/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • speech responses in dominant and nondominant hemispheresThe source states that speech impairments were evoked in both nondominant and dominant hemispheres for language.PDF p.5, Other Insular Responses
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Language abnormalitiesThe review reports language abnormalities in 10% of unselected seizures and 50% of temporal-lobe seizures in video-EEG cohorts, including ictal speech, ictal or postictal aphasia, paraphasias, and anomia.PDF p.5, section 1.9
Reported values
  • 50% of temporal-lobe seizuresLanguage abnormalitiesPercentage · Video-EEG cohorts; unselected seizures and temporal-lobe seizures · temporal-lobe seizures · ictal or postictalPDF p.5, section 1.9
  • 10% of unselected seizuresLanguage abnormalitiesPercentage · Video-EEG cohorts; unselected seizures and temporal-lobe seizures · unselected seizures · ictal or postictalPDF p.5, section 1.9
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 7 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • speech disturbancesTwenty-seven speech disturbances (5%) comprised speech arrest (18), slowing (2), slurred speech (4), or lowered voice intensity (3); they were evoked in both nondominant (51.8%) and dominant (48.2%) language hemispheres and had a widespread insular distribution with middle-upper and posterior-inferior predominance.PDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
Reported values
  • 51.8% in nondominant language hemispherespeech disturbancesPercentage · 27 speech-disturbance responses in the 550-response series · Nondominant language hemisphere · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
  • Lowered voice intensity 3/27speech disturbancesCount · n/N 3/27 · 27 speech-disturbance responses in the 550-response series · Speech disturbances · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
  • Speech slowing 2/27speech disturbancesCount · n/N 2/27 · 27 speech-disturbance responses in the 550-response series · Speech disturbances · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
  • Speech arrest 18/27speech disturbancesCount · n/N 18/27 · 27 speech-disturbance responses in the 550-response series · Speech disturbances · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
  • Slurred speech 4/27speech disturbancesCount · n/N 4/27 · 27 speech-disturbance responses in the 550-response series · Speech disturbances · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
  • 48.2% in dominant language hemispherespeech disturbancesPercentage · 27 speech-disturbance responses in the 550-response series · Dominant language hemisphere · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
  • Speech disturbances 27/550 (5%)speech disturbancesPercentage · n/N 27/550 · 27 speech-disturbance responses in the 550-response series · stimulation-evoked speech disturbancePDF p.3, Results and Table 1; PDF p.6, continuation and Fig. 5D
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfIndependent primary study · 1 finding · 7 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Independent primary study · Class II · Evidence weight 3.22 · 2 × 0.9 × 1.79
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • speech disturbance; pre-operative interictal spike dischargesAcross Groups A and B, Table IV reports dysphasia-associated EEG discharges in 15 patients exclusively left-sided, 18 bilateral, and 1 exclusively right-sided; speech-automatism-associated discharges were 4 exclusively left-sided, 20 bilateral, and 13 exclusively right-sided, with 1 additional speech-automatism patient having a normal EEG.PDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
Reported values
  • Speech automatism: 1/38 normal EEGspeech disturbance; pre-operative interictal spike dischargesCount · n/N 1/38 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Speech automatism · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
  • Speech automatism: 4/38 exclusively left-sided dischargesspeech disturbance; pre-operative interictal spike dischargesCount · n/N 4/38 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Speech automatism · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
  • Dysphasia: 18/34 bilateral dischargesspeech disturbance; pre-operative interictal spike dischargesCount · n/N 18/34 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Dysphasia · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
  • Dysphasia: 1/34 exclusively right-sided dischargespeech disturbance; pre-operative interictal spike dischargesCount · n/N 1/34 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Dysphasia · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
  • Speech automatism: 13/38 exclusively right-sided dischargesspeech disturbance; pre-operative interictal spike dischargesCount · n/N 13/38 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Speech automatism · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
  • Dysphasia: 15/34 exclusively left-sided dischargesspeech disturbance; pre-operative interictal spike dischargesCount · n/N 15/34 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Dysphasia · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns
  • Speech automatism: 20/38 bilateral dischargesspeech disturbance; pre-operative interictal spike dischargesCount · n/N 20/38 · Groups A and B combined; 34 dysphasia patients and 38 speech-automatism patients · Speech automatism · Pre-operative interictal EEGPDF p.12, Table IV, Groups A and B rows; PDF p.13, summary of pre-operative EEG patterns

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal loss of consciousnessReported: Ipsilateral10 manuscripts · 75 findings · 54 reported values
Weighted evidence supportevidence weight 18.86 across 10 manuscripts · 2 manuscript weight pending · 1 independent primary study · 2 structured design not resolved · 3 systematic review or meta-analysis · 4 narrative, educational, or cited context

The adapted table explicitly labels the dialeptic seizure pattern non-lateralising. The review states that isolated dialeptic seizures provide no useful lateralizing information. No hemisphere or body-side direction is reported. The TL-versus-T+ comparison contains no hemisphere or body-side direction. No hemisphere-direction relationship is reported. Case 5 propagation anatomy is reported without hemisphere or body-side direction. Case 6 propagation is described without hemisphere or body-side direction. No hemisphere or side-relative direction is reported. The temporal lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The frontal lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The occipital lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The parietal lobe distribution estimate for dialeptic/LOA semiology contains no hemisphere or body-side direction. The review reports no hemisphere or body-side association for dialeptic seizures. No lateralization axis information is reported for loss of consciousness versus affective/autonomic aura. Figure 6 reports OR 2.3 for Affective/autonomic aura relative to Loss of consciousness, with no hemisphere or lateralization direction.

Source-defined result groups 15
Localization: hypothalamusSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: atypical anterior cingulate lesion groupObserved proportion 100.0%All reported · typical anterior preserved awareness · patients1 manuscript · 1 reported value · not pooled
Localization: PCEObserved proportion 28.6%All reported · automotor seizures · patients1 manuscript · 1 reported value · not pooled
Localization: posterior cingulate lesion groupObserved proportion 50.0%All reported · posterior patients with automatisms · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given LOA/dialeptic semiology · localizing data point1 manuscript · 1 reported value · not pooled
Localization: ACC seizure casesSource-defined values retained separatelypatient-level frequency synthesized across eligible studies1 manuscript · 1 reported value · not pooled
Localization: cingulateSource-defined values retained separatelycingulate localization · localizing data point1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 94.9% · seizures1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given LOA/dialeptic semiology · localizing data point1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyregional localization distribution · localizing data point1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · patients with the ictal symptom1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ 100% · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 10

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 23 findings · 12 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • dialeptic-LOA-LOCTable 1 defines or exemplifies the the source's own semiology category “dialeptic-LOA-LOC” as Blank stare, loss of awareness, loss of contact, psychomotor arrest, distant gaze, dreamy state, loss of consciousness excluding generalized seizures, or dyscognitive states.PDF p.7, Table 1 Semiology descriptions and frequencies
  • dialeptic-LOA-LOCDialeptic-LOA-LOC comprised 8.3% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • dialeptic/LOA; Figure 3 all-data subsetFigure 3 reports N = 753 for the all-data dialeptic/LOA panel.PDF p.9, Figure 3 and caption
  • dialeptic/LOA; Figure 3 non-topological subsetFigure 3 reports N = 291 for the non-topological dialeptic/LOA panel.PDF p.9, Figure 3 and caption
  • dialeptic/LOA; temporal lobeLoss-of-awareness/dialeptic semiology was temporal in origin in 42%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; temporal lobeThe 95% CI for dialeptic/LOA; temporal lobe was 36%–49%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; frontal lobeLoss-of-awareness/dialeptic semiology was frontal in origin in 28%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; frontal lobeThe 95% CI for dialeptic/LOA; frontal lobe was 23%–34%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; cingulatedialeptic/LOA semiology was cingulate in 3%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; cingulateThe 95% CI for dialeptic/LOA; cingulate was 1%–4%.PDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; occipital lobedialeptic/LOA localizing distribution included occipital lobe at 9%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; occipital lobeThe 95% CI for the occipital lobe dialeptic/LOA distribution was 6%–11%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; parietal lobedialeptic/LOA localizing distribution included parietal lobe at 8%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; parietal lobeThe 95% CI for the parietal lobe dialeptic/LOA distribution was 5%–11%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; hypothalamusdialeptic/LOA localizing distribution included hypothalamus at 8%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; hypothalamusThe 95% CI for the hypothalamus dialeptic/LOA distribution was 5%–10%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; cingulatedialeptic/LOA localizing distribution included cingulate at under 5%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; cingulateThe 95% CI for the cingulate dialeptic/LOA distribution was 1%–4%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; insuladialeptic/LOA localizing distribution included insula at under 5%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; insulaThe 95% CI for the insula dialeptic/LOA distribution was 1%–4%.PDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; temporal cited resultA cited study is restated as reporting 35% of cases with dialeptic/altered-consciousness seizures involving the temporal region.PDF p.12, Localizing probabilities
  • dialeptic/LOA; frontal cited resultA cited study is restated as reporting 16% of cases with dialeptic/altered-consciousness seizures involving the frontal region.PDF p.12, Localizing probabilities
  • dialeptic/LOA; parieto-occipital cited resultA cited study is restated as reporting 5% of cases with dialeptic/altered-consciousness seizures involving the parieto-occipital region.PDF p.12, Localizing probabilities
Reported values
  • dialeptic-LOA-LOC 8.3%dialeptic-LOA-LOCPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • dialeptic/LOA; temporal lobe 42%dialeptic/LOA; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; frontal lobe 28%dialeptic/LOA; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; cingulate 3%dialeptic/LOA; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • dialeptic/LOA; occipital lobe 9%dialeptic/LOA; occipital lobePercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; parietal lobe 8%dialeptic/LOA; parietal lobePercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; hypothalamus 8%dialeptic/LOA; hypothalamusPercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; cingulate under 5%dialeptic/LOA; cingulatePercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • dialeptic/LOA; insula under 5%dialeptic/LOA; insulaPercentage · dialeptic/LOA localizing dataPDF p.12, Relative localizing values; PDF p.12, Discussion
  • temporal localization 35%dialeptic/LOA; temporal cited resultPercentage · cited altered-consciousness seizure cohortPDF p.12, Localizing probabilities
  • frontal localization 16%dialeptic/LOA; frontal cited resultPercentage · cited altered-consciousness seizure cohortPDF p.12, Localizing probabilities
  • parieto-occipital localization 5%dialeptic/LOA; parieto-occipital cited resultPercentage · cited altered-consciousness seizure cohortPDF p.12, Localizing probabilities
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 2 findings · 2 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • atypical anterior complete loss of consciousnessAll four atypical anterior patients reported complete loss of consciousness in some or all seizures.PDF p.5, Clinical Presentation
  • posterior cingulate dialeptic seizuresDialeptic seizures, defined in the figure legend as complex partial seizures without automatisms, were seen in two of four posterior cingulate patients.PDF p.5, Clinical Presentation; PDF p.4, Figure 3 legend
Reported values
  • 4/4 with complete loss of consciousnessatypical anterior complete loss of consciousnessProportion · n/N 4/4 · 4 atypical anterior cingulate cases · ictal awarenessPDF p.5, Clinical Presentation
  • 2/4 dialeptic seizuresposterior cingulate dialeptic seizuresProportion · n/N 2/4 · 4 posterior cingulate cases · ictal semiologyPDF p.5, Clinical Presentation; PDF p.4, Figure 3 legend
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 4 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.86 · 2 × 1.5 × 1.952
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • consciousness impairmentConsciousness was impaired in all but three analyzed seizures.PDF p.5, Seizure clinical semiology
  • consciousness impairmentTable 2 reports no significant difference in consciousness impairment between TL and T+ groups.PDF p.6, Table 2
Reported values
  • consciousness impaired in all but three of 80 seizuresconsciousness impairmentCount · 80 analyzed seizures, one typical seizure per patient · ictalPDF p.5, Seizure clinical semiology
  • P=0.27consciousness impairmentP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • T+ 100%consciousness impairmentPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 94.9%consciousness impairmentPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 4 findings · 2 reported values
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • loss of consciousnessTable 3 lists 9 patients for the the source's own ictal symptom “loss of consciousness”; its table phase label is propagation.PDF p.6, Table 3
  • loss of consciousnessTable 3 reports a pooled prevalence of 19% for the the source's own ictal symptom “loss of consciousness”; its table phase label is propagation.PDF p.6, Table 3
  • loss of consciousness; between-study heterogeneityThe source reports I2 heterogeneity of 30.37% for pooled loss of consciousness prevalence.PDF p.4, Results
  • loss of consciousness; heterogeneity testThe source reports p = 0.10 for the between-study heterogeneity test of pooled loss of consciousness prevalence.PDF p.4, Results
Reported values
  • 19% pooled prevalenceloss of consciousnessPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · propagationPDF p.6, Table 3
  • I2 = 30.37%loss of consciousness; between-study heterogeneityHeterogeneity I2 · Patients with SMA or pre-SMA epilepsy in the selected studies · ictal symptom prevalence analysisPDF p.4, Results
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 32 findings · 30 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • loss of consciousnessThe source reports a frequency of 35% for loss of consciousness.PDF p.13, Table 3
  • loss of consciousness; reported frequency rangeThe source reports a frequency range of 0–78% for loss of consciousness.PDF p.13, Table 3
  • loss of consciousness; ACC association gradeTable 3 assigns the source's Low overall association grade to loss of consciousness.PDF p.13, Table 3
  • loss of consciousness; Figure 4 rateFigure 4 displays a 35.5% rate for loss of consciousness.PDF p.10, Figure 4
  • pairwise OR: Loss of consciousness relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.3 for Loss of consciousness relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.4 for Loss of consciousness relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.4 for Loss of consciousness relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Autonomic signsFigure 6 reports an odds ratio of 0.6 for Loss of consciousness relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Facial expression changeFigure 6 reports an odds ratio of 0.6 for Loss of consciousness relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.7 for Loss of consciousness relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.9 for Vocalization/verbalization relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.7 for Hypermotor-complex motor behavior relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.3 for Affective/autonomic aura relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Loss of consciousnessFigure 6 reports an odds ratio of 1.7 for Autonomic signs relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Loss of consciousnessFigure 6 reports an odds ratio of 1.6 for Facial expression change relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Loss of consciousnessFigure 6 reports an odds ratio of 1.4 for Motor (gestural) automatisms relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.8 for Post-ictal confusion/behavior change disinhibition relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.5 for Chapeau de gendarme relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.4 for Dystonic posturing relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.3 for Head-eye deviation relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.3 for Laughter relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.2 for Oro-alimentary automatisms relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.2 for Tonic-clonic relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.1 for F to BTC relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 1.2 for Loss of consciousness relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 2.1 for Loss of consciousness relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Dystonic posturingFigure 6 reports an odds ratio of 2.3 for Loss of consciousness relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Head-eye deviationFigure 6 reports an odds ratio of 3.4 for Loss of consciousness relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to LaughterFigure 6 reports an odds ratio of 5.1 for Loss of consciousness relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 5.8 for Loss of consciousness relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Tonic-clonicFigure 6 reports an odds ratio of 9.6 for Loss of consciousness relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to F to BTCFigure 6 reports an odds ratio of 9.6 for Loss of consciousness relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 35% (frequency range 0–78%)loss of consciousnessPercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.13, Table 3
  • 35.5%loss of consciousness; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.10, Figure 4
  • OR 0.3pairwise OR: Loss of consciousness relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Loss of consciousness relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Loss of consciousness relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Loss of consciousness relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Loss of consciousness relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Loss of consciousness relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Vocalization/verbalization relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Hypermotor-complex motor behavior relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.3pairwise OR: Affective/autonomic aura relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Autonomic signs relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Facial expression change relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.4pairwise OR: Motor (gestural) automatisms relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Chapeau de gendarme relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Dystonic posturing relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Head-eye deviation relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Laughter relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Oro-alimentary automatisms relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Tonic-clonic relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: F to BTC relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Loss of consciousness relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Loss of consciousness relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.3pairwise OR: Loss of consciousness relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.4pairwise OR: Loss of consciousness relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.1pairwise OR: Loss of consciousness relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.8pairwise OR: Loss of consciousness relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Loss of consciousness relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Loss of consciousness relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdfStructured design not resolved · 5 findings · 2 reported values
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.423
The study enrolled seven consecutive PCE patients; six had SEEG-identified posterior cingulate ictal onset and one had an MRI-identified postcingulate tumour. Four patients underwent CCEP. SEEG and scalp EEG were retrospectively analyzed with video-documented ictal semiology; the source used the Lüders seizure-classification scheme. The posterior cingulate was operationally defined caudal to the vertical posterior commissure line.
Findings
  • dialeptic or automotor seizures in PCEFour of seven patients showed dialeptic or automotor seizures.PDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
  • dialeptic seizures in PCETwo PCE patients (Cases 5 and 6) had seizures characterized by impaired consciousness and classified as dialeptic.PDF p.5, Ictal semiology and SEEG findings
  • Case 5 dialeptic mesial temporal and occipital spreadCase 5 dialeptic seizures had spread to the hippocampus, lingual gyrus, isthmus, and cuneus.PDF p.5, Ictal semiology and SEEG findings; PDF p.4, Figure 2
  • Case 6 dialeptic inferior-parietal spreadCase 6 dialeptic seizures had spread to the inferior parietal lobule without temporal-lobe involvement.PDF p.5, Ictal semiology and SEEG findings; PDF p.4, Figure 2
  • dialeptic/automotor mesial temporal or IPL spreadThe four PCE patients with dialeptic or automotor seizures had spread to mesial temporal structures or the inferior parietal lobule.PDF p.1, Abstract; PDF p.5, Summary of ictal semiology and SEEG findings
Reported values
  • 4/7 dialeptic or automotor seizuresdialeptic or automotor seizures in PCEProportion · n/N 4/7 · 7 PCE patients · ictal semiologyPDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
  • 2/7 dialeptic seizuresdialeptic seizures in PCEProportion · n/N 2/7 · 7 PCE patients · ictal semiologyPDF p.5, Ictal semiology and SEEG findings
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • dialeptic seizuresDialeptic seizures with altered consciousness, staring, and minimal motor activity alone provide no useful localizing or lateralizing information and can arise from virtually any area, but an aura before the dialeptic phase and the subsequent ictal sequence can identify structures activated by the discharge. A dialeptic phase evolving into automotor behavior is common in TLE, whereas an isolated dialeptic phase has no localizing value.PDF p.1, section 2 General principles of ictal symptomatology; PDF p.4, section 3.4 Dialeptic seizures; PDF p.2, Table 1
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Dialeptic seizure patternTable 2 associates the dialeptic seizure pattern with limbic temporal structures, cingulum, intermediate frontal cortex (BA 8), and orbitofrontal areas and describes it as non-lateralising.PDF p.3, Table 2
  • Loss of consciousnessThe review reports that one study of 338 seizure videos in 100 patients found that seizures whose predominant semiology was loss of consciousness could originate in any lobe of the brain.PDF p.3, section 1.3
Reported values
  • Patients n=100Loss of consciousnessCount · 338 seizure videos from 100 patients; seizures with predominant loss-of-consciousness semiology · ictalPDF p.3, section 1.3
  • Seizure videos n=338Loss of consciousnessCount · 338 seizure videos from 100 patients; seizures with predominant loss-of-consciousness semiology · ictalPDF p.3, section 1.3
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 3 findings
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • dialeptic seizureThe authors coin “dialeptic seizure” for an ictal episode whose main manifestation is altered consciousness, separating a pure semiological term from electroclinical labels such as absence seizure and complex partial seizure and making it independent of associated ictal or interictal EEG changes.PDF p.1, Summary; PDF p.2, Overview; PDF p.4, Dialeptic seizures
  • dialeptic seizureFor the source’s dialeptic category, altered consciousness means unresponsiveness or decreased responsiveness not caused by motor alterations, and complete or partial amnesia for the episode is necessary to establish the diagnosis.PDF p.4, Dialeptic seizures
  • Dialeptic seizureDialeptic seizure is the authors’ term for a seizure whose predominant manifestation is altered consciousness, defined for this purpose as unresponsiveness or decreased responsiveness not caused by motor alterations; complete or partial amnesia for the episode is necessary, and the concept is independent of associated ictal or interictal EEG changes.PDF p.1, Summary; PDF p.2, Overview; PDF p.4, Dialeptic seizures
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • dialeptic seizuresThe review states that the epileptogenic zone in dialeptic seizures tends to be distant from primary or supplementary motor areas, whereas seizures originating at or near those areas tend to be predominantly motor and may have preserved consciousness; dialeptic seizures from mesial temporal structures are longer than those arising from the frontal lobe.PDF p.3, Dialeptic seizures

10 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal vocalizationReported: Dominant hemisphereAlso reported: Non-dominant hemisphereNo single reliable side7 manuscripts · 45 findings · 44 reported values
Weighted evidence supportevidence weight 18.18 across 7 manuscripts · 1 manuscript weight pending · 2 independent primary study · 1 case report or observation · 1 narrative, educational, or cited context · 2 systematic review or meta-analysis · 1 structured design not resolved

The cited study is restated as finding anterior/posterior aphasia lateralizing and vocal disturbances without lateralizing value. The qualitative table associates temporal-lobe speech vocalization with the nondominant hemisphere. Vocalization occurred in both dominant-origin (22 seizures) and nondominant-origin (14 seizures) temporal-lobe seizures; the source reports that difference as not statistically significant. The timing of vocalization relative to EEG seizure onset provides no hemispheric direction. The vocalisation frequencies report no hemisphere direction. No lateralization relationship is reported. No hemisphere or body-side direction is reported. Vocalization rates across temporal onset subtypes provide no hemisphere direction. No lateralizing direction is reported. No hemisphere-direction relationship is reported. No seizure lateralization is reported. No source-supported hemispheric or body-side lateralization is reported. No cerebral hemisphere or body-side direction is reported. The source reports OR 0.5 for motor gestural automatisms relative to vocalization/verbalization; no hemisphere direction is reported. No lateralization evidence is reported. This finding provides no lateralization information. The source reports OR <0.1 for laughter relative to vocalization/verbalization; no hemisphere direction is reported. No lateralizing semiology is reported for the tonic-clonic versus vocalization/verbalization odds comparison. No lateralization axis information is reported for vocalization/verbalization versus autonomic signs. No lateralizing semiology is reported for the reciprocal vocalization/verbalization versus tonic-clonic odds comparison.

Source-defined result groups 14
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyF to BTC · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyDominant-origin · seizure1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyNondominant-origin · Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.9%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 23.1%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 29.2%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 4 findings · 2 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • vocalization; Figure 3 all-data subsetFigure 3 reports N = 404 for the all-data vocalization panel.PDF p.9, Figure 3 and caption
  • vocalization; Figure 3 non-topological subsetFigure 3 reports N = 193 for the non-topological vocalization panel.PDF p.9, Figure 3 and caption
  • ictal vocalization with automatismsA cited study of 102 patients reported 91% sensitivity for detecting temporal-lobe seizures when ictal vocalizations co-occurred with automatisms.PDF p.12, Localizing probabilities
  • ictal vocalization with automatismsThe same cited study reported 70% specificity for detecting temporal-lobe seizures when ictal vocalizations co-occurred with automatisms.PDF p.12, Localizing probabilities
Reported values
  • sensitivity 91%ictal vocalization with automatismsSensitivity · 102 patients with ictal vocalizationPDF p.12, Localizing probabilities
  • specificity 70%ictal vocalization with automatismsSpecificity · 102 patients with ictal vocalizationPDF p.12, Localizing probabilities
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • VocalizationTable 1 contrasts temporal-lobe seizure vocalization as speech associated with the nondominant hemisphere with frontal-lobe vocalization as loud, nonspeech sounds such as grunt, scream, or moan.PDF p.2, Table 1
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 35 findings · 32 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • emotional and autonomic manifestations; vocalization; facial expression; hypermotor behaviorThe review identifies emotional/autonomic manifestations, vocalization, facial expression changes, complex automatisms, and hypermotor behavior with preserved awareness as the main ACC clinical features.PDF p.11, Anatomical and clinical correlations; PDF p.15, Conclusion
  • vocalizationThe source reports a frequency of 61% for vocalization.PDF p.13, Table 3
  • vocalization; reported frequency rangeThe source reports a frequency range of 43–80% for vocalization.PDF p.13, Table 3
  • vocalization/verbalization; Figure 4 rateFigure 4 displays a 61.3% rate for vocalization/verbalization.PDF p.10, Figure 4
  • vocalization at seizure onsetVocalizations at seizure onset were reported in 57 of 93 patients.PDF p.7, Objective symptomatology
  • vocalization/verbalization typicalityVocalization/verbalization met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • vocalization/verbalization; pairwise odds-ratio significanceVocalization/verbalization occurred significantly more often than nine of the other 15 symptoms in pairwise Holm-corrected comparisons.PDF p.10, Statistical analysis of ictal semiology
  • pairwise OR: Hypermotor-complex motor behavior relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.9 for Hypermotor-complex motor behavior relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.8 for Affective/autonomic aura relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.6 for Autonomic signs relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.5 for Facial expression change relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.5 for Motor (gestural) automatisms relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.3 for Loss of consciousness relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Laughter relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 1.1 for Vocalization/verbalization relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Affective/autonomic auraFigure 6 reports an odds ratio of 1.2 for Vocalization/verbalization relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Autonomic signsFigure 6 reports an odds ratio of 1.7 for Vocalization/verbalization relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Facial expression changeFigure 6 reports an odds ratio of 1.8 for Vocalization/verbalization relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 2.1 for Vocalization/verbalization relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.9 for Vocalization/verbalization relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 3.6 for Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 6.1 for Vocalization/verbalization relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Dystonic posturingFigure 6 reports an odds ratio of 6.5 for Vocalization/verbalization relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Head-eye deviationFigure 6 reports an odds ratio of 9.6 for Vocalization/verbalization relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to LaughterFigure 6 reports an odds ratio of 14.5 for Vocalization/verbalization relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 16.5 for Vocalization/verbalization relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Tonic-clonicFigure 6 reports an odds ratio of 27.3 for Vocalization/verbalization relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to F to BTCFigure 6 reports an odds ratio of 27.3 for Vocalization/verbalization relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 61% (frequency range 43–80%)vocalizationPercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.13, Table 3
  • 61.3%vocalization/verbalization; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.10, Figure 4
  • 57 patients (61%)vocalization at seizure onsetPercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.7, Objective symptomatology
  • 9/15 significant pairwise comparisonsvocalization/verbalization; pairwise odds-ratio significanceProportion · n/N 9/15 · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.10, Statistical analysis of ictal semiology
  • OR 0.9pairwise OR: Hypermotor-complex motor behavior relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Affective/autonomic aura relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Autonomic signs relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Facial expression change relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Motor (gestural) automatisms relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Loss of consciousness relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Dystonic posturing relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Laughter relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Vocalization/verbalization relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Vocalization/verbalization relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Vocalization/verbalization relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.8pairwise OR: Vocalization/verbalization relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Vocalization/verbalization relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Vocalization/verbalization relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.1pairwise OR: Vocalization/verbalization relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.5pairwise OR: Vocalization/verbalization relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Vocalization/verbalization relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 14.5pairwise OR: Vocalization/verbalization relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 16.5pairwise OR: Vocalization/verbalization relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 27.3pairwise OR: Vocalization/verbalization relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 27.3pairwise OR: Vocalization/verbalization relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 2 findings · 5 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.778
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • vocalizationVocalization occurred in 17 of 35 patients (48.5%) and in 36 seizures; 22 vocalization seizures arose from the dominant side and 14 from the nondominant side, a difference the source reports as not statistically significant.PDF p.1, abstract; PDF p.3, Tables 2-3 and Results; PDF p.5, Discussion
  • vocalizationVocalization was always ictal, either coinciding with EEG seizure onset or immediately preceding it and signaling a sudden change in symptomatology.PDF p.3, Results
Reported values
  • Dominant-origin vocalization seizures n=22vocalizationCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · Dominant-origin · ictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results; PDF p.5, Discussion
  • Patients with vocalization 17/35 (48.5%)vocalizationPercentage · n/N 17/35 · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · Overall · ictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results; PDF p.5, Discussion
  • Nondominant-origin vocalization seizures n=14vocalizationCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · Nondominant-origin · ictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results; PDF p.5, Discussion
  • Vocalization seizures n=36vocalizationCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · Overall · ictalPDF p.1, abstract; PDF p.3, Tables 2-3 and Results; PDF p.5, Discussion
  • 36/36 vocalization seizures were classified as ictalvocalizationCount · n/N 36/36 · 36 vocalization seizures in the 35-patient temporal-lobe epilepsy cohort · ictalPDF p.3, Results
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • anterior and posterior aphasia; vocal disturbancesThe article reports that Dussaule et al. found anterior and posterior aphasia to be lateralizing language disturbances, whereas vocal disturbances showed no lateralizing value.PDF p.3, Discussion
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • VocalisationVocalisation semiology occurred in 4/61 individuals (7%) as initial semiology and 7/61 (11%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 4/61 (7%)VocalisationPercentage · n/N 4/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 7/61 (11%)VocalisationPercentage · n/N 7/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • vocalizationVocalization over the whole seizure course did not differ significantly across M, ML, and L groups.PDF p.6, Table 3; PDF p.6, General ictal characteristics
Reported values
  • M 7/24 (29.2%)vocalizationPercentage · n/N 7/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • ML 7/18 (38.9%)vocalizationPercentage · n/N 7/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics
  • L 3/13 (23.1%)vocalizationPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.6, General ictal characteristics

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Formed semantic visual hallucinations (faces, people, scenes, objects)Source terms: Formed visual hallucinations; Formed visual hallucination; Formed semantic visual hallucinationsReported: ContralateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere8 manuscripts · 19 findings · 9 reported values
Weighted evidence supportevidence weight 18.16 across 8 manuscripts · 5 narrative, educational, or cited context · 2 independent primary study · 1 systematic review or meta-analysis

No source lateralization is reported. No hemisphere or body-side direction is reported. No hemisphere or side-relative direction is reported. The review restates stimulation findings of contralateral visual fields for elementary/intermediary hallucinations, central calcarine responses, and right-predominant associative visual effects with posterior exceptions. No lateralizing direction is reported. Across the three stimulated patients with complex visual or auditory hallucinations, the source reports composite lesion context involving nondominant inferior parieto-temporal or inferior-parieto-occipital locations and a left parietal lesion. No lateralizing direction is reported for the complex visual phenomena. The visual hallucination review synthesis reports no hemisphere or lateralizing direction. The cited table restates contralateral lateralization for complex visual aura when unilateral. The absolute right-sided stimulation site is not a lateralizing relation between the sign and seizure onset. No lateralization axis information is reported for formed visual phenomena in the cited series. The cited case of complex visual hallucinations after coloured triangles reports no hemisphere or lateralization direction. The primary result reports complex visual hallucinations after elementary visual hallucinations in 4/42 patients, with no side specified. The primary result states that all patients with complex visual hallucinations had a right occipital focus. The cited Salanova-series restatement reports right hemispheric epilepsy in all patients with complex visual auras. The cited study restatement reports complex visual aura in 5 of 42 patients with right-hemispheric epilepsy.

Source-defined result groups 5
Localization: parietal epilepsy seriesSource-defined values retained separatelyAll reported · other aura categories · aura entries1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelyAll reported · elementary/intermediary versus complex hallucinations; right versus left hemisphere; calcarine versus noncalcarine visual field · visual hallucination responses among 22 patients; exact response denominator not reported1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereSource-defined values retained separatelyAll reported · left or non-right occipital focus · patients with complex visual hallucinations1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyAll reported · left or non-right occipital focus · patients with complex visual hallucinations1 manuscript · 1 reported value · not pooled
Localization: OccipitalObserved proportion 9.5%All reported · no complex visual hallucination after elementary hallucination · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • complex visual phenomena and visual illusionsComplex visual phenomena such as dyschromatopsia or metamorphopsia are described as implying temporal or occipito-temporal seizure organization with discharge in visual associative areas rather than primary visual onset; the review distinguishes hallucination at the cortical entry from distortion or illusion at downstream interpreter sites.PDF p.3, section 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • visual association area; complex visual hallucination; kinetopsia; macropsia; micropsia; autoscopyComplex visual hallucinations in occipital epilepsy are linked to prestriate cortex or propagation to adjacent temporoparietal areas; formed hallucinations and visual distortions such as kinetopsia, macropsia, micropsia, and rarely autoscopy are described.PDF p.8, Visual association areas; PDF p.3, Figure 1
  • elementary visual aura; visual illusions/distortions; complex visual hallucinationsTable 3 maps elementary visual phenomena such as lights and shapes to primary visual cortex, visual illusions or distortions to temporo-parieto-occipital regions, and complex visual hallucinations to temporal regions.PDF p.10, Table 3; PDF p.8, Visual association areas
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • simple and complex visual aurasSimple visual auras with static, flashing, or moving lights suggest activation of the primary visual cortex and contiguous visual association areas, whereas complex visual auras involving people, scenes, objects, or illusions suggest the temporo-occipital junction or basal temporal cortex.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Complex visual hallucinations and illusionsThe review associates complex visual hallucinations with visual association cortex, including medial limbic, lateral temporal, posterior parietal, and temporo-parietal-occipital regions, and describes well-formed scenery, people, animals, faces, and distortions or illusions of object size, shape, colour, and motion.PDF p.6, section 1.12
  • Complex visual auraTable 2 associates complex visual aura with the temporo-parietal-occipital junction and basal temporal limbic/neocortical regions, with contralateral lateralisation if unilateral.PDF p.3, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Complex visual auraThe review reports that all patients with complex visual auras in the Salanova series had right hemispheric epilepsy and that complex visual auras were seen only when the lesion involved the temporal lobe.PDF p.3, section 2.5 Visual auras
  • Complex visual auraBoesebeck et al. described 5 patients with complex visual auras and right hemispheric epilepsy among 42 patients; the epileptogenic zone was determined by video/EEG and imaging, with seizure freedom after resection confirmed in 19 of 42 patients.PDF p.3, section 2.5 Visual auras
Reported values
  • Complex visual aura with right-hemispheric epilepsy 5/42Complex visual auraPercentage · n/N 5/42 · 42 patients with posterior cortical epilepsy as summarized by the review; 5 with complex visual auras and right hemispheric epilepsy · Ictal auraPDF p.3, section 2.5 Visual auras
  • Seizure freedom after resection confirmed 19/42Complex visual auraPercentage · n/N 19/42 · 42 patients with posterior cortical epilepsy as summarized by the review; 5 with complex visual auras and right hemispheric epilepsy · Ictal auraPDF p.3, section 2.5 Visual auras
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 7 findings · 4 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • elementary hallucination followed by faces or picturesIn the other cited case, spontaneous seizures began with elementary visual hallucinations followed by complex hallucinations consisting of faces or pictures, including Rembrandt’s self-portrait.PDF p.13, Cortical stimulation
  • visual experiential hallucination after right temporal stimulationIn the same cited case, stimulation of the right lateral posterior temporal cortex elicited a visual experience of a face from a picture.PDF p.13, Cortical stimulation
  • complex visual hallucinations in cited reportsThe source reports complex visual hallucinations in a range of 12% to 20% of patients in prior occipital epilepsy reports.PDF p.21, Discussion
  • formed visual phenomena in Blume et al.Blume et al. reported formed visual phenomena in six of 19 patients who underwent posterior-cortex surgery.PDF p.21, Discussion
  • coloured triangles followed by complex visual hallucinationIn one cited case, seizures began with coloured triangles followed by complex visual hallucinations of a robber with a gun or sinister characters from comic books.PDF p.13, Cortical stimulation
  • complex visual hallucinations after elementary hallucinationsIn four patients, elementary visual hallucinations were followed by complex visual hallucinations consisting mainly of familiar faces, pictures, and people.PDF p.6, Results, Visual auras
  • complex visual hallucinations and right occipital focusAll patients in the cohort with complex visual hallucinations had a right occipital focus.PDF p.6, Results, Visual auras
Reported values
  • 12%-20% reported rangecomplex visual hallucinations in cited reportsPercentage Range · cited occipital lobe epilepsy reports · seizure onset or propagationPDF p.21, Discussion
  • 6/19 patientsformed visual phenomena in Blume et al.Proportion · n/N 6/19 · cited Blume et al. posterior-cortex surgery series · seizure manifestationPDF p.21, Discussion
  • 4 patientscomplex visual hallucinations after elementary hallucinationsCount · n/N 4/42 · 42-patient cohort · seizure evolution from visual auraPDF p.6, Results, Visual auras
  • all patients with complex visual hallucinations had a right occipital focuscomplex visual hallucinations and right occipital focusProportion · four cohort patients with complex visual hallucinations · seizure onset and evolutionPDF p.6, Results, Visual auras
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 3 findings · 2 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.27 · 2 × 1.35 × 1.952
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • complex visual or auditory hallucinationsA few patients had complex visual or auditory hallucinations, interpreted by the source as suggesting spread to temporo-limbic areas.PDF p.4, Results, Aurae
  • complex visual or auditory hallucination entries in Table 1Table 1 lists five complex visual or auditory hallucination aura entries.PDF p.4, Table 1
  • complex visual or auditory hallucinations after stimulationComplex visual or auditory hallucinations occurred in three stimulated patients.PDF p.5, Electrical cortical stimulation
Reported values
  • 5 source-reported aura entriescomplex visual or auditory hallucination entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 3 patientscomplex visual or auditory hallucinations after stimulationCount · n/N 3/80 · 80 stimulated patients · stimulation response and ictal propagationPDF p.5, Electrical cortical stimulation
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • elementary, intermediary, and complex visual hallucinations; visual illusionsIn a cited depth-electrode study of 22 patients with epilepsy, the source reports that 85% of elementary and intermediary visual hallucination responses were induced from calcarine sulcus, lingual gyrus, lateral occipital cortex, fusiform gyrus, or cuneus/parieto-occipital sulcus; elementary and intermediary hallucinations were in the contralateral visual hemifield except after calcarine stimulation, when they were central. Complex meaningful hallucinations were associated with cuneus/parieto-occipital sulcus, precuneus, and fusiform gyrus, while color or spatial-background illusions were elicited from right rhinal, parahippocampal, collateral-sulcus, and fusiform regions; visual phenomena were more probable in the right than left hemisphere except at the most posterior sites.PDF p.14-15, Visual; PDF p.15, visual lateralization paragraph
Reported values
  • 85% of elementary/intermediary visual hallucination responses attributed to the listed occipital, fusiform, and cuneus/parieto-occipital siteselementary, intermediary, and complex visual hallucinations; visual illusionsPercentage · 22 patients with epilepsy in the cited depth-electrode study; exact response denominator not reported · stimulation-induced visual phenomenonPDF p.14-15, Visual; PDF p.15, visual lateralization paragraph

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal automatismsReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere14 manuscripts · 34 findings · 57 reported values
Weighted evidence supportevidence weight 18.11 across 14 manuscripts · 4 manuscript weight pending · 4 structured design not resolved · 1 independent primary study · 7 narrative, educational, or cited context · 2 systematic review or meta-analysis

Unilateral automatism was predominantly ipsilateral: 23 ipsilateral versus 3 contralateral seizures, with 6 versus 1 affected patients. Deglutition, sexual automatism, sniffing, fumbling, and spitting showed no statistically significant right-versus-left temporal-lobe-epilepsy difference. Automatisms overall were qualitatively more common in right TLE, while individual automatism categories generally did not distinguish right from left except ictal vomiting. The cited review reports disagreement about whether unilateral automatisms are ipsilateral to the seizure focus. The review links preserved awareness during automatisms and several peri-ictal autonomic/oral/urinary signs to a non-dominant focus, while rhythmic non-clonic hand motion may be contralateral. The cited study reported bilateral hypermotor automatisms; bilateral describes motor behavior and does not identify a hemisphere. The review distinguishes right-temporal tendencies for selected automatisms or well-formed ictal language, contralateral nonmanipulative movements and dystonia, ipsilateral early head turning with dystonia, and predominantly contralateral late or versive turning. Head-or-trunk automatisms did not differ significantly between right- and left-temporal seizures (23/54 versus 19/73). The supplied evidence identifies the subsequent contraversion as directed contralateral to the hemisphere of seizure onset. No cerebral-hemisphere lateralizing direction is reported. No cerebral direction or body-side result is reported. No source-supported hemispheric lateralization is reported. No seizure lateralization is reported. No lateralizing direction is reported for other automatisms. No source-supported hemispheric or body-side lateralization is reported. No lateralizing direction is reported for the other-automatisms subset. No lateralizing direction is reported for other automatisms associated with a hypothalamic source. This record provides no seizure lateralization. No lateralizing direction is reported for the hypothalamic association with other automatisms. No lateralizing direction is reported. No lateralization axis information is reported for the occipital-plus organization summary. No cerebral side or body-side result is reported.

Source-defined result groups 41
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelycontralateral · ipsilateral versus contralateral to ictal EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 1 patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 1 seizures · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%Staring with automatisms · quiet staring versus staring with automatisms before contraversion · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 1 patients · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 3 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 1 patients · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 19.8%ipsilateral · ipsilateral versus contralateral to ictal EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 3 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 2.6%contralateral · ipsilateral versus contralateral to ictal EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 0 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 6 seizures · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyQuiet staring; extratemporal origin · Temporal origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 0 patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 1 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeObserved proportion 26.0%LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 1 patients · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyQuiet staring; temporal origin · Extratemporal origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 0 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 3 patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 2 patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeObserved proportion 42.6%RTL · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 0 patients · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 4 seizures · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 3 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyLTE · RTE 1 seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 0 patients · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyRTE · LTE 3 patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyipsilateral · ipsilateral versus contralateral to ictal EEG focus · seizure, with patient count in parentheses1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 14

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 14 findings · 6 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • other automatismsTable 1 defines or exemplifies the the source's own semiology category “other automatisms” as Blinking, ictal cough, gelastic or dacrystic seizures, ictal nose wiping, or ictal face rubbing.PDF p.7, Table 1 Semiology descriptions and frequencies
  • other automatismsOther automatisms comprised 3.1% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • other automatisms; Figure 3 all-data subsetFigure 3 reports N = 347 for the all-data other automatisms panel.PDF p.9, Figure 3 and caption
  • other automatisms; Figure 3 non-topological subsetFigure 3 reports N = 108 for the non-topological other automatisms panel.PDF p.9, Figure 3 and caption
  • other automatisms; gelastic and dacrystic seizuresAmong the 108 cases categorized as other automatisms, 62 were gelastic or dacrystic seizures.PDF p.8, Seizure semiology localizing values
  • other automatisms; gelastic and dacrystic seizuresThe denominator for the reported gelastic/dacrystic subset was 108 other-automatisms cases.PDF p.8, Seizure semiology localizing values
  • other automatisms; hypothalamusOther automatisms implicated a hypothalamic source in 41% of cases.PDF p.8, Seizure semiology localizing values
  • other automatisms; hypothalamusThe 95% CI for other automatisms; hypothalamus was 30%–50%.PDF p.8, Seizure semiology localizing values
  • other automatisms; temporal lobeOther automatisms implicated a temporal-lobe source in 35% of cases.PDF p.8, Seizure semiology localizing values
  • other automatisms; temporal lobeThe 95% CI for other automatisms; temporal lobe was 24%–45%.PDF p.8, Seizure semiology localizing values
  • other automatisms; frontal lobeOther automatisms implicated a frontal-lobe source in 11% of cases.PDF p.8, Seizure semiology localizing values
  • other automatisms; frontal lobeThe 95% CI for other automatisms; frontal lobe was 5%–17%.PDF p.8, Seizure semiology localizing values
  • other automatisms; hypothalamusOther automatisms had an intrinsic localizing OR of 13.7 for the hypothalamus, reported as at least nine.PDF p.8, Relative localizing values of semiologies
  • other automatisms; hypothalamusThe 95% CI for other automatisms; hypothalamus was 9.2–20.4.PDF p.8, Relative localizing values of semiologies
Reported values
  • other automatisms 3.1%other automatismsPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • 62/108 other-automatisms casesother automatisms; gelastic and dacrystic seizuresProportion · n/N 62/108 · other automatisms category · gelastic or dacrystic seizuresPDF p.8, Seizure semiology localizing values
  • other automatisms; hypothalamus 41%other automatisms; hypothalamusPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • other automatisms; temporal lobe 35%other automatisms; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • other automatisms; frontal lobe 11%other automatisms; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 13.7other automatisms; hypothalamusOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • hypermotor bilateral automatisms group comparison (Mirandola study)The cited comparison of hypermotor bilateral automatisms is reported as statistically significant at p<.05.PDF p.7, cited-study discussion
  • hypermotor bilateral automatisms (Mirandola study)Hypermotor bilateral automatisms were observed exclusively in the PIT group, in 6 patients (43%).PDF p.7, cited-study discussion
Reported values
  • 6/14 patients (43%)hypermotor bilateral automatisms (Mirandola study)Percentage · n/N 6/14 · 14 PIT-lesion patients in the cited Mirandola comparison · ictalPDF p.7, cited-study discussion
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Less common and rare temporal-lobe automatismsThe review lists vocalizations, ictal speech, and out-of-context fear as less common automatisms associated with temporal-lobe seizures, and reports crying or dacrystic, laughing or gelastic, cursive leaving behaviours, and whistling as rarer reported behaviours or automatisms.PDF p.3, section 2.5 Automatisms
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • preserved awareness during ictal automatisms; temporal non-dominant signsPreserved awareness during ictal automatisms points to the non-dominant hemisphere; in temporal lobe epilepsy, rhythmic ictal non-clonic hand motions may be contralateral, while peri-ictal drinking, ictal spitting, ictal vomiting, and urge to urinate point to a non-dominant focus.PDF p.10, Lateralising signs; PDF p.5, Mesial temporal lobe including hippocampus
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Head or trunk automatismsHead-or-trunk automatisms did not differ significantly between RTL and LTL seizures.PDF p.4, Table 5; PDF p.4, numbered clinical-feature results
Reported values
  • LTL head-or-trunk automatisms 19/73 (34%)Head or trunk automatismsPercentage · n/N 19/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.4, Table 5; PDF p.4, numbered clinical-feature results
  • RTL head-or-trunk automatisms 23/54 (44%)Head or trunk automatismsPercentage · n/N 23/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.4, Table 5; PDF p.4, numbered clinical-feature results
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • focal impaired awareness seizures and automatismsImpaired awareness may follow FAS and is associated with unresponsiveness, motion arrest, and repetitive nonpurposeful automatisms; unlike highly localized FAS, it may reflect propagation to brainstem and thalamic arousal structures with depression of associative cortices.PDF p.8, Focal impaired awareness seizures
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal motor (automatisms)Focal motor (automatisms) semiology occurred in 2/61 individuals (3%) as initial semiology and 13/61 (21%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • 13/61 (21%) combinedFocal motor (automatisms)Percentage · n/N 13/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • 2/61 (3%) initialFocal motor (automatisms)Percentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Rudimentary automatismsRudimentary automatisms, including grasping, visual tracking, and blinking to threat, were reported in half of focal impaired-awareness seizures.PDF p.3, section 1.3
lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdfStructured design not resolved · 3 findings · 12 reported values
lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The investigators prospectively enrolled 85 consecutive adult persons with epilepsy undergoing standard-of-care SEEG evaluation in an epilepsy monitoring unit from June 2016 through April 2023. They prospectively collected 220 seizures; 39 seizures in 13 patients were excluded because breathing signals were unreliable or artifactual. The analyzed population was 179 seizures in 72 patients with reliable artifact-free respiratory signals. Real-time SEEG, video, thoracic and abdominal respiratory inductance plethysmography, oxygen saturation, heart rate, and four-channel EKG were obtained simultaneously. The analyzed cohort included 1,196 intracranial depth electrodes (mean 16.6 +/- 3.0 per patient); 55 seizures in 23 patients had ICA. All seizures were classified by seizure onset zone (SOZ), defined by the source as the cortical area from which seizures start. The source separately defined the epileptogenic zone (EZ) as the region resected to produce seizure freedom; only patients who underwent resective surgery or laser interstitial thermal therapy and had Engel class I outcome with at least six months of follow-up were classified for EZ determination. Of 31 Engel class I patients, 30 had at least six months of follow-up (mean 22.8 months +/- SD 13.1, range 6-50) and one did not. The source reports separate SOZ and EZ analyses and does not authorize conversion between their patient- and seizure-level denominators. A high-gamma analysis used a subset of 20 patients with 39 ICA seizures whose SEEG implantation sampled all regions of breathing interest; the early-onset subgroup contained 27 seizures in 13 patients and the late-onset subgroup 12 seizures in seven patients. Predictive associations were assessed with separate simple logistic-regression models; statistically significant semiologic signs were also entered as one additional predictor with ICA in multiple logistic regression. Fisher's exact test assessed ICA presence and mesial temporal sclerosis (MTS). The source used two-sided p < 0.05 for statistical significance, made no multiple-comparison correction because the study was exploratory, and treated z >= 4 as significant for the quantitative gamma analysis.
Findings
  • FOIA/FOA motor onset with automatismsFOIA/FOA motor onset with automatisms was associated with mesial temporal seizure onset with OR=3.0, 95% CI [1.1, 9.2], p=0.04, sensitivity 0.45, specificity 0.79, PPV 0.65, and NPV 0.63.PDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • ICA + FOIA/FOA motor onset with automatismsCo-occurrence of ICA and FOIA/FOA motor onset with automatisms was associated with mesial temporal seizure onset with OR=10.9, 95% CI [2.49, 57.15], p=0.001, sensitivity 0.69, specificity 0.66, PPV 0.63, and NPV 0.72.PDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • ICA with either FOIA or FOIA/FOA motor onset with automatismsWhen ICA occurred with either FOIA or FOIA/FOA motor onset with automatisms, the source reports specificity increasing up to 0.95 and sensitivity decreasing down to 0.21 for mesial temporal seizure onset.PDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones
Reported values
  • PPV 0.65FOIA/FOA motor onset with automatismsPositive predictive value · Source's seizure-onset-zone analysis; the Table 3 regression denominator is not reported · ictal FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • specificity 0.79FOIA/FOA motor onset with automatismsSpecificity · Source's seizure-onset-zone analysis; the Table 3 regression denominator is not reported · ictal FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • sensitivity 0.45FOIA/FOA motor onset with automatismsSensitivity · Source's seizure-onset-zone analysis; the Table 3 regression denominator is not reported · ictal FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • NPV 0.63FOIA/FOA motor onset with automatismsNegative predictive value · Source's seizure-onset-zone analysis; the Table 3 regression denominator is not reported · ictal FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • OR=3.0FOIA/FOA motor onset with automatismsOdds ratio · Source's seizure-onset-zone analysis; the Table 3 regression denominator is not reported · ictal FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.69ICA + FOIA/FOA motor onset with automatismsSensitivity · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.72ICA + FOIA/FOA motor onset with automatismsNegative predictive value · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.66ICA + FOIA/FOA motor onset with automatismsSpecificity · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • OR=10.9ICA + FOIA/FOA motor onset with automatismsOdds ratio · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.63ICA + FOIA/FOA motor onset with automatismsPositive predictive value · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • sensitivity down to 0.21ICA with either FOIA or FOIA/FOA motor onset with automatismsSensitivity · Source's combined occurrence analysis of ICA with either of the two listed seizure-evolution signs · ictal sequence after ICAPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones
  • specificity up to 0.95ICA with either FOIA or FOIA/FOA motor onset with automatismsSpecificity · Source's combined occurrence analysis of ICA with either of the two listed seizure-evolution signs · ictal sequence after ICAPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic seizure; automatismThe authors caution that “hyperkinetic seizure” conflates an individual semiologic feature with the description of the overall seizure and, although included in the current ILAE classification, does not correspond to a known localization, etiology, or pathophysiological correlation; they also identify “automatism” and “hyperkinetic” as terms with imprecise or nonconsensual meaning in some contexts.PDF p.12, Table 3; PDF p.13, paragraph 2
  • occipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsIn the summarized Marchi et al. study, widespread organization of the epileptogenic zone was typical in occipital or “occipital-plus” epilepsy, with temporal and/or parietal cortex commonly involved; altered conscious level was more common with widespread posterior neocortical onset, while automatic motor behavior and/or verbal automatisms were more often seen with occipitotemporal organization.PDF p.6, Table 2, Marchi et al. 2016 row
Reported values
  • 194 seizuresoccipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy; 194 seizures · Marchi et al. study · ictal onset and evolutionPDF p.6, Table 2, Marchi et al. 2016 row
  • 29 subjectsoccipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy; 194 seizures · Marchi et al. occipital-lobe epilepsy study · ictal onset and evolutionPDF p.6, Table 2, Marchi et al. 2016 row
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • temporal automatisms, dystonic posturing, and head turningOroalimentary automatisms suggest temporal involvement but are not specific; spitting, drinking, and preserved responsiveness during automatisms favor right temporal localization; manipulative automatisms alone do not lateralize, whereas nonmanipulative distal or proximal movements tend to be contralateral and may precede contralateral dystonic posturing; dystonic posturing is usually contralateral, early head turning with dystonia tends ipsilateral, late head turning is more often contralateral, and versive head turning is almost always contralateral.PDF p.50; PDF p.51
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 4 findings · 24 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • unilateral automatismTable 1 records unilateral automatism more often ipsilateral than contralateral to the ictal EEG focus, while the abstract and conclusion characterize it as an ipsilateral sign.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • other categories of automatismsThe source reports no statistically significant right-versus-left TLE difference for the listed other automatisms.PDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • overall automatisms in right versus left TLEThe authors state that automatisms overall were more common among patients with right TLE, but individual automatism categories did not clearly differentiate right from left TLE except for ictal vomiting.PDF p.7, Discussion; PDF p.4, Results/Table 2
  • unilateral automatism as an ipsilateral signThe discussion reports that some cited studies did not agree that unilateral automatism frequently indicates an ipsilateral seizure focus and cautions against treating it as a uniformly reliable sign.PDF p.6, Discussion
Reported values
  • 6 patients with ipsilateral unilateral automatismunilateral automatismCount · 19 patients with unilateral TLE; Table 1 lists 6 ipsilateral-side patients and 1 contralateral-side patient · ipsilateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • 3 contralateral seizures (3% of all 116 seizures)unilateral automatismPercentage · n/N 3/116 · 19 patients with unilateral TLE; Table 1 lists 6 ipsilateral-side patients and 1 contralateral-side patient · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • 23 ipsilateral seizures (20% of all 116 seizures)unilateral automatismPercentage · n/N 23/116 · 19 patients with unilateral TLE; Table 1 lists 6 ipsilateral-side patients and 1 contralateral-side patient · ipsilateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • 1 patient with contralateral unilateral automatismunilateral automatismCount · 19 patients with unilateral TLE; Table 1 lists 6 ipsilateral-side patients and 1 contralateral-side patient · contralateral · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • LTE 1 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 0 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 2 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 0 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 0 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 3 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 0 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 6 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 4 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 0 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • temporal-type automatisms in cited reportsThe source reports that temporal-type automatisms have been reported in a range of 29% to 88% of patients in prior occipital epilepsy series.PDF p.21, Discussion
Reported values
  • 29%-88% reported rangetemporal-type automatisms in cited reportsPercentage Range · cited occipital lobe epilepsy reports · ictal propagation or later ictal manifestationPDF p.21, Discussion
wyllie1986.pdfStructured design not resolved · 1 finding · 7 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.893
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • quiet staring and staring with automatisms before contraversionQuiet staring preceded contraversion for 8 versive seizures for 2-31 seconds (mean 17), while staring with automatisms preceded contraversion for 18 seizures for 4-227 seconds (mean 34); all seizures with automatisms before contraversion originated in temporal lobes, whereas the quiet-staring subgroup arose from temporal (25%) and extratemporal (75%) locations.PDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
Reported values
  • Quiet staring before contraversion 8/61 (13%)quiet staring and staring with automatisms before contraversionPercentage · n/N 8/61 · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring-with-automatisms duration mean 34 seconds (range 4–227)quiet staring and staring with automatisms before contraversionMean · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring subgroup temporal origin 25%quiet staring and staring with automatisms before contraversionPercentage · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring; temporal origin · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring-with-automatisms subgroup temporal origin 18/18quiet staring and staring with automatisms before contraversionPercentage · n/N 18/18 · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring duration mean 17 seconds (range 2–31)quiet staring and staring with automatisms before contraversionMean · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Quiet-staring subgroup extratemporal origin 75%quiet staring and staring with automatisms before contraversionPercentage · 26 versive seizures with a reported pre-contraversion staring phase · Quiet staring; extratemporal origin · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion
  • Staring with automatisms before contraversion 18/61 (30%)quiet staring and staring with automatisms before contraversionPercentage · n/N 18/61 · 26 versive seizures with a reported pre-contraversion staring phase · Staring with automatisms · Ictal period before contraversionPDF p.2, Table 2; PDF p.3, paragraphs reporting quiet-staring and automatisms durations and onset regions; PDF p.4, discussion of temporal localization before contraversion

14 contributing manuscripts; source-reported values remain separate and are not pooled.

facial motor signReported: Bilateral6 manuscripts · 31 findings · 17 reported values
Weighted evidence supportevidence weight 18 across 6 manuscripts · 6 systematic review or meta-analysis

The review lists multiple bilateral/symmetrical facial descriptors but explicitly warns that the labels do not always refer to the same feature. No lateralizing information is supplied. No lateralization information is reported. No source-supported hemispheric or body-side lateralization is reported. Face clonic/grimace was reported across 11.8–33.3% in the lateral-temporal studies, with an overall association grade of Low. The source reports a median onset latency of 19 seconds for Face clonic/grimace in a lateral-temporal comparison. The reported overall odds for Face clonic/grimace in lateral TLE were 0.26 with a 95% confidence interval of 0.12–0.57 and heterogeneity-test P=0.2896. The source reports a lateral-TLE Face clonic/grimace percentage range of 11.8–33.3%. The source reports a mesial-TLE Face clonic/grimace percentage range of 15–68.8%. The review classification of ictal feature categories reports no lateralizing direction. No hemisphere or body-side direction is reported for the clustered manifestations. The 23% whole-group grimace prevalence contains no hemisphere or body-side information. The subgroup grimacing prevalence contains no hemisphere or body-side direction. No lateralization relationship is reported. The emotional-grimacing association coefficient has no hemisphere or body-side information. The review does not state the side of the facial manifestations. The table does not report side. No hemisphere or body-side direction is reported.

Source-defined result groups 11
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Face clonic/grimace · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyAll reported · whole group and other network subgroup · patients in the named network subgroup1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · propagation timing · seconds from seizure onset1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · patients with the ictal symptom1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyAll reported · whole group and other network subgroup · patients in the named network subgroup1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 55.6%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 42.9%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Face clonic/grimace · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • facial somatomotor or sensory modificationsFacial somatomotor or sensory modifications were reported in 10% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Facial somato-sensory or motor (Table 3)Table 3 reports facial somato-sensory or motor signs in 8 cases (10%), more during propagation.PDF p.6, Table 3
  • Facial somato-sensory or motor (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports facial somato-sensory or motor signs in 3 cases (5%).PDF p.7, Table 4
Reported values
  • 10% facial somatomotor or sensory modificationsfacial somatomotor or sensory modificationsPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 8 cases (10%)Facial somato-sensory or motor (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 3/60 (5%)Facial somato-sensory or motor (Table 4)Percentage · n/N 3/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • grimacingTable 3 lists 5 patients for the the source's own ictal symptom “grimacing”; its table phase label is onset.PDF p.6, Table 3
  • grimacingTable 3 reports a pooled prevalence of 5% for the the source's own ictal symptom “grimacing”; its table phase label is onset.PDF p.6, Table 3
Reported values
  • 5% pooled prevalencegrimacingPercentage · Patients with SMA or pre-SMA epilepsy in the selected studies · onsetPDF p.6, Table 3
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 13 findings · 5 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Face clonic/grimaceTable 3 reports 3 studies assessing Face clonic/grimace.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports 51 patients assessed for Face clonic/grimace.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports 11.8–33.3% as the percentage range or value for Face clonic/grimace; the overall association grade is Low.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports 1 study with onset timing for Face clonic/grimace.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports an onset latency of 19 s for Face clonic/grimace.PDF p.6, Table 3
  • odds of occurrence; Face clonic/grimaceTable 4 reports overall odds of 0.26 for occurrence of Face clonic/grimace in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Face clonic/grimaceTable 4 reports a 95% confidence interval of 0.12–0.57 for the overall odds of Face clonic/grimace.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Face clonic/grimaceThe heterogeneity test for the Table 4 odds estimate for Face clonic/grimace has p=0.2896.PDF p.7, Table 4
  • Face clonic/grimace; lateral versus mesial comparisonTable 5 reports 3 studies comparing Face clonic/grimace in lateral and mesial TLE.PDF p.9, Table 5
  • Face clonic/grimace; lateral TLE patient denominatorTable 5 reports 51 lateral-TLE patients assessed for Face clonic/grimace.PDF p.9, Table 5
  • Face clonic/grimace; mesial TLE patient denominatorTable 5 reports 67 mesial-TLE patients assessed for Face clonic/grimace.PDF p.9, Table 5
  • Face clonic/grimace; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 11.8–33.3% for Face clonic/grimace.PDF p.9, Table 5
  • Face clonic/grimace; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 15–68.8% for Face clonic/grimace.PDF p.9, Table 5
Reported values
  • 11.8–33.3%Face clonic/grimacePercentage Range · Lateral temporal epilepsy patients assessed for Face clonic/grimace · ictalPDF p.6, Table 3
  • median onset latency 19 sFace clonic/grimaceMedian · Lateral temporal epilepsy study reporting onset timing for Face clonic/grimace · ictal onsetPDF p.6, Table 3
  • odds 0.26odds of occurrence; Face clonic/grimaceOdds · Lateral temporal epilepsy patients assessed for Face clonic/grimace · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 11.8–33.3%Face clonic/grimace; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Face clonic/grimace · Lateral TLE patients assessed for Face clonic/grimace · ictalPDF p.9, Table 5
  • 15–68.8%Face clonic/grimace; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Face clonic/grimace · Mesial TLE patients assessed for Face clonic/grimace · ictalPDF p.9, Table 5
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 9/21 (43%) for Elementary motor: orofacial (tonic and/or clonic, grimace); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 4/12 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the prefrontal operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Table 2 reports 5/9 patients with Elementary motor: orofacial (tonic and/or clonic, grimace) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Elementary motor: orofacial (tonic and/or clonic, grimace)Fisher's exact comparison of Elementary motor: orofacial (tonic and/or clonic, grimace) between the prefrontal and precentral Rolandic operculum groups has p=0.396.PDF p.7, Table 2
Reported values
  • 9/21 (43%)Elementary motor: orofacial (tonic and/or clonic, grimace)Percentage · n/N 9/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 4/12 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 4/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 5/9 patientsElementary motor: orofacial (tonic and/or clonic, grimace)Proportion · n/N 5/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • semiologic synonym setThe review records non-identical descriptions including “pouting,” “bilateral tonic facial contraction,” “symmetrical down-turned mouth,” “grimacing,” “inverted smile with a tearful expression,” “mouth turning down with symmetric puckering,” and “labial corners lowered with chin contraction.”PDF p.2, Introduction; PDF p.4, Study characteristics
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 8 findings · 5 reported values
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • automatisms; elementary motor; hyperkinetic; autonomic; emotional; grimace; cognitive; other subjectiveThe source classifies ictal features into automatisms, elementary motor, hyperkinetic, autonomic, emotional, grimace, cognitive, and other subjective categories for the cluster and prevalence analyses.PDF p.4, Statistical analysis
  • emotional; autonomic; cognitive; grimacing; hyperkinetic behaviorThe source identifies a main cluster containing emotional, grimacing, autonomic, cognitive, and hyperkinetic manifestations across the whole group and both subgroups.PDF p.1, Abstract; PDF p.10, Figure 3
  • emotional; autonomic; automatisms; hyperkinetic behavior; grimaceAcross groups, the source places autonomic and emotional features at seizure onset, while automatisms, hyperkinetic behavior, and grimace are associated with propagation.PDF p.2, Key points; PDF p.9, Seizure semiology
  • grimace; whole groupGrimace features were reported in 23% of the whole review group.PDF p.5, All group; PDF p.9, Figure 2
  • grimacing; fronto-temporal subgroupGrimacing was reported in 12% of the fronto-temporal subgroup (33 patients).PDF p.5, Fronto-temporal subgroup
  • grimacing; temporo-frontal subgroupGrimacing was reported in 28% of the temporo-frontal subgroup (76 patients).PDF p.5, Temporo-frontal subgroup
  • association coefficient; emotional and grimaceThe source reports an association coefficient of 0.807 for emotional and grimace in the whole group.PDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient; emotional and grimacingThe source reports an association coefficient of 0.848 for emotional and grimacing in the fronto-temporal subgroup.PDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
Reported values
  • 23%grimace; whole groupPercentage · 109 review patients, whole group · ictal propagationPDF p.5, All group; PDF p.9, Figure 2
  • 12%grimacing; fronto-temporal subgroupPercentage · 33 patients, fronto-temporal subgroup · ictal propagationPDF p.5, Fronto-temporal subgroup
  • 28%grimacing; temporo-frontal subgroupPercentage · 76 patients, temporo-frontal subgroup · ictal propagationPDF p.5, Temporo-frontal subgroup
  • association coefficient 0.807association coefficient; emotional and grimaceAssociation Coefficient · 109 review patients · ictal symptom co-occurrencePDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient 0.848association coefficient; emotional and grimacingAssociation Coefficient · 33 fronto-temporal subgroup patients · ictal symptom co-occurrencePDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Visual illusionReported: Right hemisphere5 manuscripts · 9 findings · 6 reported values
Weighted evidence supportevidence weight 17.35 across 5 manuscripts · 2 systematic review or meta-analysis · 2 independent primary study · 1 narrative, educational, or cited context

No hemisphere or body-side direction is reported. No lateralization axis information is reported for the historical lateral-temporal symptom description. The primary result reports visual illusions in 9/82 patients (11%) without an aggregated side or localization axis. The primary table lists 11 visual-illusion aura entries without an aggregated side or lateralization direction. The educational body-image/visual-illusion statement contains no lateralization evidence. The primary comparison is among medial, medial-lateral, and lateral temporal onset subtypes and reports no hemisphere-level lateralization.

Source-defined result groups 3
Localization: TemporalObserved proportion 8.3%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 16.7%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 30.8%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 5

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • elementary visual aura; visual illusions/distortions; complex visual hallucinationsTable 3 maps elementary visual phenomena such as lights and shapes to primary visual cortex, visual illusions or distortions to temporo-parieto-occipital regions, and complex visual hallucinations to temporal regions.PDF p.10, Table 3; PDF p.8, Visual association areas
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 1 finding
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • auditory hallucinations; dreamy states; visual misperceptions; language disorders; focal impaired consciousness seizuresThe source's historical lateral-temporal description includes auditory hallucinations, dreamy states, visual misperceptions, language disorders, and progression to focal impaired consciousness seizures.PDF p.1, Introduction
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • visual and vestibular illusions, including vertigoVisual and vestibular illusions, especially vertigo, are reported particularly in posterior LTLE, but the chapter states that they probably rely on propagation of ictal activity to occipital or parietal regions.PDF p.9, Focal aware seizures
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • visual hallucination or illusionVisual hallucination or illusion was numerically more frequent in L than M or ML patients, but the group difference was not statistically significant.PDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
Reported values
  • ML 3/18 (16.7%)visual hallucination or illusionPercentage · n/N 3/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • L 4/13 (30.8%)visual hallucination or illusionPercentage · n/N 4/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • M 2/24 (8.3%)visual hallucination or illusionPercentage · n/N 2/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 5 findings · 3 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • visual illusionsVisual illusions were reported by nine patients and corresponded to 11% of the cohort.PDF p.3, Results, Aurae; PDF p.9, Discussion
  • visual illusion entries in Table 1Table 1 lists 11 visual-illusion aura entries.PDF p.4, Table 1
  • visual illusion as parietal association symptomatologyThe source states that disturbance of body image or visual illusion may indicate an epileptogenic zone in parietal association cortex.PDF p.8, Discussion
  • visual illusion formsThe source describes visual illusions in which figures looked larger, were maloriented in space, or perceived images or objects were moving.PDF p.9, Discussion
  • area 5b visual illusion responseIn Case 4, stimulation of area 5b produced an aura in which things looked smaller or far away.PDF p.9, Discussion
Reported values
  • 9/82 (11%) patientsvisual illusionsPercentage · n/N 9/82 · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae; PDF p.9, Discussion
  • 11 source-reported aura entriesvisual illusion entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 1 casearea 5b visual illusion responseCount · n/N 1/1 · patient 4 cited by the source · stimulation responsePDF p.9, Discussion

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Dreamy state / panoramic consciousness (Jackson)Source terms: Dreamy state; Dreamy state / panoramic consciousnessReported: Non-dominant hemisphere7 manuscripts · 10 findings · 7 reported values
Weighted evidence supportevidence weight 17.07 across 7 manuscripts · 3 systematic review or meta-analysis · 3 narrative, educational, or cited context · 1 independent primary study

No lateralization axis information is reported for the historical lateral-temporal symptom description. No lateralization axis information is reported for the déjà vu, dreamy-state, and scene-reminiscence stimulation summary. No lateralizing direction is reported. The review table reports déjà-vu, dreamy state, or reminiscence in 12 basal-temporal cases (14%) with no hemisphere direction. The review table reports déjà-vu, dreamy state, or reminiscence in 4/60 high- or very-high-confidence basal-temporal EZ cases (7%) with no hemisphere direction. No lateralizing information is present. No hemisphere direction is reported. No seizure lateralization is reported. No hemisphere or lateralizing direction is reported. The review describes dysmnesic manifestations as characteristic of MTLE and reports déjà vu more often with nondominant MTLE.

Source-defined result groups 3
Localization: TemporalObserved proportion 27.8%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 29.2%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • déjà-vu and dreamy statesDéjà-vu and dreamy states were reported at 14% in the cognitive-disturbance summary.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Déjà-vu/dreamy state/reminiscence (Table 3)Table 3 reports déjà-vu, dreamy state, or reminiscence in 12 cases (14%), more at seizure onset.PDF p.6, Table 3
  • Déjà-vu/dreamy state/reminiscence (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports déjà-vu, dreamy state, or reminiscence in 4 cases (7%).PDF p.7, Table 4
Reported values
  • 14% déjà-vu/dreamy statesdéjà-vu and dreamy statesPercentage · reviewed basal temporal seizure cases · ictal onset in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 12 cases (14%)Déjà-vu/dreamy state/reminiscence (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 4/60 (7%)Déjà-vu/dreamy state/reminiscence (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • dreamy state and perirhinal stimulationIn a cited case of temporal epilepsy with dreamy state, perirhinal stimulation elicited reminiscence of memories and after-discharge cross-correlation increased between rhinal cortices and hippocampus, hippocampus and amygdala, and perirhinal and visual cortex, specifically in the theta band.PDF p.5, section 7; PDF p.6, section 7
Reported values
  • One cited casedreamy state and perirhinal stimulationCount · One cited case of temporal epilepsy with dreamy state; exact patient details are not reported in this review · temporal epilepsy with dreamy state · Electrical stimulation and after-dischargePDF p.5, section 7; PDF p.6, section 7
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 1 finding
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • auditory hallucinations; dreamy states; visual misperceptions; language disorders; focal impaired consciousness seizuresThe source's historical lateral-temporal description includes auditory hallucinations, dreamy states, visual misperceptions, language disorders, and progression to focal impaired consciousness seizures.PDF p.1, Introduction
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • dysmnesic manifestations, déjà vu, jamais vu, prescience, and “dreamy state”Dysmnesic manifestations are characteristic of MTLE; déjà vu has been reported as predominant in nondominant MTLE, prescience is rarely described, and the “dreamy state” may include déjà vu, strangeness or unreality, and complex auditory or visual hallucinations.PDF p.7, Focal cognitive seizures
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • dreamy stateDreamy state was reported in M and ML patients but not L patients, without a statistically significant group difference.PDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.9, Trends toward other electroclinical correlations, Dreamy state
  • pure sensory hallucinations and dreamy stateThe authors distinguish pure sensory illusions or hallucinations from complex or mnemonic experiential phenomena, interpreting pure sensory hallucinations as related to a neocortical epileptogenic network and dreamy state as tending to a network including temporolimbic structures.PDF p.9, Trends toward other electroclinical correlations, Dreamy state
Reported values
  • L 0/13 (0%)dreamy statePercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.9, Trends toward other electroclinical correlations, Dreamy state
  • M 7/24 (29.2%)dreamy statePercentage · n/N 7/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.9, Trends toward other electroclinical correlations, Dreamy state
  • ML 5/18 (27.8%)dreamy statePercentage · n/N 5/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2; PDF p.9, Trends toward other electroclinical correlations, Dreamy state
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • epigastric sensation; dreamy states; oro-alimentary automatisms; long seizure durationThe source states that focal-aware epigastric sensation, dreamy states, oro-alimentary automatisms, and long seizure duration are shared with medial temporal seizures.PDF p.5, Discussion
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • déjà vu; “dreamy state”; reminiscence of scenesThe source’s selected stimulation literature associates déjà vu or a “dreamy state” with hippocampus and amygdala stimulation and with lateral temporal stimulation spreading to medial temporal regions; a rhinal-cortex study localized déjà vu to entorhinal, perirhinal, hippocampal, and amygdalar sites, with the sensation more common after entorhinal stimulation, and localized reminiscence of scenes to perirhinal cortex.PDF p.18, Table 10.1, Consciousness/Mental Phenomenology

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Experiential / memory flashback aura (panoramic)Source terms: Experiential/memory aura; Experiential / memory flashback auraReported: Non-dominant hemisphereAlso reported: Right hemisphere8 manuscripts · 18 findings · 17 reported values
Weighted evidence supportevidence weight 16.65 across 8 manuscripts · 1 independent primary study · 2 systematic review or meta-analysis · 5 narrative, educational, or cited context

Dysmnesic-aura subcategories did not differ significantly between TL and T+ groups; no hemisphere or body-side direction is reported. The mesiotemporal-versus-lateral temporal comparison contains no hemisphere direction. No seizure lateralization is reported. Lateral-temporal versus mesial-temporal is a localization comparison, not a cerebral hemisphere direction. No lateralization axis information is reported for the déjà vu, dreamy-state, and scene-reminiscence stimulation summary. The review table reports déjà-vu, dreamy state, or reminiscence in 12 basal-temporal cases (14%) with no hemisphere direction. The review table reports déjà-vu, dreamy state, or reminiscence in 4/60 high- or very-high-confidence basal-temporal EZ cases (7%) with no hemisphere direction. No lateralizing direction is reported for the approximate experiential-sign prevalence statement. The cited déjà-vu network report gives no side or lateralization direction. No hemisphere direction is reported. Two cited Penfield and Perot cases reportedly had stimulation-elicited hallucinations; the detailed case description is right temporal. The review describes dysmnesic manifestations as characteristic of MTLE and reports déjà vu more often with nondominant MTLE.

Source-defined result groups 3
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Experiential aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Experiential aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 9 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • dysmnesic auraDysmnesic auras did not differ significantly between TL and T+ groups across familiarity illusion, memory flashback, and dreamy state subcategories.PDF p.6, Table 2
Reported values
  • T+ 0%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 3.4%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • T+ 13%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • T+ 4.3%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • P=0.2dysmnesic auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
  • TL 5.1%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • TL 1.7%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • T+ 8.7%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 0%dysmnesic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Déjà-vu/dreamy state/reminiscence (Table 3)Table 3 reports déjà-vu, dreamy state, or reminiscence in 12 cases (14%), more at seizure onset.PDF p.6, Table 3
  • Déjà-vu/dreamy state/reminiscence (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports déjà-vu, dreamy state, or reminiscence in 4 cases (7%).PDF p.7, Table 4
  • experiential signsThe review states that experiential signs such as déjà vu or reminiscences occurred in approximately 15% of cases.PDF p.8, Discussion
Reported values
  • 12 cases (14%)Déjà-vu/dreamy state/reminiscence (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 4/60 (7%)Déjà-vu/dreamy state/reminiscence (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
  • approximately 15% experiential signsexperiential signsPercentage · reviewed basal temporal seizure cases · ictalPDF p.8, Discussion
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • déjà vu and recollective experienceA cited series of patients with déjà vu showed transient functional coupling between amygdala and hippocampus and between hippocampus and rhinal cortex, particularly in the theta band, when déjà vu was provoked by electrical stimulation; the review relates déjà vu and recollection to increased hippocampus–cortex synchrony, with recollection involving a larger associative network.PDF p.6, section 7
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • abdominal aura; experiential phenomena; elemental auditory auraIn a cited study of 187 temporal lobe seizures assessed with intracranial stereo-EEG, abdominal aura and experiential phenomena such as fear, déjà vu, and jamais vu indicated mesiotemporal seizures, whereas elemental auditory aura indicated lateral onset involving Heschl’s gyrus/primary auditory cortex.PDF p.5, Auras
  • abdominal aura; experiential phenomena; elemental auditory auraIn a cited study of 187 temporal lobe seizures assessed by intracranial stereo-EEG, abdominal aura and experiential phenomena including fear, déjà vu, and jamais vu indicated mesiotemporal seizures, whereas elemental auditory aura indicated lateral onset involving Heschl’s gyrus or primary auditory cortex.PDF p.5, Auras
Reported values
  • Qualitative association in 187 seizuresabdominal aura; experiential phenomena; elemental auditory auraCount · 187 temporal lobe seizures assessed by intracranial stereo-EEG · Aura and ictal onsetPDF p.5, Auras
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 8 findings · 3 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Experiential auraTable 3 reports 1 studies assessing Experiential aura.PDF p.6, Table 3
  • Experiential auraTable 3 reports 19 patients assessed for Experiential aura.PDF p.6, Table 3
  • Experiential auraTable 3 reports 47.3% as the percentage range or value for Experiential aura; the overall association grade is Low.PDF p.6, Table 3
  • Experiential aura; lateral versus mesial comparisonTable 5 reports 1 studies comparing Experiential aura in lateral and mesial TLE.PDF p.9, Table 5
  • Experiential aura; lateral TLE patient denominatorTable 5 reports 19 lateral-TLE patients assessed for Experiential aura.PDF p.9, Table 5
  • Experiential aura; mesial TLE patient denominatorTable 5 reports 16 mesial-TLE patients assessed for Experiential aura.PDF p.9, Table 5
  • Experiential aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 47.3% for Experiential aura.PDF p.9, Table 5
  • Experiential aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0% for Experiential aura.PDF p.9, Table 5
Reported values
  • 47.3%Experiential auraPercentage · Lateral temporal epilepsy patients assessed for Experiential aura · ictalPDF p.6, Table 3
  • 47.3%Experiential aura; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Experiential aura · Lateral TLE patients assessed for Experiential aura · ictalPDF p.9, Table 5
  • 0%Experiential aura; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Experiential aura · Mesial TLE patients assessed for Experiential aura · ictalPDF p.9, Table 5
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • dysmnesic manifestations, déjà vu, jamais vu, prescience, and “dreamy state”Dysmnesic manifestations are characteristic of MTLE; déjà vu has been reported as predominant in nondominant MTLE, prescience is rarely described, and the “dreamy state” may include déjà vu, strangeness or unreality, and complex auditory or visual hallucinations.PDF p.7, Focal cognitive seizures
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • experimental hallucinations after lateral posterior temporal stimulationIn two patients previously discussed by Penfield and Perot, experimental hallucinations were elicited by stimulation of the lateral posterior temporal cortex.PDF p.13, Cortical stimulation
Reported values
  • 2 casesexperimental hallucinations after lateral posterior temporal stimulationCount · n/N 2/2 · two patients in the cited Penfield and Perot report · stimulation response and seizure evolutionPDF p.13, Cortical stimulation
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • déjà vu; “dreamy state”; reminiscence of scenesThe source’s selected stimulation literature associates déjà vu or a “dreamy state” with hippocampus and amygdala stimulation and with lateral temporal stimulation spreading to medial temporal regions; a rhinal-cortex study localized déjà vu to entorhinal, perirhinal, hippocampal, and amygdalar sites, with the sensation more common after entorhinal stimulation, and localized reminiscence of scenes to perirhinal cortex.PDF p.18, Table 10.1, Consciousness/Mental Phenomenology

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal emotional behaviorReported: ContralateralAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere8 manuscripts · 48 findings · 44 reported values
Weighted evidence supportevidence weight 16.62 across 8 manuscripts · 1 manuscript weight pending · 3 systematic review or meta-analysis · 1 independent primary study · 3 narrative, educational, or cited context · 1 structured design not resolved

Cited-study restatement combines nondominant ictal smile, contralateral lower facial asymmetry, and qualitative frontal associations. Ictal smile has been associated with possible right-hemispheric lateralization. No hemispheric lateralization is reported. This record provides no hemispheric lateralization. No hemisphere or body-side direction is reported. Emotional signs preceding hyperkinetic behavior provide no lateralizing information. The cited frontal rostrocaudal gradient is not lateralizing. Emotional manifestations in SHE provide no lateralizing information here. The rostrocaudal cluster gradient is not lateralizing. This record provides no seizure lateralization. No lateralizing direction is reported. No seizure lateralization is reported. No lateralization axis information is reported for facial expression change versus autonomic signs. No lateralization axis information is reported for affective/autonomic aura versus facial expression change. No lateralization axis information is reported for autonomic signs versus facial expression change. The source reports OR 0.9 for motor gestural automatisms relative to facial expression change; no hemisphere direction is reported. No lateralization evidence is reported. This finding provides no lateralization information. The claim states OR 0.2 for laughter relative to facial expression change, while the supplied statistic record states OR 0.1; no hemisphere direction is reported. No lateralizing semiology is reported for the tonic-clonic versus facial-expression-change odds comparison. No lateralizing semiology is reported for the reciprocal facial-expression-change versus tonic-clonic odds comparison. No body-side, seizure-onset side, or seizure-lateralization direction is reported.

Source-defined result groups 15
Localization: Frontal / TemporalObserved proportion 83.3%frontal SHE · other frontal SOZ · emotional manifestation1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 16.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 9.5%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelypatient-level frequency synthesized across eligible studies1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelytemporal SHE emotional manifestations · frontal and other SHE · patient subgroup count as reported in Table 21 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyfrontal SHE emotional manifestations · temporal and other SHE · patient subgroup count as reported in Table 21 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelypairwise comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 36 findings · 31 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • anterior cingulate cortex; emotional manifestationsACC seizures are described as having predominant emotional and behavioral manifestations, but their broad connectivity makes primary versus secondary involvement difficult to distinguish clinically.PDF p.13, ACC seizures as an emotional behavior pattern
  • emotional and autonomic manifestations; vocalization; facial expression; hypermotor behaviorThe review identifies emotional/autonomic manifestations, vocalization, facial expression changes, complex automatisms, and hypermotor behavior with preserved awareness as the main ACC clinical features.PDF p.11, Anatomical and clinical correlations; PDF p.15, Conclusion
  • facial expression changeThe source reports a frequency of 46% for facial expression change.PDF p.13, Table 3
  • facial expression change; reported frequency rangeThe source reports a frequency range of 0–100% for facial expression change.PDF p.13, Table 3
  • facial expression change; ACC association gradeTable 3 assigns the source's High overall association grade to facial expression change.PDF p.13, Table 3
  • facial expression change; Figure 4 rateFigure 4 displays a 46.2% rate for facial expression change.PDF p.10, Figure 4
  • facial expression change typicalityFacial expression change met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • facial expression change; pairwise odds-ratio significancefacial expression change showed eight significant pairwise odds-ratio comparisons after Holm correction.PDF p.10, Statistical analysis of ictal semiology
  • pairwise OR: Facial expression change relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.5 for Facial expression change relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.6 for Facial expression change relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.7 for Facial expression change relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Autonomic signsFigure 6 reports an odds ratio of 0.9 for Facial expression change relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Facial expression changeFigure 6 reports an odds ratio of 1.8 for Vocalization/verbalization relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Facial expression changeFigure 6 reports an odds ratio of 1.7 for Hypermotor-complex motor behavior relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Facial expression changeFigure 6 reports an odds ratio of 1.5 for Affective/autonomic aura relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Facial expression changeFigure 6 reports an odds ratio of 1.1 for Autonomic signs relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Facial expression changeFigure 6 reports an odds ratio of 0.9 for Motor (gestural) automatisms relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Facial expression changeFigure 6 reports an odds ratio of 0.6 for Loss of consciousness relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Facial expression changeFigure 6 reports an odds ratio of 0.5 for Post-ictal confusion/behavior change disinhibition relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Facial expression changeFigure 6 reports an odds ratio of 0.3 for Chapeau de gendarme relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Facial expression changeFigure 6 reports an odds ratio of 0.3 for Dystonic posturing relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Facial expression changeFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Facial expression changeFigure 6 reports an odds ratio of 0.2 for Laughter relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Facial expression changeFigure 6 reports an odds ratio of 0.1 for Oro-alimentary automatisms relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Facial expression changeFigure 6 reports an odds ratio of 0.1 for Tonic-clonic relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Facial expression changeFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 1.1 for Facial expression change relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Loss of consciousnessFigure 6 reports an odds ratio of 1.6 for Facial expression change relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 1.9 for Facial expression change relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 3.3 for Facial expression change relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Dystonic posturingFigure 6 reports an odds ratio of 3.6 for Facial expression change relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Head-eye deviationFigure 6 reports an odds ratio of 5.2 for Facial expression change relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to LaughterFigure 6 reports an odds ratio of 7.9 for Facial expression change relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 9 for Facial expression change relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Tonic-clonicFigure 6 reports an odds ratio of 14.9 for Facial expression change relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to F to BTCFigure 6 reports an odds ratio of 14.9 for Facial expression change relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 46% (frequency range 0–100%)facial expression changePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.13, Table 3
  • 46.2%facial expression change; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.10, Figure 4
  • 8 significant pairwise comparisonsfacial expression change; pairwise odds-ratio significanceCount · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.10, Statistical analysis of ictal semiology
  • OR 0.5pairwise OR: Facial expression change relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Facial expression change relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Facial expression change relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Facial expression change relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.8pairwise OR: Vocalization/verbalization relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Hypermotor-complex motor behavior relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Affective/autonomic aura relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Autonomic signs relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Motor (gestural) automatisms relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Loss of consciousness relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Chapeau de gendarme relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Dystonic posturing relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Laughter relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Oro-alimentary automatisms relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Facial expression change relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Facial expression change relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.9pairwise OR: Facial expression change relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.3pairwise OR: Facial expression change relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Facial expression change relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.2pairwise OR: Facial expression change relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.9pairwise OR: Facial expression change relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9pairwise OR: Facial expression change relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 14.9pairwise OR: Facial expression change relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 14.9pairwise OR: Facial expression change relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • emotional facial expression and facial asymmetryIctal smile suggests nondominant-hemisphere onset in children with parieto-occipital epilepsy and FLE; lower facial asymmetry occurs in 70% of patients with TLE and is usually contralateral to the epileptogenic zone. Ictal crying is rare in temporal or mesial frontal epilepsy, and facial expressions of fear or anger suggest frontal-lobe origin.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • Lower facial asymmetry in 70% of TLE patientsemotional facial expression and facial asymmetryPercentage · children with parieto-occipital epilepsy or FLE; patients with TLE; patients with temporal or mesial frontal epilepsy · ictalPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 3 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 4.62 · 2 × 1.5 × 1.54
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • emotional manifestationEmotional manifestations were observed only in frontal and temporal SHE; 10/12 emotional symptoms in frontal SHE were associated with an SOZ in the anterior frontal region.PDF p.6, Table 2; PDF p.7, section 3.3
Reported values
  • emotional n=12 frontalemotional manifestationCount · Frontal and temporal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists emotional n=12 frontal and n=2 temporal · frontal SHE emotional manifestations · early nonmotor manifestationPDF p.6, Table 2; PDF p.7, section 3.3
  • 10/12emotional manifestationPercentage · n/N 10/12 · Frontal and temporal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists emotional n=12 frontal and n=2 temporal · frontal SHE · early nonmotor manifestationPDF p.6, Table 2; PDF p.7, section 3.3
  • emotional n=2 temporalemotional manifestationCount · Frontal and temporal SHE patients in the 115-patient semiology-analysis cohort; Table 2 lists emotional n=12 frontal and n=2 temporal · temporal SHE emotional manifestations · early nonmotor manifestationPDF p.6, Table 2; PDF p.7, section 3.3
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Facial distressTable 2 reports 2/21 (10%) for Facial distress; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Facial distressTable 2 reports 2/12 patients with Facial distress in the prefrontal operculum group.PDF p.7, Table 2
  • Facial distressTable 2 reports 0/9 patients with Facial distress in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Facial distressFisher's exact comparison of Facial distress between the prefrontal and precentral Rolandic operculum groups has p=0.486.PDF p.7, Table 2
Reported values
  • 2/21 (10%)Facial distressPercentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 2/12 patientsFacial distressProportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 0/9 patientsFacial distressProportion · n/N 0/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal smileIctal smile has been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 5 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • elementary motor signs; gestural motor behavior; emotional expressionThe review reports that Bonini, McGonigal et al. (2014) identified four frontal-lobe semiologic groups along a rostro-caudal gradient: Group 1 had elementary motor signs without gestural motor behavior; Group 2 combined elementary and gestural motor signs, often with mainly proximal tonic signs and facial contraction; Group 3 had no elementary motor signs and often distal, integrated gestural behavior; and Group 4 had no elementary motor signs with integrated gestural behavior in an emotional, usually fearful, context.PDF p.6, Table 2, Frontal lobe row
  • elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresIn the summarized Bonini, McGonigal et al. study, automated clustering of clinical signs and brain areas involved in seizure onset and early propagation found a rostrocaudal frontal gradient with four groups: elementary motor signs without gestural behavior; elementary plus gestural signs with mainly proximal tonic signs and facial contraction; gestural behavior without elementary signs and often distal or integrated; and gestural behavior in an emotional, often fearful, context with an integrated appearance.PDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
Reported values
  • 374 seizureselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • 54 subjectselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • Semiology clusters n=4elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Patients in semiology series n=54elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Seizures in semiology series n=374elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • fear; anxiety; facial expression of fear/horror; orbitofrontal cortex; amygdalaThe source states that hyperkinetic behavior following intense fear or anxiety with facial fear/horror expression has been related to limbic imbalance, particularly decoupling between orbitofrontal cortex and amygdala.PDF p.12, Discussion
  • hyperkinetic behavior preceded by emotional signsThe source states that hyperkinetic behavior could be preceded by emotional signs in 31% of cases.PDF p.12, Discussion
Reported values
  • 31%hyperkinetic behavior preceded by emotional signsPercentage · Source-described hyperkinetic-behavior cases · ictal onset before hyperkinetic propagationPDF p.12, Discussion
simone-anatomo-functional-organization-insular-networks-2025.pdfStructured design not resolved · 1 finding
simone-anatomo-functional-organization-insular-networks-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The paper summarizes prior macaque ICMS mapping performed with 200-microsecond biphasic pulses at 50 Hz, 4 mA, for 3 seconds; a behavior entered the dataset when two observers recognized it and it was evoked in more than 50% of trials. The present analyses used ICMS maps and insular tracer injections in two male rhesus macaques (Mk1 and Mk2), indirect tracer data from 22 additional animals, and resting-state fMRI from 12 male macaques aged 4-8 years. The authors warped the ICMS maps and injection sites onto the INIA19 macaque template and delineated six insular fields. No seizure cohort, ictal or postictal observations, or clinical localization reference standard was studied.
Findings
  • emotional field; lip-smacking; discomfort reactionsThe macaque ventral middle insula was defined as an ICMS emotion-related field in which stimulation elicited lip-smacking, described as an affiliative gesture during emotionally salient social situations; intermingled stimulation sites also produced difficult-to-interpret discomfort reactions ranging from postural adjustments to psychomotor agitation. The discussion reports lip-smacking during direct eye contact with a specific experimenter and notes that the behavior can also occur during anxiety or fear.PDF p.5, Fig. 1C, E and caption; PDF p.10, Fig. 5B, C and caption; PDF p.12, §4.4.1; PDF p.19, §5.3

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal negative motor phenomenon (inhibitory arrest of contralateral limb)Source terms: Ictal negative motor phenomenonReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere11 manuscripts · 27 findings · 18 reported values
Weighted evidence supportevidence weight 16.6 across 11 manuscripts · 2 independent primary study · 1 systematic review or meta-analysis · 6 narrative, educational, or cited context · 2 case report or observation

The repeated narrative percentage is not lateralizing. The cited review describes unilateral ictal paresis or an immobile limb as contralateral to the seizure focus. Captured flaccid left upper-extremity paralysis was contralateral to a right parietal ictal onset. Ictal and postictal paresis are difficult to distinguish but are said to convey the same unspecified lateralization. The cited table labels myoclonic/negative myoclonus contralateral when unilateral. Myoclonic seizures are usually generalized or bilateral, while unilateral myoclonus is described as contralateral to primary motor or premotor cortex. The cited review describes unilateral ictal or postictal limb immobility as contralateral to the epileptogenic zone in almost all cases. The review describes unilateral ictal akinesia as contralateral to the epileptogenic zone despite low and variable frequency. Oestreich et al. observed contralateral ictal limb immobility in 5/94 consecutive focal-epilepsy patients. The cited series observed contralateral ictal limb immobility in four seizure-free surgical patients. Ictal akinesia was contralateral to the suspected epileptogenic zone in all six lesion-defined cases and all three additional cases. Ictal limb immobility was reported as always contralateral in a 328-patient MRI-and-EEG cohort, with frequency 24.6%. The narrative frequency is not lateralizing. Three parietal-epilepsy patients reported inability to move one extremity or hand weakness contralateral to the epileptogenic zone. The cited table lists limb paresis as contralateral. This finding provides no lateralization information. No manifestation-side direction is reported; right applies only to the pathway. No lateralization information is supplied. No lateralization information is reported. No resolved lateralization direction is reported.

Source-defined result groups 4
Localization: FrontalObserved proportion 9.5%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 22.2%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · no negative-motor or weakness aura · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 11

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Unilateral ictal paresis or immobile limbUnilateral ictal paresis or “immobile limb” is an infrequent sign contralateral to the seizure focus and involves sudden loss of tone in one upper limb while the other maintains tone and movement or an automatism.PDF p.5, unilateral ictal paresis paragraph; PDF p.4, Table 2
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • pre-SMA speech and movement arrest / negative motor areasSeizures arising from rostral SMA or pre-SMA may consist of speech arrest, optional quavering vocalization, movement arrest, or subtle leg repositioning; when the examiner raises the arms they gradually drop back, a negative motor phenomenon associated with dorsal or ventral premotor areas.PDF p.3, section 4
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 2 findings · 3 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • myoclonic and negative myoclonus seizuresMyoclonic seizures are usually generalized or bilateral but can be focal; unilateral myoclonic seizures are generated from the primary motor or premotor cortex contralateral to the seizure. Negative myoclonus is brief muscle atonia during contraction, and negative epileptic myoclonus is rarely observed in perirolandic epilepsy.PDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
  • unilateral ictal or postictal immobile limbA sudden loss of tone in one upper limb while the opposite side expresses automatisms was observed in 5–28% of focal seizures, usually with temporal-lobe origin, and was contralateral to the epileptogenic zone in almost all cases.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • Myoclonic duration shorter than 400 msmyoclonic and negative myoclonus seizuresDuration · patients with focal or generalized epilepsy · Myoclonic seizure · ictal motorPDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
  • Negative myoclonus duration 20–400 msmyoclonic and negative myoclonus seizuresRange · patients with focal or generalized epilepsy · Negative myoclonus · ictal motorPDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
  • Observed in 5–28% of focal seizuresunilateral ictal or postictal immobile limbPercentage · patients with focal seizures · ictal or postictalPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 6 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • negative motor signs during seizure propagationDuring seizure propagation, the source reports negative motor signs in 12% of patients.PDF p.6, Anatomical and clinical correlations
  • negative motor signs during seizure propagationDuring seizure propagation, negative motor signs were observed in two patients.PDF p.6, Anatomical and clinical correlations
  • Negative motorTable 2 reports 2/21 (10%) for Negative motor; timing is late, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Negative motorTable 2 reports 0/12 patients with Negative motor in the prefrontal operculum group.PDF p.7, Table 2
  • Negative motorTable 2 reports 2/9 patients with Negative motor in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Negative motorFisher's exact comparison of Negative motor between the prefrontal and precentral Rolandic operculum groups has p=0.171.PDF p.7, Table 2
Reported values
  • 2 patients (12%)negative motor signs during seizure propagationPercentage · Included fronto-opercular epilepsy patients with propagation data · Included fronto-opercular epilepsy patients with propagation data · ictal propagationPDF p.6, Anatomical and clinical correlations
  • 2/21 (10%)Negative motorPercentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · LatePDF p.7, Table 2
  • 0/12 patientsNegative motorProportion · n/N 0/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · LatePDF p.7, Table 2
  • 2/9 patientsNegative motorProportion · n/N 2/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · LatePDF p.7, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 3 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Ictal and postictal paresisThe review states that ictal and postictal paresis are difficult to distinguish but provide the same lateralisation information.PDF p.4, section 1.6
  • Myoclonic/negative myoclonusTable 2 associates myoclonic/negative myoclonus with primary motor cortex (BA 4), premotor cortex (BA 6), and primary somatosensory area and lists contralateral lateralisation if unilateral.PDF p.3, Table 2
  • Paresis of limbTable 3 associates limb paresis with M1 or premotor exhaustion or activation of negative motor areas including primary motor cortex, SMA, and cingulum and lists contralateral lateralisation.PDF p.4, Table 3
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 5 findings · 7 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral ictal akinesiaUnilateral ictal limb immobility occurs in a minority of focal epilepsy patients and lateralizes contralateral to the epileptogenic zone.PDF p.9, section 3.16
  • unilateral ictal limb immobilityOestreich et al. observed contralateral ictal limb immobility in 5 of 94 consecutive focal-epilepsy patients.PDF p.9, section 3.16
  • ictal limb immobilityBleasel et al. observed contralateral ictal limb immobility in four seizure-free surgical patients.PDF p.9, section 3.16
  • ictal akinesiaNoachtar and Luders reported ictal akinesia contralateral to the suspected epileptogenic zone in every reported case group.PDF p.9, section 3.16
  • ictal limb immobilityIctal limb immobility was reported as always contralateral in a 328-patient MRI-and-EEG cohort.PDF p.9, section 3.16
Reported values
  • reported frequency 5-24%unilateral ictal akinesiaPercentage · patients with focal epilepsy · ictalPDF p.9, section 3.16
  • 5/94unilateral ictal limb immobilityCount · n/N 5/94 · 94 consecutive patients with focal epilepsy evaluated presurgically · ictalPDF p.9, section 3.16
  • 34/54 had temporal epilepsyictal limb immobilityPercentage · n/N 34/54 · 54 patients with focal epilepsy and postoperative seizure freedom, including 34 with temporal epilepsy · temporal epilepsy · ictalPDF p.9, section 3.16
  • 4/54 with contralateral immobilityictal limb immobilityPercentage · n/N 4/54 · 54 patients with focal epilepsy and postoperative seizure freedom, including 34 with temporal epilepsy · seizure-free surgical patients · ictalPDF p.9, section 3.16
  • Additional ictal-akinesia cases contralateral 3/3ictal akinesiaPercentage · n/N 3/3 · 6 cases with contralateral lesions by EEG or neuroimaging plus 3 additional cases · Additional case group · ictalPDF p.9, section 3.16
  • Lesion-defined ictal-akinesia cases contralateral 6/6ictal akinesiaPercentage · n/N 6/6 · 6 cases with contralateral lesions by EEG or neuroimaging plus 3 additional cases · EEG/neuroimaging lesion group · ictalPDF p.9, section 3.16
  • 24.6%ictal limb immobilityPercentage · 328 patients evaluated by MRI and EEG · MRI-and-EEG cohort · ictalPDF p.9, section 3.16
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 2 findings
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • inhibitory right parietal seizure with flaccid left armIn the illustrated case with recurrent flaccid left-arm weakness and later violent shaking, video-EEG confirmed rare inhibitory seizures with right parietal onset at P8 and P4 greater than T8 and C4, producing focal ictal paralysis; the patient also had coexisting psychogenic nonepileptic events.PDF p.413; PDF p.414; PDF p.415
  • supplementary negative motor and frontal hypermotor seizuresSupplementary sensorimotor seizures may produce ictal paralysis or other negative motor symptoms, often with no scalp EEG because of mesial frontal dipole orientation; bizarre hypermotor seizures can arise from cingulate or orbitofrontal regions or appear after extrafrontal spread, with unilateral posturing and axial rotation favoring mesial frontal origin, severe agitation favoring orbitofrontal localization, and a longer electrical-to-hypermotor latency suggesting extrafrontal onset.PDF p.52; PDF p.53
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 3 findings · 3 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • inability to move or weakness of one extremityThree patients complained of inability to move one extremity or a feeling of weakness in the hand contralateral to the epileptogenic zone.PDF p.3, Results, Aurae
  • inability-to-move aura entries in Table 1Table 1 lists four aura entries for feeling of inability to move one extremity.PDF p.4, Table 1
  • negative motor manifestationsTwo patients had negative motor manifestations.PDF p.4, Results, Other seizure characteristics
Reported values
  • 3 patientsinability to move or weakness of one extremityCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae
  • 4 source-reported aura entriesinability-to-move aura entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 2 patientsnegative motor manifestationsCount · 82-patient parietal epilepsy series · ictal motor phasePDF p.4, Results, Other seizure characteristics
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding · 1 reported value
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • short negative motor seizureSpontaneous seizures persisted after surgery but had lessened in frequency and severity; they were characterized by short negative motor seizures with movement stopping instantly, occurring once every 2 or 3 days.PDF p.2, Case Report
Reported values
  • Short negative motor semiology and source-reported occurrence once every 2 or 3 daysshort negative motor seizureCount · Single reported patient · One-year postoperative follow-upPDF p.2, Case Report
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • focal clonic movement; negative motor responses; tonic posturing; palilaliaThe source reports that central-region pulse or short-train stimulation is used to induce focal clonic movement, that negative motor responses are seen in the pre-SMA region, and that SMA-proper stimulation induces positive motor behaviors such as tonic posturing or palilalia.PDF p.13, Motor Behaviors
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • motor arrest and staringTable 2 records motor arrest or staring as an early seizure sign in multiple cases.PDF p.6, Table 2 cases 1, 4, and 5
  • object dropping during visual-obscuration seizureTable 2 records motor arrest with object dropping after visual obscuration in Case 8.PDF p.7, Table 2 Case 8

11 contributing manuscripts; source-reported values remain separate and are not pooled.

Elementary visual phenomena (phosphenes, flickering lights, geometric forms, fortification spectra)Source terms: Elementary visual phenomena; Elementary visual auraReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere9 manuscripts · 25 findings · 9 reported values
Weighted evidence supportevidence weight 16.4 across 9 manuscripts · 3 independent primary study · 5 narrative, educational, or cited context · 1 systematic review or meta-analysis

The case records yellow-green spots in the right visual field; this is a visual-field frame, not an inferred cerebral side. The review restates stimulation findings of contralateral visual fields for elementary/intermediary hallucinations, central calcarine responses, and right-predominant associative visual effects with posterior exceptions. The review restates that a left visual-field elementary hallucination indicates right infra-calcarine discharge and is contralateral to the relevant visual cortex. The table reports elementary visual aura as contralateral. Visual phenomena are usually contralateral to seizure onset, with up to 30% described as more diffuse. one hemi-field or quadrant is interpreted relative to the contralateral occipital lobe and supra- or infracalcarine fissure left occipital pole Where side data were available, elementary visual hallucinations were contralateral to the epileptogenic side. The review reports unilateral visual auras in the contralateral visual field in 6/25 occipital-lobe epilepsy patients. No source lateralization is reported. No seizure lateralization is reported. No lateralizing direction is reported. No hemisphere or body-side direction is reported. The cited case of complex visual hallucinations after coloured triangles reports no hemisphere or lateralization direction.

Source-defined result groups 2
Localization: OccipitalSource-defined values retained separatelyAll reported · nonvisual reproduced aura · reproduced habitual aura1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelyAll reported · elementary/intermediary versus complex hallucinations; right versus left hemisphere; calcarine versus noncalcarine visual field · visual hallucination responses among 22 patients; exact response denominator not reported1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • elementary visual hallucinationsThe review reports that an elementary visual hallucination such as colored circles, twinkling stars, or moving flies in the left superior visual-field quadrant indicates discharge in the right infra-calcarine cortex, and that elementary hallucinations do not arise in spontaneous seizures beginning in structures distant from visual cortex.PDF p.2, section 4; PDF p.3, section 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 3 findings · 4 reported values
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • occipital lobe seizures; elementary visual auraOccipital lobe seizures are usually characterized by visual aura in 40%-75% of patients, or less commonly oculomotor features, and primary visual cortex seizures produce brief elementary visual auras, usually less than 2 minutes; in most patients the visual phenomena are lateralized and contralateral to seizure onset, but up to 30% have more diffuse visual changes.PDF p.8, Occipital lobe seizures; PDF p.8, Primary visual cortex
  • primary visual cortex; elementary visual auraSeizures arising from primary visual (calcarine) cortex cause elementary visual aura and tend to be brief, usually less than 2 minutes; flashing coloured or bright white lights are described, and lateral occipital cortex is said to probably produce pulsating visual features.PDF p.8, Primary visual cortex; PDF p.3, Figure 1
  • elementary visual aura; visual illusions/distortions; complex visual hallucinationsTable 3 maps elementary visual phenomena such as lights and shapes to primary visual cortex, visual illusions or distortions to temporo-parieto-occipital regions, and complex visual hallucinations to temporal regions.PDF p.10, Table 3; PDF p.8, Visual association areas
Reported values
  • up to 30% diffuse visual changesoccipital lobe seizures; elementary visual auraPercentage · Patients with occipital lobe epilepsy; exact cohort Not reported · Aura and ictal onsetPDF p.8, Occipital lobe seizures; PDF p.8, Primary visual cortex
  • Visual aura in 40%-75% of patientsoccipital lobe seizures; elementary visual auraPercentage · Patients with occipital lobe epilepsy; exact cohort Not reported · Aura and ictal onsetPDF p.8, Occipital lobe seizures; PDF p.8, Primary visual cortex
  • primary visual aura usually <2 minoccipital lobe seizures; elementary visual auraCount · Patients with occipital lobe epilepsy; exact cohort Not reported · Aura and ictal onsetPDF p.8, Occipital lobe seizures; PDF p.8, Primary visual cortex
  • duration usually <2 minprimary visual cortex; elementary visual auraDuration Threshold · occipital lobe seizure literature · ictal auraPDF p.8, Primary visual cortex; PDF p.3, Figure 1
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 2 findings
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • lateralized visual phenomena and visual field aurasVisual phenomena lateralized to one hemi-field as an early ictal manifestation are highly suggestive of onset in the contralateral occipital lobe. Symptoms restricted to the lower or upper quadrant are reported to localize to the contralateral supra- or infracalcarine fissure, respectively.PDF p.2, section 3.1 Auras
  • simple and complex visual aurasSimple visual auras with static, flashing, or moving lights suggest activation of the primary visual cortex and contiguous visual association areas, whereas complex visual auras involving people, scenes, objects, or illusions suggest the temporo-occipital junction or basal temporal cortex.PDF p.2, section 3.1 Auras; PDF p.2, Table 1
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 2 findings
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Elementary visual auraTable 2 associates elementary visual aura with the primary visual cortex (BA 17, 18, 19) and contralateral lateralisation.PDF p.3, Table 2
  • Elementary visual phenomenaThe review states that elementary visual hallucinations are typically associated with seizures originating in primary visual cortex (V1) and may be positive geometric shapes, lines, blobs, or flashes, or negative visual-field deficits, blurred vision, or cortical blindness.PDF p.6, section 1.12
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Unilateral visual auraWilliamson et al. reported unilateral visual auras in the contralateral visual field in 6 of 25 patients with occipital lobe epilepsy, with the diagnosis determined by semiology, EEG, and imaging features.PDF p.3, section 2.5 Visual auras
Reported values
  • 6 of 25 patientsUnilateral visual auraCount · n/N 6/25 · 25 patients with occipital lobe epilepsy · Ictal auraPDF p.3, section 2.5 Visual auras
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 8 findings · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • coloured lights elicited from left occipital poleIn patient 4, cortical stimulation of the left occipital pole elicited the habitual aura of coloured lights that whirled as usual.PDF p.18, Fig. 4
  • contralateral elementary visual hallucinationsWhere data were available, elementary visual hallucinations were contralateral to the epileptogenic side.PDF p.4, Results, Visual auras
  • elementary visual hallucination elicited by stimulationAll stimulation-reproduced habitual auras were elementary visual hallucinations.PDF p.13, Cortical stimulation
  • coloured triangles followed by complex visual hallucinationIn one cited case, seizures began with coloured triangles followed by complex visual hallucinations of a robber with a gun or sinister characters from comic books.PDF p.13, Cortical stimulation
  • elementary hallucination followed by faces or picturesIn the other cited case, spontaneous seizures began with elementary visual hallucinations followed by complex hallucinations consisting of faces or pictures, including Rembrandt’s self-portrait.PDF p.13, Cortical stimulation
  • stimulation-reproduced elementary visual hallucinationsThe source states that elementary visual hallucinations have been reproduced by cortical stimulation in prior reports.PDF p.2, Introduction
  • elementary visual hallucinationsElementary visual hallucinations were the most common visual aura in the cohort.PDF p.4, Results, Visual auras
  • co-occurring elementary hallucinations and ictal blindnessElementary visual hallucinations and ictal blindness could occur in the same patient at different times.PDF p.6, Results, Visual auras
Reported values
  • all stimulation-reproduced habitual auras were elementary visual hallucinationselementary visual hallucination elicited by stimulationProportion · patients with stimulation-reproduced habitual auras · stimulation responsePDF p.13, Cortical stimulation
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • elementary visual hallucination entriesTable 1 lists six elementary visual-hallucination aura entries.PDF p.4, Table 1
Reported values
  • 6 source-reported aura entrieselementary visual hallucination entriesCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • elementary, intermediary, and complex visual hallucinations; visual illusionsIn a cited depth-electrode study of 22 patients with epilepsy, the source reports that 85% of elementary and intermediary visual hallucination responses were induced from calcarine sulcus, lingual gyrus, lateral occipital cortex, fusiform gyrus, or cuneus/parieto-occipital sulcus; elementary and intermediary hallucinations were in the contralateral visual hemifield except after calcarine stimulation, when they were central. Complex meaningful hallucinations were associated with cuneus/parieto-occipital sulcus, precuneus, and fusiform gyrus, while color or spatial-background illusions were elicited from right rhinal, parahippocampal, collateral-sulcus, and fusiform regions; visual phenomena were more probable in the right than left hemisphere except at the most posterior sites.PDF p.14-15, Visual; PDF p.15, visual lateralization paragraph
Reported values
  • 85% of elementary/intermediary visual hallucination responses attributed to the listed occipital, fusiform, and cuneus/parieto-occipital siteselementary, intermediary, and complex visual hallucinations; visual illusionsPercentage · 22 patients with epilepsy in the cited depth-electrode study; exact response denominator not reported · stimulation-induced visual phenomenonPDF p.14-15, Visual; PDF p.15, visual lateralization paragraph
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 6 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • yellow-green visual hallucinations in right visual fieldTable 2 records elementary visual hallucinations of yellow-green spots in the right visual field in Case 6 Sz1.PDF p.6, Table 2 Case 6 Sz1
  • elementary visual hallucinationsElementary visual hallucinations occurred in six of 19 patients (31.6%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
  • pure visual phenotypePhenotype I is defined by exclusive subjective visual auras, including elementary visual hallucinations, amaurosis, or visual obscuration, without objective motor or autonomic progression.PDF p.9, Phenotype I
  • elementary visual hallucination color progressionTable 2 records elementary visual hallucinations progressing from black/white spots to enlarging spots and colored spots, followed by headache.PDF p.6, Table 2 Case 3
  • white-flash visual hallucinationsTable 2 records elementary visual hallucinations of white flashes followed by headache in Case 10.PDF p.7, Table 2 Case 10
  • dizziness with or without colored lightsTable 2 records dizziness with or without colored lights as an aura in Case 13.PDF p.7, Table 2 Case 13
Reported values
  • 6/19 (31.6%) elementary visual hallucinationselementary visual hallucinationsPercentage · n/N 6/19 · 19 patients monitored with SEEG · aura/ictal semiologyPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Preserved responsiveness during automatisms (AAPR)Source terms: Preserved responsiveness during automatismsReported: ContralateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side8 manuscripts · 17 findings · 21 reported values
Weighted evidence supportevidence weight 16.36 across 8 manuscripts · 1 manuscript weight pending · 3 systematic review or meta-analysis · 2 narrative, educational, or cited context · 1 independent primary study · 1 structured design not resolved · 1 case report or observation

The review links preserved awareness during automatisms and several peri-ictal autonomic/oral/urinary signs to a non-dominant focus, while rhythmic non-clonic hand motion may be contralateral. Automatisms with preserved responsiveness were reported as lateralizing to the non-dominant hemisphere, right in the described right-handed subgroup, with one left-language-dominant left temporal exception. The review distinguishes dominant-hemisphere dysphasia, nondominant ictal speech or preserved awareness, contralateral RINCH motions, and nonlateralizing speech arrest. The cited study attributes preserved responsiveness during oral or manual automatisms to nondominant temporal onset. The review states that automatisms with preserved responsiveness generally lateralize temporal seizures to the nondominant hemisphere, with one reported exception. The cited study restatement reports preserved-responsiveness automatisms exclusively in right nondominant temporal seizures and not in left temporal seizures. The additional case of automatisms with preserved consciousness was reported in right temporal lobe epilepsy. A case was reported with left hemispheric epilepsy and right-sided language dominance. The case reports a right temporal seizure focus with right-sided language dominance, a dominant-temporal exception to the usual nondominant pattern. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. No hemisphere or body-side direction is reported. No lateralizing direction is reported for complex behavior with preserved awareness.

Source-defined result groups 11
Lateralization: Left hemisphereObserved proportion 100.0%All reported · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Right hemisphereObserved proportion 100.0%All reported · usual nondominant-hemisphere association · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Non-dominant hemisphere / Right hemisphereSource-defined values retained separatelyAll reported · Lobar subgroup comparison within the surgical cohort. · Seizure and patient counts for sign occurrence; narrative subgroup includes seizures and patients.1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 61.9%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · usual nondominant-hemisphere association · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 55.6%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · patient1 manuscript · 1 reported value · not pooled
Localization: typical anterior cingulate lesion groupObserved proportion 0.0%All reported · complete loss of consciousness · patients1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 100.0%All reported · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Non-dominant hemisphere / Right hemisphereObserved proportion range 75.0–80.0% (median 77.5%)narrative right-handed subgroup · Lobar subgroup comparison within the surgical cohort. · Seizure and patient counts for sign occurrence; narrative subgroup includes seizures and patients.1 manuscript · 2 reported values · not pooled
Localization: FrontalObserved proportion 66.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 1 finding · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.389
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior preserved consciousnessNone of the six typical anterior patients reported complete loss of consciousness during seizures.PDF p.5, Clinical Presentation
Reported values
  • 0/6 with complete loss of consciousnesstypical anterior preserved consciousnessProportion · n/N 0/6 · 6 typical anterior cingulate cases · ictal awarenessPDF p.5, Clinical Presentation
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • preserved awareness; complex behaviorStriking complex behavior with preserved awareness is described as highly suggestive of ACC involvement.PDF p.1, Abstract; PDF p.15, Conclusion
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • preserved awareness during ictal automatisms; temporal non-dominant signsPreserved awareness during ictal automatisms points to the non-dominant hemisphere; in temporal lobe epilepsy, rhythmic ictal non-clonic hand motions may be contralateral, while peri-ictal drinking, ictal spitting, ictal vomiting, and urge to urinate point to a non-dominant focus.PDF p.10, Lateralising signs; PDF p.5, Mesial temporal lobe including hippocampus
  • ictal/postictal dysphasia; ictal speech; preserved awareness; RINCH motionsIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value and must be distinguished from non-lateralising speech arrest; formed nonsensical ictal speech and preserved awareness during ictal automatisms point to the nondominant hemisphere, while rhythmic ictal non-clonic hand motions may be contralateral in temporal lobe epilepsy and peri-ictal drinking, spitting, vomiting, or urge to urinate point to a nondominant focus.PDF p.10, Lateralising signs
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 8 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 4.36 · 2 × 1.5 × 1.452
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Automatisms with preserved responsivenessAutomatisms with preserved responsiveness were reported as lateralizing to the non-dominant hemisphere with 62% PPV and inter-observer kappa of 0.89, with a right-hemisphere pattern in the described right-handed subgroup and one left-language-dominant exception.PDF p.3, Table 1; PDF p.3, §5.1
Reported values
  • frontal PPV 0%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 4/5 patientsAutomatisms with preserved responsivenessPercentage · n/N 4/5 · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · narrative right-handed subgroup · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • 6/8 seizuresAutomatisms with preserved responsivenessPercentage · n/N 6/8 · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · narrative right-handed subgroup · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • overall PPV 62%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • occipital PPV 100%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • temporal PPV 60%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • inter-observer kappa 0.89Automatisms with preserved responsivenessKappa · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
  • parietal PPV 100%Automatisms with preserved responsivenessPositive predictive value · Sign-positive occurrences included 21 seizures in 17 patients overall; temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. The narrative additionally describes 6/8 seizures in 4/5 right-handed patients and one left-temporal seizure with left hemispheric language dominance by fMRI. · IctalPDF p.3, Table 1; PDF p.3, §5.1
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • automatisms with preserved responsivenessOral or manual automatisms with preserved responsiveness reliably localize seizure onset to the nondominant temporal lobe because seizure propagation does not reach the language-dominant temporal lobe or extratemporal structures.PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • Preserved consciousnessTable 2 reports 13/21 (62%) for Preserved consciousness; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Preserved consciousnessTable 2 reports 8/12 patients with Preserved consciousness in the prefrontal operculum group.PDF p.7, Table 2
  • Preserved consciousnessTable 2 reports 5/9 patients with Preserved consciousness in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Preserved consciousnessFisher's exact comparison of Preserved consciousness between the prefrontal and precentral Rolandic operculum groups has p=0.673.PDF p.7, Table 2
Reported values
  • 13/21 (62%)Preserved consciousnessPercentage · n/N 13/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 8/12 patientsPreserved consciousnessProportion · n/N 8/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 5/9 patientsPreserved consciousnessProportion · n/N 5/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • preserved awareness in insular seizuresPreserved awareness is reported as common in insular seizures.PDF p.2, Clinical Features
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfCase report or observation · 5 findings · 9 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • automatisms with preserved responsivenessAutomatisms with preserved responsiveness generally lateralize temporal lobe seizures to the nondominant hemisphere, with one reported exception.PDF p.6, section 3.10; PDF p.7, section 3.10 continuation; PDF p.12, Table 1
  • automatisms with preserved responsivenessEbner et al. observed automatisms with preserved responsiveness exclusively in right nondominant temporal seizures and not in left temporal seizures.PDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • automatisms with preserved consciousnessAn additional case of automatisms with preserved consciousness was reported in right temporal lobe epilepsy.PDF p.7, section 3.10
  • automatisms with preserved responsivenessA case was reported with left hemispheric epilepsy and right-sided language dominance.PDF p.7, section 3.10
  • automatisms with preserved responsiveness and ictal dysphasiaJanszky et al. reported a dominant-temporal exception to the usual nondominant lateralization of preserved-responsive automatisms.PDF p.7, section 3.10; PDF p.12, Table 1
Reported values
  • 100% nondominantautomatisms with preserved responsivenessPercentage · patients with temporal lobe epilepsy · TLE with preserved-responsive automatisms · ictalPDF p.12, Table 1
  • 5.7%automatisms with preserved responsivenessPercentage · patients with temporal lobe epilepsy · temporal lobe epilepsy · ictalPDF p.12, Table 1
  • one exceptionautomatisms with preserved responsivenessCount · patients with temporal lobe epilepsy · reported exception · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation; PDF p.12, Table 1
  • none observed in left temporal seizuresautomatisms with preserved responsivenessCount · 123 patients with temporal lobe epilepsy diagnosed by video/EEG and MRI · left temporal seizures · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • 7/123 (5.7%) overallautomatisms with preserved responsivenessPercentage · n/N 7/123 · 123 patients with temporal lobe epilepsy diagnosed by video/EEG and MRI · all TLE patients · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • 10% of right nondominant TLE patientsautomatisms with preserved responsivenessPercentage · 123 patients with temporal lobe epilepsy diagnosed by video/EEG and MRI · right nondominant TLE · ictalPDF p.6, section 3.10; PDF p.7, section 3.10 continuation
  • 1 caseautomatisms with preserved consciousnessCount · n/N 1/1 · one patient with right temporal lobe epilepsy · ictalPDF p.7, section 3.10
  • 1 caseautomatisms with preserved responsivenessCount · n/N 1/1 · one patient with left hemispheric epilepsy · ictalPDF p.7, section 3.10
  • 1 caseautomatisms with preserved responsiveness and ictal dysphasiaCount · n/N 1/1 · one 25-year-old woman with right temporal lobe epilepsy · ictalPDF p.7, section 3.10; PDF p.12, Table 1

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Figure-of-4 sign (extended arm + flexed arm asymmetric tonic)Source terms: Figure-of-4 signReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere11 manuscripts · 21 findings · 46 reported values
Weighted evidence supportevidence weight 16.22 across 11 manuscripts · 2 manuscript weight pending · 6 narrative, educational, or cited context · 2 independent primary study · 2 structured design not resolved · 1 systematic review or meta-analysis

A right middle frontal gyrus lesion case had left-face/left-arm clonic spread and fencing posture, with semiology and ictal EEG interpreted as right frontocentral onset. The review describes a component-specific lateralizing pattern within asymmetric bilateral tonic seizures. In one case with a left amygdala/hippocampal cavernoma and left temporal EEG onset, right head/eye version and a figure-of-4 posture preceded rare focal-to-bilateral tonic-clonic seizures. The review states that the extended arm in the figure-of-four sign is contralateral to seizure onset. Figure-of-4 posturing lateralized the seizure focus contralateral to the extended limb, with overall PPV 92%; reported lobar PPVs were temporal 100%, frontal 86%, and occipital 100%. The review table lists fencing (M2E) as contralateral. The review states that seizure onset is contralateral to the extended arm in the figure-of-4 sign. Both handbook tables list Figure of 4 as contralateral. The extended elbow was contralateral to the source-reported ictal-onset side in 35 of 39 patients with ATLP. In this single case, left face and arm clonic spread and subsequent left-arm extension were contralateral to the right frontocentral ictal EEG onset. Right head/eye version and right-arm extension in the figure-of-4 posture were contralateral to the case's left-hemisphere onset. The review describes robust motor signs as predominantly contralateral to onset, with the last clonic jerk as an ipsilateral sign. In this case, right head version and right-arm extension were contralateral to left onset, while the left last clonic jerk was ipsilateral to left onset. The review defines the initial figure-of-4 posture as extension of the limb contralateral to the epileptogenic hemisphere with flexion of the ipsilateral limb and reports 90% correct lateralization. The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. The cited rule lateralizes seizure onset contralateral to the initially extended tonic arm in the figure-of-4 sign. The review describes the extended limb in the figure-of-four posture as contralateral to the seizure focus. The review reports that the extended elbow in asymmetric tonic limb posturing is predominantly contralateral to seizure onset, with ipsilateral and bilateral exceptions. The cited series predominantly associated the extended elbow component with the hemisphere contralateral to seizure onset. The frontal-versus-temporal statement contains no lateralization information. The arm was on the side of contraversion, but no relation to seizure-onset side is supplied.

Source-defined result groups 11
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 89.7%All reported · ictal-onset side · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · Lobar subgroup comparison within the surgical cohort. · Seizure and patient counts for sign occurrence; PPV analysis unit not otherwise reported.1 manuscript · 4 reported values · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 89.7%asymmetric tonic limb posturing · non-contralateral · case1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 11

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 2 findings
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Fencing (M2E)The fencing (M2E) posture is listed as contralateral and associated with a supplementary motor localization.PDF p.4, Table 2
  • Figure-of-4 signAsymmetric tonic limb posturing or the figure-of-4 sign is usually observed during the early tonic phase just before secondary generalization, and seizure onset is contralateral to the extended arm.PDF p.4, Table 2; PDF p.5, figure-of-4 paragraph
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 8 findings · 1 reported value
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • aura; behavioural arrest; left-face clonic activity; fencing postureIn an illustrative 50-year-old man with a right middle frontal gyrus cystic lesion, a seizure evolved from an aura to behavioural arrest, left-face clonic movements spreading over the left arm, and left-arm extension in a fencing posture before secondary generalisation; the authors state that the semiology and ictal EEG supported right frontocentral onset.PDF p.3, Video case 1 and Figure 1; PDF p.3, Figure 2 caption
  • supplementary motor area seizure; fencing postureSupplementary motor area seizures are characterized by asymmetric bilateral tonic posturing, with or without impaired awareness; the source describes contralateral upper-limb extension, ipsilateral upper-limb flexion as a fencing posture, and contralateral head and eye deviation, while noting that extrafrontal seizures can also produce asymmetric tonic posturing.PDF p.3, Supplementary motor area; PDF p.4, Other frontal regions; PDF p.3, Figure 1
  • psychic aura; abdominal aura; automotor seizure; figure-of-4 signIn an illustrative 36-year-old right-handed man with a left amygdala/hippocampal cavernoma, seizures began with déjà vu and epigastric rising, evolved to automotor features and rarely focal-to-bilateral tonic-clonic seizures, and showed right head/eye version plus a figure-of-4 posture before generalisation; left temporal EEG onset and the posture were consistent with left hemispheric onset.PDF p.5, Video case 3; PDF p.6, Video case 3 and Figure 4 caption
  • figure-of-4 signBefore secondary generalisation, a figure-of-4 sign in which the extended arm is contralateral to seizure onset is described as a lateralising motor phenomenon.PDF p.10, Lateralising signs; PDF p.6, Video case 3
  • fencing posture; Jacksonian spreadIn the review’s video case 1, a 50-year-old man with a cystic lesion in the right middle frontal gyrus had an aura followed by behavioural arrest, left-face clonic movements spreading over the left arm, then left-arm extension in a fencing posture before secondary generalisation; the semiology and ictal EEG pointed to right frontocentral/right hemispheric onset.PDF p.3, Video case 1; PDF p.4, Figure 2 and Video case 1 description
  • psychic and abdominal aura; figure-of-4 signIn video case 3, a 36-year-old right-handed man with a left amygdala/hippocampal-head cavernoma had déjà vu and epigastric rising followed by oral and manual automatisms and loss of awareness; before generalization, right head and eye version and a figure-of-4 posture with the left arm flexed and right arm extended lateralised onset to the left hemisphere, concordant with left temporal EEG onset.PDF p.6, Video case 3 and Figure 4
  • robust lateralising motor signs; figure-of-4 sign; Todd’s paresisThe review describes unilateral clonic movements, unilateral tonic or dystonic posturing, and early head version as robust lateralising motor signs with positive predictive value greater than 80%, all contralateral to onset; it also states that before secondary generalization the extended arm in a figure-of-4 sign is contralateral, the last clonic jerk is ipsilateral, and postictal Todd’s paresis is contralateral to seizure onset.PDF p.10, Lateralising signs
  • head version; figure-of-4 sign; last clonic jerkIn video case 7, a 33-year-old man with left temporal hypometabolism had head version to the right followed by right-arm extension in a figure-of-4 posture, indicating left hemispheric onset; in one seizure the last clonic jerk was on the left, also pointing to left onset, while ictal EEG was non-localisable in one seizure and lateralised left in another.PDF p.10, Video case 7
Reported values
  • Positive predictive value >80% for the listed robust motor signsrobust lateralising motor signs; figure-of-4 sign; Todd’s paresisPercentage · Patients with focal seizures in the cited motor-sequence literature; exact cohort Not reported · Ictal onset, pre-generalization, generalized phase ending, and postictal periodPDF p.10, Lateralising signs
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 7 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Figure 4 posturingFigure 4 posturing was reported as contralateral to the extended limb with 92% PPV and inter-observer kappa of 0.81 overall.PDF p.3, Table 1; PDF p.5, §7
Reported values
  • 13 seizures with Figure 4 posturingFigure 4 posturingCount · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
  • occipital PPV 100%Figure 4 posturingPositive predictive value · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
  • temporal PPV 100%Figure 4 posturingPositive predictive value · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
  • inter-observer kappa 0.81Figure 4 posturingKappa · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
  • frontal PPV 86%Figure 4 posturingPositive predictive value · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
  • 9 patients with Figure 4 posturingFigure 4 posturingCount · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
  • overall PPV 92%Figure 4 posturingPositive predictive value · Sign-positive occurrences included 13 seizures in 9 patients overall; temporal 5 seizures/3 patients, frontal 7/5, parietal 0/0, and occipital 1/1. · Ictal or secondarily generalized seizure sequence as reported for the sign.PDF p.3, Table 1; PDF p.5, §7
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Figure of 4Both tables list Figure of 4 as Contralateral.PDF p.2, Lateralizing signs/Localization table row "Figure of 4" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Figure of 4" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • asymmetric tonic limb posturing or figure-4 signAsymmetric tonic limb posturing is a figure-4 posture in which the elbow contralateral to the epileptogenic hemisphere is extended and the ipsilateral limb flexes over the chest during the tonic phase of an SGTCS. The sign provides correct lateralization in 90% of cases, is most common in temporal-lobe seizures, and can change sides, so only its initial appearance should be used for lateralization.PDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
Reported values
  • Correct lateralization in 90% of casesasymmetric tonic limb posturing or figure-4 signPercentage · patients with secondarily generalized tonic-clonic seizures · initial tonic phase of SGTCSPDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • asymmetric tonic limb posturing (“figure-of-4” sign)During the tonic phase of a focal to bilateral tonic-clonic seizure, asymmetric tonic limb posturing, also called the “figure-of-4” sign, is described as contralateral to the seizure focus.PDF p.9, Focal to bilateral tonic-clonic seizures
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfNarrative, educational, or cited context · 1 finding
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • fencing posture and postictal confusionThe source states that adopting a fencing posture and the duration of postictal confusion have been demonstrated to distinguish frontal-lobe from temporal-lobe epilepsy.PDF p.4, Discussion
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 1 finding · 1 reported value
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.796
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • asymmetric tonic limb posturing (ATLP) / “Figure 4 Sign”The article summary reports that the extended elbow was contralateral to the side of ictal onset in 35 of 39 patients who had ATLP during their seizures.PDF p.1, Summary—Results
Reported values
  • 35 of 39 patientsasymmetric tonic limb posturing (ATLP) / “Figure 4 Sign”Count · n/N 35/39 · Patients with ATLP across the two analyzed groups; aggregate construction Not reported · Tonic phase of a secondarily generalized GTC seizurePDF p.1, Summary—Results
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 8 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Asymmetric tonic limb posturing (figure-of-4 sign)The review describes asymmetric tonic limb posturing before bilateral tonic arm posturing as a lateralizing sign in which the extended elbow is usually contralateral to seizure onset; Table 1 summarizes 17.7% in temporal and 15% in extratemporal lobe epilepsy and 89% contralateral.PDF p.5, section 3.6 Asymmetric tonic limb posturing; PDF p.5, section 3.6.1 Mechanism; PDF p.12, Table 1
  • Asymmetric tonic limb posturing (figure-of-4 sign)Kotagal et al. retrospectively reviewed 59 secondary generalized tonic-clonic seizures in 31 patients seizure free after surgery and prospectively analyzed 64 seizures in 26 patients; the extended elbow was contralateral to seizure onset in 35 of 39 cases.PDF p.5, section 3.6 Asymmetric tonic limb posturing
Reported values
  • 15%Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · extratemporal lobe epilepsy · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.12, Table 1
  • 17.7%Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · temporal lobe epilepsy · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.12, Table 1
  • 35 of 39 (89%)Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · n/N 35/39 · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · asymmetric tonic limb posturing · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing; PDF p.5, section 3.6.1 Mechanism; PDF p.12, Table 1
  • 26 prospective patientsAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · prospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 64 prospective seizuresAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · prospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • extended elbow contralateral in 35/39 casesAsymmetric tonic limb posturing (figure-of-4 sign)Percentage · n/N 35/39 · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 59 retrospective seizuresAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · retrospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 31 retrospective patientsAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · retrospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 2 findings · 25 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • figure of 4 sign; asymmetric tonic limb posturingThe current paper reports that figure of 4 has been described as having approximately 90% contralateral lateralizing value and attributes to the original Kotagal report the rule that the initial tonic arm extension is the component to use because a later figure of 4 may appear on the opposite side.PDF p.7, figure of 4 definition and cited value; PDF p.8, cited initial-component rule; PDF p.12, discussion of the source definition
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • Approximately 90% contralateral lateralizing valuefigure of 4 sign; asymmetric tonic limb posturingPercentage · Cited source population as summarized in the current paper; Not reported · Beginning of the tonic phase of a secondary generalized tonic-clonic seizurePDF p.7, figure of 4 definition and cited value; PDF p.8, cited initial-component rule; PDF p.12, discussion of the source definition
wyllie1986.pdfStructured design not resolved · 1 finding · 3 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • fencing position and M2e postureIn 23 versive seizures from 14 patients, arm posturing included the “fencing position” with elbow flexion followed by approximately 90-degree shoulder abduction; the authors state that M2e posturing was common in temporal and extratemporal onset versive seizures without ictal activity localized to the supplementary motor areas and probably reflected widespread ictal involvement of precentral contraversive and arm/face motor areas rather than localized supplementary motor activation.PDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization
Reported values
  • Versive seizures with fencing posturing n=23fencing position and M2e postureCount · 23 versive seizures from 14 patients; temporal and extratemporal onset versive seizures in the authors’ discussion · During contraversionPDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization
  • Shoulder abduction approximately 90 degreesfencing position and M2e postureOther reported value · 23 versive seizures from 14 patients; temporal and extratemporal onset versive seizures in the authors’ discussion · During contraversionPDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization
  • Patients with fencing posturing n=14fencing position and M2e postureCount · 23 versive seizures from 14 patients; temporal and extratemporal onset versive seizures in the authors’ discussion · During contraversionPDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization

11 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal apneaReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphere7 manuscripts · 34 findings · 86 reported values
Weighted evidence supportevidence weight 15.6 across 7 manuscripts · 1 manuscript weight pending · 1 systematic review or meta-analysis · 2 independent primary study · 3 narrative, educational, or cited context · 1 structured design not resolved

The illustrated late-onset ICA seizure had right anterobasal EEG onset. The illustrated early-onset ICA seizure had left mesial-temporal EEG onset. The illustrated apnea occurred during one source-labeled left frontotemporal seizure. No lateralization axis information is reported for choking, dyspnea, apnea, or throat constriction. No lateralization axis information is reported for the prefrontal-operculum choking/dyspnea/apnea/throat-constriction result. No lateralization axis information is reported for the precentral Rolandic-operculum choking/dyspnea/apnea/throat-constriction result. The primary choking/dyspnea/apnea/throat-constriction comparison reports no hemisphere or lateralization direction. This record provides no seizure lateralization. No hemisphere or body-side result is reported. No lateralizing direction is reported for ictal versus postictal central apnoea. No seizure lateralization is reported. No lateralizing direction is reported for the mesial-temporal/amygdalar association. No fixed cerebral side or body-side direction is reported. No lateralizing direction is reported for ICA presence frequency. No lateralizing direction is reported for patient-level ICA occurrence. No lateralizing direction is reported for ICA as the first clinical feature versus aura first. No cerebral lateralization or symptomatic body-side result is reported. No source-supported hemispheric lateralization is reported. No cerebral direction or body-side result is reported. No lateralizing semiology is reported for the MTS-versus-ICA association test. No cerebral lateralization or body-side result is shown. No body side or cerebral hemisphere result is reported. No lateralizing direction is reported for ictal central apnea frequency. No lateralizing semiology is reported for the apnea-time and oxygen-desaturation correlation.

Source-defined result groups 48
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 30.0%Temporal pole and anterior basotemporal · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 23.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 16.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 0.0%lateral temporal · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 47.1%mesial temporal · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 28.6%occipital · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizures without ICA and the source-defined non-mesial-temporal SOZ categories, as applicable to the reported comparison1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 27.3%Parietal · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%amygdala · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizures without ICA and the source-defined non-mesial-temporal SOZ categories, as applicable to the reported comparison1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelyparietal · other displayed EZ categories · seizure with ICA; exact source unit not further reported1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 0.0%Lateral temporal · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 16.7%parietal · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 0.0%central · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizures without ICA and the source-defined non-mesial-temporal SOZ categories, as applicable to the reported comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 6.2%mesial temporal seizures · seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 0.0%Insula · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal EZ categories · patient subgroup as described for EZ determination; the reported regression denominator is not stated1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizures without ICA and the source-defined non-mesial-temporal SOZ categories, as applicable to the reported comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 25.0%temporal pole and anterior basotemporal · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 12.5%frontal · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 100.0%posterior basotemporal · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 12.0%Frontal · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Ictal EEG onset preceding ICA onset · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 93.3%hippocampus · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyICA + FOIA/FOA motor onset with automatisms · non-mesial-temporal SOZ categories · source-defined SOZ analysis1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelytemporal pole and anterior basotemporal · other displayed EZ categories · seizure with ICA; exact source unit not further reported1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 0.0%Central · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelyposterior basotemporal · other displayed EZ categories · seizure with ICA; exact source unit not further reported1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 71.4%Posterior basotemporal · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelyoccipital · other displayed EZ categories · seizure with ICA; exact source unit not further reported1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 42.9%Occipital · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 0.0%insula · The other source-reported EZ categories1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / Occipital / Parietal / TemporalObserved proportion 43.2%Mesial temporal · Other SOZ categories · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported1 manuscript · 1 reported value · not pooled
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelymesial temporal · other displayed EZ categories · seizure with ICA; exact source unit not further reported1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · The source-defined non-mesial-temporal SOZ categories1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizures without ICA and the source-defined non-mesial-temporal SOZ categories, as applicable to the reported comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfNarrative, educational, or cited context · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • early apnoea and tachycardia; amygdala involvementThe review states that early apnoea and tachycardia in mesial temporal lobe seizures indicate involvement of the amygdala.PDF p.5, Mesial temporal lobe including hippocampus
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal hyperventilation, apnea, dyspnea, and stridorIctal hyperventilation, defined as at least a 10% increase in respiratory rate from baseline, was observed in seizures of more than 50% of children in one series and was more common in temporal than frontal lobe epilepsy. In adults with TLE it is more common with mesial than neocortical onset; ictal apnea is most common in infants and neonates, while ictal dyspnea and stridor are rare and occur primarily during the tonic phase of GTCSs.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
Reported values
  • at least a 10% increaseictal hyperventilation, apnea, dyspnea, and stridorThreshold · children with focal seizures; adults with TLE; infants and neonates · ictal hyperventilation definition · ictal, with dyspnea and stridor primarily tonic phase of GTCSPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • more than 50%ictal hyperventilation, apnea, dyspnea, and stridorOther reported value · children with focal seizures; adults with TLE; infants and neonates · children in one cited series · ictal, with dyspnea and stridor primarily tonic phase of GTCSPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Choking, dyspnea, apnea, throat constrictionTable 2 reports 5/21 (24%) for Choking, dyspnea, apnea, throat constriction; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Choking, dyspnea, apnea, throat constrictionTable 2 reports 2/12 patients with Choking, dyspnea, apnea, throat constriction in the prefrontal operculum group.PDF p.7, Table 2
  • Choking, dyspnea, apnea, throat constrictionTable 2 reports 3/9 patients with Choking, dyspnea, apnea, throat constriction in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Choking, dyspnea, apnea, throat constrictionFisher's exact comparison of Choking, dyspnea, apnea, throat constriction between the prefrontal and precentral Rolandic operculum groups has p=0.611.PDF p.7, Table 2
Reported values
  • 5/21 (24%)Choking, dyspnea, apnea, throat constrictionPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 2/12 patientsChoking, dyspnea, apnea, throat constrictionProportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 3/9 patientsChoking, dyspnea, apnea, throat constrictionProportion · n/N 3/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdfStructured design not resolved · 20 findings · 63 reported values
lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The investigators prospectively enrolled 85 consecutive adult persons with epilepsy undergoing standard-of-care SEEG evaluation in an epilepsy monitoring unit from June 2016 through April 2023. They prospectively collected 220 seizures; 39 seizures in 13 patients were excluded because breathing signals were unreliable or artifactual. The analyzed population was 179 seizures in 72 patients with reliable artifact-free respiratory signals. Real-time SEEG, video, thoracic and abdominal respiratory inductance plethysmography, oxygen saturation, heart rate, and four-channel EKG were obtained simultaneously. The analyzed cohort included 1,196 intracranial depth electrodes (mean 16.6 +/- 3.0 per patient); 55 seizures in 23 patients had ICA. All seizures were classified by seizure onset zone (SOZ), defined by the source as the cortical area from which seizures start. The source separately defined the epileptogenic zone (EZ) as the region resected to produce seizure freedom; only patients who underwent resective surgery or laser interstitial thermal therapy and had Engel class I outcome with at least six months of follow-up were classified for EZ determination. Of 31 Engel class I patients, 30 had at least six months of follow-up (mean 22.8 months +/- SD 13.1, range 6-50) and one did not. The source reports separate SOZ and EZ analyses and does not authorize conversion between their patient- and seizure-level denominators. A high-gamma analysis used a subset of 20 patients with 39 ICA seizures whose SEEG implantation sampled all regions of breathing interest; the early-onset subgroup contained 27 seizures in 13 patients and the late-onset subgroup 12 seizures in seven patients. Predictive associations were assessed with separate simple logistic-regression models; statistically significant semiologic signs were also entered as one additional predictor with ICA in multiple logistic regression. Fisher's exact test assessed ICA presence and mesial temporal sclerosis (MTS). The source used two-sided p < 0.05 for statistical significance, made no multiple-comparison correction because the study was exploratory, and treated z >= 4 as significant for the quantitative gamma analysis.
Findings
  • late-onset ictal central apnea illustrative seizureFigure 1 illustrates Patient 35, seizure 1, with right implantation: right anterobasal low-amplitude fast activity at EEG onset spread rapidly to the temporal pole, and ICA emerged after mesial temporal involvement of amygdala, anterior hippocampus, and posterior hippocampus, 21 seconds after ictal EEG onset.PDF p.15, Figure 1A-C; PDF p.16, Figure 1 caption continuation
  • early-onset ictal central apnea illustrative seizureFigure 2 illustrates Patient 25, seizure 1, with bilateral implantation: left mesial temporal low-amplitude fast activity at EEG onset in the left anterior hippocampus, left posterior hippocampus, and left amygdala was followed by ICA within two seconds after ictal EEG onset.PDF p.17, Figure 2A-C; PDF p.18, Figure 2 caption continuation
  • ictal central apnea (ICA)ICA occurred in 55/179 (30.7%) of the analyzed seizures.PDF p.3, Abstract; PDF p.6, Results; PDF p.7, Ictal central apnea presence and characteristics
  • ICA occurrence in patientsAt least one ICA-positive seizure occurred in 23/72 (31.5%) of the analyzed patients.PDF p.7, Ictal central apnea presence and characteristics; PDF p.22, Table 2
  • ICA as first clinical featureICA was the first clinical feature in 49/55 (89.1%) ICA-positive seizures, while aura was the first clinical symptom in the remaining 6/55 (10.9%) seizures.PDF p.7, Ictal central apnea presence and characteristics
  • ICA as the only clinical signICA was the only clinical sign in 10/179 (5.6%) of all analyzed seizures, 5/81 (6.8%) mesial temporal seizures, and 10/55 (18.2%) ICA-positive seizures.PDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea
  • ICA duration and onset intervalsIn the source's ICA cohort, Table 2 reports mean ICA duration of 26.4 +/- 19.1 seconds, mean time from SEEG onset to ICA onset of 6.4 +/- 9.5 seconds, and mean time from ICA onset to clinical onset of 0.6 +/- 3.5 seconds.PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • ICA by seizure onset zoneTable 2 reports ICA in mesial temporal 35/81 (43.2%), frontal 3/25 (12%), insula 0/24 (0%), occipital 6/14 (42.8%), parietal 3/11 (27.3%), temporal pole and anterior basotemporal 3/10 (30%), posterior basotemporal 5/7 (71.4%), lateral temporal 0/6 (0%), and central 0/1 (0%) seizures.PDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • mesial temporal involvement at ICA onsetWithin the mesial temporal row of Table 2, amygdala involvement at ICA onset was reported in 30/30 (100%) and hippocampus involvement at ICA onset in 28/30 (93.3%).PDF p.7, Quantitative Analysis of SEEG Data; PDF p.9, Quantitative analysis of video-SEEG recordings; PDF p.22, Table 2
  • ICA by epileptogenic zoneTable 2 reports ICA in mesial temporal 16/34 (47.1%), frontal 1/8 (12.5%), insula 0/8 (0%), occipital 2/7 (28.6%), parietal 1/6 (16.7%), temporal pole and anterior basotemporal 1/4 (25%), posterior basotemporal 2/2 (100%), lateral temporal 0/3 (0%), and central 0/1 (0%) source-defined epileptogenic-zone categories.PDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • ICA predicting mesial temporal seizure onsetICA predicted mesial temporal seizure onset with OR=3.8, 95% CI [1.3, 11.6], p=0.01, sensitivity 0.45, specificity 0.82, PPV 0.68, and NPV 0.64.PDF p.3, Abstract; PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • ICA + FOIA non-motor onsetCo-occurrence of ICA and FOIA non-motor onset was associated with mesial temporal seizure onset with OR=30.0, 95% CI [5.5, 221.7], p<0.001, sensitivity 0.85, specificity 0.64, PPV 0.67, and NPV 0.83.PDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • ICA + FOIA/FOA motor onset with automatismsCo-occurrence of ICA and FOIA/FOA motor onset with automatisms was associated with mesial temporal seizure onset with OR=10.9, 95% CI [2.49, 57.15], p=0.001, sensitivity 0.69, specificity 0.66, PPV 0.63, and NPV 0.72.PDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • ICA with either FOIA or FOIA/FOA motor onset with automatismsWhen ICA occurred with either FOIA or FOIA/FOA motor onset with automatisms, the source reports specificity increasing up to 0.95 and sensitivity decreasing down to 0.21 for mesial temporal seizure onset.PDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones
  • ICA and mesial temporal epileptogenic zoneThe relationship between ICA and mesial temporal epileptogenic zone was not statistically significant: OR=2.7, 95% CI [0.5, 15.0], p=0.25.PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea
  • ICA features and seizure evolution timingNo association was found between ICA features, including total ICA duration and time from ICA onset to the next clinical seizure sign.PDF p.7, Visual analysis of SEEG data
  • MTS and ICA presenceNo association was found between MTS and ICA presence (p=0.34).PDF p.6, Statistical analysis; PDF p.7, Visual analysis of SEEG data
  • ICA seizures classified by seizure onset zone in Figure 3AFigure 3A displays the distribution of seizures with ICA by SOZ as mesial temporal 63.6%, parietal 5.5%, temporal pole and anterior basotemporal 5.5%, posterior basotemporal 9%, frontal 5.5%, and occipital 10.9%.PDF p.19, Figure 3A
  • ICA seizures classified by epileptogenic zone in Figure 3BFigure 3B displays the distribution of seizures with ICA by EZ as mesial temporal 50%, parietal 12.5%, temporal pole and anterior basotemporal 5.5%, posterior basotemporal 12.5%, and occipital 12.5%.PDF p.19, Figure 3B
  • ICA in a prior small series of mesial temporal lobe seizuresThe current article states that simultaneous respiratory monitoring revealed ICA in 70% of seizures in a small prior series of mesial temporal lobe seizures.PDF p.4, Introduction
Reported values
  • 21 seconds from ictal EEG onset to ICA onsetlate-onset ictal central apnea illustrative seizureCount · One illustrative SEEG-recorded seizure, Patient 35 seizure 1 · late-onset ICA after ictal EEG onsetPDF p.15, Figure 1A-C; PDF p.16, Figure 1 caption continuation
  • ICA presence frequency 30.7%ictal central apnea (ICA)Percentage · n/N 55/179 · 179 seizures in 72 adult patients with reliable artifact-free respiratory signals; 55 ICA-positive seizures · ictal ICA occurrencePDF p.3, Abstract; PDF p.6, Results; PDF p.7, Ictal central apnea presence and characteristics
  • patient-level ICA occurrence 31.5%ICA occurrence in patientsPercentage · n/N 23/72 · 72 analyzed adult patients with reliable artifact-free respiratory signals · ictal ICA occurrencePDF p.7, Ictal central apnea presence and characteristics; PDF p.22, Table 2
  • Aura first clinical symptom 6/55 (10.9%)ICA as first clinical featurePercentage · n/N 6/55 · 55 ICA-positive seizures in 23 patients · Aura first · first ictal clinical featurePDF p.7, Ictal central apnea presence and characteristics
  • ICA first clinical feature 49/55 (89.1%)ICA as first clinical featurePercentage · n/N 49/55 · 55 ICA-positive seizures in 23 patients · ICA first · first ictal clinical featurePDF p.7, Ictal central apnea presence and characteristics
  • 5/81 (6.8%)ICA as the only clinical signPercentage · n/N 5/81 · All analyzed seizures; mesial temporal SOZ seizures; and ICA-positive seizures, respectively · mesial temporal seizures · ictal clinical manifestationPDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea
  • 10/179 (5.6%)ICA as the only clinical signPercentage · n/N 10/179 · All analyzed seizures; mesial temporal SOZ seizures; and ICA-positive seizures, respectively · all analyzed seizures · ictal clinical manifestationPDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea
  • 10/55 (18.2%)ICA as the only clinical signPercentage · n/N 10/55 · All analyzed seizures; mesial temporal SOZ seizures; and ICA-positive seizures, respectively · ICA-positive seizures · ictal clinical manifestationPDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea
  • ICA-onset-to-clinical-onset interval 0.6 secondsICA duration and onset intervalsMean · Patients and seizures with ICA as presented in Table 2 · ictal ICA duration and timing relative to SEEG and clinical onsetPDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • SEEG-onset-to-ICA-onset interval 6.4 secondsICA duration and onset intervalsMean · Patients and seizures with ICA as presented in Table 2 · ictal ICA duration and timing relative to SEEG and clinical onsetPDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • ICA duration 26.4 secondsICA duration and onset intervalsMean · Patients and seizures with ICA as presented in Table 2 · ictal ICA duration and timing relative to SEEG and clinical onsetPDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Central ICA 0/1 (0%)ICA by seizure onset zonePercentage · n/N 0/1 · Analyzed seizures classified by source-defined seizure onset zone · Central · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Mesial temporal ICA 35/81 (43.2%)ICA by seizure onset zonePercentage · n/N 35/81 · Analyzed seizures classified by source-defined seizure onset zone · Mesial temporal · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Insula ICA 0/24 (0%)ICA by seizure onset zonePercentage · n/N 0/24 · Analyzed seizures classified by source-defined seizure onset zone · Insula · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Lateral temporal ICA 0/6 (0%)ICA by seizure onset zonePercentage · n/N 0/6 · Analyzed seizures classified by source-defined seizure onset zone · Lateral temporal · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Parietal ICA 3/11 (27.3%)ICA by seizure onset zonePercentage · n/N 3/11 · Analyzed seizures classified by source-defined seizure onset zone · Parietal · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Temporal pole and anterior basotemporal ICA 3/10 (30%)ICA by seizure onset zonePercentage · n/N 3/10 · Analyzed seizures classified by source-defined seizure onset zone · Temporal pole and anterior basotemporal · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Occipital ICA 6/14 (42.8%)ICA by seizure onset zonePercentage · n/N 6/14 · Analyzed seizures classified by source-defined seizure onset zone · Occipital · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Frontal ICA 3/25 (12%)ICA by seizure onset zonePercentage · n/N 3/25 · Analyzed seizures classified by source-defined seizure onset zone · Frontal · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • Posterior basotemporal ICA 5/7 (71.4%)ICA by seizure onset zonePercentage · n/N 5/7 · Analyzed seizures classified by source-defined seizure onset zone · Posterior basotemporal · ictal ICA presencePDF p.7, Ictal central apnea presence and characteristics; PDF p.8, The localizing value of ictal central apnea; PDF p.22, Table 2
  • 30/30 (100%)mesial temporal involvement at ICA onsetPercentage · n/N 30/30 · Source-reported mesial temporal seizures with ICA and sampled mesial temporal structures · amygdala · ICA onsetPDF p.7, Quantitative Analysis of SEEG Data; PDF p.9, Quantitative analysis of video-SEEG recordings; PDF p.22, Table 2
  • 28/30 (93.3%)mesial temporal involvement at ICA onsetPercentage · n/N 28/30 · Source-reported mesial temporal seizures with ICA and sampled mesial temporal structures · hippocampus · ICA onsetPDF p.7, Quantitative Analysis of SEEG Data; PDF p.9, Quantitative analysis of video-SEEG recordings; PDF p.22, Table 2
  • temporal pole and anterior basotemporal 1/4 (25%)ICA by epileptogenic zonePercentage · n/N 1/4 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · temporal pole and anterior basotemporal · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • frontal 1/8 (12.5%)ICA by epileptogenic zonePercentage · n/N 1/8 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · frontal · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • insula 0/8 (0%)ICA by epileptogenic zonePercentage · n/N 0/8 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · insula · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • parietal 1/6 (16.7%)ICA by epileptogenic zonePercentage · n/N 1/6 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · parietal · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • central 0/1 (0%)ICA by epileptogenic zonePercentage · n/N 0/1 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · central · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • posterior basotemporal 2/2 (100%)ICA by epileptogenic zonePercentage · n/N 2/2 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · posterior basotemporal · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • mesial temporal 16/34 (47.1%)ICA by epileptogenic zonePercentage · n/N 16/34 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · mesial temporal · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • lateral temporal 0/3 (0%)ICA by epileptogenic zonePercentage · n/N 0/3 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · lateral temporal · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • occipital 2/7 (28.6%)ICA by epileptogenic zonePercentage · n/N 2/7 · Source-defined epileptogenic-zone classification in the Engel class I/minimum-six-month follow-up subgroup, as presented in the ICA table · occipital · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.22, Table 2
  • NPV 0.64ICA predicting mesial temporal seizure onsetNegative predictive value · Source's all-patient/all-analyzed-seizure seizure-onset-zone analysis; the report contains 179 analyzed seizures in 72 patients but does not state a Table 3 regression denominator · ictal ICA presencePDF p.3, Abstract; PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • Specificity 0.82ICA predicting mesial temporal seizure onsetSpecificity · Source's all-patient/all-analyzed-seizure seizure-onset-zone analysis; the report contains 179 analyzed seizures in 72 patients but does not state a Table 3 regression denominator · ictal ICA presencePDF p.3, Abstract; PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • OR=3.8ICA predicting mesial temporal seizure onsetOdds ratio · Source's all-patient/all-analyzed-seizure seizure-onset-zone analysis; the report contains 179 analyzed seizures in 72 patients but does not state a Table 3 regression denominator · ictal ICA presencePDF p.3, Abstract; PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • Sensitivity 0.45ICA predicting mesial temporal seizure onsetSensitivity · Source's all-patient/all-analyzed-seizure seizure-onset-zone analysis; the report contains 179 analyzed seizures in 72 patients but does not state a Table 3 regression denominator · ictal ICA presencePDF p.3, Abstract; PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • PPV 0.68ICA predicting mesial temporal seizure onsetPositive predictive value · Source's all-patient/all-analyzed-seizure seizure-onset-zone analysis; the report contains 179 analyzed seizures in 72 patients but does not state a Table 3 regression denominator · ictal ICA presencePDF p.3, Abstract; PDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • OR=30ICA + FOIA non-motor onsetOdds ratio · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ictal co-occurrence/evolution of ICA and FOIA non-motor onsetPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • Sensitivity 0.85ICA + FOIA non-motor onsetSensitivity · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ictal co-occurrence/evolution of ICA and FOIA non-motor onsetPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • PPV 0.67ICA + FOIA non-motor onsetPositive predictive value · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ictal co-occurrence/evolution of ICA and FOIA non-motor onsetPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • Specificity 0.64ICA + FOIA non-motor onsetSpecificity · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ictal co-occurrence/evolution of ICA and FOIA non-motor onsetPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • NPV 0.83ICA + FOIA non-motor onsetNegative predictive value · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ictal co-occurrence/evolution of ICA and FOIA non-motor onsetPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.14, Summary for Social Media; PDF p.23, Table 3
  • 0.69ICA + FOIA/FOA motor onset with automatismsSensitivity · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.72ICA + FOIA/FOA motor onset with automatismsNegative predictive value · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.66ICA + FOIA/FOA motor onset with automatismsSpecificity · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • OR=10.9ICA + FOIA/FOA motor onset with automatismsOdds ratio · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • 0.63ICA + FOIA/FOA motor onset with automatismsPositive predictive value · Source's co-occurrence analysis of ICA and one additional semiologic sign for seizure-onset-zone prediction · ICA + FOIA/FOA motor onset with automatisms · ictal co-occurrence/evolution of ICA and FOIA/FOA motor onset with automatismsPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones; PDF p.23, Table 3
  • sensitivity down to 0.21ICA with either FOIA or FOIA/FOA motor onset with automatismsSensitivity · Source's combined occurrence analysis of ICA with either of the two listed seizure-evolution signs · ictal sequence after ICAPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones
  • specificity up to 0.95ICA with either FOIA or FOIA/FOA motor onset with automatismsSpecificity · Source's combined occurrence analysis of ICA with either of the two listed seizure-evolution signs · ictal sequence after ICAPDF p.7, Visual analysis of SEEG data; PDF p.9, Seizure evolution features further increase odds of mesial temporal ictal onset zones
  • OR=2.7ICA and mesial temporal epileptogenic zoneOdds ratio · Source-defined EZ subgroup of patients with resection or LITT, Engel class I outcome, and at least six months of follow-up · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea
  • p=0.25ICA and mesial temporal epileptogenic zoneP value · Source-defined EZ subgroup of patients with resection or LITT, Engel class I outcome, and at least six months of follow-up · ictal ICA presencePDF p.7, Visual analysis of SEEG data; PDF p.8, The localizing value of ictal central apnea
  • p=0.34MTS and ICA presenceP value · Analyzed cohort used for the MTS and ICA presence comparison · ictal ICA presencePDF p.6, Statistical analysis; PDF p.7, Visual analysis of SEEG data
  • Posterior basotemporal 9%ICA seizures classified by seizure onset zone in Figure 3APercentage · Seizures with ICA classified by source-defined seizure onset zone · Posterior basotemporal · ictal ICAPDF p.19, Figure 3A
  • Mesial temporal 63.6%ICA seizures classified by seizure onset zone in Figure 3APercentage · Seizures with ICA classified by source-defined seizure onset zone · Mesial temporal · ictal ICAPDF p.19, Figure 3A
  • Occipital 10.9%ICA seizures classified by seizure onset zone in Figure 3APercentage · Seizures with ICA classified by source-defined seizure onset zone · Occipital · ictal ICAPDF p.19, Figure 3A
  • Temporal pole and anterior basotemporal 5.5%ICA seizures classified by seizure onset zone in Figure 3APercentage · Seizures with ICA classified by source-defined seizure onset zone · Temporal pole and anterior basotemporal · ictal ICAPDF p.19, Figure 3A
  • Parietal 5.5%ICA seizures classified by seizure onset zone in Figure 3APercentage · Seizures with ICA classified by source-defined seizure onset zone · Parietal · ictal ICAPDF p.19, Figure 3A
  • Frontal 5.5%ICA seizures classified by seizure onset zone in Figure 3APercentage · Seizures with ICA classified by source-defined seizure onset zone · Frontal · ictal ICAPDF p.19, Figure 3A
  • 12.5%ICA seizures classified by epileptogenic zone in Figure 3BPercentage · Seizures with ICA classified by source-defined epileptogenic zone · posterior basotemporal · ictal ICAPDF p.19, Figure 3B
  • 50%ICA seizures classified by epileptogenic zone in Figure 3BPercentage · Seizures with ICA classified by source-defined epileptogenic zone · mesial temporal · ictal ICAPDF p.19, Figure 3B
  • 5.5%ICA seizures classified by epileptogenic zone in Figure 3BPercentage · Seizures with ICA classified by source-defined epileptogenic zone · temporal pole and anterior basotemporal · ictal ICAPDF p.19, Figure 3B
  • 12.5%ICA seizures classified by epileptogenic zone in Figure 3BPercentage · Seizures with ICA classified by source-defined epileptogenic zone · occipital · ictal ICAPDF p.19, Figure 3B
  • 12.5%ICA seizures classified by epileptogenic zone in Figure 3BPercentage · Seizures with ICA classified by source-defined epileptogenic zone · parietal · ictal ICAPDF p.19, Figure 3B
  • ICA frequency 70%ICA in a prior small series of mesial temporal lobe seizuresPercentage · Cited small series of mesial temporal lobe seizures; further cohort details are not given in the current article · ictal ICAPDF p.4, Introduction
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 3 findings · 7 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 4.80 · 2 × 1.2 × 2
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • ictal apnea extending into the postictal period in case MO#12In the illustrated MO#12 left frontotemporal seizure, apnea began 20 seconds before scalp EEG seizure onset, persisted for about 15 seconds after EEG termination, and was followed by two brief postictal apnea episodes with progressive oxygen desaturation to below 80%.PDF p.7, Figure 2A caption
  • ictal central apnea (ICA)ICA occurred in 71 of 406 analyzed focal-onset seizures and in 27 of 69 analyzed patients.PDF p.1, Abstract Results; PDF p.3, Results, ICA in Focal Seizures; PDF p.5, Table 1
  • apnea time and oxygen-desaturation durationApnea time was significantly correlated with duration of oxygen desaturation in seizures with PICA.PDF p.6, Results after Table 2
Reported values
  • below 80%ictal apnea extending into the postictal period in case MO#12Threshold · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • two brief postictal apnea episodesictal apnea extending into the postictal period in case MO#12Count · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • approximately 15 secondsictal apnea extending into the postictal period in case MO#12Other reported value · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • 20 seconds beforeictal apnea extending into the postictal period in case MO#12Other reported value · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • ICA in 27/69 patients (39%)ictal central apnea (ICA)Percentage · n/N 27/69 · 69 patients and 406 focal-onset seizures without secondary bilateral tonic-clonic evolution · ictalPDF p.1, Abstract Results; PDF p.3, Results, ICA in Focal Seizures; PDF p.5, Table 1
  • ICA in 71/406 seizures (17.5%)ictal central apnea (ICA)Percentage · n/N 71/406 · 69 patients and 406 focal-onset seizures without secondary bilateral tonic-clonic evolution · ictalPDF p.1, Abstract Results; PDF p.3, Results, ICA in Focal Seizures; PDF p.5, Table 1
  • p < 0.001apnea time and oxygen-desaturation durationP value · Seizures with PICA · peri-ictal and postictalPDF p.6, Results after Table 2
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdfIndependent primary study · 4 findings · 11 reported values
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf
Independent primary study · Class II · Evidence weight 4.80 · 2 × 1.2 × 2
The study enrolled 2632 children and adults with epilepsy at nine epilepsy-monitoring centres in the USA and UK between 2011 and 2021; 164 were lost to follow-up and 2468 participants were included in the primary follow-up analyses. There were 38 SUDEP outcomes and two near-SUDEP events. During admission, 1660 participants had seizures captured, 1432 had analysable seizures, and the report describes 1091 analysable generalised convulsive seizures and 2117 non-convulsive seizures. The primary endpoint was time to SUDEP or censoring due to other causes. Cox proportional hazards models assessed clinical and electroclinical predictors; repeated seizure predictors were aggregated to the most severe feature per patient, using the maximum for continuous features or presence for categorical features. Analyses used prolonged video-EEG, ECG, pulse oximetry, and chest/abdominal inductance plethysmography. Statistical significance in primary analyses required two-sided p<0.05 after Bonferroni correction; the report states that secondary-analysis confidence intervals were not intended for hypothesis testing. Main-text results include varying denominators and missing data, which are retained below.
Findings
  • ictal central apnoeaIctal central apnoea was present in 9/25 (36%) of SUDEP-or-near-SUDEP participants with available data versus 344/799 (43%) of non-SUDEP participants, but median duration was longer at 44 seconds (IQR 28-49) versus 17 seconds (10-27); each 10-second increase was associated with higher SUDEP risk in the primary Cox model, HR 1.11 (95% CI 1.05-1.18; p<0.0001), while the 5-year risk was 7.4% (1.3-13.1) for median duration >17 seconds versus 3.7% (1.3-6.1) for <=17 seconds, a threshold comparison with p=0.11. The adjusted association was not significant after clinical covariate adjustment, and exclusion of possible and near-SUDEP cases gave HR 1.06 (0.82-1.37).PDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • ictal central apnoeaThe Discussion restates that brief ictal central apnoea is commonly seen in about 37% of temporal lobe seizures, whereas prolonged ictal central apnoea is less common.PDF p.9, Discussion
  • ictal central apnoea; postictal central apnoeaThe Discussion restates that ictal central apnoea is associated with postictal central apnoea, suggesting that individuals with ictal central apnoea are more likely to develop postictal breathing cessation.PDF p.9, Discussion
  • ictal central apnoea; amygdala; hippocampus; mesial temporal poleAccording to brain electrical stimulation studies cited by the authors, ictal central apnoea likely arises from seizure discharges invading respiratory-modulating structures including the amygdala, hippocampus, and mesial temporal pole.PDF p.9, Discussion
Reported values
  • median duration 17 secondsictal central apnoeaMedian · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · median duration ≤17 seconds · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 5-year risk 3.7%ictal central apnoeaPercentage · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · median duration ≤17 seconds · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • median duration 44 secondsictal central apnoeaMedian · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · SUDEP or near-SUDEP · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 344/799 (43%) with ictal central apnoeaictal central apnoeaPercentage · n/N 344/799 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · non-SUDEP · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • HR 1.11 per 10-second increaseictal central apnoeaHazard ratio · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · primary Cox model · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 9/25 (36%) with ictal central apnoeaictal central apnoeaPercentage · n/N 9/25 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · SUDEP or near-SUDEP · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 5-year risk 7.4%ictal central apnoeaPercentage · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · median duration >17 seconds · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 608/1432 had missing ictal-apnoea dataictal central apnoeaPercentage · n/N 608/1432 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · overall cohort · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • HR 1.06 after excluding possible and near-SUDEP casesictal central apnoeaHazard ratio · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · exclusion analysis · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • p=0.11ictal central apnoeaP value · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • About 37% for brief ictal central apnoeaictal central apnoeaPercentage · Temporal lobe seizures in the cited prior literature · ictalPDF p.9, Discussion
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • central apnea and oxygen desaturation; amygdala stimulationThe source reports that amygdala stimulation induced central apnea and oxygen desaturation, most frequently after stimulation of medial-most amygdalar contacts located in the central nucleus, and states that these findings highlight a role for the amygdala in voluntary respiratory control.PDF p.14, Cardiorespiratory response; PDF p.25, cited references 114-117

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Complex auditory hallucinations (formed music, songs, melodies)Source terms: Complex auditory hallucinationsReported: ContralateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere7 manuscripts · 10 findings · 11 reported values
Weighted evidence supportevidence weight 15.34 across 7 manuscripts · 4 narrative, educational, or cited context · 2 independent primary study · 1 case report or observation

Across the three stimulated patients with complex visual or auditory hallucinations, the source reports composite lesion context involving nondominant inferior parieto-temporal or inferior-parieto-occipital locations and a left parietal lesion. The review restates that noises evoked from the medial primary auditory site were perceived in the ear contralateral to stimulation. The table restates contralateral lateralization for complex auditory aura when the phenomenon is unilateral. The synthesis reports a right-hemisphere stimulation predominance for verbal hallucinations, with no general hemisphere rule for all auditory percept types. No hemisphere or sign-side direction is reported. No lateralizing direction is reported. No hemisphere direction is reported. No sign-specific lateralizing rule is present.

Source-defined result groups 4
Localization: TemporalObserved proportion 4.2%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: parietal epilepsy seriesSource-defined values retained separatelyAll reported · other aura categories · aura entries1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 46.2%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 11.1%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • auditory illusion versus auditory hallucinationThe source reports Bancaud's assumption that auditory illusions occur preferentially with widely extended discharges over the superior temporal gyrus, whereas auditory hallucinations are likely when discharges are more spatially limited.PDF p.8, auditory aura discussion
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • auditory hallucinations and illusionsThe review reports a stimulation comparison in which the medial transverse gyrus of Heschl produced auditory hallucinations in 80% of patients, mostly high-frequency or broadband noise, whereas stimulation of the lateral transverse gyrus, anterior superior temporal gyrus, or planum temporale produced more illusions in 41–55%; from medial to lateral sites, hallucination content changed from high- to low-frequency noises, and primary-site noises were perceived in the contralateral ear.PDF p.3, section 4 and Fig. 1; PDF p.3, Fig. 1 caption
Reported values
  • medial Heschl auditory hallucinations 80%auditory hallucinations and illusionsPercentage · Patients undergoing superior temporal gyrus and planum temporale stimulation; total patient denominator is not reported in this review · medial transverse gyrus of Heschl · Stimulation-evoked auditory experiencePDF p.3, section 4 and Fig. 1; PDF p.3, Fig. 1 caption
  • lateral transverse gyrus/anterior STG/planum temporale illusions 41–55%auditory hallucinations and illusionsRange · Patients undergoing superior temporal gyrus and planum temporale stimulation; total patient denominator is not reported in this review · lateral or associative auditory sites · Stimulation-evoked auditory experiencePDF p.3, section 4 and Fig. 1; PDF p.3, Fig. 1 caption
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 2 findings · 4 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)In the cortical-stimulation synthesis, SH were mainly induced by posterior insula and Heschl’s gyrus (HG); CH by STG, STS, mesiotemporal structures, and insula; I by STG, HG, STS, and temporal plane with about one-third from extratemporal structures; VH included 60% produced by right-hemisphere stimulation, mostly STG; MH involved STG, HG, temporal plane, and SMG; HD involved temporal structures and insula, especially PLST, posterior STG, and HG; and few PAL reports were identified.PDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • auditory hallucinations and illusions induced by direct intracortical electrical stimulationThe review states that Jaroszynski et al. induced AP in 50 patients undergoing presurgical assessment for focal drug-resistant epilepsy and reported a large overlap between regions producing hallucinations and illusions.PDF p.4, section 5, Jaroszynski paragraph
Reported values
  • Verbal hallucinations from right-hemisphere stimulation 60%simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Verbal hallucinations · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • Auditory illusions from extratemporal stimulation about one-thirdsimple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Auditory illusions · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • large overlap, with no overlap numerator reported in this reviewauditory hallucinations and illusions induced by direct intracortical electrical stimulationCount · Cited Jaroszynski et al. presurgical focal drug-resistant epilepsy cohort · Direct intracortical stimulationPDF p.4, section 5, Jaroszynski paragraph
  • 50 patientsauditory hallucinations and illusions induced by direct intracortical electrical stimulationCount · Cited Jaroszynski et al. presurgical focal drug-resistant epilepsy cohort · Direct intracortical stimulationPDF p.4, section 5, Jaroszynski paragraph
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Complex auditory auraTable 2 associates complex auditory aura with auditory association cortex (BA 42, 22) and contralateral lateralisation if unilateral.PDF p.3, Table 2
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • auditory hallucination or illusionInitial auditory hallucination or illusion was more frequent in L than in M or ML patients.PDF p.5, Semiologic analysis; PDF p.5, Table 2
Reported values
  • 2/18 (11.1%)auditory hallucination or illusionPercentage · n/N 2/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2
  • 6/13 (46.2%)auditory hallucination or illusionPercentage · n/N 6/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2
  • 1/24 (4.2%)auditory hallucination or illusionPercentage · n/N 1/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfNarrative, educational, or cited context · 1 finding
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • auditory experiential hallucination after right temporal stimulationIn one cited case, stimulation of the right lateral posterior temporal cortex elicited singing as an experiential auditory phenomenon.PDF p.13, Cortical stimulation
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 3 findings · 2 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.27 · 2 × 1.35 × 1.952
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • complex visual or auditory hallucinations after stimulationComplex visual or auditory hallucinations occurred in three stimulated patients.PDF p.5, Electrical cortical stimulation
  • complex visual or auditory hallucinationsA few patients had complex visual or auditory hallucinations, interpreted by the source as suggesting spread to temporo-limbic areas.PDF p.4, Results, Aurae
  • complex visual or auditory hallucination entries in Table 1Table 1 lists five complex visual or auditory hallucination aura entries.PDF p.4, Table 1
Reported values
  • 3 patientscomplex visual or auditory hallucinations after stimulationCount · n/N 3/80 · 80 stimulated patients · stimulation response and ictal propagationPDF p.5, Electrical cortical stimulation
  • 5 source-reported aura entriescomplex visual or auditory hallucination entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal emotional auraReported: Left hemisphereAlso reported: Right hemisphere5 manuscripts · 14 findings · 19 reported values
Weighted evidence supportevidence weight 15.11 across 5 manuscripts · 2 independent primary study · 2 systematic review or meta-analysis · 1 narrative, educational, or cited context

The cited stimulation study reports predominantly negative emotions with right-amygdala stimulation and pleasant or unpleasant emotions with left-amygdala stimulation, with no right positive-emotion effect in the cited table. No lateralizing direction is reported for emotional auras across TL and T+ groups. No cerebral hemisphere or body-side direction is reported. No source-supported hemispheric or body-side lateralization is reported. No lateralizing direction is reported for the emotional-aura denominator. No lateralizing direction is reported for emotional subjective symptoms. No lateralizing direction is reported for the emotional symptom row.

Source-defined result groups 5
Localization: FrontalObserved proportion 4.9%All reported · individual1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 3.3%All reported · individual1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Emotional aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Emotional aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 5

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 11 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • emotional auraEmotional auras did not differ significantly between TL and T+ groups across fear, anxiety, anger, and pleasure subcategories.PDF p.6, Table 2
Reported values
  • T+ anxiety 21.7%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • TL anger 3.4%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
  • TL fear 22%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
  • T+ pleasure 0%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • T+ fear 13%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • P=0.6emotional auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
  • TL 33.9%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
  • T+ anger 4.3%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • TL pleasure 0%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
  • T+ 39.1%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictal onsetPDF p.6, Table 2
  • TL anxiety 11.9%emotional auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictal onsetPDF p.6, Table 2
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • emotional subjective symptomsEmotional subjective symptoms were reported in 8% of cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Emotional (Table 3)Table 3 reports emotional symptoms in 7 cases (8%), more at seizure onset.PDF p.6, Table 3
  • Emotional (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports emotional symptoms in 9 cases (15%).PDF p.7, Table 4
Reported values
  • 8% emotional subjective symptomsemotional subjective symptomsPercentage · reviewed basal temporal seizure cases · ictal onsetPDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 7 cases (8%)Emotional (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 9/60 (15%)Emotional (Table 4)Percentage · n/N 9/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 8 findings · 3 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Emotional auraTable 3 reports 1 studies assessing Emotional aura.PDF p.6, Table 3
  • Emotional auraTable 3 reports 8 patients assessed for Emotional aura.PDF p.6, Table 3
  • Emotional auraTable 3 reports 12.5% as the percentage range or value for Emotional aura; the overall association grade is Low.PDF p.6, Table 3
  • Emotional aura; lateral versus mesial comparisonTable 5 reports 1 studies comparing Emotional aura in lateral and mesial TLE.PDF p.9, Table 5
  • Emotional aura; lateral TLE patient denominatorTable 5 reports 8 lateral-TLE patients assessed for Emotional aura.PDF p.9, Table 5
  • Emotional aura; mesial TLE patient denominatorTable 5 reports 20 mesial-TLE patients assessed for Emotional aura.PDF p.9, Table 5
  • Emotional aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 12.5% for Emotional aura.PDF p.9, Table 5
  • Emotional aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 15% for Emotional aura.PDF p.9, Table 5
Reported values
  • 12.5%Emotional auraPercentage · Lateral temporal epilepsy patients assessed for Emotional aura · ictalPDF p.6, Table 3
  • 12.5%Emotional aura; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Emotional aura · Lateral TLE patients assessed for Emotional aura · ictalPDF p.9, Table 5
  • 15%Emotional aura; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Emotional aura · Mesial TLE patients assessed for Emotional aura · ictalPDF p.9, Table 5
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal non-motor (emotional)Focal non-motor (emotional) semiology occurred in 2/61 individuals (3%) as initial semiology and 3/61 (5%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Combined 3/61 (5%)Focal non-motor (emotional)Percentage · n/N 3/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Initial 2/61 (3%)Focal non-motor (emotional)Percentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • experience of negative and positive emotions; amygdala stimulationThe source reports different emotional valence by amygdala side: right-amygdala stimulation induced negative emotions, especially fear and sadness, whereas left-amygdala stimulation induced either pleasant happiness or unpleasant fear, anxiety, or sadness; Table 10.1 lists negative-emotion responses from both sides and no right-hemisphere positive-emotion effect in the cited study.PDF p.13, Socio-emotional function; PDF p.18, Table 10.1, Emotional Responses

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Tonic posturingReported: Contralateral7 manuscripts · 7 findings · 4 reported values
Weighted evidence supportevidence weight 14.54 across 7 manuscripts · 2 independent primary study · 4 narrative, educational, or cited context · 1 systematic review or meta-analysis

The discussion restates greater lateralizing value for dystonic than tonic posturing without stating the lateralizing direction. The source describes visual aura followed by head-eye deviation and contralateral tonic posturing as activity propagates through dorsal parietal nodes toward premotor areas. The cited table associates tonic posturing with contralateral lateralisation. No lateralization information is reported. No lateralization is reported. No lateralizing direction is reported for the tonic-to-clonic propagation description. The cited anterior-versus-posterior insular comparison provides no lateralizing information.

Source-defined result groups 1
Localization: ParietalObserved proportion 60.9%All reported · tonic-posturing patients without superior parietal involvement · patients with tonic posturing1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review searched PubMed and Embase through December 2023, used adapted QUADAS-2 and GRADE assessments, and included primary adult/pediatric presurgical or surgical studies with explicit anatomo-electroclinical correlations. Fresh text from all 10 pages was read, and the abstract, PRISMA flow, individual-study table, aggregate table, symptom meta-analysis table, and discussion layouts were visually inspected. Table 1 cells are retained as cited-study restatements; Table 2 and Table 3 aggregate cells are retained as primary review results. Each count, percentage, subgroup component, confidence category, heterogeneity statistic, and p value is represented independently.
Findings
  • tonic posturing; clonic jerksThe source describes clonic jerks following focal tonic manifestations as likely reflecting propagation from the SMA to the primary motor area.PDF p.7, Discussion
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Tonic posturingTable 3 associates tonic posturing with SSMA, basal ganglia, cingulum, and primary motor cortex (M1) and contralateral lateralisation.PDF p.4, Table 3
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • dystonic versus tonic posturingThe discussion distinguishes tonic from dystonic posturing, states that dystonia has greater lateralizing value, and reports that Kotagal et al. (1989) observed unilateral dystonia in 15% of patients with TLE.PDF p.5, Discussion
Reported values
  • 15% of patients with TLE, as reported for Kotagal et al. (1989)dystonic versus tonic posturingPercentage · Cited TLE study as described by the current source; not independently reviewed · ictal motor posturingPDF p.5, Discussion
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 4.54 · 2 × 1.35 × 1.681
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • superior parietal epileptogenic zone with tonic posturingFourteen of 23 patients with tonic posturing had epileptogenic zones including the superior parietal lobule.PDF p.4, Results, Other seizure characteristics; PDF p.6, Discussion
Reported values
  • 14/23 (61%) patientssuperior parietal epileptogenic zone with tonic posturingPercentage · n/N 14/23 · 23 patients with tonic posturing · ictal motor phase and seizure-onset localizationPDF p.4, Results, Other seizure characteristics; PDF p.6, Discussion
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • focal clonic movement; negative motor responses; tonic posturing; palilaliaThe source reports that central-region pulse or short-train stimulation is used to induce focal clonic movement, that negative motor responses are seen in the pre-SMA region, and that SMA-proper stimulation induces positive motor behaviors such as tonic posturing or palilalia.PDF p.13, Motor Behaviors
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • dorsal parietal to premotor motor evolutionThe authors link rapid motor evolution after visual aura to propagation to dorsal parietal nodes and then premotor areas.PDF p.13, Phenotype III discussion

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal speech productionReported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side9 manuscripts · 10 findings · 14 reported values
Weighted evidence supportevidence weight 14.11 across 9 manuscripts · 1 manuscript weight pending · 1 independent primary study · 6 narrative, educational, or cited context · 1 structured design not resolved · 1 systematic review or meta-analysis

The educational table assigns ictal speech to the nondominant hemisphere. Ictal verbalization tends to occur with nondominant-hemisphere onset, whereas pure vocalization is described as non-lateralizing. The review distinguishes dominant-hemisphere dysphasia, nondominant ictal speech or preserved awareness, contralateral RINCH motions, and nonlateralizing speech arrest. The review cites ictal speech in 10 of 12 nondominant temporal-lobe cases and in 12 of 13 right temporal-lobe cases. Comprehensible stereotyped ictal speech is described as suggesting a nondominant focus, while dominant-hemisphere lateralization of vocalizations remains controversial. Ictal speech is restated as generally associated with the nondominant hemisphere, with 83% nondominant among patients with ictal speech. Among temporal-lobe epilepsy cases with ictal speech, more than 80% were reported to have nondominant-hemisphere lateralization. Identifiable speech during seizures occurred in 10 of 12 patients with nondominant temporal-lobe onset and 2 of 12 with dominant temporal-lobe onset. The cited ictal-speech cohort had left-sided seizures in 12 of 13 cases; Wada language representation was a separate contextual distribution. This finding provides no lateralization information.

Source-defined result groups 3
Localization: FrontalObserved proportion 0.0%initial semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 3.3%combined set-of-semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereObserved proportion 83.3%nondominant-origin seizures · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • ictal/postictal dysphasia; ictal speech; preserved awareness; RINCH motionsIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value and must be distinguished from non-lateralising speech arrest; formed nonsensical ictal speech and preserved awareness during ictal automatisms point to the nondominant hemisphere, while rhythmic ictal non-clonic hand motions may be contralateral in temporal lobe epilepsy and peri-ictal drinking, spitting, vomiting, or urge to urinate point to a nondominant focus.PDF p.10, Lateralising signs
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • ictal speechThe p.2 table lists ictal speech as Nondominant hemisphere.PDF p.2, Lateralizing signs/Localization table entry "ictal speech" (printed p.7)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal speech in cited studiesThe current paper reports that Gabr et al. (1989) found ictal speech in 12 patients, 10 of whom had seizure onset in the nondominant temporal lobe, and that Koerner and Laxer (1988) described ictal speech in 13 patients, 12 of whom had RTLE.PDF p.5, Discussion, ictal-speech paragraph
Reported values
  • 10 of 12Ictal speech in cited studiesPercentage · n/N 10/12 · Cited patient series as restated by the current paper · Gabr et al. 1989; ictal speech · IctalPDF p.5, Discussion, ictal-speech paragraph
  • 12 of 13Ictal speech in cited studiesPercentage · n/N 12/13 · Cited patient series as restated by the current paper · Koerner and Laxer 1988; ictal speech · IctalPDF p.5, Discussion, ictal-speech paragraph
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal speech, verbal automatisms, and ictal vocalizationsIctal vocalizations and ictal speech are reported in TLE but are not exclusive to it; comprehensible stereotyped speech, including rare second-language automatisms, suggests a nondominant-hemisphere focus, whereas the lateralizing value of vocalizations toward the dominant hemisphere remains controversial.PDF p.8, Focal impaired awareness seizures
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 2 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.54
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • ictal identifiable speechAmong the 12 patients with ictal identifiable speech, 10 (83%) had seizures of nondominant origin and 2 had seizures of dominant origin; the difference was statistically significant (chi-square p = 0.013).PDF p.1, abstract; PDF p.3, Table 4 and Results; PDF p.5, Discussion and conclusion
Reported values
  • 2/12ictal identifiable speechPercentage · n/N 2/12 · 12 patients with ictal identifiable speech in the 35-patient temporal-lobe epilepsy cohort · dominant-origin seizures · ictalPDF p.1, abstract; PDF p.3, Table 4 and Results; PDF p.5, Discussion and conclusion
  • 10/12 (83%)ictal identifiable speechPercentage · n/N 10/12 · 12 patients with ictal identifiable speech in the 35-patient temporal-lobe epilepsy cohort · nondominant-origin seizures · ictalPDF p.1, abstract; PDF p.3, Table 4 and Results; PDF p.5, Discussion and conclusion
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Ictal speechIctal speech was absent as initial semiology (0/61, 0%) and occurred in 2/61 individuals (3%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Combined 2/61 (3%)Ictal speechPercentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Initial 0/61 (0%)Ictal speechPercentage · n/N 0/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Ictal speechThe review reports that one-third of temporal-lobe epilepsy cases demonstrate ictal speech and that more than 80% of those cases have non-dominant-hemisphere lateralisation.PDF p.6, section 1.9
Reported values
  • Ictal-speech cases with non-dominant-hemisphere lateralisation >80%Ictal speechPercentage · Temporal-lobe epilepsy cases · TLE cases with ictal speech · ictalPDF p.6, section 1.9
  • Temporal-lobe epilepsy cases with ictal speech: one-thirdIctal speechPercentage · Temporal-lobe epilepsy cases · All TLE cases · ictalPDF p.6, section 1.9
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal speechIctal speech is generally associated with seizures from the nondominant hemisphere.PDF p.9, section 4.1; PDF p.12, Table 1
  • ictal speechKoerner and Laxer found left-sided seizures in 12 of 13 focal-seizure patients with ictal speech.PDF p.9, section 4.1
Reported values
  • 34.2% of EMU patientsictal speechPercentage · epilepsy monitoring unit patients with ictal speech · EMU patients · ictalPDF p.9, section 4.1; PDF p.12, Table 1
  • 83% nondominantictal speechPercentage · epilepsy monitoring unit patients with ictal speech · patients with ictal speech · ictalPDF p.9, section 4.1; PDF p.12, Table 1
  • Ictal-speech patients with bilateral-language representation 3/13ictal speechPercentage · n/N 3/13 · 84 patients with focal seizures, including 13 with ictal speech · Patients with ictal speech · ictalPDF p.9, section 4.1
  • Ictal-speech patients with left-language dominance 10/13ictal speechPercentage · n/N 10/13 · 84 patients with focal seizures, including 13 with ictal speech · Patients with ictal speech · ictalPDF p.9, section 4.1
  • Patients with ictal speech 13/84ictal speechPercentage · n/N 13/84 · 84 patients with focal seizures, including 13 with ictal speech · ictalPDF p.9, section 4.1
  • Ictal-speech patients with left-sided seizures 12/13ictal speechPercentage · n/N 12/13 · 84 patients with focal seizures, including 13 with ictal speech · Patients with ictal speech · ictalPDF p.9, section 4.1
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal speechThe review defines ictal verbalization as clearly intelligible speech when the patient is already unresponsive or has clear distal automatisms and states that it tends to lateralize temporal-lobe epilepsy to the non-dominant hemisphere. Exceptions are not infrequent, making it poorly reliable; pure vocalization has no lateralizing significance.PDF p.6, Ictal speech

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Simple auditory aura (tones, buzzing, hissing, roaring)Source terms: Simple auditory auraReported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side9 manuscripts · 18 findings · 76 reported values
Weighted evidence supportevidence weight 14.11 across 9 manuscripts · 1 manuscript weight pending · 4 narrative, educational, or cited context · 1 independent primary study · 1 structured design not resolved · 2 case report or observation · 1 systematic review or meta-analysis

The review states that rhythmic non-clonic hand motion may be contralateral and that rare unilateral simple auditory aura is contralateral. The cited stimulation series describes left superior temporal stimulation effects that vary by task and subregion, including auditory phenomena, phonological errors, and naming or reading deficits. Right facial pain, right-ear ringing, right hemibody and foot manifestations predominated in the early sequence, while left-sided stiffening occurred in half of seizures. The cited table restates contralateral lateralisation for a unilateral simple auditory aura. The review gives contralateral direction for hemifield visual aura, simple unilateral auditory aura, and the fast nystagmus component, but ipsilateral direction for unilateral eye blinking. The synthesis reports a right-hemisphere stimulation predominance for verbal hallucinations, with no general hemisphere rule for all auditory percept types. The review synthesis reports a left probable SOZ predominance overall (123/200 versus 77/200), with equal left/right counts for illusions and an abstract/Table 2 percentage discrepancy. Perceived auditory seizures were reported in the right ear, left ear, bilaterally, or inside the head; subtype patterns differed and other types had no clear ear-side tendency. The review restates that perceived auditory side may be contralateral to the SOZ in a small set of previously published cases. Auditory laterality is subtype-dependent: unilateral auditory symptoms are described as contralateral, while complex verbal hallucinations or negative auditory illusions may indicate dominant-hemisphere involvement. The cited study restatement reports no clear contralateral-temporal lateralization for auditory sensation. No seizure lateralization is reported. No lateralization axis information is reported for focal sensory auditory semiology. The mesiotemporal-versus-lateral temporal comparison contains no hemisphere direction. No lateralizing direction is reported. No lateralization axis information is reported for the siren aura. No hemisphere direction is reported. No source lateralization is reported.

Source-defined result groups 1
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft-sided stiffening · Early diurnal versus later nocturnal/postoperative semiology · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • gustatory, vestibular, and auditory symptomsThe source states that the localizing significance of gustatory, vestibular, and auditory symptoms remains uncertain in the cited literature.PDF p.7, Auras
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 5 findings · 1 reported value
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • rhythmic ictal non-clonic hand motion; unilateral elementary auditory auraRhythmic ictal non-clonic hand motions may be a contralateral sign in temporal lobe epilepsy, and a simple unilateral auditory aura, described as rare, is also a contralateral sign.PDF p.10, Lateralising signs; PDF p.6, Lateral/neocortical temporal lobe
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmus; unilateral auditory auraA hemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; the fast component of epileptic nystagmus is contralateral to seizure onset; and a simple unilateral auditory aura, which the review notes is rare, is contralateral.PDF p.6, Lateral/neocortical temporal lobe; PDF p.8, Parieto-occipital junction; PDF p.10, Lateralising signs
  • abdominal aura; experiential phenomena; elemental auditory auraIn a cited study of 187 temporal lobe seizures assessed with intracranial stereo-EEG, abdominal aura and experiential phenomena such as fear, déjà vu, and jamais vu indicated mesiotemporal seizures, whereas elemental auditory aura indicated lateral onset involving Heschl’s gyrus/primary auditory cortex.PDF p.5, Auras
  • elementary auditory aura; auditory illusion/distortionTable 3 maps elementary auditory aura to Heschl’s gyrus or superior temporal regions and auditory illusions or distortions to lateral temporal regions or insula.PDF p.10, Table 3; PDF p.6, Lateral/neocortical temporal lobe
  • abdominal aura; experiential phenomena; elemental auditory auraIn a cited study of 187 temporal lobe seizures assessed by intracranial stereo-EEG, abdominal aura and experiential phenomena including fear, déjà vu, and jamais vu indicated mesiotemporal seizures, whereas elemental auditory aura indicated lateral onset involving Heschl’s gyrus or primary auditory cortex.PDF p.5, Auras
Reported values
  • Qualitative association in 187 seizuresabdominal aura; experiential phenomena; elemental auditory auraCount · 187 temporal lobe seizures assessed by intracranial stereo-EEG · Aura and ictal onsetPDF p.5, Auras
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 6 findings · 67 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)In the cortical-stimulation synthesis, SH were mainly induced by posterior insula and Heschl’s gyrus (HG); CH by STG, STS, mesiotemporal structures, and insula; I by STG, HG, STS, and temporal plane with about one-third from extratemporal structures; VH included 60% produced by right-hemisphere stimulation, mostly STG; MH involved STG, HG, temporal plane, and SMG; HD involved temporal structures and insula, especially PLST, posterior STG, and HG; and few PAL reports were identified.PDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • lateralization of the probable SOZ in auditory seizuresIn the review’s 200-AS synthesis, the probable SOZ was more often left (123/200, 62%) than right (77/200, 39% in Table 2; 38% in the abstract), with left predominance for most AS types and equal left/right counts for illusions.PDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • lateralization of the perceived auditory seizure (AS)Among 114 AS with perceived-side data, AS were heard in the right ear in 33%, left ear in 26%, bilaterally in 31%, and inside the head in 10%; illusions were all bilateral, HD was mostly bilateral (70%), and other AS types showed no clear ear-side tendency.PDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • contralateral auditory seizures in a cited 2009 reviewThe review states that a 2009 review of previously published cases supported AS being contralateral to the SOZ, but that the total number of cases was small.PDF p.5, section 6.1
  • lateralizing value of the auditory aura in a cited 36-case studyThe review states that a larger cited study of 36 cases found that AS did not clearly lateralize to the contralateral temporal cortex.PDF p.5, section 6.1
  • extratemporal seizure-onset-zone localization in auditory seizuresApproximately 30% of AS originated outside the temporal lobe, mainly in parietal, frontal, and insular regions with few occipital cases; IFG was the most frequently reported frontal structure, parietal localization was often unspecified or involved AG/PoG, and insular AS were rare despite frequent insular AP in stimulation studies.PDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
Reported values
  • Verbal hallucinations from right-hemisphere stimulation 60%simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Verbal hallucinations · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • Auditory illusions from extratemporal stimulation about one-thirdsimple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Auditory illusions · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • R8lateralization of the probable SOZ in auditory seizuresCount · n/N 8/21 · 174 reviewed cases comprising 200 AS, classified by AS type where available · PAL · Ictal ASPDF p.7, Table 2
  • L5lateralization of the probable SOZ in auditory seizuresCount · n/N 5/9 · 174 reviewed cases comprising 200 AS, classified by AS type where available · NS · Ictal ASPDF p.7, Table 2
  • 38%lateralization of the probable SOZ in auditory seizuresPercentage · n/N 77/200 · 174 reviewed cases comprising 200 AS, classified by AS type where available · I · Ictal ASPDF p.1, Abstract
  • L22lateralization of the probable SOZ in auditory seizuresCount · n/N 22/32 · 174 reviewed cases comprising 200 AS, classified by AS type where available · MH · Ictal ASPDF p.7, Table 2
  • L25lateralization of the probable SOZ in auditory seizuresCount · n/N 25/42 · 174 reviewed cases comprising 200 AS, classified by AS type where available · VH · Ictal ASPDF p.7, Table 2
  • L11lateralization of the probable SOZ in auditory seizuresCount · n/N 11/15 · 174 reviewed cases comprising 200 AS, classified by AS type where available · HD · Ictal ASPDF p.7, Table 2
  • L7lateralization of the probable SOZ in auditory seizuresCount · n/N 7/14 · 174 reviewed cases comprising 200 AS, classified by AS type where available · I · Ictal ASPDF p.7, Table 2
  • R4lateralization of the probable SOZ in auditory seizuresCount · n/N 4/15 · 174 reviewed cases comprising 200 AS, classified by AS type where available · HD · Ictal ASPDF p.7, Table 2
  • 123/200 (62%)lateralization of the probable SOZ in auditory seizuresPercentage · n/N 123/200 · 174 reviewed cases comprising 200 AS, classified by AS type where available · all AS; left probable SOZ · Ictal ASPDF p.1, Abstract; PDF p.7, Table 2
  • L28lateralization of the probable SOZ in auditory seizuresCount · n/N 28/49 · 174 reviewed cases comprising 200 AS, classified by AS type where available · SH · Ictal ASPDF p.7, Table 2
  • R6lateralization of the probable SOZ in auditory seizuresCount · n/N 6/18 · 174 reviewed cases comprising 200 AS, classified by AS type where available · CH · Ictal ASPDF p.7, Table 2
  • L13lateralization of the probable SOZ in auditory seizuresCount · n/N 13/21 · 174 reviewed cases comprising 200 AS, classified by AS type where available · PAL · Ictal ASPDF p.7, Table 2
  • R10lateralization of the probable SOZ in auditory seizuresCount · n/N 10/32 · 174 reviewed cases comprising 200 AS, classified by AS type where available · MH · Ictal ASPDF p.7, Table 2
  • L12lateralization of the probable SOZ in auditory seizuresCount · n/N 12/18 · 174 reviewed cases comprising 200 AS, classified by AS type where available · CH · Ictal ASPDF p.7, Table 2
  • R7lateralization of the probable SOZ in auditory seizuresCount · n/N 7/14 · 174 reviewed cases comprising 200 AS, classified by AS type where available · I · Ictal ASPDF p.7, Table 2
  • 77/200 (39%)lateralization of the probable SOZ in auditory seizuresPercentage · n/N 77/200 · 174 reviewed cases comprising 200 AS, classified by AS type where available · all AS; right probable SOZ · Ictal ASPDF p.7, Table 2
  • R21lateralization of the probable SOZ in auditory seizuresCount · n/N 21/49 · 174 reviewed cases comprising 200 AS, classified by AS type where available · SH · Ictal ASPDF p.7, Table 2
  • R17lateralization of the probable SOZ in auditory seizuresCount · n/N 17/42 · 174 reviewed cases comprising 200 AS, classified by AS type where available · VH · Ictal ASPDF p.7, Table 2
  • R4lateralization of the probable SOZ in auditory seizuresCount · n/N 4/9 · 174 reviewed cases comprising 200 AS, classified by AS type where available · NS · Ictal ASPDF p.7, Table 2
  • PAL left ear 4/17lateralization of the perceived auditory seizure (AS)Count · n/N 4/17 · AS with reported perceived side in the review synthesis · PAL · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • MH left ear 5/15lateralization of the perceived auditory seizure (AS)Count · n/N 5/15 · AS with reported perceived side in the review synthesis · MH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • SH left ear 11/33lateralization of the perceived auditory seizure (AS)Count · n/N 11/33 · AS with reported perceived side in the review synthesis · SH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • VH bilateral 3/22lateralization of the perceived auditory seizure (AS)Count · n/N 3/22 · AS with reported perceived side in the review synthesis · VH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • MH right ear 4/15lateralization of the perceived auditory seizure (AS)Count · n/N 4/15 · AS with reported perceived side in the review synthesis · MH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • HD inside head 0/10lateralization of the perceived auditory seizure (AS)Count · n/N 0/10 · AS with reported perceived side in the review synthesis · HD · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • SH bilateral 8/33lateralization of the perceived auditory seizure (AS)Count · n/N 8/33 · AS with reported perceived side in the review synthesis · SH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • NS right ear 2/3lateralization of the perceived auditory seizure (AS)Count · n/N 2/3 · AS with reported perceived side in the review synthesis · NS · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • MH bilateral 4/15lateralization of the perceived auditory seizure (AS)Count · n/N 4/15 · AS with reported perceived side in the review synthesis · MH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • CH bilateral 3/8lateralization of the perceived auditory seizure (AS)Count · n/N 3/8 · AS with reported perceived side in the review synthesis · CH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • VH left ear 5/22lateralization of the perceived auditory seizure (AS)Count · n/N 5/22 · AS with reported perceived side in the review synthesis · VH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • HD right ear 2/10lateralization of the perceived auditory seizure (AS)Count · n/N 2/10 · AS with reported perceived side in the review synthesis · HD · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • MH inside head 2/15lateralization of the perceived auditory seizure (AS)Count · n/N 2/15 · AS with reported perceived side in the review synthesis · MH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • I left ear 0/6lateralization of the perceived auditory seizure (AS)Count · n/N 0/6 · AS with reported perceived side in the review synthesis · I · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • NS bilateral 1/3lateralization of the perceived auditory seizure (AS)Count · n/N 1/3 · AS with reported perceived side in the review synthesis · NS · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • PAL right ear 9/17lateralization of the perceived auditory seizure (AS)Count · n/N 9/17 · AS with reported perceived side in the review synthesis · PAL · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • SH inside head 1/33lateralization of the perceived auditory seizure (AS)Count · n/N 1/33 · AS with reported perceived side in the review synthesis · SH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • PAL bilateral 3/17lateralization of the perceived auditory seizure (AS)Count · n/N 3/17 · AS with reported perceived side in the review synthesis · PAL · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • VH inside head 6/22lateralization of the perceived auditory seizure (AS)Count · n/N 6/22 · AS with reported perceived side in the review synthesis · VH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • VH right ear 8/22lateralization of the perceived auditory seizure (AS)Count · n/N 8/22 · AS with reported perceived side in the review synthesis · VH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • SH right ear 13/33lateralization of the perceived auditory seizure (AS)Count · n/N 13/33 · AS with reported perceived side in the review synthesis · SH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • I right ear 0/6lateralization of the perceived auditory seizure (AS)Count · n/N 0/6 · AS with reported perceived side in the review synthesis · I · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • CH right ear 0/8lateralization of the perceived auditory seizure (AS)Count · n/N 0/8 · AS with reported perceived side in the review synthesis · CH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • NS left ear 0/3lateralization of the perceived auditory seizure (AS)Count · n/N 0/3 · AS with reported perceived side in the review synthesis · NS · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • PAL inside head 1/17lateralization of the perceived auditory seizure (AS)Count · n/N 1/17 · AS with reported perceived side in the review synthesis · PAL · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • CH left ear 4/8lateralization of the perceived auditory seizure (AS)Count · n/N 4/8 · AS with reported perceived side in the review synthesis · CH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • 114 AS with perceived-side datalateralization of the perceived auditory seizure (AS)Count · AS with reported perceived side in the review synthesis · I · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • All types left ear 30/114 (26%)lateralization of the perceived auditory seizure (AS)Percentage · n/N 30/114 · AS with reported perceived side in the review synthesis · All types · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • CH inside head 1/8lateralization of the perceived auditory seizure (AS)Count · n/N 1/8 · AS with reported perceived side in the review synthesis · CH · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • I inside head 0/6lateralization of the perceived auditory seizure (AS)Count · n/N 0/6 · AS with reported perceived side in the review synthesis · I · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • I bilateral 6/6 (100%)lateralization of the perceived auditory seizure (AS)Percentage · n/N 6/6 · AS with reported perceived side in the review synthesis · I · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • NS inside head 0/3lateralization of the perceived auditory seizure (AS)Count · n/N 0/3 · AS with reported perceived side in the review synthesis · NS · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • HD bilateral 7/10 (70%)lateralization of the perceived auditory seizure (AS)Percentage · n/N 7/10 · AS with reported perceived side in the review synthesis · HD · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • HD left ear 1/10lateralization of the perceived auditory seizure (AS)Count · n/N 1/10 · AS with reported perceived side in the review synthesis · HD · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • All types bilateral 35/114 (31%)lateralization of the perceived auditory seizure (AS)Percentage · n/N 35/114 · AS with reported perceived side in the review synthesis · All types · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • All types inside head 11/114 (10%)lateralization of the perceived auditory seizure (AS)Percentage · n/N 11/114 · AS with reported perceived side in the review synthesis · All types · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • All types right ear 38/114 (33%)lateralization of the perceived auditory seizure (AS)Percentage · n/N 38/114 · AS with reported perceived side in the review synthesis · All types · Ictal ASPDF p.6, section 6.1; PDF p.7, Table 2; PDF p.9, Conclusion
  • no clear contralateral-temporal lateralizationlateralizing value of the auditory aura in a cited 36-case studyCount · Cited 36-case auditory-aura study · Ictal auditory aura/ASPDF p.5, section 6.1
  • 36 caseslateralizing value of the auditory aura in a cited 36-case studyCount · Cited 36-case auditory-aura study · Ictal auditory aura/ASPDF p.5, section 6.1
  • Review corpus auditory seizures n=200extratemporal seizure-onset-zone localization in auditory seizuresCount · AS cases in the review’s localization synthesis · Review corpus · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
  • Occipital regional classifications n=5extratemporal seizure-onset-zone localization in auditory seizuresCount · AS cases in the review’s localization synthesis · Occipital · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
  • Auditory seizures originating outside temporal lobe approximately 30%extratemporal seizure-onset-zone localization in auditory seizuresPercentage · AS cases in the review’s localization synthesis · Extratemporal SOZ · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
  • Cingulate regional classifications n=3extratemporal seizure-onset-zone localization in auditory seizuresCount · AS cases in the review’s localization synthesis · Cingulate · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
  • Parietal regional classifications n=26extratemporal seizure-onset-zone localization in auditory seizuresCount · AS cases in the review’s localization synthesis · Parietal · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
  • Frontal regional classifications n=15extratemporal seizure-onset-zone localization in auditory seizuresCount · AS cases in the review’s localization synthesis · Frontal · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
  • Insula regional classifications n=12extratemporal seizure-onset-zone localization in auditory seizuresCount · AS cases in the review’s localization synthesis · Insula · Ictal ASPDF p.1, Abstract; PDF p.8, section 6.2.2 and Figure 3; PDF p.9, section 6.2.2; PDF p.10, Conclusion
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • focal auditory seizures in LTLEFocal auditory seizures are the most suggestive symptom of LTLE: elementary sounds implicate Heschl’s gyrus and primary auditory cortex, complex voices or music implicate secondary auditory cortex, and auditory illusions represent distorted perception of real sounds; unilateral auditory symptoms arise from the contralateral hemisphere, while complex verbal hallucinations and negative auditory illusions may indicate dominant-hemisphere involvement.PDF p.9, Lateral temporal lobe epilepsy; PDF p.9, Focal aware seizures
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal sensory (auditory)Focal sensory (auditory) semiology occurred in 1/61 individuals (2%) both as initial semiology and in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 1/61 (2%)Focal sensory (auditory)Percentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 1/61 (2%)Focal sensory (auditory)Percentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Simple auditory auraTable 2 associates simple auditory aura with primary auditory cortex (BA 41), and lists lateral temporal cortex and insula for auditory illusions, with contralateral lateralisation if unilateral.PDF p.3, Table 2
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding · 5 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyCase 2 was a 46-year-old right-handed man whose seizures began with lancinating right facial pain followed within 2 seconds by high-pitched right-ear ringing descending along the right hemibody to the foot, sometimes with right-foot tremor, witnessed erratic right-sided and truncal movements, and left-sided stiffening in half the seizures; he was usually conscious without postictal paresis, had 10–15-second events up to 100 times per day triggered by sounds, and could develop hypersalivation, speech difficulty, later nocturnal hypermotor seizures, and urinary incontinence.PDF p.11, Case 2; PDF p.13, continuation of Case 2
Reported values
  • within 2 secondsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyDuration · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · early sensory sequence · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 10–15-second eventsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · habitual events · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 2–3 per monthCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · youth · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • in half the seizuresCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyOther reported value · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · left-sided stiffening · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • up to 100 times per dayCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyFrequency · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · later high-frequency period · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • hallucinations or illusions; auditory symptoms; articulatory or phonological errors; naming or reading deficitsIn the posterior left superior temporal region, the source reports task- and subregion-specific effects: word-repetition stimulation of Heschl’s gyrus induced hallucinations or illusions without language deficit; planum temporale stimulation induced auditory symptoms with comprehension deficit; left planum temporale or Spt stimulation during word or pseudoword repetition elicited articulatory or phonological errors and difficulty maintaining the phonological loop; and posterior left STS stimulation during naming or reading produced naming or reading deficits without positive auditory symptoms, including the source’s reported “graphene” decoding, comprehension, and “graphene to phoneme” deficits.PDF p.7, posterior left superior temporal gyrus paragraph; PDF p.8, Fig. 10.3 caption
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 1 finding · 1 reported value
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • siren aura in hypermotor seizureOne hypermotor patient reported sirens as an aura.PDF p.4, Seizure semiology on video-EEG recording; PDF p.3, Table 1
Reported values
  • 1/4 hypermotor patients with siren aurasiren aura in hypermotor seizureProportion · n/N 1/4 · 4 hypermotor patients · auraPDF p.4, Seizure semiology on video-EEG recording; PDF p.3, Table 1

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Head versionReported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphere8 manuscripts · 24 findings · 27 reported values
Weighted evidence supportevidence weight 14.11 across 8 manuscripts · 2 manuscript weight pending · 2 structured design not resolved · 1 independent primary study · 3 narrative, educational, or cited context · 2 systematic review or meta-analysis

ATLP was usually on the same side as version, with one complex two-direction version exception; the head was midline or returning to midline when ATLP appeared. In the unilateral TLE cohort, head version occurred only contralateral to the EEG seizure focus. The educational tables list asymmetric ending as ipsilateral but do not report the reference side or viewpoint. The reproduced table associates head version with a contralateral direction. No hemisphere or body-side direction is reported. This educational statement supplies no lateralizing direction. The educational definition of head version gives no hemisphere or lateralizing direction. No lateralization axis information is reported for the 4.3% head-version frequency. The all-data head-version panel sample size N=597 provides no lateralization result. The non-topological head-version panel sample size N=151 provides no lateralization result. No lateralization axis information is reported for head version with temporal-lobe localization. No lateralization axis information is reported for head version with frontal-lobe localization. No lateralization axis information is reported for the conditional frontal head-version probability. No lateralization axis information is reported for the conditional temporal head-version probability. No lateralization axis information is reported for the frontal head-version odds interval. No lateralization axis information is reported for the temporal head-version odds interval. No cerebral lateralization axis information is reported for head version or orientation. No lateralizing direction is reported for version or ATLP.

Source-defined result groups 6
Localization: TemporalSource-defined values retained separatelytemporal localization relative to EUD-Loc · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / IpsilateralSource-defined values retained separatelyAll reported · ATLP side versus version side and EEG laterality · instance1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization relative to EUD-Loc · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given head version · localizing data point1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / IpsilateralSource-defined values retained separatelyGroup II with ATLP and version · ATLP side versus version side and EEG laterality · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyfrontal localization given head version · localizing data point1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 16 findings · 7 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • head versionTable 1 defines or exemplifies the the source's own semiology category “head version” as Forced head deviation over the shoulder or extreme head turn.PDF p.7, Table 1 Semiology descriptions and frequencies
  • head versionHead version comprised 4.3% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • head version; Figure 3 all-data subsetFigure 3 reports N = 597 for the all-data head version panel.PDF p.9, Figure 3 and caption
  • head version; Figure 3 non-topological subsetFigure 3 reports N = 151 for the non-topological head version panel.PDF p.9, Figure 3 and caption
  • head version; temporal lobeHead version implicated the temporal lobe in 46%.PDF p.8, Seizure semiology localizing values
  • head version; temporal lobeThe 95% CI for head version; temporal lobe was 36%–57%.PDF p.8, Seizure semiology localizing values
  • head version; frontal lobeHead version implicated the frontal lobe in 33%.PDF p.8, Seizure semiology localizing values
  • head version; frontal lobeThe 95% CI for head version; frontal lobe was 24%–41%.PDF p.8, Seizure semiology localizing values
  • head version; frontal lobeHead version had a probability of 0.33 for frontal localization in the non-topological estimate.PDF p.8, Relative localizing values
  • head version; frontal lobeThe interval for the head-version frontal localization given head version probability was 0.24–0.41.PDF p.8, Relative localizing values
  • head version; temporal lobeHead version had a probability of 0.46 for temporal localization in the non-topological estimate.PDF p.8, Relative localizing values
  • head version; temporal lobeThe interval for the head-version temporal localization given head version probability was 0.36–0.57.PDF p.8, Relative localizing values
  • head version; frontal lobeHead version had an OR of 0.9 for frontal localization relative to the EUD-Loc prior.PDF p.8, Relative localizing values of semiologies
  • head version; frontal lobeThe 95% CI for head version; frontal lobe was 0.7–1.2.PDF p.8, Relative localizing values of semiologies
  • head version; temporal lobeHead version had an OR of 1.21 for temporal localization relative to the EUD-Loc prior.PDF p.8, Relative localizing values of semiologies
  • head version; temporal lobeThe 95% CI for head version; temporal lobe was 0.9–1.6.PDF p.8, Relative localizing values of semiologies
Reported values
  • head version 4.3%head versionPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • head version; temporal lobe 46%head version; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • head version; frontal lobe 33%head version; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • probability 0.33head version; frontal lobeProbability · non-topological localizing data pointsPDF p.8, Relative localizing values
  • probability 0.46head version; temporal lobeProbability · non-topological localizing data pointsPDF p.8, Relative localizing values
  • OR 0.9head version; frontal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
  • OR 1.21head version; temporal lobeOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • head version or orientationHead version or orientation was reported in 30% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
Reported values
  • 30% head orientationhead version or orientationPercentage · reviewed basal temporal seizure cases · ictal propagation in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Asymmetric ending seizure (subentries: Terminal clonus; p.3 additionally Versive)The tables list an asymmetric ending seizure as Ipsilateral; p.2 shows the subentry Terminal clonus, whereas p.3 shows Terminal clonus and Versive.PDF p.2, Lateralizing signs/Localization table row "Asymmetric ending seizure" with subentry "Terminal clonus" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Asymmetric ending seizure" with subentries "Terminal clonus" and "Versive" (printed p.5)
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Head versionHead-version semiology occurred in 1/61 individuals (2%) as initial semiology and 12/61 (20%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 1/61 (2%)Head versionPercentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 12/61 (20%)Head versionPercentage · n/N 12/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Head versionTable 3 associates head version during secondary generalized tonic-clonic seizures with premotor area (BA 6 and 8) and contralateral lateralisation.PDF p.4, Table 3
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 2 findings · 14 reported values
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.707
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • ATLP following head and eye versionAt the time of ATLP, the head was midline or returning to midline from version in all instances, and ATLP was on the same side as version in all but one Group II patient; the exception had left version followed by right version, right ATLP, and generalized clonic movements, with EEG higher over the left hemisphere.PDF p.3, Other characteristics of ATLP—item 2
  • ATLP and versionTable 1 reports patient-level joint version/ATLP categories as TLE: version+ATLP 8/16, version without ATLP 1/16, ATLP without version 4/16, neither 3/16; XTLE: 4/15, 4/15, 4/15, 3/15; Group II: 10/26, 12/26, 9/26, 0, respectively.PDF p.3, Table 1—Version and ATLP
Reported values
  • Head midline or returning to midline at ATLP in all instancesATLP following head and eye versionPercentage · Group II patients with ATLP and version; one symptomatic generalized epilepsy exception is described · ATLP after version and before generalized clonic movementsPDF p.3, Other characteristics of ATLP—item 2
  • ATLP on same side as version in all but one Group II patientATLP following head and eye versionPercentage · Group II patients with ATLP and version; one symptomatic generalized epilepsy exception is described · Group II with ATLP and version · ATLP after version and before generalized clonic movementsPDF p.3, Other characteristics of ATLP—item 2
  • XTLE Version + ATLP 4/15ATLP and versionPercentage · n/N 4/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; Version + ATLPPDF p.3, Table 1—Version and ATLP
  • Group II Version + ATLP 10/26ATLP and versionPercentage · n/N 10/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; Version + ATLPPDF p.3, Table 1—Version and ATLP
  • XTLE ATLP without version 4/15ATLP and versionPercentage · n/N 4/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; ATLP without versionPDF p.3, Table 1—Version and ATLP
  • TLE ATLP without version 4/16ATLP and versionPercentage · n/N 4/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; ATLP without versionPDF p.3, Table 1—Version and ATLP
  • XTLE Neither 3/15ATLP and versionPercentage · n/N 3/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; NeitherPDF p.3, Table 1—Version and ATLP
  • TLE Neither 3/16ATLP and versionPercentage · n/N 3/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; NeitherPDF p.3, Table 1—Version and ATLP
  • TLE Version + ATLP 8/16ATLP and versionPercentage · n/N 8/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; Version + ATLPPDF p.3, Table 1—Version and ATLP
  • Group II Version without ATLP 12/26ATLP and versionPercentage · n/N 12/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; Version without ATLPPDF p.3, Table 1—Version and ATLP
  • TLE Version without ATLP 1/16ATLP and versionPercentage · n/N 1/16 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · TLE; Version without ATLPPDF p.3, Table 1—Version and ATLP
  • Group II Neither 0/26ATLP and versionPercentage · n/N 0/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; NeitherPDF p.3, Table 1—Version and ATLP
  • XTLE Version without ATLP 4/15ATLP and versionPercentage · n/N 4/15 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · XTLE; Version without ATLPPDF p.3, Table 1—Version and ATLP
  • Group II ATLP without version 9/26ATLP and versionPercentage · n/N 9/26 · Group I TLE, Group I XTLE, and Group II patients represented in Table 1 · Group II; ATLP without versionPDF p.3, Table 1—Version and ATLP
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 1 finding · 3 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • head versionIn the unilateral TLE cohort, head version occurred only on the side contralateral to the EEG seizure focus.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
Reported values
  • 6 patientshead versionCount · n/N 6/19 · 19 patients with unilateral TLE; head version occurred in 6 patients · patients with head version · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 0 ipsilateral seizureshead versionCount · n/N 0/116 · 19 patients with unilateral TLE; head version occurred in 6 patients · ipsilateral to EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
  • 14 contralateral seizures (12% of all 116 seizures)head versionPercentage · n/N 14/116 · 19 patients with unilateral TLE; head version occurred in 6 patients · contralateral to EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfNarrative, educational, or cited context · 1 finding
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • adversive head and eye movement after parietal spreadThe source suggests that adversive head and eye movements may reflect spread from the superior parietal lobule to the frontal lobe.PDF p.10, Discussion

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal verbal automatismsReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side10 manuscripts · 14 findings · 21 reported values
Weighted evidence supportevidence weight 14.07 across 10 manuscripts · 4 case report or observation · 5 narrative, educational, or cited context · 1 independent primary study

The article restates that ictal speech automatisms are significantly more frequent with nondominant than dominant temporal-lobe seizure origin. The review restates left temporal resection association for dysphasia and a non-lateralizing result for speech automatisms. The review states that ictal foreign-language speech automatisms may occur with seizures originating in the nondominant hemisphere. The cited Hecaen and Angelergues report describes 32 ictal speech-automatism cases among 208 patients: EEG focus was left in 11, right in 13, and undecided in 8; 176/208 remaining cases were dysphasic. The cited review associates temporal verbal automatisms with the non-dominant language hemisphere and describes speech arrest/vocalization in cortical language areas. The cited Bingley study reported ictal speech automatisms more often with a unilateral nondominant EEG focus (10/17, 59%) than with a unilateral dominant focus (6/24, 25%; P=0.01). In the cited 32-patient series, EEG focus was right-lateralized in 13, left-lateralized in 11, and undecided in 8. The paper restates older studies as finding ictal speech automatism only slightly more common in the source-termed 'recessive temporal lobe' and of little lateralizing value. Comprehensible stereotyped ictal speech is described as suggesting a nondominant focus, while dominant-hemisphere lateralization of vocalizations remains controversial. No hemisphere or body-side direction is reported. No hemisphere or body-side direction is reported for the initial clinical semiology.

Source-defined result groups 6
Localization: TemporalObserved proportion 27.8%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 11.1%ML · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%L · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 12.5%M · M versus ML versus L · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 10

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • ictal speech arrest, vocalization, and verbal automatismsThe review states that most seizures involving cortical language areas reduce to speech arrest or vocalization depending on the involved area and its distance from ventral central regions; verbal automatisms occur in temporal seizures and are associated with the non-dominant language hemisphere, while aphasia-like abnormal production is less frequent.PDF p.7, section 8
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal speech automatism in cited studiesThe current paper reports that Serafetinides and Falconer (1963) found ictal speech automatism only slightly more common in the “recessive temporal lobe” and considered it of little lateralizing value, with similar results reported by Currie et al. (1971).PDF p.5, Discussion, ictal-speech paragraph
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal speech, verbal automatisms, and ictal vocalizationsIctal vocalizations and ictal speech are reported in TLE but are not exclusive to it; comprehensible stereotyped speech, including rare second-language automatisms, suggests a nondominant-hemisphere focus, whereas the lateralizing value of vocalizations toward the dominant hemisphere remains controversial.PDF p.8, Focal impaired awareness seizures
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfNarrative, educational, or cited context · 2 findings · 6 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • ictal speech automatismsThe source reports that Bingley observed ictal speech automatisms in 29 of 74 patients (39%) with nontumorous temporal-lobe epilepsy, including 6 of 24 (25%) with a unilateral dominant EEG focus and 10 of 17 (59%) with a unilateral nondominant EEG focus (p = 0.01).PDF p.5, Discussion
  • ictal speech automatismsThe source reports that Hecaen and Angelergues described 32 patients with ictal speech automatisms: 11 had a left-lateralized EEG focus, 13 a right-lateralized focus, and 8 were undecided.PDF p.5, Discussion
Reported values
  • Unilateral nondominant EEG focus 10/17 (59%)ictal speech automatismsPercentage · n/N 10/17 · Patients with nontumorous temporal-lobe epilepsy in the cited Bingley report · Unilateral nondominant EEG focus · ictalPDF p.5, Discussion
  • Ictal speech automatisms overall 29/74 (39%)ictal speech automatismsPercentage · n/N 29/74 · Patients with nontumorous temporal-lobe epilepsy in the cited Bingley report · Overall nontumorous TLE · ictalPDF p.5, Discussion
  • Unilateral dominant EEG focus 6/24 (25%)ictal speech automatismsPercentage · n/N 6/24 · Patients with nontumorous temporal-lobe epilepsy in the cited Bingley report · Unilateral dominant EEG focus · ictalPDF p.5, Discussion
  • 13/32ictal speech automatismsPercentage · n/N 13/32 · 32 patients with ictal speech automatisms in the cited Hecaen and Angelergues report · right-lateralized EEG focus · ictalPDF p.5, Discussion
  • 8/32ictal speech automatismsPercentage · n/N 8/32 · 32 patients with ictal speech automatisms in the cited Hecaen and Angelergues report · undecided EEG focus · ictalPDF p.5, Discussion
  • 11/32ictal speech automatismsPercentage · n/N 11/32 · 32 patients with ictal speech automatisms in the cited Hecaen and Angelergues report · left-lateralized EEG focus · ictalPDF p.5, Discussion
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • dysphasia; speech automatismsThe article reports that the Serafetinides and Falconer series described dysphasia as predominantly associated with left temporal resection, whereas speech automatisms did not show a lateralizing value.PDF p.3, Discussion
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 7 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • early verbal automatismsEarly verbal automatisms occurred only in ML patients in the displayed comparison, but the source reports discrepant p values for the same result: p=0.028 in Table 4 and p=0.004 in the adjacent Results prose.PDF p.6, Table 4; PDF p.6, Early features
  • late verbal automatismsLate verbal automatisms did not differ significantly across M, ML, and L groups.PDF p.7, Table 5; PDF p.7, Later features
Reported values
  • 5/18 (27.8%)early verbal automatismsPercentage · n/N 5/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 0/24 (0%)early verbal automatismsPercentage · n/N 0/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 0/13 (0%)early verbal automatismsPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • p=0.4late verbal automatismsP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
  • L=0/13 (0%)late verbal automatismsPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
  • ML=2/18 (11.1%)late verbal automatismsPercentage · n/N 2/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
  • M=3/24 (12.5%)late verbal automatismsPercentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 2 findings · 1 reported value
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • ictal speech automatismsThe article states that these automatisms are significantly more frequent in seizures originating from the non-dominant than the dominant temporal lobe.PDF p.1, left column, paragraph beginning “Ictal speech automatisms”
  • ictal speech automatisms or verbalisationsThe article states that ictal speech automatisms or verbalisations occur in 12%–39% of patients with drug-resistant temporal lobe epilepsy.PDF p.1, left column, paragraph beginning “Ictal speech automatisms”
Reported values
  • 12%–39% occurrence rangeictal speech automatisms or verbalisationsPercentage · patients with drug-resistant temporal lobe epilepsy · ictalPDF p.1, left column, paragraph beginning “Ictal speech automatisms”
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding · 2 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 1 gelastic, singing, whistling, and verbal-automatism semiologyCase 1 was a 27-year-old right-handed woman whose seizures began at age 9 with uncontrollable laughter without associated emotion, sometimes singing or whistling, and sometimes repeated vocalizations such as “it doesn’t matter” or “no, no”; she could have a nonspecific “lucidity” warning, was usually aware with possible cognitive slowing, had nocturnal predominance without postictal deficit, and had 10–25-second seizures occurring 1–4 times per day.PDF p.8, Case 1; PDF p.8, Video-EEG data
Reported values
  • Seizure duration 10–25 secondsCase 1 gelastic, singing, whistling, and verbal-automatism semiologyRange · Individual Case 1; 27-year-old right-handed woman, seizure onset age 9 · Ictal; aura/warning and postictal observationPDF p.8, Case 1; PDF p.8, Video-EEG data
  • Seizure frequency 1–4 per dayCase 1 gelastic, singing, whistling, and verbal-automatism semiologyRange · Individual Case 1; 27-year-old right-handed woman, seizure onset age 9 · Ictal; aura/warning and postictal observationPDF p.8, Case 1; PDF p.8, Video-EEG data
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfNarrative, educational, or cited context · 1 finding · 5 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • ictal speech automatism; dysphasic speech disorderThe current article reports that Hecaen and Angelergues described 32 cases of ictal speech automatism among 208 epileptic patients with paroxysmal speech disorders; EEG focus was left-sided in 11, right-sided in 13, and undecided in 8, while the remaining 176 cases were dysphasic.PDF p.10, discussion of prior speech-automatism reports
Reported values
  • 13 of 32ictal speech automatism; dysphasic speech disorderPercentage · n/N 13/32 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · speech automatism; right-sided EEG focus · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 8 of 32ictal speech automatism; dysphasic speech disorderPercentage · n/N 8/32 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · speech automatism; undecided EEG focus · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 32 cases ... among 208ictal speech automatism; dysphasic speech disorderPercentage · n/N 32/208 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · ictal speech automatism · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 176/208ictal speech automatism; dysphasic speech disorderPercentage · n/N 176/208 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · dysphasic speech disorder · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
  • 11 of 32ictal speech automatism; dysphasic speech disorderPercentage · n/N 11/32 · Hecaen and Angelergues’ cited 208 epileptic patients with paroxysmal speech disorders · speech automatism; left-sided EEG focus · Ictal speech automatism or dysphasic speech disorderPDF p.10, discussion of prior speech-automatism reports
unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 2 findings
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • ictal foreign language speech automatismsThe review states that ictal foreign language speech automatisms may complicate seizures originating in the non-dominant hemisphere.PDF p.2, §2 paragraph beginning “Speech automatisms may be divided”
  • ictal speech automatismsThe review identifies singing, humming, and laughing as typical ictal speech automatisms and describes reiterative neologisms as rare ictal speech automatisms.PDF p.2, §2 paragraph beginning “Speech automatisms may be divided”

10 contributing manuscripts; source-reported values remain separate and are not pooled.

Chapeau de gendarme sign (bilateral forced lip-corner retraction)Source terms: Chapeau de gendarme signReported: BilateralAlso reported: Ipsilateral4 manuscripts · 127 findings · 96 reported values
Weighted evidence supportevidence weight 14.01 across 4 manuscripts · 1 independent primary study · 3 systematic review or meta-analysis

The review describes bilateral lip and chin contraction in chapeau de gendarme or ictal pout, with no source-supported hemispheric direction. The canonical definition requires symmetrical lowering of the labial commissures with chin contraction. The review reports no apparent lateralizing value for Chapeau de gendarme semiology. left anterior/middle cingulate, central operculum, and insula on FDG-PET; hemisphere source-explicit The illustrated case is source-explicitly left-sided through the left cingulate discharge context. left anterior/middle cingulate gyrus, central operculum, and insula The case context is explicitly left-sided. The case retains a left-side context for the cingulate-onset seizure with secondary opercular propagation. The source supports unilateral/asymmetric-bilateral perioral activity and reports three ipsilateral cases, but the ipsilateral reference side is not defined at the result locus. The review lists multiple bilateral/symmetrical facial descriptors but explicitly warns that the labels do not always refer to the same feature. No lateralizing direction is reported for the frontal-localization restatement. No source lateralization is reported. The educational differentiation framework contains no lateralization evidence. No lateralization evidence is reported. The temporal timing table gives no hemisphere or body-side direction. The unknown-timing category gives no hemisphere or body-side direction. The basal-frontal EZ distribution gives no hemisphere direction. The lateral-frontal EZ distribution gives no hemisphere direction. The nonspecific frontal EZ category gives no hemisphere direction. The temporal EZ distribution gives no hemisphere direction. The temporo-parietal EZ distribution gives no hemisphere direction. The high-confidence lateral-frontal EZ distribution gives no hemisphere direction. The high-confidence temporal EZ distribution gives no hemisphere direction. The low-confidence mesial-frontal EZ distribution gives no hemisphere direction. The low-confidence lateral-frontal EZ distribution gives no hemisphere direction. The mesial-versus-lateral frontal occurrence ratio gives no hemisphere direction. The mesial-frontal versus insulo-opercular ratio gives no hemisphere direction. No lateralizing direction is reported. The cited emotional-expression statement reports no hemisphere or lateralization direction. Left-side context is not treated as a separate source-stated lateralization assertion. No independent lateralization evidence is reported for the FCD2A pathology finding. No lateralization result is reported. The cited patient count gives no hemisphere or lateralization information. No lateralization axis information is reported for chapeau de gendarme versus affective/autonomic aura. No hemisphere or body-side direction is reported. Figure 6 reports OR 4.9 for Affective/autonomic aura relative to Chapeau de gendarme, with no hemisphere or lateralization direction.

Source-defined result groups 29
Localization: FrontalSource-defined values retained separatelyAll reported · propagation and unknown timing · cases1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · other regions among very-high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · onset and unknown timing · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · onset and propagation · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · onset and propagation · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · other regions among very-high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · propagation and unknown timing · cases1 manuscript · 1 reported value · not pooled
Localization: Parietal / TemporalSource-defined values retained separatelyAll reported · other reported brain regions · patients/cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · other reported brain regions · patients/cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · propagation and unknown timing · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · other regions among very-high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · insulo-opercular, lateral frontal, basal frontal, temporal, and temporo-parietal regions · patients/cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · onset and propagation · cases1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other regions among high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other regions among very-high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · other reported brain regions · patients/cases1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 5.0%All reported · other Cebeci study patients · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 11.8%All reported · other Zhang study patients · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · lateral frontal region · region occurrence rate1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / IpsilateralObserved proportion 50.0%unilateral or asymmetric bilateral perioral focal tonic seizures · symmetric facial tonic contraction · patient1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · other regions among high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: Frontal / Parietal / TemporalSource-defined values retained separatelyAll reported · other regions among very-high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other reported brain regions · patients/cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · onset and unknown timing · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · insulo-opercular region · region occurrence rate1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · other regions among very-high-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · onset and unknown timing · cases1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · lateral frontal and insulo-opercular regions among low-confidence cases · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyAll reported · mesial frontal and insulo-opercular regions among low-confidence cases · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 4

Alphabetical by manuscript.

chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 32 findings · 30 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • chapeau de gendarme; ictal poutingThe source reports a frequency of 20% for chapeau de gendarme; ictal pouting.PDF p.13, Table 3
  • chapeau de gendarme; ictal pouting; reported frequency rangeThe source reports a frequency range of 0–100% for chapeau de gendarme; ictal pouting.PDF p.13, Table 3
  • chapeau de gendarme; ictal pouting; ACC association gradeTable 3 assigns the source's High overall association grade to chapeau de gendarme; ictal pouting.PDF p.13, Table 3
  • chapeau de gendarme; Figure 4 rateFigure 4 displays a 20.4% rate for chapeau de gendarme.PDF p.10, Figure 4
  • pairwise OR: Chapeau de gendarme relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Autonomic signsFigure 6 reports an odds ratio of 0.3 for Chapeau de gendarme relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Facial expression changeFigure 6 reports an odds ratio of 0.3 for Chapeau de gendarme relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.3 for Chapeau de gendarme relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.5 for Chapeau de gendarme relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.6 for Chapeau de gendarme relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 6.1 for Vocalization/verbalization relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 5.8 for Hypermotor-complex motor behavior relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 4.9 for Affective/autonomic aura relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 3.6 for Autonomic signs relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 3.3 for Facial expression change relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 2.9 for Motor (gestural) automatisms relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 2.1 for Loss of consciousness relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 1.7 for Post-ictal confusion/behavior change disinhibition relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.9 for Dystonic posturing relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.6 for Head-eye deviation relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.4 for Laughter relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.4 for Oro-alimentary automatisms relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.4 for Tonic-clonic relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.2 for F to BTC relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Dystonic posturingFigure 6 reports an odds ratio of 1.1 for Chapeau de gendarme relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Head-eye deviationFigure 6 reports an odds ratio of 1.6 for Chapeau de gendarme relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to LaughterFigure 6 reports an odds ratio of 2.4 for Chapeau de gendarme relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 2.7 for Chapeau de gendarme relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Tonic-clonicFigure 6 reports an odds ratio of 4.5 for Chapeau de gendarme relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to F to BTCFigure 6 reports an odds ratio of 4.5 for Chapeau de gendarme relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 20% (frequency range 0–100%)chapeau de gendarme; ictal poutingPercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.13, Table 3
  • 20.4%chapeau de gendarme; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.10, Figure 4
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Chapeau de gendarme relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Chapeau de gendarme relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Chapeau de gendarme relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Chapeau de gendarme relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Chapeau de gendarme relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.1pairwise OR: Vocalization/verbalization relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.8pairwise OR: Hypermotor-complex motor behavior relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.9pairwise OR: Affective/autonomic aura relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Autonomic signs relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.3pairwise OR: Facial expression change relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Motor (gestural) automatisms relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Loss of consciousness relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Dystonic posturing relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Head-eye deviation relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Laughter relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Oro-alimentary automatisms relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Tonic-clonic relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: F to BTC relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Chapeau de gendarme relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Chapeau de gendarme relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.4pairwise OR: Chapeau de gendarme relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.7pairwise OR: Chapeau de gendarme relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.5pairwise OR: Chapeau de gendarme relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.5pairwise OR: Chapeau de gendarme relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • chapeau de gendarme; ictal pout signThe chapeau de gendarme or ictal pout sign is a downturned mouth caused by bilateral lip and chin contraction and, when seen early in a seizure, is described as highly localising to frontal onset, particularly anterior cingulate, orbitofrontal, mesio-prefrontal, or premotor cortex.PDF p.9, Chapeau de gendarme
  • chapeau de gendarme; ictal pout signThe chapeau de gendarme or ictal pout sign is a downturned mouth caused by bilateral lip and chin contraction and, when seen early in a seizure, is described as highly localising to frontal onset, particularly anterior cingulate, orbitofrontal, mesio-prefrontal, or premotor cortex.PDF p.9, Chapeau de gendarme
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 92 findings · 63 reported values
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • chapeau de gendarme canonical definitionThe source gives the original definition as symmetrical and sustained (>5 s) lowering of the labial commissures with chin contraction, mimicking fear, disgust, or menace.PDF p.4, Study characteristics; PDF p.13, Limitations
  • lateralizing valueThe review states that no apparent lateralizing value has been attributed to the chapeau de gendarme semiology.PDF p.12, Discussion
  • figure 2 chapeau de gendarme caseFigure 2 describes a 16-year-old girl with sleep-related hypermotor epilepsy and the chapeau de gendarme sign.PDF p.7, Figure 2
  • early chapeau de gendarme timing in figure 2 caseIn the Figure 2 case, the sign occurred five seconds after the first clinical change.PDF p.7, Figure 2
  • sustained component duration in figure 2 caseThe sustained component of the sign lasted seven seconds in the Figure 2 case.PDF p.7, Figure 2
  • FDG-PET localization in figure 2 caseFDG-PET showed hypometabolic areas involving the anterior/middle cingulate gyrus, central operculum, and insula on the left side.PDF p.7, Figure 2
  • cingulate discharge origin in figure 2 caseSEEG in the Figure 2 case showed discharge originating in the cingulate gyrus at the junction of the anterior and middle cingulate parts.PDF p.7, Figure 2
  • secondary opercular propagation in figure 2 casePropagation to the opercular areas occurred secondarily in the Figure 2 case.PDF p.7, Figure 2
  • semiologic synonym setThe review records non-identical descriptions including “pouting,” “bilateral tonic facial contraction,” “symmetrical down-turned mouth,” “grimacing,” “inverted smile with a tearful expression,” “mouth turning down with symmetric puckering,” and “labial corners lowered with chin contraction.”PDF p.2, Introduction; PDF p.4, Study characteristics
  • chapeau de gendarme / ictal poutingThe review describes the “chapeau de gendarme” sign, also known as ictal pouting, as a distinctive focal-epilepsy facial expression with a turned-down mouth and symmetrical contraction of the lips and chin.PDF p.1, Abstract; PDF p.2, Introduction
  • timing and duration of mouth contractionThe review states that primary versus secondary occurrence, brief versus prolonged duration, and associated facial-expression or motor behavior must be considered when differentiating mouth-contraction manifestations.PDF p.4, Study characteristics
  • focal cortical dysplasia histopathologyFCD was the most common histopathological finding and was identified in 75% of resected cases.PDF p.6, Patient characteristics; PDF p.12, Substrate discussion
  • prodromal componentA video-analysis study described a prodromal component marked by vertical constriction of the lips and chin resembling forced mouth closure.PDF p.4, Study characteristics
  • major componentThe same video-analysis study described a major component with symmetrical downward contraction of the mouth corners.PDF p.4, Study characteristics
  • FCD type 2 histopathologyThe review reports that 59% of the histopathological cases were FCD type 2.PDF p.6, Patient characteristics; PDF p.12, Substrate discussion
  • FCD type 1 histopathologyThe review reports that 11% of the histopathological cases were FCD type 1.PDF p.6, Patient characteristics
  • FCD not further specifiedThe review reports that 23% of the histopathological cases were FCD not further specified.PDF p.6, Patient characteristics
  • tumors or vascular malformationsThe review reports that the remaining 7% of histopathological cases included tumors or vascular malformations.PDF p.6, Patient characteristics
  • mesial frontal EZ localizationThe EZ was localized to the mesial frontal region in 43% of cases.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • insulo-opercular EZ localizationThe EZ was localized to the insulo-opercular region in 21% of cases.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • lateral frontal EZ localizationThe EZ was localized to the lateral frontal region in 15% of cases.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • basal frontal EZ localizationThe EZ was localized to the basal frontal region in 10% of cases.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • temporal EZ localizationThe EZ was localized to the temporal region in 10% of cases.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • temporo-parietal EZ localizationThe EZ was localized to the temporo-parietal region in 1% of cases.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • mesial frontal seizure onsetAmong mesial frontal cases with timing information, 38% were associated with seizure onset.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • mesial frontal propagationAmong mesial frontal cases with timing information, 17% were associated with propagation.PDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • mesial frontal timing unknownTiming relative to seizure onset was unknown in 45% of mesial frontal cases in Table 6.PDF p.12, Table 6
  • basal frontal seizure onsetAmong basal frontal cases with timing information, 14% were associated with seizure onset.PDF p.12, Table 6
  • basal frontal propagationAmong basal frontal cases with timing information, 29% were associated with propagation.PDF p.12, Table 6
  • basal frontal timing unknownTiming relative to seizure onset was unknown in 57% of basal frontal cases in Table 6.PDF p.12, Table 6
  • lateral frontal seizure onsetAmong lateral frontal cases with timing information, 50% were associated with seizure onset.PDF p.12, Table 6
  • lateral frontal propagationAmong lateral frontal cases with timing information, 20% were associated with propagation.PDF p.12, Table 6
  • lateral frontal timing unknownTiming relative to seizure onset was unknown in 30% of lateral frontal cases in Table 6.PDF p.12, Table 6
  • insulo-opercular seizure onsetAmong insulo-opercular cases with timing information, 7% were associated with seizure onset.PDF p.12, Table 6
  • insulo-opercular propagationAmong insulo-opercular cases with timing information, 21% were associated with propagation.PDF p.12, Table 6
  • insulo-opercular timing unknownTiming relative to seizure onset was unknown in 72% of insulo-opercular cases in Table 6.PDF p.12, Table 6
  • temporal seizure onsetAmong temporal cases with timing information, 29% were associated with seizure onset.PDF p.12, Table 6
  • temporal propagationAmong temporal cases with timing information, 14% were associated with propagation.PDF p.12, Table 6
  • temporal timing unknownTiming relative to seizure onset was unknown in 57% of temporal cases in Table 6.PDF p.12, Table 6
  • temporo-parietal propagationThe temporo-parietal EZ case was classified as propagation rather than seizure onset in Table 6.PDF p.12, Table 6
  • very-high EZ confidenceEZ localization confidence was rated very high in 72% of patients.PDF p.7, Anatomo-clinical correlations
  • mesial frontal among very-high-confidence casesMesial frontal localization represented 41% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • basal frontal among very-high-confidence casesBasal frontal localization represented 14% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • lateral frontal among very-high-confidence casesLateral frontal localization represented 14% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • frontal without sublobar specification among very-high-confidence casesFrontal localization without sublobar specification represented 6% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • insulo-opercular among very-high-confidence casesInsulo-opercular localization represented 17% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • temporal among very-high-confidence casesTemporal localization represented 6% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • temporo-parietal among very-high-confidence casesTemporo-parietal localization represented 2% of the very-high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • high EZ confidenceEZ localization confidence was rated high in 22% of patients.PDF p.7, Anatomo-clinical correlations
  • mesial frontal among high-confidence casesMesial frontal localization represented 38% of the high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • lateral frontal among high-confidence casesLateral frontal localization represented 12% of the high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • insulo-opercular among high-confidence casesInsulo-opercular localization represented 25% of the high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • temporal among high-confidence casesTemporal localization represented 25% of the high-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • mesial frontal among low-confidence casesMesial frontal localization represented 50% of the low-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • lateral frontal among low-confidence casesLateral frontal localization represented 25% of the low-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • insulo-opercular among low-confidence casesInsulo-opercular localization represented 25% of the low-confidence EZ cases.PDF p.7, Anatomo-clinical correlations
  • mesial frontal occurrence ratioThe mesial frontal occurrence rate was 4.14 times higher than the basal frontal and temporal occurrence rates.PDF p.7, Pairwise analysis
  • mesial frontal versus basal/temporal occurrence p valueThe pairwise difference between mesial frontal and basal frontal/temporal occurrence rates had p < .001.PDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • mesial frontal occurrence ratio versus lateral frontalThe mesial frontal occurrence rate was 2.90 times higher than the lateral frontal occurrence rate.PDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • mesial frontal versus lateral frontal occurrence p valueThe pairwise difference between mesial frontal and lateral frontal occurrence rates had p = .0049.PDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • mesial frontal occurrence ratio versus insulo-opercularThe mesial frontal occurrence rate was 2.07 times higher than the insulo-opercular occurrence rate.PDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • mesial frontal versus insulo-opercular occurrence p valueThe pairwise difference between mesial frontal and insulo-opercular occurrence rates had p = .07.PDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • other brain-region pairwise differencesNo significant differences were detected among the other brain regions in the pairwise analysis.PDF p.7, Pairwise analysis
  • frontal and mesial frontal associationThe review assigns strong evidence associating the sign with frontal EZ localization, particularly mesial frontal localization.PDF p.7, Overall summary of evidence; PDF p.13, Conclusion
  • insulo-opercular associationThe review assigns moderate evidence suggesting potential involvement or origin in the insulo-opercular cortex.PDF p.7, Overall summary of evidence; PDF p.13, Conclusion
  • first localizing study cohortThe first study describing chapeau de gendarme as a localizing feature included 11 cases.PDF p.8, Discussion
  • ACC primary generation in first studyACC was the primary region of generation in all but one case of the 11-case first study, corresponding to 10/11 cases under the source wording.PDF p.8, Discussion
  • insulo-opercular origin with spread to ACCIn the remaining case of the first study, the sign originated in the insulo-opercular cortex with secondary spread to the ACC.PDF p.8, Discussion
  • negative emotional expressionsThe first study associated the sign with negative emotions including disgust, distress, displeasure, disappointment, disapproval, disagreement, and doubt.PDF p.8, Discussion
  • affective ACC expressionStronger emotional expressions such as fear or menace, with open eyes, hypermotor, and autonomic features, were linked to the rostroventral “affective” ACC.PDF p.8, Discussion
  • cognitive ACC expressionMilder expressions such as discontent, disappointment, disagreement, or doubt, with closed eyes and without hypermotor features, were linked to the dorsal “cognitive” ACC.PDF p.8, Discussion
  • SSMA-associated chapeau de gendarmeThe sign was observed in tonic seizures arising from the supplementary sensorimotor area in nine cases.PDF p.8, Discussion
  • SSMA feature specificityThe review characterizes the sign as a common but non-specific feature of SSMA epilepsy.PDF p.8, Discussion
  • FCD type 2 association cautionThe review states that the observed FCD pattern does not imply a specific link between the sign and FCD, particularly FCD type 2.PDF p.12, Substrate discussion
  • multimodal presurgical evaluationThe review recommends evaluating the sign with electrophysiological and neuroimaging data, including EEG, MRI, and FDG-PET, especially when MRI is negative.PDF p.13, Clinical value; PDF p.13, Conclusion
  • non-painful sensation in the eyesThe first clinical symptom in the Figure 2 case was a non-painful sensation in the eyes.PDF p.7, Figure 2
  • hand-to-eye movementA hand-to-eye movement followed the non-painful eye sensation in the Figure 2 case.PDF p.7, Figure 2
  • forced eye closureForced eye closure preceded or accompanied the chapeau de gendarme sign in the Figure 2 case.PDF p.7, Figure 2
  • persistence during hypermotor phaseThe chapeau de gendarme sign persisted during the hypermotor phase and correlated with extensive mesial frontal involvement in the Figure 2 case.PDF p.7, Figure 2
  • FCD type IIA in figure 2 caseHistopathology in the Figure 2 case confirmed focal cortical dysplasia type IIA (FCD2A).PDF p.7, Figure 2
  • Sitthinamsuwan chapeau de gendarme regional-linkage casesTable 1 reports nine Sitthinamsuwan patients in whom chapeau de gendarme semiology could be linked to a specific brain region.PDF p.5, Table 1
  • Sitthinamsuwan chapeau de gendarme described casesThe Sitthinamsuwan study described the sign in 12 patients.PDF p.5, Table 1
  • Souirti chapeau de gendarme casesTable 1 reports 11 Souirti patients with chapeau de gendarme.PDF p.5, Table 1
  • Lu chapeau de gendarme casesTable 1 reports 10 Lu patients with chapeau de gendarme.PDF p.5, Table 1
  • Yu chapeau de gendarme casesTable 1 reports seven Yu patients with chapeau de gendarme.PDF p.5, Table 1
  • Zhao chapeau de gendarme casesTable 1 reports four Zhao patients with chapeau de gendarme.PDF p.5, Table 1
  • Xu chapeau de gendarme casesTable 1 reports three Xu patients with chapeau de gendarme.PDF p.5, Table 1
  • Cebeci chapeau de gendarme casesTable 1 reports three Cebeci patients with chapeau de gendarme.PDF p.5, Table 1
  • Wang 2019 chapeau de gendarme casesTable 1 reports two Wang 2019 patients with chapeau de gendarme.PDF p.5, Table 1
  • Zhang chapeau de gendarme casesTable 1 reports two Zhang patients with chapeau de gendarme.PDF p.5, Table 1
  • Chibane chapeau de gendarme casesTable 1 reports two Chibane patients with chapeau de gendarme.PDF p.5, Table 1
  • van Dalen chapeau de gendarme casesTable 1 reports two van Dalen patients with chapeau de gendarme.PDF p.5, Table 1
Reported values
  • >5 secondschapeau de gendarme canonical definitionDuration Threshold · the source's own semiology definition · ictal; duration criterion explicitPDF p.4, Study characteristics; PDF p.13, Limitations
  • 5 seconds after first clinical changeearly chapeau de gendarme timing in figure 2 caseLatency · one 16-year-old girl in Figure 2 · early ictalPDF p.7, Figure 2
  • 7 secondssustained component duration in figure 2 caseDuration · one 16-year-old girl in Figure 2 · ictalPDF p.7, Figure 2
  • 75% FCD histopathologyfocal cortical dysplasia histopathologyPercentage · patients undergoing resective epilepsy surgery with histopathology · postoperative pathologyPDF p.6, Patient characteristics; PDF p.12, Substrate discussion
  • 59% FCD type 2FCD type 2 histopathologyPercentage · resected cases with histopathological findings · postoperative pathologyPDF p.6, Patient characteristics; PDF p.12, Substrate discussion
  • 11% FCD type 1FCD type 1 histopathologyPercentage · resected cases with histopathological findings · postoperative pathologyPDF p.6, Patient characteristics
  • 23% FCD not further specifiedFCD not further specifiedPercentage · resected cases with histopathological findings · postoperative pathologyPDF p.6, Patient characteristics
  • 7% tumors or vascular malformationstumors or vascular malformationsPercentage · resected cases with histopathological findings · postoperative pathologyPDF p.6, Patient characteristics
  • 43% mesial frontal localizationmesial frontal EZ localizationPercentage · review cases with EZ localization · EZ localizationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 21% insulo-opercular localizationinsulo-opercular EZ localizationPercentage · review cases with EZ localization · EZ localizationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 15% lateral frontal localizationlateral frontal EZ localizationPercentage · review cases with EZ localization · EZ localizationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 10% basal frontal localizationbasal frontal EZ localizationPercentage · review cases with EZ localization · EZ localizationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 10% temporal localizationtemporal EZ localizationPercentage · review cases with EZ localization · EZ localizationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 1% temporo-parietal localizationtemporo-parietal EZ localizationPercentage · review cases with EZ localization · EZ localizationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 38% onsetmesial frontal seizure onsetPercentage · mesial frontal EZ cases with onset/propagation timing information · seizure onsetPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 17% propagationmesial frontal propagationPercentage · mesial frontal EZ cases with onset/propagation timing information · propagationPDF p.6, Anatomo-clinical correlations; PDF p.12, Table 6
  • 45% timing unknownmesial frontal timing unknownPercentage · mesial frontal EZ cases with onset/propagation timing assessment · timing unknownPDF p.12, Table 6
  • 14% onsetbasal frontal seizure onsetPercentage · basal frontal EZ cases with onset/propagation timing information · seizure onsetPDF p.12, Table 6
  • 29% propagationbasal frontal propagationPercentage · basal frontal EZ cases with onset/propagation timing information · propagationPDF p.12, Table 6
  • 57% timing unknownbasal frontal timing unknownPercentage · basal frontal EZ cases with onset/propagation timing assessment · timing unknownPDF p.12, Table 6
  • 50% onsetlateral frontal seizure onsetPercentage · lateral frontal EZ cases with onset/propagation timing information · seizure onsetPDF p.12, Table 6
  • 20% propagationlateral frontal propagationPercentage · lateral frontal EZ cases with onset/propagation timing information · propagationPDF p.12, Table 6
  • 30% timing unknownlateral frontal timing unknownPercentage · lateral frontal EZ cases with onset/propagation timing assessment · timing unknownPDF p.12, Table 6
  • 7% onsetinsulo-opercular seizure onsetPercentage · insulo-opercular EZ cases with onset/propagation timing information · seizure onsetPDF p.12, Table 6
  • 21% propagationinsulo-opercular propagationPercentage · insulo-opercular EZ cases with onset/propagation timing information · propagationPDF p.12, Table 6
  • 72% timing unknowninsulo-opercular timing unknownPercentage · insulo-opercular EZ cases with onset/propagation timing assessment · timing unknownPDF p.12, Table 6
  • 29% onsettemporal seizure onsetPercentage · temporal EZ cases with onset/propagation timing information · seizure onsetPDF p.12, Table 6
  • 14% propagationtemporal propagationPercentage · temporal EZ cases with onset/propagation timing information · propagationPDF p.12, Table 6
  • 57% timing unknowntemporal timing unknownPercentage · temporal EZ cases with onset/propagation timing assessment · timing unknownPDF p.12, Table 6
  • 72% very-high confidencevery-high EZ confidencePercentage · review patients with EZ confidence grading · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 41% of very-high-confidence casesmesial frontal among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 14% of very-high-confidence casesbasal frontal among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 14% of very-high-confidence caseslateral frontal among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 6% of very-high-confidence casesfrontal without sublobar specification among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 17% of very-high-confidence casesinsulo-opercular among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 6% of very-high-confidence casestemporal among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 2% of very-high-confidence casestemporo-parietal among very-high-confidence casesPercentage · very-high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 22% high confidencehigh EZ confidencePercentage · review patients with EZ confidence grading · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 38% of high-confidence casesmesial frontal among high-confidence casesPercentage · high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 12% of high-confidence caseslateral frontal among high-confidence casesPercentage · high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 25% of high-confidence casesinsulo-opercular among high-confidence casesPercentage · high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 25% of high-confidence casestemporal among high-confidence casesPercentage · high-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 50% of low-confidence casesmesial frontal among low-confidence casesPercentage · low-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 25% of low-confidence caseslateral frontal among low-confidence casesPercentage · low-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • 25% of low-confidence casesinsulo-opercular among low-confidence casesPercentage · low-confidence EZ cases · EZ confidence assessmentPDF p.7, Anatomo-clinical correlations
  • ratio 4.14mesial frontal occurrence ratioRatio · brain-region EZ occurrence comparisons · pairwise analysisPDF p.7, Pairwise analysis
  • ratio 2.90mesial frontal occurrence ratio versus lateral frontalRatio · brain-region EZ occurrence comparisons · pairwise analysisPDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • ratio 2.07mesial frontal occurrence ratio versus insulo-opercularRatio · brain-region EZ occurrence comparisons · pairwise analysisPDF p.7, Pairwise analysis; PDF p.12, Figure 5
  • all but one case in an 11-case studyACC primary generation in first studyProportion · 11-case Souirti et al. cohort · seizure generationPDF p.8, Discussion
  • 1 caseinsulo-opercular origin with spread to ACCCount · n/N 1/11 · one case in the 11-case Souirti et al. cohort · seizure onset and propagationPDF p.8, Discussion
  • 9 casesSSMA-associated chapeau de gendarmeCount · Sitthinamsuwan et al. SSMA-origin tonic seizure series · tonic ictal seizuresPDF p.8, Discussion
  • 9 patients with regional linkageSitthinamsuwan chapeau de gendarme regional-linkage casesCount · n/N 9/22 · Sitthinamsuwan 2016 study population · study cohortPDF p.5, Table 1
  • 12 patients with chapeau de gendarmeSitthinamsuwan chapeau de gendarme described casesCount · n/N 12/22 · Sitthinamsuwan 2016 study population · study cohortPDF p.5, Table 1
  • 11 patients with chapeau de gendarmeSouirti chapeau de gendarme casesCount · n/N 11/36 · Souirti 2014 study population · study cohortPDF p.5, Table 1
  • 10 patients with chapeau de gendarmeLu chapeau de gendarme casesCount · n/N 10/10 · Lu 2021 study population · study cohortPDF p.5, Table 1
  • 7 patients with chapeau de gendarmeYu chapeau de gendarme casesCount · n/N 7/13 · Yu 2018 study population · study cohortPDF p.5, Table 1
  • 4 patients with chapeau de gendarmeZhao chapeau de gendarme casesCount · n/N 4/27 · Zhao 2021 study population · study cohortPDF p.5, Table 1
  • 3 patients with chapeau de gendarmeXu chapeau de gendarme casesCount · n/N 3/3 · Xu 2021 study population · study cohortPDF p.5, Table 1
  • 3 patients with chapeau de gendarmeCebeci chapeau de gendarme casesCount · n/N 3/60 · Cebeci 2019 study population · study cohortPDF p.5, Table 1
  • 2 patients with chapeau de gendarmeWang 2019 chapeau de gendarme casesCount · n/N 2/22 · Wang 2019 study population · study cohortPDF p.5, Table 1
  • 2 patients with chapeau de gendarmeZhang chapeau de gendarme casesCount · n/N 2/17 · Zhang 2019 study population · study cohortPDF p.5, Table 1
  • 2 patients with chapeau de gendarmeChibane chapeau de gendarme casesCount · n/N 2/16 · Chibane 2017 study population · study cohortPDF p.5, Table 1
  • 2 patients with chapeau de gendarmevan Dalen chapeau de gendarme casesCount · n/N 2/50 · van Dalen 2024 study population · study cohortPDF p.5, Table 1
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 3 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • focal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionFocal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas occurred in 11 patients, with ipsilateral involvement reported in three, while four patients had symmetric facial tonic contraction including pouting, grimace, or bilateral eyelid tonic closure.PDF p.3, Results—Seizure semiology; PDF p.5, Table 1
Reported values
  • four (18%)focal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionPercentage · n/N 4/22 · 22 patients with insulo-opercular epilepsy · symmetric facial tonic contraction · early ictal motor signPDF p.3, Results—Seizure semiology; PDF p.5, Table 1
  • 11/22 (50%)focal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionPercentage · n/N 11/22 · 22 patients with insulo-opercular epilepsy · unilateral or asymmetric bilateral perioral focal tonic seizures · early ictal motor signPDF p.3, Results—Seizure semiology; PDF p.5, Table 1
  • three patientsfocal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionCount · 22 patients with insulo-opercular epilepsy · ipsilateral involvement within the perioral group · early ictal motor signPDF p.3, Results—Seizure semiology; PDF p.5, Table 1

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal tachycardiaReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side8 manuscripts · 14 findings · 11 reported values
Weighted evidence supportevidence weight 14 across 8 manuscripts · 1 independent primary study · 2 systematic review or meta-analysis · 5 narrative, educational, or cited context

The cited series reports tachycardia or bradycardia with bilateral insular stimulation, with posterior-versus-anterior subregional differences and mild left-right asymmetry. The cited table describes tachycardia/hyperventilation as non-lateralising and often right. The cited review reports tachycardia above 100 bpm in more than 50% of seizures, greater early tachycardia in temporal than extratemporal epilepsy with right MTLE emphasis, and no localizing or lateralizing value for bradycardia below 60 bpm. The review describes ictal tachycardia/bradycardia as more frequent in temporal impaired-awareness seizures, particularly left-hemisphere cases, with slight MTLE predominance in some studies. No sign-specific hemisphere direction is reported; left is retained only as the source-side case context. No sign-specific hemisphere direction is reported; right is retained only as the source-side case context. No lateralizing direction is reported for the vegetative-sign result. No seizure lateralization is reported. No lateralizing direction is reported. No lateralizing direction is reported for the restricted high/very-high-confidence subset. No lateralizing direction is reported for the mesial-temporal/amygdalar association.

Source-defined result groups 3
Localization: FrontalObserved proportion 9.5%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 8.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 11.1%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Tachycardia (Table 3)Table 3 reports tachycardia in 3 cases (4%), more at seizure onset.PDF p.6, Table 3
  • Tachycardia (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports tachycardia in 4 cases (7%).PDF p.7, Table 4
Reported values
  • 3 cases (4%)Tachycardia (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 4/60 (7%)Tachycardia (Table 4)Percentage · n/N 4/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfNarrative, educational, or cited context · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • early apnoea and tachycardia; amygdala involvementThe review states that early apnoea and tachycardia in mesial temporal lobe seizures indicate involvement of the amygdala.PDF p.5, Mesial temporal lobe including hippocampus
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal tachycardia, bradycardia, asystole, and arrhythmiaIctal tachycardia, defined in the review as heart rate above 100 bpm, is reported in more than 50% of seizures and early significant tachycardia is more common in temporal than extratemporal epilepsy, particularly right MTLE. Ictal bradycardia below 60 bpm is less common and has not shown localizing or lateralizing value; ictal asystole and arrhythmia are rare and are implicated in SUDEP pathogenesis.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
Reported values
  • Ictal tachycardia in more than 50% of seizuresictal tachycardia, bradycardia, asystole, and arrhythmiaPercentage · patients with focal epilepsy and otherwise subclinical seizures · Ictal tachycardia · ictal autonomicPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • Ictal tachycardia defined as heart rate >100 bpmictal tachycardia, bradycardia, asystole, and arrhythmiaThreshold · patients with focal epilepsy and otherwise subclinical seizures · Ictal tachycardia · ictal autonomicPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • Ictal bradycardia defined as heart rate <60 bpmictal tachycardia, bradycardia, asystole, and arrhythmiaThreshold · patients with focal epilepsy and otherwise subclinical seizures · Ictal bradycardia · ictal autonomicPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal tachycardia, bradycardia, and asystoleIctal tachycardia and bradycardia, which may lead to ictal asystole, are described as more frequent in temporal focal seizures with impaired awareness than in extratemporal seizures, particularly when seizures originate from the left hemisphere; some studies report a slight MTLE predominance.PDF p.8, Focal autonomic seizures
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • vegetative signs; tachycardia; bradycardia; rubefactionThe source reports vegetative signs including tachycardia, bradycardia, and rubefaction in 5 of 21 patients (25%).PDF p.6, Anatomical and clinical correlations
  • TachycardiaTable 2 reports 2/21 (10%) for Tachycardia; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • TachycardiaTable 2 reports 1/12 patients with Tachycardia in the prefrontal operculum group.PDF p.7, Table 2
  • TachycardiaTable 2 reports 1/9 patients with Tachycardia in the precentral Rolandic operculum group.PDF p.7, Table 2
  • TachycardiaFisher's exact comparison of Tachycardia between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 5/21 (25%)vegetative signs; tachycardia; bradycardia; rubefactionPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
  • 2/21 (10%)TachycardiaPercentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 1/12 patientsTachycardiaProportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 1/9 patientsTachycardiaProportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Tachycardia/hyperventilationTable 2 associates autonomic tachycardia/hyperventilation with amygdala, insula, anterior cingulum, ventro-medial prefrontal cortex, and hippocampus and describes it as non-lateralising, often right.PDF p.3, Table 2
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • tachycardia and bradycardia; insular stimulationThe source reports that right and left insular stimulation can induce tachycardia or bradycardia; tachycardia predominated in posterior insula sites, whereas bradycardia sites were more anterior in the median insula, with mild left-right asymmetry. Tachycardia was accompanied by increased LF/HF ratio and bradycardia tended to be accompanied by increased HF.PDF p.14, Cardiorespiratory response
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings · 2 reported values
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • tachycardia in Case 4Table 2 records tachycardia in approximately 30% of Case 4 seizures or observations as shown in the symptom sequence.PDF p.6, Table 2 Case 4
  • tachycardia in Case 5Table 2 records tachycardia in approximately 80% of Case 5 seizures or observations as shown in the symptom sequence.PDF p.6, Table 2 Case 5
Reported values
  • ~30%tachycardia in Case 4Percentage · Table 2 Case 4 seizures · ictal autonomic signPDF p.6, Table 2 Case 4
  • ~80%tachycardia in Case 5Percentage · Table 2 Case 5 seizures · ictal autonomic signPDF p.6, Table 2 Case 5

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Automotor seizureReported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereNo single reliable side10 manuscripts · 18 findings · 6 reported values
Weighted evidence supportevidence weight 13 across 10 manuscripts · 1 manuscript weight pending · 1 independent primary study · 1 structured design not resolved · 7 narrative, educational, or cited context · 1 systematic review or meta-analysis

Focal motor seizures are described as contralateral to the involved primary motor cortex. In one case with a left amygdala/hippocampal cavernoma and left temporal EEG onset, right head/eye version and a figure-of-4 posture preceded rare focal-to-bilateral tonic-clonic seizures. Both educational tables list automotor with dialepsis as associated with the dominant hemisphere. Both handbook tables associate automotor seizures without dialepsis with the nondominant hemisphere. The adapted table describes automotor focal-onset seizures with automatisms as non-lateralising. The review states that unilateral automatisms more often indicate an ipsilateral epileptogenic zone, whereas preserved consciousness during automotor seizures is associated almost exclusively with non-dominant mesial temporal epilepsy. The review states that awareness is generally impaired during automotor seizures, except that it may be preserved when seizures remain restricted to the nondominant temporal lobe. Preserved consciousness during an automotor seizure may occur particularly with origin from the nondominant hemisphere. Preserved consciousness during an automotor seizure is associated particularly with origin from the nondominant hemisphere. The lateral-occipital-to-TPOJ pathway interpretation reports no hemisphere direction. The probability statement contains no lateralization information. No hemisphere-direction relationship is reported. The Case 4 propagation observation reports no side direction. No hemisphere or side-relative direction is reported. The educational manifestation list reports no hemisphere direction. The probability estimates contain no lateralization information. No hemisphere or body-side relation is reported.

Evidence by contributing manuscript 10

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfNarrative, educational, or cited context · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • posterior cingulate simple motor and automotor seizuresThe three posterior cingulate patients with motor phenomena presented with different seizure types including simple motor and automotor seizures.PDF p.5, Clinical Presentation
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • focal motor seizure; automotor seizureThe review describes focal motor seizures arising from contralateral primary motor cortex as highly specific or pathognomonic for that region, while automotor seizures are less localising because they can arise from different brain regions.PDF p.2, Introduction
  • psychic aura; abdominal aura; automotor seizure; figure-of-4 signIn an illustrative 36-year-old right-handed man with a left amygdala/hippocampal cavernoma, seizures began with déjà vu and epigastric rising, evolved to automotor features and rarely focal-to-bilateral tonic-clonic seizures, and showed right head/eye version plus a figure-of-4 posture before generalisation; left temporal EEG onset and the posture were consistent with left hemispheric onset.PDF p.5, Video case 3; PDF p.6, Video case 3 and Figure 4 caption
  • abdominal aura evolving to automotor seizureThe review states that evolution of an abdominal aura into an automotor seizure increases the probability of temporal lobe epilepsy to 98%.PDF p.5, Auras
  • abdominal aura; automotor evolutionAn abdominal aura, such as a rising epigastric sensation or abdominal discomfort, is reported as highly associated with temporal lobe epilepsy with a probability of 74%, and evolution of the abdominal aura into an automotor seizure increases the probability to 98%.PDF p.5, Auras
Reported values
  • probability of temporal lobe epilepsy 98%abdominal aura evolving to automotor seizurePercentage · focal epilepsy patients with abdominal aura in the cited study · aura to ictal evolutionPDF p.5, Auras
  • 98%abdominal aura; automotor evolutionPercentage · Patients with focal epilepsies in the cited study; exact cohort Not reported · abdominal aura evolving into automotor seizure · Aura and subsequent ictal automotor evolutionPDF p.5, Auras
  • 74%abdominal aura; automotor evolutionPercentage · Patients with focal epilepsies in the cited study; exact cohort Not reported · abdominal aura alone · Aura and subsequent ictal automotor evolutionPDF p.5, Auras
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdfStructured design not resolved · 4 findings · 2 reported values
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.423
The study enrolled seven consecutive PCE patients; six had SEEG-identified posterior cingulate ictal onset and one had an MRI-identified postcingulate tumour. Four patients underwent CCEP. SEEG and scalp EEG were retrospectively analyzed with video-documented ictal semiology; the source used the Lüders seizure-classification scheme. The posterior cingulate was operationally defined caudal to the vertical posterior commissure line.
Findings
  • dialeptic or automotor seizures in PCEFour of seven patients showed dialeptic or automotor seizures.PDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
  • automotor seizures in PCETwo PCE patients (Cases 4 and 7) had automotor seizures.PDF p.5, Ictal semiology and SEEG findings
  • Case 4 automotor mesial temporal spreadCase 4 automotor symptoms occurred with spread to the amygdala, hippocampus, and entorhinal cortex.PDF p.5, Ictal semiology and SEEG findings; PDF p.4, Figure 2
  • dialeptic/automotor mesial temporal or IPL spreadThe four PCE patients with dialeptic or automotor seizures had spread to mesial temporal structures or the inferior parietal lobule.PDF p.1, Abstract; PDF p.5, Summary of ictal semiology and SEEG findings
Reported values
  • 4/7 dialeptic or automotor seizuresdialeptic or automotor seizures in PCEProportion · n/N 4/7 · 7 PCE patients · ictal semiologyPDF p.1, Abstract; PDF p.5, Ictal semiology and SEEG findings
  • 2/7 automotor seizuresautomotor seizures in PCEProportion · n/N 2/7 · 7 PCE patients · ictal semiologyPDF p.5, Ictal semiology and SEEG findings
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 2 findings
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Automotor with dialepsisBoth tables list Automotor with dialepsis as Dominant hemisphere.PDF p.2, Lateralizing signs/Localization table row "Automotor with dialepsis" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Automotor with dialepsis" (printed p.5)
  • Automotor without dialepsisBoth tables list Automotor without dialepsis as Nondominant hemisphere.PDF p.2, Lateralizing signs/Localization table row "Automotor without dialepsis" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Automotor without dialepsis" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • automotor seizuresAutomotor seizures consist of repetitive, stereotyped, semipurposeful oral, lingual, or distal-limb behaviors. Awareness is generally impaired except in seizures restricted to the nondominant temporal lobe; prolonged homogeneous perseverative, complex-gesture, and upper-limb automatisms characterize TLE, whereas frontal automatisms are more hyperkinetic and irregular, involve proximal limbs, and genital manipulations are rare in frontal and temporal seizures.PDF p.3, section 3.3 Complex motor seizures; PDF p.4, section 3.3 Complex motor seizures; PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • automotor behaviorAutomotor behavior is among the clinical manifestations reported with insular seizures.PDF p.2, Clinical Features
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Automotor seizureTable 2 associates an automotor focal-onset seizure with automatisms with mesial temporal and anterior cingulum regions and SSMA and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 2 findings
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • automotor seizureAutomotor seizures are complex motor seizures dominated by automatisms of the distal hands or feet or the mouth and tongue; consciousness is usually affected but may be preserved, particularly when the seizure originates from the nondominant hemisphere.PDF p.5, Complex motor seizures
  • Automotor seizureAutomotor seizures are complex motor seizures whose main manifestations are automatisms involving distal hands, feet, mouth, or tongue; consciousness is usually affected but may be preserved, particularly when the seizure originates from the nondominant hemisphere.PDF p.5, Complex motor seizures, Automotor seizures; PDF p.2, Table 1
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • automotor seizuresThe review states that automotor seizures consist mainly of distal hand, foot, mouth, and tongue automatisms and are typical of temporal-lobe epilepsy, although they can occur in frontal-lobe seizures; frontal automotor seizures tend to be shorter. Unilateral automatisms are more frequently associated with an ipsilateral epileptogenic zone, possibly because contralateral limb dystonia interrupts distal automatisms. Altered consciousness accompanies 95% of automotor seizures, while preserved consciousness is observed almost exclusively in non-dominant mesial temporal epilepsy.PDF p.5, Automotor seizures
Reported values
  • 95% of automotor seizures associated with altered consciousnessautomotor seizuresPercentage · Patients with automotor seizures, compared between temporal/frontal and dominant/non-dominant mesial temporal epilepsy; denominator not reported · IctalPDF p.5, Automotor seizures
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • TPOJ oculomotor and automotor signsIn Pattern IV, rapid TPOJ engagement is associated with early oculomotor and automotor signs.PDF p.14, Key Hubs Act as Accelerators and Switches

10 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal piloerection (goosebumps)Source terms: PiloerectionReported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere9 manuscripts · 12 findings · 19 reported values
Weighted evidence supportevidence weight 13 across 9 manuscripts · 1 independent primary study · 7 narrative, educational, or cited context · 1 systematic review or meta-analysis

The review lists piloerection as tending toward a left-sided temporal origin. The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. Pilomotor seizures are described as tending to be ipsilateral to the seizure-onset zone. Thermoregulatory change and piloerection provide no lateralizing information in this record. No lateralizing relationship is reported for piloerection. No lateralizing direction is reported. The adapted table describes unilateral goosebumps as ipsilateral. The review assigns ipsilateral direction to marching piloerection, left-temporal onset context to pallor in one pediatric series, and no lateralizing value to flushing. The chapter reports that ictal piloerection has been described ipsilateral to the seizure-onset zone. Unilateral or initially unilateral ictal piloerection was ipsilateral to the seizure focus in 16 of 19 summarized patients (84%). Unilateral or initially unilateral ictal piloerection was ipsilateral to the seizure focus in 4 of 5 recent-series cases and 12 of 14 literature-review cases.

Source-defined result groups 2
Localization: T+ group / TL groupSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 3 findings · 10 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • thermoregulatory change and piloerectionThermoregulatory changes did not differ overall between TL and T+ groups, but piloerection was more frequent in T+ seizures.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • piloerection localizationThe source states that epileptic piloerection occurs predominantly in patients with TL seizures but has also been reported from frontal, fronto-parietal, fronto-temporal, parieto-occipital, and insular cortices.PDF p.8, Autonomic symptoms
  • piloerection and central autonomic networkThe source states that piloerection generators seem to lie near structures in the central autonomic network and that a pivotal role for the insula remains debatable.PDF p.8, Autonomic symptoms
Reported values
  • TL thermoregulatory 20.3%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ pilo-erection 13%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ sensation of heat or cold 13%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • TL sweat 3.4%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ sweat 4.3%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • P=0.03thermoregulatory change and piloerectionP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • TL sensation of heat or cold 15.3%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ thermoregulatory 30.4%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • TL pilo-erection 1.7%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • P=0.33thermoregulatory change and piloerectionP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • PiloerectionPiloerection is listed as localizing to a left temporal-lobe focus.PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal piloerection, pallor, and flushingIctal piloerection presents as marching goose bumps involving a limb ipsilateral to seizure onset and is most common in TLE. Ictal pallor, usually occurring with other cutaneous signs, was associated with left temporal onset in one pediatric series, whereas ictal flushing involving mainly the face has no localizing value.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal piloerectionIctal piloerection is described as a relatively rare manifestation and has been reported on the side ipsilateral to the seizure-onset zone.PDF p.8, Focal autonomic seizures
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • piloerection autonomic symptomPiloerection is among the autonomic symptoms reported with insular seizures.PDF p.2, Clinical Features
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • GoosebumpsTable 2 associates goosebumps with mesial frontal and anterior cingulate regions and describes ipsilateral lateralisation.PDF p.3, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 9 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Ictal piloerectionThe review presents unilateral or initially unilateral ictal piloerection as usually ipsilateral to the seizure focus in the summarized series and literature, while noting that the underlying central autonomic network mechanism is not fully established.PDF p.3, section 2.6 Ipsilateral ictal piloerection; PDF p.3, section 2.6.1 Mechanism
  • Ictal piloerectionLoddenkemper et al. observed ictal piloerection in 14 of 3500 patients undergoing video/EEG monitoring; 5 of 14 had unilateral or initially unilateral piloerection, and 4 of these 5 were ipsilateral to the seizure focus, alongside 12 of 14 ipsilateral cases in the literature review.PDF p.3, section 2.6 Ipsilateral ictal piloerection
Reported values
  • four of fiveIctal piloerectionPercentage · n/N 4/5 · Patients undergoing video/EEG monitoring and patients in published piloerection reports · reported series · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection; PDF p.3, section 2.6.1 Mechanism
  • 84%Ictal piloerectionPercentage · n/N 16/19 · Patients undergoing video/EEG monitoring and patients in published piloerection reports · reported series plus literature review · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection; PDF p.3, section 2.6.1 Mechanism
  • 0.15%Ictal piloerectionPercentage · Patients undergoing video/EEG monitoring and patients in published piloerection reports · patients undergoing video/EEG monitoring · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection; PDF p.3, section 2.6.1 Mechanism
  • 12 of 14Ictal piloerectionPercentage · n/N 12/14 · Patients undergoing video/EEG monitoring and patients in published piloerection reports · additional literature review · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection; PDF p.3, section 2.6.1 Mechanism
  • 5 of 14 unilateral or initially unilateralIctal piloerectionPercentage · n/N 5/14 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · unilateral or initially unilateral · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 12 of 14 literature-review cases ipsilateralIctal piloerectionPercentage · n/N 12/14 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · literature review · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 84% as reportedIctal piloerectionPercentage · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · combined summary · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 4 of 5 recent-series cases ipsilateralIctal piloerectionPercentage · n/N 4/5 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · recent series · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 14 of 3500Ictal piloerectionPercentage · n/N 14/3500 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · ictal piloerection · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • pilomotor seizuresThe review states that pilomotor seizures have a somatotopic distribution and may spread in a Jacksonian-march-like pattern; they tend to be ipsilateral to the seizure-onset zone, but their localization value is poor.PDF p.3, Autonomic seizures

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictus emeticus (ictal vomiting with nausea)Source terms: Ictus emeticusReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side9 manuscripts · 15 findings · 18 reported values
Weighted evidence supportevidence weight 12.65 across 9 manuscripts · 1 manuscript weight pending · 1 independent primary study · 1 structured design not resolved · 6 narrative, educational, or cited context · 1 case report or observation

The sole observed vomiting seizure occurred with right temporal lobe seizure onset. The discussion restates prior reports describing ictal vomiting predominantly in the right temporal region. The review lists ictal emeticus and ictal urinary urge as localizing to a right temporal focus. Both educational tables list ictal emesis with the nondominant hemisphere, with one table explicitly marking it not highly reliable. The review states that ictal vomiting and retching have no definite lateralizing value. The cited review describes ictal vomiting as often associated with nondominant temporal seizure origin. The cited study is restated as showing ictal emesis predominantly in right temporal seizures. Ictal vomiting was associated with the nondominant hemisphere in 81% of cited cases but was not exclusive to it. Kramer et al. found right-lateralized EEG seizures in all nine ictal-vomiting patients among 450 monitored patients. Both cases had left temporal onset; one vomited during spread to the right temporal lobe, while the other had right-sided language dominance. The cited synthesis found right lateralization in 14/16 published ictal-emesis cases. In two cited left-temporal, left-language-dominant cases, ictal emesis accompanied left-to-right propagation and bitemporal activity. The cited Mayo series included two left-hemispheric ictal-vomiting cases, including one left temporal case in a left-language-dominant patient. No lateralization information is reported.

Source-defined result groups 5
Localization: TemporalSource-defined values retained separatelyAll reported · right TLE versus left TLE · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereSource-defined values retained separatelyAll reported · right TLE versus left TLE · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 0% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ 0% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · right temporal cases · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 9

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • vomitingVomiting was absent in both groups in the reported Table 2 frequencies, with no significant group difference.PDF p.6, Table 2
Reported values
  • TL 0%vomitingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 0%vomitingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • P=0.73vomitingP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal emeticus and ictal urinary urgeIctal emeticus and ictal urinary urge are each listed as localizing to a right temporal-lobe focus.PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Ictal emesisBoth tables list Ictal emesis as Nondominant hemisphere; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Ictal emesis*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Ictal emesis" (printed p.5)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal emesis in a cited studyThe current paper suggests that ictal spitting and coughing may be related to ictal emesis and reports that ictal emesis appeared to occur predominantly in RTL seizures in Kramer et al. (1988).PDF p.5, Discussion, automisms paragraph
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal vomitingIctal vomiting usually occurs without other gastrointestinal symptoms during unresponsiveness and is followed by postictal amnesia; it is often a sign of nondominant temporal seizure origin and can also be an early manifestation of benign childhood epilepsies.PDF p.5, section 5 Nondominant temporal signs; PDF p.4, section 3.5 Autonomic seizures; PDF p.5, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • vomiting autonomic symptomVomiting is among the autonomic symptoms reported with insular seizures.PDF p.2, Clinical Features
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfCase report or observation · 6 findings · 14 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal vomitingIctal vomiting is uncommon and usually associated with the nondominant hemisphere, but it is not exclusive to that hemisphere.PDF p.8, section 3.13; PDF p.12, Table 1
  • ictal vomitingKramer et al. found right-lateralized EEG seizures in all nine patients with ictal vomiting.PDF p.8, section 3.13
  • ictal vomiting in left temporal lobe epilepsyDevinsky et al. reported two left temporal cases; one vomited as the seizure spread left to right, and the other had right-sided language dominance.PDF p.8, section 3.13
  • ictal emesis in published casesDevinsky et al. found right lateralization in 14 of 16 previously reported ictal-emesis cases.PDF p.8, section 3.13
  • ictal emesisChen et al. reported ictal emesis in 3 of 156 monitored patients, including two left temporal, left-language-dominant cases whose vomiting accompanied left-to-right spread and bitemporal discharges.PDF p.8, section 3.13
  • ictal vomitingThe Mayo Clinic series included two left-hemispheric seizure cases among 11 patients with ictal vomiting.PDF p.8, section 3.13
Reported values
  • Ictal vomiting nondominant-associated in 81%ictal vomitingPercentage · epilepsy monitoring unit patients with ictal vomiting · Ictal-vomiting cases · ictalPDF p.8, section 3.13; PDF p.12, Table 1
  • Ictal vomiting in 2% of EMU patientsictal vomitingPercentage · epilepsy monitoring unit patients with ictal vomiting · Epilepsy monitoring unit · ictalPDF p.8, section 3.13; PDF p.12, Table 1
  • all nineictal vomitingPercentage · n/N 9/9 · 450 patients undergoing video/EEG monitoring · ictal-vomiting cases · ictalPDF p.8, section 3.13
  • 9/450 (2%)ictal vomitingPercentage · n/N 9/450 · 450 patients undergoing video/EEG monitoring · ictal-vomiting cases · ictalPDF p.8, section 3.13
  • 2 casesictal vomiting in left temporal lobe epilepsyCount · n/N 2/2 · two patients with left temporal lobe epilepsy and ictal vomiting · ictalPDF p.8, section 3.13
  • 14/16 right lateralizedictal emesis in published casesCount · n/N 14/16 · 16 previously reported cases, including the Kramer et al. cases · ictalPDF p.8, section 3.13
  • bothictal emesisCount · n/N 2/2 left-onset cases · 156 consecutive monitoring-unit patients; 3 with ictal emesis · left-onset ictal-emesis cases · ictalPDF p.8, section 3.13
  • 2/3ictal emesisPercentage · n/N 2/3 · 156 consecutive monitoring-unit patients; 3 with ictal emesis · ictal-emesis cases · ictalPDF p.8, section 3.13
  • 3 of 156ictal emesisPercentage · n/N 3/156 · 156 consecutive monitoring-unit patients; 3 with ictal emesis · monitoring-unit cohort · ictalPDF p.8, section 3.13
  • 2ictal emesisPercentage · n/N 2/3 · 156 consecutive monitoring-unit patients; 3 with ictal emesis · left temporal and left-language-dominant cases · ictalPDF p.8, section 3.13
  • 1ictal emesisCount · n/N 1/2 left-onset cases · 156 consecutive monitoring-unit patients; 3 with ictal emesis · left temporal and left-language-dominant cases · ictalPDF p.8, section 3.13
  • bothictal emesisCount · n/N 2/2 left-onset cases · 156 consecutive monitoring-unit patients; 3 with ictal emesis · left-onset ictal-emesis cases · ictalPDF p.8, section 3.13
  • 1 case documented with bilateral temporal depth electrodesictal vomitingCount · 11 patients with ictal vomiting · depth-electrode documented · ictalPDF p.8, section 3.13
  • 2/11 left hemisphericictal vomitingPercentage · n/N 2/11 · 11 patients with ictal vomiting · left-hemispheric · ictalPDF p.8, section 3.13
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 2 findings · 1 reported value
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • ictal vomitingActual vomiting was observed in only one seizure arising from right temporal lobe epilepsy in this study.PDF p.4, Results; PDF p.7, Discussion
  • ictal vomiting in prior reportsThe discussion reports that ictal vomiting was observed predominantly in the right temporal region in prior reports.PDF p.7, Discussion
Reported values
  • 1 seizure with actual vomiting in right TLEictal vomitingCount · 19 patients with unilateral TLE; right-versus-left TLE comparison · ictalPDF p.4, Results; PDF p.7, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal vomiting and ictal retchingThe review states that ictal vomiting and retching are observed mainly in adult temporal lobe seizures, have no definite lateralizing value, and have some evidence supporting a role for the insula as visceral sensory cortex.PDF p.3, Autonomic seizures

9 contributing manuscripts; source-reported values remain separate and are not pooled.

Asymmetric clonic endingReported: ContralateralAlso reported: Ipsilateral7 manuscripts · 8 findings · 32 reported values
Weighted evidence supportevidence weight 12.22 across 7 manuscripts · 5 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 independent primary study

The review restates an ipsilateral last clonic jerk and contralateral postictal Todd's paresis as lateralizing signs. Ipsilateral focus. Exhaustion of hemisphere of seizure onset; ipsilateral Persistent ending activity suggests ipsilateral seizure onset; proposed mechanism involves ongoing activity in the hemisphere contralateral to seizure origin The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. Ipsilateral hemisphere relative to the last outlasting clonic activity The cited Trinka result reports the last clonic jerk ipsilateral to the seizure onset zone in 17/23 patients. The educational tables list asymmetric ending as ipsilateral but do not report the reference side or viewpoint.

Source-defined result groups 8
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Asymmetrical clonic endingAsymmetrical clonic ending is listed as ipsilateral to the seizure focus.PDF p.4, Table 2
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • asymmetric clonic ending; postictal Todd’s paresisThe source states that an asymmetric clonic ending of the generalised phase, with the last clonic jerk ipsilateral to seizure onset, and postictal Todd’s paresis contralateral to seizure onset are lateralising signs; these signs do not distinguish frontal from extrafrontal onset.PDF p.10, Lateralising signs
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Asymmetric ending seizure (subentries: Terminal clonus; p.3 additionally Versive)The tables list an asymmetric ending seizure as Ipsilateral; p.2 shows the subentry Terminal clonus, whereas p.3 shows Terminal clonus and Versive.PDF p.2, Lateralizing signs/Localization table row "Asymmetric ending seizure" with subentry "Terminal clonus" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Asymmetric ending seizure" with subentries "Terminal clonus" and "Versive" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • asymmetric ending of clonic jerksPersistent asymmetric clonic activity at seizure termination is attributed to ongoing ictal activity in the hemisphere contralateral to the seizure origin after activity ends in the epileptogenic hemisphere; persistent clonic activity therefore suggests ipsilateral seizure onset.PDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Asymmetric termination of clonic jerksTable 3 associates asymmetric termination of clonic jerks during secondary generalized tonic-clonic seizures with exhaustion of the hemisphere of seizure onset and ipsilateral lateralisation.PDF p.4, Table 3
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 7 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Asymmetric clonic endingTrinka et al. analyzed 57 patients with temporal lobe epilepsy; 29 were seizure free for at least 1 year after surgery, and among 28 diagnosed by presurgical evaluation, 23 had an asymmetric generalized tonic-clonic ending. The last jerk was ipsilateral to the seizure onset zone in 17 of 23 patients.PDF p.5, section 3.4 Significance of last clonic jerk
Reported values
  • 23/28 with asymmetric endingAsymmetric clonic endingPercentage · n/N 23/28 · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · patients with asymmetric ending · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 17/23 last jerks ipsilateralAsymmetric clonic endingPercentage · n/N 17/23 · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · patients with asymmetric ending · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 28 diagnosed by presurgical evaluationAsymmetric clonic endingCount · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · presurgical-evaluation subgroup · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 57 patients with temporal lobe epilepsyAsymmetric clonic endingCount · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • 29 seizure-free for at least 1 yearAsymmetric clonic endingCount · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · postoperative seizure-free · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • P<0.001Asymmetric clonic endingP value · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
  • interobserver agreement kappa=1.0Asymmetric clonic endingKappa · 57 patients with temporal lobe epilepsy; 29 seizure free for at least 1 year after surgery and 28 diagnosed by presurgical evaluation including video/EEG and MRI · End of generalized tonic-clonic seizurePDF p.5, section 3.4 Significance of last clonic jerk
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 2 findings · 25 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • asymmetric clonic endingThe current paper reports that previous studies found asymmetric clonic activity of this type to have 83% specificity for lateralizing the EZ to the ipsilateral hemisphere.PDF p.8, asymmetric clonic ending definition and cited specificity; PDF p.11, discussion comparing the current PPV with prior literature
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • Specificity 83%asymmetric clonic endingPercentage · Cited-study populations as summarized in the current paper; Not reported · End of the clonic phase of a secondary generalized tonic-clonic seizurePDF p.8, asymmetric clonic ending definition and cited specificity; PDF p.11, discussion comparing the current PPV with prior literature

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Tonic-clonic seizureReported: Bilateral5 manuscripts · 38 findings · 35 reported values
Weighted evidence supportevidence weight 12.13 across 5 manuscripts · 2 independent primary study · 2 narrative, educational, or cited context · 1 systematic review or meta-analysis

Tonic-clonic manifestations and focal-to-bilateral tonic-clonic seizures were rare in the anterior cingulate review. No hemisphere or body-side direction is reported. This record provides no seizure lateralization. Symmetrical tonic-clonic onset is contrasted with asymmetric focal tonic onset, but no hemisphere direction is reported. This finding provides no lateralization information. No source-supported hemispheric lateralization is reported. No lateralizing direction is reported for the tonic-clonic manifestation range. No lateralizing direction is reported for the low ACC association grade assigned to tonic-clonic manifestations. No lateralizing semiology is reported for the tonic-clonic versus vocalization/verbalization odds comparison. No lateralizing direction is reported. No lateralization axis information is reported for tonic-clonic activity versus affective/autonomic aura. No lateralizing semiology is reported for the tonic-clonic versus autonomic-sign odds comparison. No lateralizing semiology is reported for the tonic-clonic versus facial-expression-change odds comparison. No seizure lateralization is reported. No lateralizing semiology is reported for the tonic-clonic versus head-eye-deviation odds comparison. No lateralizing semiology is reported for the reciprocal vocalization/verbalization versus tonic-clonic odds comparison. Figure 6 reports OR 21.9 for Affective/autonomic aura relative to Tonic-clonic, with no hemisphere or lateralization direction. No lateralizing semiology is reported for the reciprocal autonomic-signs versus tonic-clonic odds comparison. No lateralizing semiology is reported for the reciprocal facial-expression-change versus tonic-clonic odds comparison. No lateralizing semiology is reported for the reciprocal head-eye-deviation versus tonic-clonic odds comparison. No lateralizing semiology is reported for the F-to-BTC versus tonic-clonic odds comparison. No lateralizing semiology is reported for the reciprocal tonic-clonic versus F-to-BTC odds comparison. No lateralizing direction is reported for the generalized tonic-clonic evolution definition.

Source-defined result groups 1
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyTonic-clonic · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 5

Alphabetical by manuscript.

asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • tonic-clonic seizuresSixteen of 18 patients had tonic-clonic seizures before surgery.PDF p.1, Abstract; PDF p.2, Results
Reported values
  • 16/18 (88%) tonic-clonic seizurestonic-clonic seizuresPercentage · n/N 16/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · preoperative seizure historyPDF p.1, Abstract; PDF p.2, Results
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 32 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • tonic-clonic manifestations; prolonged seizureTonic-clonic manifestations and focal to bilateral tonic-clonic seizures were rare, occurring in 5% and only occasionally in prolonged seizures.PDF p.9, Objective symptomatology
  • dystonic posturing; head-eye deviation; tonic-clonic manifestationsThe review links dystonic posturing, head/eye deviation, and tonic-clonic manifestations to propagation rather than the earliest seizure phase.PDF p.11, Anatomical and clinical correlations
  • tonic-clonic manifestationsThe source reports a frequency of 5% for tonic-clonic manifestations.PDF p.13, Table 3
  • tonic-clonic manifestations; reported frequency rangeThe source reports a frequency range of 0–40% for tonic-clonic manifestations.PDF p.13, Table 3
  • tonic-clonic manifestations; ACC association gradeTable 3 assigns the source's Low overall association grade to tonic-clonic manifestations.PDF p.13, Table 3
  • tonic-clonic manifestations; Figure 4 rateFigure 4 displays a 5.4% rate for tonic-clonic manifestations.PDF p.10, Figure 4
  • pairwise OR: Tonic-clonic relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Affective/autonomic auraFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Autonomic signsFigure 6 reports an odds ratio of 0.1 for Tonic-clonic relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Facial expression changeFigure 6 reports an odds ratio of 0.1 for Tonic-clonic relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 0.1 for Tonic-clonic relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Loss of consciousnessFigure 6 reports an odds ratio of 0.2 for Tonic-clonic relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 0.2 for Tonic-clonic relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 0.4 for Tonic-clonic relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Dystonic posturingFigure 6 reports an odds ratio of 0.4 for Tonic-clonic relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Head-eye deviationFigure 6 reports an odds ratio of 0.6 for Tonic-clonic relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to LaughterFigure 6 reports an odds ratio of 0.9 for Tonic-clonic relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 1.1 for Tonic-clonic relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Tonic-clonicFigure 6 reports an odds ratio of 27.3 for Vocalization/verbalization relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Tonic-clonicFigure 6 reports an odds ratio of 25.7 for Hypermotor-complex motor behavior relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Tonic-clonicFigure 6 reports an odds ratio of 21.9 for Affective/autonomic aura relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Tonic-clonicFigure 6 reports an odds ratio of 16.2 for Autonomic signs relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Tonic-clonicFigure 6 reports an odds ratio of 14.9 for Facial expression change relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Tonic-clonicFigure 6 reports an odds ratio of 13.1 for Motor (gestural) automatisms relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Tonic-clonicFigure 6 reports an odds ratio of 9.6 for Loss of consciousness relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Tonic-clonicFigure 6 reports an odds ratio of 7.6 for Post-ictal confusion/behavior change disinhibition relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Tonic-clonicFigure 6 reports an odds ratio of 4.5 for Chapeau de gendarme relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Tonic-clonicFigure 6 reports an odds ratio of 4.2 for Dystonic posturing relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Tonic-clonicFigure 6 reports an odds ratio of 2.8 for Head-eye deviation relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Tonic-clonicFigure 6 reports an odds ratio of 2.6 for Laughter relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Tonic-clonicFigure 6 reports an odds ratio of 1.9 for Oro-alimentary automatisms relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Tonic-clonicFigure 6 reports an odds ratio of 1.7 for F to BTC relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to F to BTCFigure 6 reports an odds ratio of 1.7 for Tonic-clonic relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 5%tonic-clonic manifestations; prolonged seizurePercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • 5%tonic-clonic manifestations; prolonged seizurePercentage · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.9, Objective symptomatology
  • 5% (frequency range 0–40%)tonic-clonic manifestationsPercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.13, Table 3
  • 5.4%tonic-clonic manifestations; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.10, Figure 4
  • OR <0.1pairwise OR: Tonic-clonic relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Tonic-clonic relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Tonic-clonic relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Tonic-clonic relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Tonic-clonic relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Tonic-clonic relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Tonic-clonic relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Tonic-clonic relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 27.3pairwise OR: Vocalization/verbalization relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 25.7pairwise OR: Hypermotor-complex motor behavior relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 21.9pairwise OR: Affective/autonomic aura relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 16.2pairwise OR: Autonomic signs relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 14.9pairwise OR: Facial expression change relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.1pairwise OR: Motor (gestural) automatisms relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Loss of consciousness relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.6pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.5pairwise OR: Chapeau de gendarme relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.2pairwise OR: Dystonic posturing relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.8pairwise OR: Head-eye deviation relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.9pairwise OR: Laughter relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Oro-alimentary automatisms relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1pairwise OR: F to BTC relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1pairwise OR: Tonic-clonic relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Tonic-clonic seizureGeneralized tonic-clonic seizures begin with tonic posturing of all limbs and evolve to a clonic phase whose contractions progressively decrease in frequency until disappearing; the muscles involved in the tonic and clonic phases should be essentially the same, and focal motor seizures with this evolution are described as infrequent.PDF p.4, Simple motor seizures, Tonic-clonic seizures; PDF p.2, Table 1
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfIndependent primary study · 1 finding · 2 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Independent primary study · Class II · Evidence weight 3.22 · 2 × 0.9 × 1.79
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • paroxysmal dysphasia; ictal speech automatism; grand mal attacksThe authors report that more than three-quarters of the 34 patients with paroxysmal dysphasia also had grand mal attacks, whereas slightly less than half of the patients with ictal speech automatism had these major seizures.PDF p.11, discussion of seizure severity
Reported values
  • slightly less than half of 38 speech-automatism patientsparoxysmal dysphasia; ictal speech automatism; grand mal attacksPercentage · Patients with pre-operative paroxysmal dysphasia and patients with pre-operative ictal speech automatisms · ictal speech automatism · Pre-operative seizure historyPDF p.11, discussion of seizure severity
  • more than three-quarters of 34 dysphasia patientsparoxysmal dysphasia; ictal speech automatism; grand mal attacksPercentage · Patients with pre-operative paroxysmal dysphasia and patients with pre-operative ictal speech automatisms · paroxysmal dysphasia · Pre-operative seizure historyPDF p.11, discussion of seizure severity
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • tonic-clonic seizuresThe review reserves the expression “tonic-clonic seizures” for generalized tonic-clonic seizures and states that onset with relatively symmetrical involvement of all limbs is highly suggestive of generalized epilepsy; focal epilepsies can also produce generalized tonic-clonic seizures, but these are almost always preceded by other seizure types and have a usually asymmetric tonic phase.PDF p.4, Tonic-clonic seizures

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Early non-forced head turning (<30s, ipsilateral, exploratory)Source terms: Non-forced head turning; Early non-forced head turningReported: ContralateralAlso reported: IpsilateralNo single reliable side7 manuscripts · 7 findings · 7 reported values
Weighted evidence supportevidence weight 12.07 across 7 manuscripts · 1 manuscript weight pending · 4 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 independent primary study · 1 structured design not resolved

The review restates that nonversive head turning is usually ipsilateral to the epileptogenic zone, including 94% ipsilateral same-direction turns without secondary generalization, while a two-turn pre-SGTCS sequence changes from ipsilateral first to contralateral second. The review conclusion says nonversive head deviation and turning may have stage-dependent lateralizing value. Cerebral lateralization: these signs are contralateral to seizure onset; target lobe is not differentiated by these signs alone. The review restates that early nonforced head turning is usually ipsilateral, whereas later forceful involuntary version is most often contralateral to the seizure focus. The handbook lists early head deviation as ipsilateral. No head/eye direction relative to the seizure hemisphere is reported. The two mixed-sequence seizures show ipsilateral early nonversive movement and contralateral later version, with nonversive movement itself nonlateralizing.

Source-defined result groups 5
Localization: L onset subtype / M onset subtype / ML onset subtypeObserved proportion 22.2%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelystudy versive seizures · after secondary generalization · seizure1 manuscript · 1 reported value · not pooled
Localization: L onset subtype / M onset subtype / ML onset subtypeObserved proportion 12.5%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Ipsilateral / Does not lateralizeSource-defined values retained separatelyseizures containing both movement types · early nonversive versus later versive movement; pre-generalization versus post-generalization direction · seizure1 manuscript · 1 reported value · not pooled
Localization: L onset subtype / M onset subtype / ML onset subtypeObserved proportion 23.1%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Early head turn and late versionAn early nonforced head turn or head tilt, especially with preserved consciousness, is usually ipsilateral to seizure onset, whereas later, more forceful involuntary version is most often contralateral to the seizure focus.PDF p.4, Table 2; PDF p.4, section 4 Lateralizing Features in Temporal Lobe Epilepsy
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionThe review describes unilateral clonic movements, unilateral tonic or dystonic posturing, and early forced head version as robust lateralising motor signs with positive predictive value greater than 80%, and states that these signs are contralateral to the side of seizure onset.PDF p.10, Lateralising signs
Reported values
  • positive predictive value >80%unilateral clonic movement; unilateral tonic/dystonic posturing; early head versionPositive predictive value · focal seizure literature · ictal onset/early ictalPDF p.10, Lateralising signs
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Early head deviationBoth tables list Early head deviation as Ipsilateral; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Early head deviation*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Early head deviation" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • nonversive head turningNonversive head turning is a natural, unforced lateral movement reported in temporal and frontal epilepsy and usually occurs ipsilateral to the epileptogenic hemisphere. Without secondary generalization, one or two turns in the same direction were ipsilateral to the EZ in 94% of seizures; before an SGTCS, the first of two turns was ipsilateral and the second contralateral.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • 94% ipsilateral for one or two same-direction turns without secondary generalizationnonversive head turningPercentage · patients with temporal or frontal epilepsy; seizures with or without secondary generalization · ictal; before SGTCS when two turns occurPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • nonversive head deviation and turningNonversive head deviation and turning during different stages of focal seizures may have lateralizing value.PDF p.12, Conclusion
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • early head and/or eyes deviationEarly head and/or eyes deviation did not differ significantly across M, ML, and L groups.PDF p.6, Table 4; PDF p.6, Early features
Reported values
  • 4/18 (22.2%)early head and/or eyes deviationPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 3/24 (12.5%)early head and/or eyes deviationPercentage · n/N 3/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • 3/13 (23.1%)early head and/or eyes deviationPercentage · n/N 3/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
wyllie1986.pdfStructured design not resolved · 1 finding · 2 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • ipsiversive and contraversive sequence of movementsIn the two seizures that contained both movement types, an early nonversive movement was ipsilateral and the later forced versive movement was contralateral; ipsiversion did not occur before secondary generalization in the study seizures.PDF p.2, results paragraph; PDF p.3, discussion paragraph on ipsiversion
Reported values
  • two seizuresipsiversive and contraversive sequence of movementsCount · n/N 2/2 mixed-pattern seizures · Two seizures with both versive and nonversive head and eye turning; study versive seizures for the pre-generalization null observation · seizures containing both movement types · Early ictal movement, later contraversion, and before secondary generalizationPDF p.2, results paragraph; PDF p.3, discussion paragraph on ipsiversion
  • no ipsiversionipsiversive and contraversive sequence of movementsCount · Two seizures with both versive and nonversive head and eye turning; study versive seizures for the pre-generalization null observation · study versive seizures · Early ictal movement, later contraversion, and before secondary generalizationPDF p.2, results paragraph; PDF p.3, discussion paragraph on ipsiversion

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Impaired awarenessReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereNo single reliable side8 manuscripts · 9 findings · 7 reported values
Weighted evidence supportevidence weight 12.01 across 8 manuscripts · 1 independent primary study · 6 narrative, educational, or cited context · 1 case report or observation

Both educational tables list automotor with dialepsis as associated with the dominant hemisphere. The review concludes that altered awareness is not reliably lateralising. A cited study is restated as finding alteration of consciousness more frequent in left and bilateral temporal seizures. Right-sided hemorrhage/encephalomalacia is lesion context; no auditory laterality or ictal hemisphere was established for the episodes. No hemisphere or body-side direction is reported. The cited temporal-like insular semiology has no hemisphere or body-side direction. The educational duration description provides no lateralizing direction. No source-supported lateralizing direction is reported for the cited occipital-plus organization summary. No lateralization axis information is reported for the occipital-plus organization summary.

Source-defined result groups 2
Localization: FrontalObserved proportion 41.0%combined set-of-semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 19.7%initial semiology · Initial semiology versus combined set-of-semiology · individual1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Behavioural arrest and staring with altered consciousnessCPSs are described as associated with altered consciousness and amnesia, typically with behavioural arrest and staring lasting 30 seconds to 1–2 minutes.PDF p.2, section 2.3 Altered Consciousness
Reported values
  • 30 seconds to 1–2 minutesBehavioural arrest and staring with altered consciousnessCount · Patients with CPSs as described in the review; no single cohort reported. · IctalPDF p.2, section 2.3 Altered Consciousness
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Automotor with dialepsisBoth tables list Automotor with dialepsis as Dominant hemisphere.PDF p.2, Lateralizing signs/Localization table row "Automotor with dialepsis" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Automotor with dialepsis" (printed p.5)
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • altered awareness temporal-like symptomTemporal-like insular seizures may include altered awareness.PDF p.2, Clinical Features
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Impaired awarenessImpaired awareness was the most common initial semiology, occurring in 12/61 individuals (20%), and occurred in 25/61 (41%) in the combined set-of-semiology.PDF p.3, Results; PDF p.5, Table 2
Reported values
  • Initial 12/61 (20%)Impaired awarenessPercentage · n/N 12/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
  • Combined 25/61 (41%)Impaired awarenessPercentage · n/N 25/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Altered awarenessThe review concludes that altered awareness in seizures associated with impaired awareness is not reliably lateralising or localising; the particular aura and ictal sequence may add localization information, and more reliable localising and lateralising information can be obtained once awareness is established.PDF p.4, section 1.3
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfNarrative, educational, or cited context · 1 finding
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • alteration of consciousness in left and bilateral temporal lobe seizuresThe discussion reports that a prior study found alteration of consciousness more frequent in left and bilateral temporal lobe seizures and used a broader definition including orientation, speech, and postictal memory; the current study’s loss-of-contact definition was narrower.PDF p.8, Initial loss of contact
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 4 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • altered conscious level; automatic motor behavior; verbal automatismsThe review reports that Marchi et al. (2016) found widespread epileptogenic-zone organization typical of occipital-plus epilepsy, with temporal and/or parietal cortex commonly involved; altered conscious level was more common with widespread posterior neocortical onset, while automatic motor behavior and/or verbal automatisms were more often seen with occipitotemporal organization.PDF p.6, Table 2, Occipital lobe row
  • occipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsIn the summarized Marchi et al. study, widespread organization of the epileptogenic zone was typical in occipital or “occipital-plus” epilepsy, with temporal and/or parietal cortex commonly involved; altered conscious level was more common with widespread posterior neocortical onset, while automatic motor behavior and/or verbal automatisms were more often seen with occipitotemporal organization.PDF p.6, Table 2, Marchi et al. 2016 row
Reported values
  • 29 subjectsaltered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy and 194 seizures · occipital-lobe epilepsy study · Seizure onset and semiologic expressionPDF p.6, Table 2, Occipital lobe row
  • 194 seizuresaltered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy and 194 seizures · occipital-lobe epilepsy study · Seizure onset and semiologic expressionPDF p.6, Table 2, Occipital lobe row
  • 194 seizuresoccipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy; 194 seizures · Marchi et al. study · ictal onset and evolutionPDF p.6, Table 2, Marchi et al. 2016 row
  • 29 subjectsoccipital epilepsy; occipital-plus epilepsy; altered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy; 194 seizures · Marchi et al. occipital-lobe epilepsy study · ictal onset and evolutionPDF p.6, Table 2, Marchi et al. 2016 row
palinacousis-seven-new-cases.pdfCase report or observation · 1 finding
palinacousis-seven-new-cases.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • repeating voices during altered responsiveness without electrographic seizureA man with a right intracranial hemorrhage in childhood had brief episodes of altered responsiveness off anti-seizure medication, repeatedly said shh, and later described surrounding people's voices repeating, although EEG showed no electrographic seizures; tachycardia accompanied the episodes.PDF p.2, Table 1 case 7 and caption; PDF p.3, case 7

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal nose wiping / nose rubbingSource terms: Postictal nose wipingReported: ContralateralAlso reported: Ipsilateral8 manuscripts · 17 findings · 29 reported values
Weighted evidence supportevidence weight 12 across 8 manuscripts · 1 systematic review or meta-analysis · 1 independent primary study · 6 narrative, educational, or cited context

Postictal nose wiping was predominantly ipsilateral to the epileptogenic zone (overall PPV 62%), with six false-lateralized patients. The review restates that postictal nose rubbing or wiping is usually ipsilateral to the seizure focus. The educational tables label postictal nose wiping as ipsilateral. Nose wiping was reported to use the hand ipsilateral to the epileptogenic temporal lobe in 75–90% of cases. The chapter restates that postictal hemiparesis is contralateral, whereas the nose-wiping hand is ipsilateral to the seizure focus. Postictal nosewiping was predominantly ipsilateral to seizure onset in the reviewed temporal-lobe epilepsy data. Within 60 seconds postictally, nosewiping was ipsilateral in 92% of the cited TLE subgroup; repeated wiping was always ipsilateral. The review restates ipsilateral postictal nose wiping in 86.5% of TLE patients and 54.5% of ETLE patients. The review card contains incompatible ipsilateral and contralateral statements for postictal nose-wipe side relative to seizure onset. This finding provides no hemispheric lateralization information. This finding provides no lateralization information.

Source-defined result groups 15
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyParietal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Nose wiping · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Nose wiping · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyParietal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyTemporal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · seizure1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyOccipital lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · seizure1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyParietal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · sign-positive lateralization1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyOccipital lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · patient1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyOccipital lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · sign-positive lateralization1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyFrontal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · patient1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyOverall · Lobar subgroup comparison within the surgical cohort. · sign-positive lateralization1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyTemporal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · patient1 manuscript · 1 reported value · not pooled
Lateralization: IpsilateralSource-defined values retained separatelyTemporal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · sign-positive lateralization1 manuscript · 1 reported value · not pooled
Localization: Frontal lobe epilepsy / Occipital lobe epilepsy / Parietal lobe epilepsy / Temporal lobe epilepsySource-defined values retained separatelyFrontal lobe epilepsy · Lobar subgroup comparison within the surgical cohort. · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Postictal nose wipingPostictal nose rubbing or wiping is usually associated with an ipsilateral temporal-lobe focus.PDF p.4, Table 2; PDF p.4, section 4; PDF p.5, section 6
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 8 findings · 3 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Nose wipingTable 3 reports 1 studies assessing Nose wiping.PDF p.6, Table 3
  • Nose wipingTable 3 reports 17 patients assessed for Nose wiping.PDF p.6, Table 3
  • Nose wipingTable 3 reports 11.8% as the percentage range or value for Nose wiping; the overall association grade is Low.PDF p.6, Table 3
  • Nose wiping; lateral versus mesial comparisonTable 5 reports 1 studies comparing Nose wiping in lateral and mesial TLE.PDF p.9, Table 5
  • Nose wiping; lateral TLE patient denominatorTable 5 reports 17 lateral-TLE patients assessed for Nose wiping.PDF p.9, Table 5
  • Nose wiping; mesial TLE patient denominatorTable 5 reports 20 mesial-TLE patients assessed for Nose wiping.PDF p.9, Table 5
  • Nose wiping; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 11.8% for Nose wiping.PDF p.9, Table 5
  • Nose wiping; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 30% for Nose wiping.PDF p.9, Table 5
Reported values
  • 11.8%Nose wipingPercentage · Lateral temporal epilepsy patients assessed for Nose wiping · ictalPDF p.6, Table 3
  • 11.8%Nose wiping; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Nose wiping · Lateral TLE patients assessed for Nose wiping · ictalPDF p.9, Table 5
  • 30%Nose wiping; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Nose wiping · Mesial TLE patients assessed for Nose wiping · ictalPDF p.9, Table 5
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 17 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Post ictal nose wipingPostictal nose wiping was reported as an ipsilateral lateralizing sign with 62% PPV and inter-observer kappa of 0.71, despite the source describing false lateralization in six patients.PDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
Reported values
  • 3 patients in Occipital lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Occipital lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 17 patients overallPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Overall · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • Parietal PPV 100%Post ictal nose wipingPositive predictive value · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Parietal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 1 seizures in Parietal lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Parietal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 15 seizures in Temporal lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Temporal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 3 seizures in Occipital lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Occipital lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • Temporal PPV 60%Post ictal nose wipingPositive predictive value · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Temporal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 21 seizures overallPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Overall · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • false lateralization in 6 patientsPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Overall · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • Overall PPV 62% (ipsilateral)Post ictal nose wipingPositive predictive value · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Overall · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • inter-observer kappa 0.71Post ictal nose wipingKappa · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • Occipital PPV 100%Post ictal nose wipingPositive predictive value · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Occipital lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 2 seizures in Frontal lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Frontal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 1 patients in Parietal lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Parietal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • Frontal PPV 0%Post ictal nose wipingPositive predictive value · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Frontal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 2 patients in Frontal lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Frontal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
  • 11 patients in Temporal lobe epilepsyPost ictal nose wipingCount · The sign was seen in 17 patients, including 11 with temporal lobe epilepsy; Table 1 gives 21 seizures in 17 patients overall and subgroup occurrences temporal 15/11, frontal 2/2, parietal 1/1, and occipital 3/3. · Temporal lobe epilepsy · PostictalPDF p.3, Table 1; PDF p.3, §5.1; PDF p.3, §5.2
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Postictal nose wipingBoth tables list Postictal nose wiping as Ipsilateral; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Postictal nose wiping*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Postictal nose wiping" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • nose wipingNose wiping, defined as wiping or rubbing the nose during or within 60 seconds of seizure termination, is most common in mesial temporal seizures in 50–85% of cases and is performed with the hand ipsilateral to the epileptogenic temporal lobe in 75–90% of cases.PDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • during or within 60 seconds of seizure terminationnose wipingOther reported value · patients with focal epilepsy, especially mesial temporal seizures · ictal or within 60 seconds postictalPDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • 50–85% occurrence in mesial temporal seizuresnose wipingRange · patients with focal epilepsy, especially mesial temporal seizures · mesial temporal seizures · ictal or within 60 seconds postictalPDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
  • 75–90% ipsilateral hand usenose wipingRange · patients with focal epilepsy, especially mesial temporal seizures · nose-wiping cases · ictal or within 60 seconds postictalPDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal hemiparesis and nose wipingPostictal hemiparesis reflects a contralateral seizure focus, whereas postictal nose wiping affects the hand ipsilateral to the seizure focus.PDF p.9, Postictal state
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal nosewipingPostictal nosewiping after temporal lobe seizures generally lateralizes ipsilateral to seizure onset.PDF p.10, section 5.4; PDF p.12, Table 1
  • postictal nosewiping within 60 secondsHirsch et al. found postictal nosewiping within 60 seconds in 53% of TLE patients and ipsilateral in 92%; repeated wiping was always ipsilateral.PDF p.10, section 5.4; PDF p.12, Table 1
  • postictal nosewipingLeutmezer et al. reported a higher ipsilateral value in temporal than extratemporal lobe epilepsy.PDF p.10, section 5.4
Reported values
  • Postictal nosewiping ipsilateral in 92%postictal nosewipingPercentage · patients with temporal lobe epilepsy · TLE with postictal nosewiping · postictalPDF p.10, section 5.4; PDF p.12, Table 1
  • Postictal nosewiping in 53.2% of TLEpostictal nosewipingPercentage · patients with temporal lobe epilepsy · Temporal lobe epilepsy · postictalPDF p.10, section 5.4; PDF p.12, Table 1
  • 53%postictal nosewiping within 60 secondsPercentage · 87 patients with temporal or extratemporal lobe epilepsy · temporal lobe epilepsy · postictal within 60 secondsPDF p.10, section 5.4; PDF p.12, Table 1
  • 92%postictal nosewiping within 60 secondsPercentage · 87 patients with temporal or extratemporal lobe epilepsy · TLE patients with postictal nosewiping · postictal within 60 secondsPDF p.10, section 5.4; PDF p.12, Table 1
  • 54.5% ipsilateral in ETLEpostictal nosewipingPercentage · patients with temporal or extratemporal lobe epilepsy · ETLE · postictalPDF p.10, section 5.4
  • 86.5% ipsilateral in TLEpostictal nosewipingPercentage · patients with temporal or extratemporal lobe epilepsy · TLE · postictalPDF p.10, section 5.4
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • post-ictal nose wipeThe review states that postictal nose wiping lateralizes temporal-lobe epilepsy to the ipsilateral hemisphere and reports the assumption that the hemisphere contralateral to the nose wipe, which is the seizure-onset hemisphere, suffers from postictal neglect.PDF p.6, Post-ictal nose wipe

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal amaurosis / visual field lossSource terms: Ictal amaurosisReported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere6 manuscripts · 13 findings · 11 reported values
Weighted evidence supportevidence weight 11.7 across 6 manuscripts · 2 independent primary study · 2 case report or observation · 1 systematic review or meta-analysis · 1 narrative, educational, or cited context

The review restates three source-relative relations: hemifield visual aura contralateral to occipital onset, unilateral eye blinking ipsilateral to the blinking eye, and epileptic-nystagmus fast component contralateral to the seizure-onset hemisphere. The case reports left occipital ictal discharges with a right homonymous hemianopia, a contralateral relationship. This case links a left visual-field aura with right-hemisphere EEG findings and a source-suggested, not definitive, right-sided interpretation. The review gives contralateral direction for hemifield visual aura, simple unilateral auditory aura, and the fast nystagmus component, but ipsilateral direction for unilateral eye blinking. one hemi-field or quadrant is interpreted relative to the contralateral occipital lobe and supra- or infracalcarine fissure No source lateralization is reported. No seizure lateralization is reported. No lateralizing direction is reported. No hemisphere or body-side direction is reported. The case had a left medial occipital lesion, but the blindness itself is not reported with a unilateral visual-field or body-side direction.

Source-defined result groups 5
Localization: OccipitalSource-defined values retained separatelyright parieto-occipital maximum · left parieto-occipital and right temporal maxima · regional discharge observation1 manuscript · 1 reported value · not pooled
Localization: OccipitalObserved proportion 28.6%All reported · no ictal blindness · patients1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyAll reported · no ictal blindness · patients1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyright parieto-occipital maximum · left parieto-occipital and right temporal maxima · regional discharge observation1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 83.3%right-hemisphere fast activity · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmusHemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; and in epileptic nystagmus the fast component is contralateral to the seizure-onset hemisphere.PDF p.10, Lateralising signs; PDF p.8, Parieto-occipital junction
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmus; unilateral auditory auraA hemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; the fast component of epileptic nystagmus is contralateral to seizure onset; and a simple unilateral auditory aura, which the review notes is rare, is contralateral.PDF p.6, Lateral/neocortical temporal lobe; PDF p.8, Parieto-occipital junction; PDF p.10, Lateralising signs
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfCase report or observation · 1 finding · 6 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • Case Study 3 left visual-field aura and right occipital findingsIn Case Study 3, a woman experienced multicolored bright stars moving in the left visual field for about 30 seconds followed by headache, later eye blinking, vocalization, and unresponsiveness, sometimes with secondary generalized tonic-clonic activity. Video EEG showed frequent multiregional discharges maximal in the right parieto-occipital region (65%), left parieto-occipital region (25%), and right temporal region (10%); ten seizures had fast activity over the right hemisphere and two had generalized posteriorly predominant rhythmic activity. The discussion stated that the left visual aura and right occipital polyspikes suggested right occipital lobe epilepsy, while further invasive evaluation was needed to delineate the zone.PDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
Reported values
  • 2/12Case Study 3 left visual-field aura and right occipital findingsPercentage · n/N 2/12 · Single illustrative case, 23-year-old ambidextrous woman with recurrent seizures · generalized posteriorly predominant rhythmic activity · aura and ictalPDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
  • about 30 secondsCase Study 3 left visual-field aura and right occipital findingsDuration · Single illustrative case, 23-year-old ambidextrous woman with recurrent seizures · multicolored bright stars in the left visual field · aura and ictalPDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
  • 65%Case Study 3 left visual-field aura and right occipital findingsPercentage · Single illustrative case, 23-year-old ambidextrous woman with recurrent seizures · right parieto-occipital maximum · aura and ictalPDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
  • 10/12Case Study 3 left visual-field aura and right occipital findingsPercentage · n/N 10/12 · Single illustrative case, 23-year-old ambidextrous woman with recurrent seizures · right-hemisphere fast activity · aura and ictalPDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
  • 10%Case Study 3 left visual-field aura and right occipital findingsPercentage · Single illustrative case, 23-year-old ambidextrous woman with recurrent seizures · right temporal maximum · aura and ictalPDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
  • 25%Case Study 3 left visual-field aura and right occipital findingsPercentage · Single illustrative case, 23-year-old ambidextrous woman with recurrent seizures · left parieto-occipital maximum · aura and ictalPDF p.14, Case Study 3, clinical history and video-EEG findings; PDF p.14, Case Study 3, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • lateralized visual phenomena and visual field aurasVisual phenomena lateralized to one hemi-field as an early ictal manifestation are highly suggestive of onset in the contralateral occipital lobe. Symptoms restricted to the lower or upper quadrant are reported to localize to the contralateral supra- or infracalcarine fissure, respectively.PDF p.2, section 3.1 Auras
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • left occipital ictal discharges with transient hemianopiaIn the illustrated nonketotic-hyperglycemia case, recurrent left occipital ictal discharges accompanied a right homonymous hemianopia and visual-spatial symptoms; the source describes 19 discharges over 2 hours, resolution of ictal discharges after correction of hyperglycemia, and resolution of the hemianopia over several days, while noting that occipital seizures can produce either positive visual phenomena or negative field loss and that hemianopia may also be postictal.PDF p.391; PDF p.392; PDF p.394
Reported values
  • 19 recurrent ictal discharges in 2 hoursleft occipital ictal discharges with transient hemianopiaCount · 51-year-old man with glucose 542 and transient right homonymous hemianopia · recurrent ictal activity and postictal visual deficitPDF p.391; PDF p.392; PDF p.394
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 6 findings · 3 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • ictal blindness cited rangeThe source reports that prior authors described ictal blindness in as many as 40% of patients with occipital lobe epilepsy.PDF p.2, Introduction
  • ictal blindnessIctal blindness occurred in 12 of 42 patients.PDF p.4, Results, Visual auras
  • blacking out or graying outThe the source's own descriptions of ictal blindness included “blacking out” and “graying out.”PDF p.6, Results, Visual auras
  • prolonged ictal blindnessIctal blindness lasted several minutes on some occasions.PDF p.6, Results, Visual auras
  • co-occurring elementary hallucinations and ictal blindnessElementary visual hallucinations and ictal blindness could occur in the same patient at different times.PDF p.6, Results, Visual auras
  • prolonged blindness as sole manifestationOne patient had prolonged ictal blindness lasting several minutes as the sole seizure manifestation for several years before complex partial seizures developed.PDF p.11, Results, Aetiology of the seizures
Reported values
  • up to 40%ictal blindness cited rangeUpper-bound percentage · cited occipital lobe epilepsy reports · seizure onset or ictal evolutionPDF p.2, Introduction
  • 12/42 (29%) patientsictal blindnessPercentage · n/N 12/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.4, Results, Visual auras
  • 28% with ictal blindness as an initial manifestationictal blindnessPercentage · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.19, Discussion
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • amaurosisAmaurosis occurred in four of 19 patients (21.1%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
  • pure visual phenotypePhenotype I is defined by exclusive subjective visual auras, including elementary visual hallucinations, amaurosis, or visual obscuration, without objective motor or autonomic progression.PDF p.9, Phenotype I
Reported values
  • 4/19 (21.1%) amaurosisamaurosisPercentage · n/N 4/19 · 19 patients monitored with SEEG · aura/ictal semiologyPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Auditory illusions (sounds distorted in quality, loudness, or distance)Source terms: Auditory illusionsReported: ContralateralAlso reported: Right hemisphere5 manuscripts · 7 findings · 18 reported values
Weighted evidence supportevidence weight 11.07 across 5 manuscripts · 2 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 independent primary study · 1 case report or observation

The review restates that noises evoked from the medial primary auditory site were perceived in the ear contralateral to stimulation. The synthesis reports a right-hemisphere stimulation predominance for verbal hallucinations, with no general hemisphere rule for all auditory percept types. No hemisphere or sign-side direction is reported. No lateralizing direction is reported. No hemisphere direction is reported. No lateralization result is reported in this corpus-size finding.

Source-defined result groups 3
Localization: TemporalObserved proportion 4.2%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 46.2%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 11.1%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 5

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • auditory illusion versus auditory hallucinationThe source reports Bancaud's assumption that auditory illusions occur preferentially with widely extended discharges over the superior temporal gyrus, whereas auditory hallucinations are likely when discharges are more spatially limited.PDF p.8, auditory aura discussion
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • auditory hallucinations and illusionsThe review reports a stimulation comparison in which the medial transverse gyrus of Heschl produced auditory hallucinations in 80% of patients, mostly high-frequency or broadband noise, whereas stimulation of the lateral transverse gyrus, anterior superior temporal gyrus, or planum temporale produced more illusions in 41–55%; from medial to lateral sites, hallucination content changed from high- to low-frequency noises, and primary-site noises were perceived in the contralateral ear.PDF p.3, section 4 and Fig. 1; PDF p.3, Fig. 1 caption
Reported values
  • medial Heschl auditory hallucinations 80%auditory hallucinations and illusionsPercentage · Patients undergoing superior temporal gyrus and planum temporale stimulation; total patient denominator is not reported in this review · medial transverse gyrus of Heschl · Stimulation-evoked auditory experiencePDF p.3, section 4 and Fig. 1; PDF p.3, Fig. 1 caption
  • lateral transverse gyrus/anterior STG/planum temporale illusions 41–55%auditory hallucinations and illusionsRange · Patients undergoing superior temporal gyrus and planum temporale stimulation; total patient denominator is not reported in this review · lateral or associative auditory sites · Stimulation-evoked auditory experiencePDF p.3, section 4 and Fig. 1; PDF p.3, Fig. 1 caption
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • elementary auditory aura; auditory illusion/distortionTable 3 maps elementary auditory aura to Heschl’s gyrus or superior temporal regions and auditory illusions or distortions to lateral temporal regions or insula.PDF p.10, Table 3; PDF p.6, Lateral/neocortical temporal lobe
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 3 findings · 13 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)In the cortical-stimulation synthesis, SH were mainly induced by posterior insula and Heschl’s gyrus (HG); CH by STG, STS, mesiotemporal structures, and insula; I by STG, HG, STS, and temporal plane with about one-third from extratemporal structures; VH included 60% produced by right-hemisphere stimulation, mostly STG; MH involved STG, HG, temporal plane, and SMG; HD involved temporal structures and insula, especially PLST, posterior STG, and HG; and few PAL reports were identified.PDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • auditory seizures (AS) and auditory phenomena (AP)The review analyzed 174 cases comprising 200 AS from 70 articles; Level A covered 115 cases/131 AS, Level B covered 59 cases/69 AS, and the SOZ-to-perceived-side lateralization analysis included 99 cases comprising 114 AS.PDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • auditory hallucinations and illusions induced by direct intracortical electrical stimulationThe review states that Jaroszynski et al. induced AP in 50 patients undergoing presurgical assessment for focal drug-resistant epilepsy and reported a large overlap between regions producing hallucinations and illusions.PDF p.4, section 5, Jaroszynski paragraph
Reported values
  • Verbal hallucinations from right-hemisphere stimulation 60%simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Verbal hallucinations · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • Auditory illusions from extratemporal stimulation about one-thirdsimple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Auditory illusions · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • 70 articlesauditory seizures (AS) and auditory phenomena (AP)Count · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · overall review corpus · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 99 casesauditory seizures (AS) and auditory phenomena (AP)Count · n/N 99/174 cases · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · paired SOZ-to-perceived-side lateralization analysis · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 59 casesauditory seizures (AS) and auditory phenomena (AP)Count · n/N 59/174 cases · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level B · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 131 ASauditory seizures (AS) and auditory phenomena (AP)Count · n/N 131/200 AS · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level A · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 200 ASauditory seizures (AS) and auditory phenomena (AP)Count · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · overall review corpus · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 69 ASauditory seizures (AS) and auditory phenomena (AP)Count · n/N 69/200 AS · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level B · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 174 casesauditory seizures (AS) and auditory phenomena (AP)Count · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · overall review corpus · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 115 casesauditory seizures (AS) and auditory phenomena (AP)Count · n/N 115/174 cases · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · Level A · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • 114 ASauditory seizures (AS) and auditory phenomena (AP)Count · n/N 114/200 AS · Literature case reports and series for AS, with a separate cortical-stimulation literature synthesis for AP · paired SOZ-to-perceived-side lateralization analysis · Ictal AS; electrically induced AP analyzed separatelyPDF p.1, Abstract; PDF p.2, Methods sections 2.1-2.3; PDF p.5, section 6
  • large overlap, with no overlap numerator reported in this reviewauditory hallucinations and illusions induced by direct intracortical electrical stimulationCount · Cited Jaroszynski et al. presurgical focal drug-resistant epilepsy cohort · Direct intracortical stimulationPDF p.4, section 5, Jaroszynski paragraph
  • 50 patientsauditory hallucinations and illusions induced by direct intracortical electrical stimulationCount · Cited Jaroszynski et al. presurgical focal drug-resistant epilepsy cohort · Direct intracortical stimulationPDF p.4, section 5, Jaroszynski paragraph
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • auditory hallucination or illusionInitial auditory hallucination or illusion was more frequent in L than in M or ML patients.PDF p.5, Semiologic analysis; PDF p.5, Table 2
Reported values
  • 2/18 (11.1%)auditory hallucination or illusionPercentage · n/N 2/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2
  • 6/13 (46.2%)auditory hallucination or illusionPercentage · n/N 6/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2
  • 1/24 (4.2%)auditory hallucination or illusionPercentage · n/N 1/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Semiologic analysis; PDF p.5, Table 2

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Deja vuSource terms: Déjà vuReported: Non-dominant hemisphereNo single reliable side7 manuscripts · 7 findings · 2 reported values
Weighted evidence supportevidence weight 11.01 across 7 manuscripts · 1 independent primary study · 5 narrative, educational, or cited context · 1 case report or observation

The cited table describes déjà vu/jamais vu aura as non-lateralising. The review table labels both fear and déjà vu/jamais vu as nonlateralizing, while noting an often-nondominant tendency only for déjà vu/jamais vu. The review describes dysmnesic manifestations as characteristic of MTLE and reports déjà vu more often with nondominant MTLE. No hemisphere or body-side direction is reported. No lateralization axis information is reported for the déjà vu, dreamy-state, and scene-reminiscence stimulation summary. The cited déjà-vu network report gives no side or lateralization direction. The case lists déjà vu, jamais vu, and abdominal aura terms without a side or lateralization direction.

Evidence by contributing manuscript 7

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 13 déjà/jamais/abdominal auraDéjà vu, jamais vu, and abdominal aura terms were listed for patient 13.PDF p.4, Figure 3
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • déjà vu and recollective experienceA cited series of patients with déjà vu showed transient functional coupling between amygdala and hippocampus and between hippocampus and rhinal cortex, particularly in the theta band, when déjà vu was provoked by electrical stimulation; the review relates déjà vu and recollection to increased hippocampus–cortex synchrony, with recollection involving a larger associative network.PDF p.6, section 7
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • fear and déjà vu or jamais vu auras in Table 1Table 1 lists fear as arising from the amygdala, hippocampus, and mesial frontal lobe and as nonlateralizing; it lists déjà vu or jamais vu as arising from the uncus, entorhinal cortex, and temporal neocortex and as nonlateralizing, often nondominant.PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • dysmnesic manifestations, déjà vu, jamais vu, prescience, and “dreamy state”Dysmnesic manifestations are characteristic of MTLE; déjà vu has been reported as predominant in nondominant MTLE, prescience is rarely described, and the “dreamy state” may include déjà vu, strangeness or unreality, and complex auditory or visual hallucinations.PDF p.7, Focal cognitive seizures
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal cognitive (deja vu/jamais vu)Focal cognitive (deja vu/jamais vu) semiology occurred in 6/61 individuals (10%) both as initial semiology and in the combined set-of-semiology.PDF p.3, Results; PDF p.5, Table 2
Reported values
  • Initial 6/61 (10%)Focal cognitive (deja vu/jamais vu)Percentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
  • Combined 6/61 (10%)Focal cognitive (deja vu/jamais vu)Percentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Deja vu/jamais vu auraTable 2 associates deja vu/jamais vu aura with uncus, entorhinal/perirhinal cortex, and temporal neocortex and describes it as non-lateralising.PDF p.3, Table 2
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • déjà vu; “dreamy state”; reminiscence of scenesThe source’s selected stimulation literature associates déjà vu or a “dreamy state” with hippocampus and amygdala stimulation and with lateral temporal stimulation spreading to medial temporal regions; a rhinal-cortex study localized déjà vu to entorhinal, perirhinal, hippocampal, and amygdalar sites, with the sensation more common after entorhinal stimulation, and localized reminiscence of scenes to perirhinal cortex.PDF p.18, Table 10.1, Consciousness/Mental Phenomenology

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Peri-ictal headache / postictal headache (occipital type)Source terms: Peri-ictal headacheReported: Ipsilateral5 manuscripts · 21 findings · 26 reported values
Weighted evidence supportevidence weight 10.92 across 5 manuscripts · 1 independent primary study · 1 systematic review or meta-analysis · 3 narrative, educational, or cited context

Both handbook tables list peri-ictal headache as ipsilateral, with a p.2 reliability caution and no reported reference side. The cited study reports headache more likely ipsilateral to the seizure-onset focus in temporal lobe epilepsy, while headache in non-temporal lobe epilepsy was not lateralizing. The cited review reports peri-ictal headache in 47%, pre-ictal headache in 11%, and some qualified lateralizing value for temporal-lobar focus without a direction. The cited review says ICHD-3 regarded headache ipsilateral to concurrent ictal discharge, or headache ending with seizure cessation, as useful diagnostic features, while pain location itself had poor localizing value in the cited IEH review. No hemisphere or body-side direction is reported. No lateralization axis information is reported for the headache study count. No lateralization axis information is reported for the 22-patient headache denominator. The review reports post-ictal headache as the most common epilepsy-related headache with prevalence of 10%-50% and no lateralization information. The cited headache review reports no hemisphere or lateralization direction. The review describes ictal epilepsy-related headache as rare when it is the main or sole manifestation, at 3%-5% of people with epilepsy or fewer, without lateralization information. The cited EMU review reports headache as a seizure aura in 6/831 patients (0.7%) without side information. No lateralization is reported. The cited study comparison of post-ictal headache in occipital- versus temporal-lobe epilepsy reports no left/right direction. The review states that generalized convulsions may be more often associated with post-ictal headache but gives no lateralization information. The review says children may experience seizure-associated headaches more often than adults and gives no lateralization information.

Evidence by contributing manuscript 5

Alphabetical by manuscript.

doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 3 findings · 1 reported value
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • HeadacheTable 3 reports 1 studies assessing Headache.PDF p.6, Table 3
  • HeadacheTable 3 reports 22 patients assessed for Headache.PDF p.6, Table 3
  • HeadacheTable 3 reports 4.5% as the percentage range or value for Headache; the overall association grade is Low.PDF p.6, Table 3
Reported values
  • 4.5%HeadachePercentage · Lateral temporal epilepsy patients assessed for Headache · ictalPDF p.6, Table 3
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Peri-ictal headacheBoth tables list Peri-ictal headache as Ipsilateral; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Peri-ictal headache*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Peri-ictal headache" (printed p.5)
hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 15 findings · 21 reported values
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • peri-ictal headache and temporal lateralizationIn standardized interviews of 100 medically refractory patients with epilepsy, peri-ictal headache was self-reported by 47%, mostly as post-ictal headache, and pre-ictal headache occurring up to 1 day before was reported by 11%; the review states that peri- or post-ictal headache had some lateralizing value for a temporal-lobar seizure focus but not for other seizure types.PDF p.2, Headache as a Symptom of Seizures, Description
  • IEH pain location and localization valueThe review states that pain location in the cited IEH literature review did not appear to have good localizing value for lesion or seizure focus, whereas the ICHD-3 committee judged ipsilateral headache or termination with seizure cessation to be a useful diagnostic feature.PDF p.2, Headache as a Symptom of Seizures, Description; PDF p.2, Table 2
  • post-ictal headacheThe review states that post-ictal headache is the most common epilepsy-related headache and that reported prevalence is 10% to 50% in patients with epilepsy.PDF p.2, Headache as a Symptom of Seizures, Description
  • seizure-associated headache timing and typeThe review reports that a study of 110 patients with epilepsy found seizure-associated headache in 43%, with most having exclusively post-ictal headache; only 3 patients had both pre- and post-ictal headache, one had pre-ictal headache alone, and post-ictal migraine and tension-like headache each comprised about one-third of classifiable headache types.PDF p.2, Headache as a Symptom of Seizures, Description
  • pre-ictal, ictal, and post-ictal headache prevalenceIn a retrospective cohort of 388 patients with epilepsy, the review reports pre-ictal headache up to 24 hours before seizure in 6.7%, ictal headache in 0.8%, and post-ictal headache in 19.1%.PDF p.2, Headache as a Symptom of Seizures, Description
  • ictal epileptic headache (IEH) as main or sole manifestationThe review describes IEH as a rare phenomenon when it is the main feature or sole manifestation during an active seizure, occurring in 3% to 5% of patients with epilepsy or fewer.PDF p.2, Headache as a Symptom of Seizures, Description
  • headache during active seizureThe review reports that retrospective review of EEG recordings from nearly 4,800 patients admitted to an EMU identified headache during the active seizure in only 5 patients; the headaches were tension-type or migrainous and terminated immediately with seizure cessation.PDF p.2, Headache as a Symptom of Seizures, Description
  • headache as aura of seizureThe review reports that a retrospective review of 831 consecutive patients with epilepsy admitted to an EMU found headache as a seizure aura in 6 patients, or 0.7%.PDF p.2, Headache as a Symptom of Seizures, Description
  • IEH literature case count and accompanying symptomsThe review reports that a 2017 review identified 32 cases in the literature since 1971 of IEH defined as head pain caused by a simultaneous epileptic discharge, occurring alone or before other epileptic symptoms; accompanying symptoms were described in half of the patients.PDF p.2, Headache as a Symptom of Seizures, Description
  • occipital and non-occipital headache-associated seizuresSeveral authors proposed that seizures involving occipital head regions may be more likely to activate headache, although the review also reports headache with temporal, frontal, and parietal seizure localizations.PDF p.3, Localization
  • post-ictal headache in occipital versus temporal epilepsyThe review reports that a study of 109 patients with occipital or temporal lobe epilepsy found post-ictal headache in 62% of patients with occipital lobe epilepsy versus 23% of those with temporal lobe epilepsy.PDF p.3, Localization
  • generalized convulsions and post-ictal headacheThe review states that generalized convulsions seem to be more often associated with post-ictal headache than other seizure types.PDF p.3, Localization
  • age and seizure-associated headacheThe review states that children may experience seizure-associated headaches more often than adults, possibly reflecting more autonomic symptoms or greater susceptibility to headache.PDF p.3, Localization
  • Gastaut syndrome headache-associated seizure semiologyThe review describes Gastaut syndrome as rare and usually occurring in the first decade; seizures begin with visual symptoms such as scintillating scotomas or hallucinations and eye deviation, then evolve to impaired awareness and focal motor activity, with migraine headaches common after seizures.PDF p.3, Localization; PDF p.4, Localization (continued)
  • ictal headache and seizure-focus physiologyThe review links epileptic headaches to local vasodilation of large pial vessels and dura over epileptic foci with trigeminovascular and sensory pain-pathway activation; it also states that simultaneous EEG-fMRI shows regional blood-flow changes correlating with interictal spikes, ictal SPECT or PET shows increased blood flow and metabolism at a seizure focus, and chronic spike locations tend to correlate with decreased metabolism.PDF p.3, Pathophysiology
Reported values
  • Peri-ictal headache 47%peri-ictal headache and temporal lateralizationPercentage · 100 medically refractory patients with epilepsy · Pre-ictal, peri-ictal, and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • pre-ictal headache 11%peri-ictal headache and temporal lateralizationPercentage · 100 medically refractory patients with epilepsy · Pre-ictal, peri-ictal, and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • mostly post-ictal within the peri-ictal groupperi-ictal headache and temporal lateralizationCount · 100 medically refractory patients with epilepsy · Pre-ictal, peri-ictal, and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • 10%-50% prevalencepost-ictal headachePercentage · Patients with epilepsy · Post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • 1 with pre-ictal headache aloneseizure-associated headache timing and typeCount · 110 patients with epilepsy · pre-ictal only · Pre-ictal and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • post-ictal migraine about one-thirdseizure-associated headache timing and typePercentage · 110 patients with epilepsy · post-ictal migraine · Pre-ictal and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • 3 with both pre- and post-ictal headacheseizure-associated headache timing and typeCount · 110 patients with epilepsy · both pre- and post-ictal · Pre-ictal and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • tension-like headache about one-thirdseizure-associated headache timing and typePercentage · 110 patients with epilepsy · tension-like headache · Pre-ictal and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • 43% seizure-associated headacheseizure-associated headache timing and typePercentage · 110 patients with epilepsy · epilepsy cohort · Pre-ictal and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • Postictal headache 19.1% of 388pre-ictal, ictal, and post-ictal headache prevalencePercentage · 388 patients with epilepsy in a retrospective cohort · Pre-ictal, ictal, and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • Ictal headache 0.8% of 388pre-ictal, ictal, and post-ictal headache prevalencePercentage · 388 patients with epilepsy in a retrospective cohort · Pre-ictal, ictal, and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • Pre-ictal headache 6.7% of 388pre-ictal, ictal, and post-ictal headache prevalencePercentage · 388 patients with epilepsy in a retrospective cohort · Pre-ictal, ictal, and post-ictalPDF p.2, Headache as a Symptom of Seizures, Description
  • 3%-5% of PWE or fewerictal epileptic headache (IEH) as main or sole manifestationPercentage · Patients with epilepsy · IctalPDF p.2, Headache as a Symptom of Seizures, Description
  • tension-type or migrainous characterheadache during active seizureCount · n/N 5/4800 · Nearly 4,800 EMU admissions in the cited retrospective EEG review · Active ictal periodPDF p.2, Headache as a Symptom of Seizures, Description
  • immediate termination with seizure cessationheadache during active seizureCount · n/N 5/4800 · Nearly 4,800 EMU admissions in the cited retrospective EEG review · Active ictal periodPDF p.2, Headache as a Symptom of Seizures, Description
  • 5 patients with active-seizure headacheheadache during active seizureCount · n/N 5/4800 · Nearly 4,800 EMU admissions in the cited retrospective EEG review · Active ictal periodPDF p.2, Headache as a Symptom of Seizures, Description
  • 6/831 patients (0.7%)headache as aura of seizurePercentage · n/N 6/831 · 831 consecutive patients with epilepsy admitted to an EMU · Aura or pre-ictal seizure phasePDF p.2, Headache as a Symptom of Seizures, Description
  • 32 literature casesIEH literature case count and accompanying symptomsCount · 32 IEH cases reported in the literature since 1971 · Simultaneous ictal discharge; may precede other epileptic symptomsPDF p.2, Headache as a Symptom of Seizures, Description
  • accompanying symptoms in half of the casesIEH literature case count and accompanying symptomsCount · 32 IEH cases reported in the literature since 1971 · Simultaneous ictal discharge; may precede other epileptic symptomsPDF p.2, Headache as a Symptom of Seizures, Description
  • 62% occipital-lobe epilepsypost-ictal headache in occipital versus temporal epilepsyPercentage · 109 patients with occipital or temporal lobe epilepsy assessed by clinical symptoms, EEG, and neuroimaging · occipital-lobe epilepsy · Post-ictalPDF p.3, Localization
  • 23% temporal-lobe epilepsypost-ictal headache in occipital versus temporal epilepsyPercentage · 109 patients with occipital or temporal lobe epilepsy assessed by clinical symptoms, EEG, and neuroimaging · temporal-lobe epilepsy · Post-ictalPDF p.3, Localization
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Peri-ictal headacheBernasconi et al. reported peri-ictal headache in 47 of 100 patients; in temporal lobe epilepsy the headache was more likely ipsilateral to the seizure onset focus in 90% of cases, whereas headache in non-temporal lobe epilepsy was not lateralizing.PDF p.2, section 2.3 Peri-ictal headache
Reported values
  • 47 of 100Peri-ictal headachePercentage · n/N 47/100 · 100 patients with partial epilepsy; temporal and non-temporal lobe epilepsy subgroups · partial epilepsy cohort · Peri-ictalPDF p.2, section 2.3 Peri-ictal headache
  • 90%Peri-ictal headachePercentage · 100 patients with partial epilepsy; temporal and non-temporal lobe epilepsy subgroups · temporal lobe epilepsy cases with peri-ictal headache · Peri-ictalPDF p.2, section 2.3 Peri-ictal headache
  • 68%Peri-ictal headachePercentage · 100 patients with partial epilepsy; temporal and non-temporal lobe epilepsy subgroups · study patients; exact referent retained as reported · Peri-ictalPDF p.2, section 2.3 Peri-ictal headache
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • headacheHeadache occurred in two of 19 patients (10.5%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
Reported values
  • 2/19 (10.5%) headacheheadachePercentage · n/N 2/19 · 19 patients monitored with SEEG · ictal/postictal symptom as reportedPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal nystagmusReported: ContralateralAlso reported: Ipsilateral5 manuscripts · 10 findings · 7 reported values
Weighted evidence supportevidence weight 10.89 across 5 manuscripts · 3 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 independent primary study

The review restates contralateral fast and ipsilateral slow nystagmus components relative to the seizure-onset hemisphere. The review restates three source-relative relations: hemifield visual aura contralateral to occipital onset, unilateral eye blinking ipsilateral to the blinking eye, and epileptic-nystagmus fast component contralateral to the seizure-onset hemisphere. The cited review restates that the fast phase of ictal nystagmus was opposite the seizure focus. The review states that the fast phase of epileptic nystagmus is typically contralateral and the slow component ipsilateral to the seizure-onset hemisphere. The review gives contralateral direction for hemifield visual aura, simple unilateral auditory aura, and the fast nystagmus component, but ipsilateral direction for unilateral eye blinking. The review states that the fast phase of epileptic nystagmus is usually contralateral to the epileptogenic zone. Contralateral nystagmoid eye movements occurred in three of 42 patients (7%). The review synthesis reports EEG changes contralateral to the fast phase of ictal nystagmus. The cited series reports the fast phase of epileptic nystagmus as contralateral to the epileptogenic zone in all nine cases. No lateralizing direction is reported for the cited nystagmoid eye-movement percentage.

Source-defined result groups 1
Lateralization: ContralateralObserved proportion 7.1%All reported · no nystagmoid eye movements · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 5

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 4 findings · 1 reported value
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • epileptic nystagmus; parieto-occipital junctionEye version, blinking, and nystagmus may occur with parieto-occipital seizures; epileptic nystagmus is described as having a fast phase toward the hemisphere contralateral to seizure onset and a slow component toward the ipsilateral side.PDF p.8, Parieto-occipital junction; PDF p.10, Lateralising signs
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmusHemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; and in epileptic nystagmus the fast component is contralateral to the seizure-onset hemisphere.PDF p.10, Lateralising signs; PDF p.8, Parieto-occipital junction
  • eye blinking; epileptic nystagmusIn a cited large series, 20% of patients had eye blinking at seizure onset; the review also states that eye version can occur with occipital-localized ictal discharges and that epileptic nystagmus typically has its fast phase contralateral and slow component ipsilateral to the seizure-onset hemisphere.PDF p.8, Parieto-occipital junction
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmus; unilateral auditory auraA hemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; the fast component of epileptic nystagmus is contralateral to seizure onset; and a simple unilateral auditory aura, which the review notes is rare, is contralateral.PDF p.6, Lateral/neocortical temporal lobe; PDF p.8, Parieto-occipital junction; PDF p.10, Lateralising signs
Reported values
  • Eye blinking at onset in 20% of the cited serieseye blinking; epileptic nystagmusPercentage · Patients in the cited occipital epilepsy series and reported nystagmus cases; exact cohorts Not reported · Ictal onset and ictal evolutionPDF p.8, Parieto-occipital junction
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • nystagmusNystagmus is rare and is observed predominantly in parieto-occipital epilepsies; the fast phase is usually contralateral to the epileptogenic zone.PDF p.5, section 4 Lateralizing motor signs in complex motor seizures
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 4 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • epileptic nystagmusIctal nystagmus is often associated with posterior-head-region seizures, with EEG changes contralateral to the fast phase.PDF p.8, section 3.15
  • epileptic nystagmus fast phaseIn the authors' cited series, the fast phase of epileptic nystagmus was always contralateral to the epileptogenic zone.PDF p.8, section 3.15
Reported values
  • 9/1838 casesepileptic nystagmus fast phasePercentage · n/N 9/1838 · 1838 epilepsy patients, including 9 with epileptic nystagmus · epileptic nystagmus · ictalPDF p.8, section 3.15
  • fast phase always contralateralepileptic nystagmus fast phasePercentage · 1838 epilepsy patients, including 9 with epileptic nystagmus · epileptic nystagmus cases · ictalPDF p.8, section 3.15
  • 6 imaging-plus-EEG confirmedepileptic nystagmus fast phaseCount · 1838 epilepsy patients, including 9 with epileptic nystagmus · neuroimaging plus EEG · ictalPDF p.8, section 3.15
  • 3 surgically confirmedepileptic nystagmus fast phaseCount · 1838 epilepsy patients, including 9 with epileptic nystagmus · seizure-freedom confirmation · ictalPDF p.8, section 3.15
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 2 findings · 2 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • contralateral nystagmoid eye movementsContralateral nystagmoid eye movements occurred in three of 42 patients.PDF p.6, Results, Non-visual manifestations
  • nystagmoid eye movements in Ludwig and Ajmone-MarsanThe source reports nystagmoid eye movements in 9% of the cited Ludwig and Ajmone-Marsan patients.PDF p.20, Discussion
Reported values
  • 3/42 (7%) patientscontralateral nystagmoid eye movementsPercentage · n/N 3/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.6, Results, Non-visual manifestations
  • 9%nystagmoid eye movements in Ludwig and Ajmone-MarsanPercentage · cited Ludwig and Ajmone-Marsan occipital epilepsy series · ictal manifestationPDF p.20, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal nystagmusThe review states that most described ictal nystagmus is predominantly horizontal and binocular, with the fast phase opposite the seizure focus; it reports origins from either the occipital lobe or temporo-occipital junction and frequent association with ictal vertigo.PDF p.6, Ictal nystagmus

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Somatosensory warmth / burning / thermal sensation (dysesthetic)Source terms: Somatosensory warmth / burning / thermal sensation; Thermal somatosensory auraReported: Left hemisphereAlso reported: Non-dominant hemisphere6 manuscripts · 7 findings · 4 reported values
Weighted evidence supportevidence weight 10.5 across 6 manuscripts · 4 narrative, educational, or cited context · 1 independent primary study · 1 systematic review or meta-analysis

The chapter restates that painful sensation has been described more frequently in the nondominant hemisphere. Ictal cold is suspected to show left-hemispheric predominance. This finding provides no lateralization information. No thermal-response-specific lateralization result is supplied.

Source-defined result groups 4
Localization: InsularObserved proportion 11.6%all thermal responses · warm versus cold sensations · evoked thermal response1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · no thermal sensation · patients1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelywarm sensations · warm versus cold sensations · evoked thermal response1 manuscript · 1 reported value · not pooled
Localization: InsularSource-defined values retained separatelycold sensations · warm versus cold sensations · evoked thermal response1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • pain; warmth auraTable 3 lists pain or warmth aura as localising to secondary somatosensory cortex or insula.PDF p.10, Table 3
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • thermal sensations after paresthesiasThermal sensations followed paresthesias in the qualitative ordering of somatosensory stimulation responses.PDF p.5, Somatosensory Sensations
  • thermal response around insular central sulcusThermal responses were evoked by stimulation around the central sulcus of the insula.PDF p.5, Somatosensory Sensations
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal coldIctal cold has been suspected to show left-hemispheric predominance.PDF p.12, Conclusion
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • thermal sensationsThermal sensations numbered 64 (11.7%) and were evoked mainly around the central sulcus in the median insula; warm sensations were more frequent than cold sensations.PDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3B
Reported values
  • thermal 64/550 (11.7%)thermal sensationsPercentage · n/N 64/550 · 64 thermal responses in the 550-response series · all thermal responses · stimulation-evoked thermal sensationPDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3B
  • warm sensations 9.7%thermal sensationsPercentage · 64 thermal responses in the 550-response series · warm sensations · stimulation-evoked thermal sensationPDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3B
  • cold sensations 3.8%thermal sensationsPercentage · 64 thermal responses in the 550-response series · cold sensations · stimulation-evoked thermal sensationPDF p.3, Results and Table 1; PDF p.4, Somato-sensory Responses and Fig. 3B
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • thermal somatosensory auraThermal sensations were reported in five patients.PDF p.3, Results, Aurae; PDF p.8, Discussion
Reported values
  • 5 patientsthermal somatosensory auraCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae; PDF p.8, Discussion
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • anesthesia; paresthesia; thermic dispersion; painful sensationThe source reports anesthesia, paresthesia, or thermic dispersion mainly with parietal stimulation, with the main effect in postcentral gyrus but additional involvement of precuneus and posterior cingulum; insular stimulation induced paresthesias and localized warmth, and painful sensations were preferentially associated with the posterior two thirds of the insula and were more frequently described in the nondominant hemisphere.PDF p.14, Somato-sensory sensations and pain

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Moving visual phenomena (motion-specific: moving dots, patterns, streams - without form)Source terms: Moving visual phenomenaReported: Dominant hemisphereAlso reported: Non-dominant hemisphere5 manuscripts · 7 findings · 1 reported value
Weighted evidence supportevidence weight 10.4 across 5 manuscripts · 2 independent primary study · 2 narrative, educational, or cited context · 1 systematic review or meta-analysis

The review assigns non-dominant context to body-image distortion and dominant parietotemporal context to the distinct manifestation of reading and writing impairment; no direction is stated for kinetopsia, macropsia, or micropsia. No hemisphere or side-relative direction is reported. No lateralizing direction is reported for the sensation of objects moving during visual illusions. No lateralization relationship is reported. The review's visual-stimulation description reports no hemisphere or lateralization direction. No lateralizing direction is reported for the revolving or rotating visual image. No lateralizing direction is reported for moving lights or objects across the visual field.

Evidence by contributing manuscript 5

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • parietal association seizure; macrosomatognosis; microsomatagnosis; epileptic kinetopsia; macropsia; micropsiaThe review relates non-dominant parietal association seizures to distortions of body image, superior parietal lobule and precuneus seizures to enlarged or shrunken body-part perception, epileptic kinetopsia to superior parietal lobule/intraparietal sulcus, and macropsia or micropsia to precuneus involvement; dominant parietotemporal seizures may cause reading and writing impairment.PDF p.7, Parietal association areas; PDF p.3, Figure 1
  • visual association area; complex visual hallucination; kinetopsia; macropsia; micropsia; autoscopyComplex visual hallucinations in occipital epilepsy are linked to prestriate cortex or propagation to adjacent temporoparietal areas; formed hallucinations and visual distortions such as kinetopsia, macropsia, micropsia, and rarely autoscopy are described.PDF p.8, Visual association areas; PDF p.3, Figure 1
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • visual motion, blurry vision, and visual distortionsStimulation of the precuneus, posterior cingulum, or mesial parieto-occipital region produces blurry vision or visual motions, and visual distortions such as micropsia, macropsia, metamorphopsia, and palinopsia suggest activation near the geniculostriate radiation.PDF p.2, section 3.1 Auras
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • KinetopsiaThe review reports that ictal motion-perception distortion (kinetopsia) has been mapped to the superior parietal lobule and intraparietal sulcus and has been reported in seizures from the temporo-parietal-occipital junction.PDF p.6, section 1.12
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 2 findings · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • revolving or rotating visual imageIn the cited Penfield and Kristiansen series, five patients described the visual image as revolving or rotating.PDF p.2, Introduction
  • moving lights or objectsA few patients described lights or objects moving across the visual field.PDF p.4, Results, Visual auras
Reported values
  • 5/11 cited patientsrevolving or rotating visual imageProportion · n/N 5/11 · 11 cited patients with visual sensations · seizure onsetPDF p.2, Introduction
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • objects moving in visual illusionSome patients with visual illusions described objects moving.PDF p.3, Results, Aurae

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Psychic auraReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side6 manuscripts · 18 findings · 12 reported values
Weighted evidence supportevidence weight 10 across 6 manuscripts · 1 independent primary study · 1 systematic review or meta-analysis · 3 narrative, educational, or cited context · 1 case report or observation

In one case with a left amygdala/hippocampal cavernoma and left temporal EEG onset, right head/eye version and a figure-of-4 posture preceded rare focal-to-bilateral tonic-clonic seizures. The illustrative case reports left temporal ictal EEG onset and a left-sided structural/metabolic temporal extension. The review explicitly states that autoscopic phenomena have no lateralizing value. Right head/eye version and right-arm extension in the figure-of-4 posture were contralateral to the case's left-hemisphere onset. The review classifies fear as nonlateralizing while discussing possible temporal or frontal psychic-aura associations without a hemispheric direction. Other psychic-aura subcategories did not differ significantly between TL and T+ groups; no hemisphere or body-side direction is reported. This lateral-versus-mesial temporal statistic provides no hemispheric lateralization. The lateral-temporal prevalence range provides no hemispheric direction. The occurrence odds provide no hemispheric direction. The lateral-TLE prevalence range provides no hemispheric direction. The mesial-TLE prevalence range provides no hemispheric direction. The educational statement does not provide lateralization evidence.

Source-defined result groups 4
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Fear aura/psychic aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Fear aura/psychic aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 8 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • other psychic auraOther psychic auras did not differ significantly between TL and T+ groups across forced thinking, distortion of reality, and urge to move.PDF p.6, Table 2
Reported values
  • T+ 4.3%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • T+ 0%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 0%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • TL 3.4%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • T+ 4.3%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • T+ 0%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 3.4%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • TL 0%other psychic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfCase report or observation · 3 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • psychic aura; abdominal aura; automotor seizure; figure-of-4 signIn an illustrative 36-year-old right-handed man with a left amygdala/hippocampal cavernoma, seizures began with déjà vu and epigastric rising, evolved to automotor features and rarely focal-to-bilateral tonic-clonic seizures, and showed right head/eye version plus a figure-of-4 posture before generalisation; left temporal EEG onset and the posture were consistent with left hemispheric onset.PDF p.5, Video case 3; PDF p.6, Video case 3 and Figure 4 caption
  • psychic aura; ictal dysphasiaIn an illustrative 27-year-old woman with a non-lesional MRI and left temporal PET abnormality, seizures began with fear/anxiety and sometimes ear noise followed by difficulty speaking; she could follow visual but not verbal commands, and ictal EEG showed left temporal onset suggesting neocortical onset.PDF p.6, Video case 4; PDF p.6, Figure 5 caption
  • psychic and abdominal aura; figure-of-4 signIn video case 3, a 36-year-old right-handed man with a left amygdala/hippocampal-head cavernoma had déjà vu and epigastric rising followed by oral and manual automatisms and loss of awareness; before generalization, right head and eye version and a figure-of-4 posture with the left arm flexed and right arm extended lateralised onset to the left hemisphere, concordant with left temporal EEG onset.PDF p.6, Video case 3 and Figure 4
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Fear aura/psychic auraTable 3 reports 5 studies assessing Fear aura/psychic aura.PDF p.6, Table 3
  • Fear aura/psychic auraTable 3 reports 81 patients assessed for Fear aura/psychic aura.PDF p.6, Table 3
  • Fear aura/psychic auraTable 3 reports 0–40% as the percentage range or value for Fear aura/psychic aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Fear aura/psychic auraTable 4 reports overall odds of 0.10 for occurrence of Fear aura/psychic aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Fear aura/psychic auraTable 4 reports a 95% confidence interval of 0.02–0.45 for the overall odds of Fear aura/psychic aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Fear aura/psychic auraThe heterogeneity test for the Table 4 odds estimate for Fear aura/psychic aura has p=0.0243.PDF p.7, Table 4
  • Fear aura/psychic aura; lateral versus mesial comparisonTable 5 reports 4 studies comparing Fear aura/psychic aura in lateral and mesial TLE.PDF p.9, Table 5
  • Fear aura/psychic aura; lateral TLE patient denominatorTable 5 reports 58 lateral-TLE patients assessed for Fear aura/psychic aura.PDF p.9, Table 5
  • Fear aura/psychic aura; mesial TLE patient denominatorTable 5 reports 87 mesial-TLE patients assessed for Fear aura/psychic aura.PDF p.9, Table 5
  • Fear aura/psychic aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 0–40% for Fear aura/psychic aura.PDF p.9, Table 5
  • Fear aura/psychic aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 18.8–35.5% for Fear aura/psychic aura.PDF p.9, Table 5
Reported values
  • 0–40%Fear aura/psychic auraPercentage Range · Lateral temporal epilepsy patients assessed for Fear aura/psychic aura · ictalPDF p.6, Table 3
  • odds 0.10odds of occurrence; Fear aura/psychic auraOdds · Lateral temporal epilepsy patients assessed for Fear aura/psychic aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 0–40%Fear aura/psychic aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Fear aura/psychic aura · Lateral TLE patients assessed for Fear aura/psychic aura · ictalPDF p.9, Table 5
  • 18.8–35.5%Fear aura/psychic aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Fear aura/psychic aura · Mesial TLE patients assessed for Fear aura/psychic aura · ictalPDF p.9, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • psychic aurasPsychic auras include emotional symptoms and familiarity distortions; the symptomatogenic zone is generally temporal neocortex or mesial temporal structures, except that forced thoughts are generally observed in FLE. Fear is associated with amygdala, hippocampal, mesial frontal, or temporal-neocortical activation, and Table 1 lists fear as nonlateralizing.PDF p.3, section 3.1 Auras; PDF p.2, Table 1
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Psychic auraPsychic auras consist of complex hallucinations and illusions affecting different senses, including distortions of familiarity such as déjà vu or jamais vu, often with emotional changes such as fear and sometimes with complex visual or auditory phenomena.PDF p.3, Auras, subsection Psychic auras; PDF p.2, Table 1
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • psychic and autoscopic aurasThe review states that psychic auras include complex hallucinations or illusions such as autoscopy, fear, elation, déjà vu, and jamais vu. The temporal lobe is usually involved in autoscopic phenomena, but they have no lateralizing value; stimulation has elicited related sensations from the temporal convexity or posterior temporal-occipital/parietal junction, with mesial temporal structures concurrently involved in most cited cases.PDF p.2, Psychic auras; PDF p.3, Psychic auras (continued)

6 contributing manuscripts; source-reported values remain separate and are not pooled.

hemifacial clonic jerksReported: ContralateralAlso reported: Right hemisphere6 manuscripts · 19 findings · 6 reported values
Weighted evidence supportevidence weight 9.9 across 6 manuscripts · 2 systematic review or meta-analysis · 2 case report or observation · 2 narrative, educational, or cited context

The educational opercular-seizure description associates oral symptoms and speech difficulty with focal clonic movements of the contralateral face. The review states that focal clonic face seizures have high localizing value and involve the contralateral central (Rolandic) operculum. A right middle frontal gyrus lesion case had left-face/left-arm clonic spread and fencing posture, with semiology and ictal EEG interpreted as right frontocentral onset. Persistent focal right perioral clonic seizures were observed after resection; the cerebral reference side for the right perioral label is not stated in the figure caption. The review states that clonic facial jerking represents activation of the contralateral facial motor area in M1. No source-supported hemispheric or body-side lateralization is reported. Face clonic/grimace was reported across 11.8–33.3% in the lateral-temporal studies, with an overall association grade of Low. The source reports a median onset latency of 19 seconds for Face clonic/grimace in a lateral-temporal comparison. The reported overall odds for Face clonic/grimace in lateral TLE were 0.26 with a 95% confidence interval of 0.12–0.57 and heterogeneity-test P=0.2896. The source reports a lateral-TLE Face clonic/grimace percentage range of 11.8–33.3%. The source reports a mesial-TLE Face clonic/grimace percentage range of 15–68.8%. The ventral-versus-dorsal insular focus record provides no lateralizing information.

Source-defined result groups 6
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Face clonic/grimace · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereSource-defined values retained separatelyAll reported · single patient and postoperative seizure observation1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · propagation timing · seconds from seizure onset1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Face clonic/grimace · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfCase report or observation · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • aura; behavioural arrest; left-face clonic activity; fencing postureIn an illustrative 50-year-old man with a right middle frontal gyrus cystic lesion, a seizure evolved from an aura to behavioural arrest, left-face clonic movements spreading over the left arm, and left-arm extension in a fencing posture before secondary generalisation; the authors state that the semiology and ictal EEG supported right frontocentral onset.PDF p.3, Video case 1 and Figure 1; PDF p.3, Figure 2 caption
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 13 findings · 5 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Face clonic/grimaceTable 3 reports 3 studies assessing Face clonic/grimace.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports 51 patients assessed for Face clonic/grimace.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports 11.8–33.3% as the percentage range or value for Face clonic/grimace; the overall association grade is Low.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports 1 study with onset timing for Face clonic/grimace.PDF p.6, Table 3
  • Face clonic/grimaceTable 3 reports an onset latency of 19 s for Face clonic/grimace.PDF p.6, Table 3
  • odds of occurrence; Face clonic/grimaceTable 4 reports overall odds of 0.26 for occurrence of Face clonic/grimace in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Face clonic/grimaceTable 4 reports a 95% confidence interval of 0.12–0.57 for the overall odds of Face clonic/grimace.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Face clonic/grimaceThe heterogeneity test for the Table 4 odds estimate for Face clonic/grimace has p=0.2896.PDF p.7, Table 4
  • Face clonic/grimace; lateral versus mesial comparisonTable 5 reports 3 studies comparing Face clonic/grimace in lateral and mesial TLE.PDF p.9, Table 5
  • Face clonic/grimace; lateral TLE patient denominatorTable 5 reports 51 lateral-TLE patients assessed for Face clonic/grimace.PDF p.9, Table 5
  • Face clonic/grimace; mesial TLE patient denominatorTable 5 reports 67 mesial-TLE patients assessed for Face clonic/grimace.PDF p.9, Table 5
  • Face clonic/grimace; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 11.8–33.3% for Face clonic/grimace.PDF p.9, Table 5
  • Face clonic/grimace; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 15–68.8% for Face clonic/grimace.PDF p.9, Table 5
Reported values
  • 11.8–33.3%Face clonic/grimacePercentage Range · Lateral temporal epilepsy patients assessed for Face clonic/grimace · ictalPDF p.6, Table 3
  • median onset latency 19 sFace clonic/grimaceMedian · Lateral temporal epilepsy study reporting onset timing for Face clonic/grimace · ictal onsetPDF p.6, Table 3
  • odds 0.26odds of occurrence; Face clonic/grimaceOdds · Lateral temporal epilepsy patients assessed for Face clonic/grimace · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 11.8–33.3%Face clonic/grimace; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Face clonic/grimace · Lateral TLE patients assessed for Face clonic/grimace · ictalPDF p.9, Table 5
  • 15–68.8%Face clonic/grimace; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Face clonic/grimace · Mesial TLE patients assessed for Face clonic/grimace · ictalPDF p.9, Table 5
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 2 findings
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • oral symptoms; sialorrhea; speech difficulties; focal clonic movements of the contralateral faceThe source's introductory clinical description associates opercular seizures with oral symptoms such as sialorrhea and speech difficulties, together with focal clonic movements of the contralateral face.PDF p.2, Introduction
  • focal clonic seizures of the face; central Rolandic operculumThe discussion attributes a highly localizing value to focal clonic face seizures, stating that they always involve the contralateral central (Rolandic) operculum.PDF p.8, Discussion
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Clonic facial jerkingThe review explains that clonic jerking of the face represents activation of the contralateral facial motor area in primary motor cortex (M1).PDF p.4, section 1.6
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • focal nonmotor unaware seizures; hyperkinetic features; asymmetric tonic posturing; elementary facial contractionsThe source relates more ventrally located insular foci to focal nonmotor unaware seizures and more dorsally located foci to motor manifestations caused by propagation toward frontal areas, including often sleep-related hyperkinetic features, asymmetric tonic posturing, or elementary facial contractions; patients are frequently unaware of these manifestations.PDF p.5, Ictal Semiology; PDF p.16, Summary
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfCase report or observation · 1 finding · 1 reported value
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • right perioral clonic seizures after opercular resection in Patient 18In Patient 18, the posterior central operculum and opercular part of the central sulcus were highly epileptogenic on EI; after resection including those structures, focal right perioral clonic seizures without loss of consciousness persisted 20 months after surgery, which the authors state strongly suggested incomplete resection of the anterior central operculum.PDF p.10, Figure 4 caption; PDF p.6, Surgery resection and pathology
Reported values
  • Persistent focal right perioral clonic seizures at 20 months after surgeryright perioral clonic seizures after opercular resection in Patient 18Count · Patient 18 in the present series · ictal SEEG episode and postoperative follow-upPDF p.10, Figure 4 caption; PDF p.6, Surgery resection and pathology

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal pout (perioral dystonic protrusion/pursing - distinct from chapeau)Source terms: Ictal poutReported: Bilateral4 manuscripts · 10 findings · 2 reported values
Weighted evidence supportevidence weight 9.9 across 4 manuscripts · 1 narrative, educational, or cited context · 3 systematic review or meta-analysis

The review describes bilateral lip and chin contraction in chapeau de gendarme or ictal pout, with no source-supported hemispheric direction. The review lists multiple bilateral/symmetrical facial descriptors but explicitly warns that the labels do not always refer to the same feature. The review associations contain no lateralization information. No lateralization information is reported. No lateralizing direction is reported for the frontal-localization restatement. No source lateralization is reported. No lateralization evidence is reported.

Evidence by contributing manuscript 4

Alphabetical by manuscript.

chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 1 reported value
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • chapeau de gendarme; ictal poutingThe source reports a frequency of 20% for chapeau de gendarme; ictal pouting.PDF p.13, Table 3
  • chapeau de gendarme; ictal pouting; reported frequency rangeThe source reports a frequency range of 0–100% for chapeau de gendarme; ictal pouting.PDF p.13, Table 3
  • chapeau de gendarme; ictal pouting; ACC association gradeTable 3 assigns the source's High overall association grade to chapeau de gendarme; ictal pouting.PDF p.13, Table 3
Reported values
  • 20% (frequency range 0–100%)chapeau de gendarme; ictal poutingPercentage · Reviewed ACC seizure cases with reported semiology · ictal onset and propagationPDF p.13, Table 3
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 3 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • chapeau de gendarme; ictal pout signThe chapeau de gendarme or ictal pout sign is a downturned mouth caused by bilateral lip and chin contraction and, when seen early in a seizure, is described as highly localising to frontal onset, particularly anterior cingulate, orbitofrontal, mesio-prefrontal, or premotor cortex.PDF p.9, Chapeau de gendarme
  • focal atonic seizure; gelastic seizure; ictal poutingFocal atonic seizures may indicate involvement of negative motor areas or the supplementary motor area; gelastic seizures and ictal pouting may occur in mesiofrontal and anterior cingulate frontal seizures and are discussed as separate semiologies.PDF p.4, Other frontal regions; PDF p.3, Figure 1
  • chapeau de gendarme; ictal pout signThe chapeau de gendarme or ictal pout sign is a downturned mouth caused by bilateral lip and chin contraction and, when seen early in a seizure, is described as highly localising to frontal onset, particularly anterior cingulate, orbitofrontal, mesio-prefrontal, or premotor cortex.PDF p.9, Chapeau de gendarme
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • pouting; mimic automatismsTwo restricted-OFC cases with mimic automatisms displayed pouting.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 2 patientspouting; mimic automatismsCount · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • semiologic synonym setThe review records non-identical descriptions including “pouting,” “bilateral tonic facial contraction,” “symmetrical down-turned mouth,” “grimacing,” “inverted smile with a tearful expression,” “mouth turning down with symmetric puckering,” and “labial corners lowered with chin contraction.”PDF p.2, Introduction; PDF p.4, Study characteristics
  • chapeau de gendarme / ictal poutingThe review describes the “chapeau de gendarme” sign, also known as ictal pouting, as a distinctive focal-epilepsy facial expression with a turned-down mouth and symmetrical contraction of the lips and chin.PDF p.1, Abstract; PDF p.2, Introduction
  • major componentThe same video-analysis study described a major component with symmetrical downward contraction of the mouth corners.PDF p.4, Study characteristics

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Tonic arm posturingReported: BilateralAlso reported: Contralateral4 manuscripts · 6 findings · 4 reported values
Weighted evidence supportevidence weight 9.87 across 4 manuscripts · 2 independent primary study · 2 case report or observation

This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. With a left-sided source in Case 4, tonic posturing was recorded as bilateral with right predominance or as right-upper-limb posturing. The patient-level observation reports bilateral tonic activity with right arm extension. The case reports left upper-limb tonic posturing but no direction relative to seizure onset. The case observation reports right-arm tonic posturing but gives no direction relative to seizure onset. This finding provides no lateralization information.

Source-defined result groups 3
Localization: M, ML, and L temporal-lobe seizure-onset subtypesObserved proportion 15.4%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: M, ML, and L temporal-lobe seizure-onset subtypesObserved proportion 29.2%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: M, ML, and L temporal-lobe seizure-onset subtypesObserved proportion 27.8%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 4

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 2 bilateral tonic right-arm extensionBilateral tonic activity with right arm extension was listed for patient 2.PDF p.4, Figure 3
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • upper-limb tonic posturingUpper-limb tonic posturing over the whole seizure course did not differ significantly across M, ML, and L groups.PDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
Reported values
  • 5/18 (27.8%)upper-limb tonic posturingPercentage · n/N 5/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • 7/24 (29.2%)upper-limb tonic posturingPercentage · n/N 7/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
  • 2/13 (15.4%)upper-limb tonic posturingPercentage · n/N 2/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · ictal course, early or late combinedPDF p.6, Table 3; PDF p.9, Nondifferentiating ictal characteristics
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfCase report or observation · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • right-arm tonic posturing in Fig. 1In Figure 1, the rightward head deviation was followed by right-arm tonic posturing.PDF p.4, Fig. 1
Reported values
  • 1 caseright-arm tonic posturing in Fig. 1Count · n/N 1/1 · patient 7 (M.B.) · ictal evolutionPDF p.4, Fig. 1
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 3 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • bilateral or right upper-limb tonic posturingTable 2 records bilateral (right greater than left) or right-upper-limb tonic posturing in Case 4.PDF p.6, Table 2 Case 4
  • left upper-limb tonic posturingTable 2 records tonic posturing of the left upper limb in a seizure sequence.PDF p.6, Table 2 Case 1 Sz1

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal dysphoriaReported: IpsilateralAlso reported: Right hemisphere3 manuscripts · 4 findings · 5 reported values
Weighted evidence supportevidence weight 9.65 across 3 manuscripts · 1 independent primary study · 1 systematic review or meta-analysis · 1 narrative, educational, or cited context

The temporal-plus description preserves contraversive eye/head and ipsilateral tonic-motor relations without assigning a left/right cerebral hemisphere. The cited study restatement reports postictal flattened or depressed affect more often after right than left hemispheric seizures. No lateralizing direction is reported. The source proposes that more frequent right lateralization of T+ epilepsy might partly explain postictal dysphoria but explicitly states that the relation remains controversial.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • post-ictal dysphoric stateA dysphoric post-ictal state was more frequent in T+ than TL seizures.PDF p.1, abstract; PDF p.6, Table 2; PDF p.9, Post-ictal signs
  • post-ictal dysphoria and focus lateralizationThe source states that the association of post-ictal dysphoria with T+ epilepsy might partly reflect more frequent right lateralization of T+ epilepsy, but that the lateralization relation remains controversial.PDF p.9, Post-ictal signs
Reported values
  • TL 6.8%post-ictal dysphoric statePercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · post-ictalPDF p.1, abstract; PDF p.6, Table 2; PDF p.9, Post-ictal signs
  • T+ 39.1%post-ictal dysphoric statePercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · post-ictalPDF p.1, abstract; PDF p.6, Table 2; PDF p.9, Post-ictal signs
  • P=0.0001post-ictal dysphoric stateP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · post-ictalPDF p.1, abstract; PDF p.6, Table 2; PDF p.9, Post-ictal signs
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal flattened or depressed affectFlattened or depressed affect was more frequent after right than left hemispheric seizures.PDF p.11, section 5.6
Reported values
  • 40%postictal flattened or depressed affectPercentage · 19 patients contributing 32 right and 33 left hemispheric seizures · right hemispheric seizures · postictalPDF p.11, section 5.6
  • 12.5%postictal flattened or depressed affectPercentage · 19 patients contributing 32 right and 33 left hemispheric seizures · left hemispheric seizures · postictalPDF p.11, section 5.6
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • temporal plus epilepsy; gustatory; vestibular; auditory; contraversive eyes/head; piloerection; ipsilateral tonic motor; postictal dysphoriaThe source describes temporal-plus semiology as more often including gustatory, vestibular, or auditory symptoms, contraversive eye or head manifestations, piloerection, ipsilateral tonic motor signs, and a more dysphoric postictal phase.PDF p.2, Introduction

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal central apneaReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphere3 manuscripts · 10 findings · 19 reported values
Weighted evidence supportevidence weight 9.6 across 3 manuscripts · 1 manuscript weight pending · 2 independent primary study · 1 structured design not resolved

The illustrated late-onset ICA seizure had right anterobasal EEG onset. The illustrated early-onset ICA seizure had left mesial-temporal EEG onset. This record provides no seizure lateralization. No hemisphere or body-side result is reported. No lateralizing direction is reported for ictal versus postictal central apnoea. No seizure lateralization is reported. The authors interpret premortem peri-ictal breathing dysfunction, specifically prolonged ictal and postictal central apnoea, as a potential SUDEP risk marker and propose >14 seconds for postictal central apnoea and >17 seconds for ictal central apnoea as study-derived thresholds that could inform development of a validatable risk index; the Discussion separately describes >=15 seconds as prolonged postictal central apnoea and calls for further prospective validation. No lateralizing direction is reported for ICA presence frequency. No lateralizing direction is reported for ictal central apnea frequency. No lateralization evidence is reported.

Source-defined result groups 1
Localization: TemporalSource-defined values retained separatelyAll reported · Ictal EEG onset preceding ICA onset · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdfStructured design not resolved · 3 findings · 2 reported values
lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The investigators prospectively enrolled 85 consecutive adult persons with epilepsy undergoing standard-of-care SEEG evaluation in an epilepsy monitoring unit from June 2016 through April 2023. They prospectively collected 220 seizures; 39 seizures in 13 patients were excluded because breathing signals were unreliable or artifactual. The analyzed population was 179 seizures in 72 patients with reliable artifact-free respiratory signals. Real-time SEEG, video, thoracic and abdominal respiratory inductance plethysmography, oxygen saturation, heart rate, and four-channel EKG were obtained simultaneously. The analyzed cohort included 1,196 intracranial depth electrodes (mean 16.6 +/- 3.0 per patient); 55 seizures in 23 patients had ICA. All seizures were classified by seizure onset zone (SOZ), defined by the source as the cortical area from which seizures start. The source separately defined the epileptogenic zone (EZ) as the region resected to produce seizure freedom; only patients who underwent resective surgery or laser interstitial thermal therapy and had Engel class I outcome with at least six months of follow-up were classified for EZ determination. Of 31 Engel class I patients, 30 had at least six months of follow-up (mean 22.8 months +/- SD 13.1, range 6-50) and one did not. The source reports separate SOZ and EZ analyses and does not authorize conversion between their patient- and seizure-level denominators. A high-gamma analysis used a subset of 20 patients with 39 ICA seizures whose SEEG implantation sampled all regions of breathing interest; the early-onset subgroup contained 27 seizures in 13 patients and the late-onset subgroup 12 seizures in seven patients. Predictive associations were assessed with separate simple logistic-regression models; statistically significant semiologic signs were also entered as one additional predictor with ICA in multiple logistic regression. Fisher's exact test assessed ICA presence and mesial temporal sclerosis (MTS). The source used two-sided p < 0.05 for statistical significance, made no multiple-comparison correction because the study was exploratory, and treated z >= 4 as significant for the quantitative gamma analysis.
Findings
  • late-onset ictal central apnea illustrative seizureFigure 1 illustrates Patient 35, seizure 1, with right implantation: right anterobasal low-amplitude fast activity at EEG onset spread rapidly to the temporal pole, and ICA emerged after mesial temporal involvement of amygdala, anterior hippocampus, and posterior hippocampus, 21 seconds after ictal EEG onset.PDF p.15, Figure 1A-C; PDF p.16, Figure 1 caption continuation
  • early-onset ictal central apnea illustrative seizureFigure 2 illustrates Patient 25, seizure 1, with bilateral implantation: left mesial temporal low-amplitude fast activity at EEG onset in the left anterior hippocampus, left posterior hippocampus, and left amygdala was followed by ICA within two seconds after ictal EEG onset.PDF p.17, Figure 2A-C; PDF p.18, Figure 2 caption continuation
  • ictal central apnea (ICA)ICA occurred in 55/179 (30.7%) of the analyzed seizures.PDF p.3, Abstract; PDF p.6, Results; PDF p.7, Ictal central apnea presence and characteristics
Reported values
  • 21 seconds from ictal EEG onset to ICA onsetlate-onset ictal central apnea illustrative seizureCount · One illustrative SEEG-recorded seizure, Patient 35 seizure 1 · late-onset ICA after ictal EEG onsetPDF p.15, Figure 1A-C; PDF p.16, Figure 1 caption continuation
  • ICA presence frequency 30.7%ictal central apnea (ICA)Percentage · n/N 55/179 · 179 seizures in 72 adult patients with reliable artifact-free respiratory signals; 55 ICA-positive seizures · ictal ICA occurrencePDF p.3, Abstract; PDF p.6, Results; PDF p.7, Ictal central apnea presence and characteristics
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 2 findings · 3 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 4.80 · 2 × 1.2 × 2
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • ictal central apnea (ICA)ICA occurred in 71 of 406 analyzed focal-onset seizures and in 27 of 69 analyzed patients.PDF p.1, Abstract Results; PDF p.3, Results, ICA in Focal Seizures; PDF p.5, Table 1
  • awareness of ICANo patient reported awareness of apnea when actively tested or interrogated after seizures with ICA only.PDF p.6, Awareness of Apnea in the Postictal Period and the Role of External Interventions; PDF p.10, Discussion of unawareness
Reported values
  • ICA in 27/69 patients (39%)ictal central apnea (ICA)Percentage · n/N 27/69 · 69 patients and 406 focal-onset seizures without secondary bilateral tonic-clonic evolution · ictalPDF p.1, Abstract Results; PDF p.3, Results, ICA in Focal Seizures; PDF p.5, Table 1
  • ICA in 71/406 seizures (17.5%)ictal central apnea (ICA)Percentage · n/N 71/406 · 69 patients and 406 focal-onset seizures without secondary bilateral tonic-clonic evolution · ictalPDF p.1, Abstract Results; PDF p.3, Results, ICA in Focal Seizures; PDF p.5, Table 1
  • 0 reported awareness among 35 actively tested ICA-only seizuresawareness of ICACount · n/N 35/47 · 47 seizures with ICA only, of which 35 were actively tested/interrogated · postictalPDF p.6, Awareness of Apnea in the Postictal Period and the Role of External Interventions; PDF p.10, Discussion of unawareness
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdfIndependent primary study · 5 findings · 14 reported values
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf
Independent primary study · Class II · Evidence weight 4.80 · 2 × 1.2 × 2
The study enrolled 2632 children and adults with epilepsy at nine epilepsy-monitoring centres in the USA and UK between 2011 and 2021; 164 were lost to follow-up and 2468 participants were included in the primary follow-up analyses. There were 38 SUDEP outcomes and two near-SUDEP events. During admission, 1660 participants had seizures captured, 1432 had analysable seizures, and the report describes 1091 analysable generalised convulsive seizures and 2117 non-convulsive seizures. The primary endpoint was time to SUDEP or censoring due to other causes. Cox proportional hazards models assessed clinical and electroclinical predictors; repeated seizure predictors were aggregated to the most severe feature per patient, using the maximum for continuous features or presence for categorical features. Analyses used prolonged video-EEG, ECG, pulse oximetry, and chest/abdominal inductance plethysmography. Statistical significance in primary analyses required two-sided p<0.05 after Bonferroni correction; the report states that secondary-analysis confidence intervals were not intended for hypothesis testing. Main-text results include varying denominators and missing data, which are retained below.
Findings
  • ictal central apnoeaIctal central apnoea was present in 9/25 (36%) of SUDEP-or-near-SUDEP participants with available data versus 344/799 (43%) of non-SUDEP participants, but median duration was longer at 44 seconds (IQR 28-49) versus 17 seconds (10-27); each 10-second increase was associated with higher SUDEP risk in the primary Cox model, HR 1.11 (95% CI 1.05-1.18; p<0.0001), while the 5-year risk was 7.4% (1.3-13.1) for median duration >17 seconds versus 3.7% (1.3-6.1) for <=17 seconds, a threshold comparison with p=0.11. The adjusted association was not significant after clinical covariate adjustment, and exclusion of possible and near-SUDEP cases gave HR 1.06 (0.82-1.37).PDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • ictal central apnoeaThe Discussion restates that brief ictal central apnoea is commonly seen in about 37% of temporal lobe seizures, whereas prolonged ictal central apnoea is less common.PDF p.9, Discussion
  • ictal central apnoea; postictal central apnoeaThe Discussion restates that ictal central apnoea is associated with postictal central apnoea, suggesting that individuals with ictal central apnoea are more likely to develop postictal breathing cessation.PDF p.9, Discussion
  • ictal central apnoea; amygdala; hippocampus; mesial temporal poleAccording to brain electrical stimulation studies cited by the authors, ictal central apnoea likely arises from seizure discharges invading respiratory-modulating structures including the amygdala, hippocampus, and mesial temporal pole.PDF p.9, Discussion
  • prolonged peri-ictal central apnoeaThe authors interpret premortem peri-ictal breathing dysfunction, specifically prolonged ictal and postictal central apnoea, as a potential SUDEP risk marker and propose >14 seconds for postictal central apnoea and >17 seconds for ictal central apnoea as study-derived thresholds that could inform development of a validatable risk index; the Discussion separately describes >=15 seconds as prolonged postictal central apnoea and calls for further prospective validation.PDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion
Reported values
  • median duration 17 secondsictal central apnoeaMedian · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · median duration ≤17 seconds · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 5-year risk 3.7%ictal central apnoeaPercentage · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · median duration ≤17 seconds · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • median duration 44 secondsictal central apnoeaMedian · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · SUDEP or near-SUDEP · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 344/799 (43%) with ictal central apnoeaictal central apnoeaPercentage · n/N 344/799 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · non-SUDEP · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • HR 1.11 per 10-second increaseictal central apnoeaHazard ratio · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · primary Cox model · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 9/25 (36%) with ictal central apnoeaictal central apnoeaPercentage · n/N 9/25 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · SUDEP or near-SUDEP · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 5-year risk 7.4%ictal central apnoeaPercentage · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · median duration >17 seconds · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 608/1432 had missing ictal-apnoea dataictal central apnoeaPercentage · n/N 608/1432 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · overall cohort · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • HR 1.06 after excluding possible and near-SUDEP casesictal central apnoeaHazard ratio · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · exclusion analysis · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • p=0.11ictal central apnoeaP value · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available ictal central-apnoea data · ictalPDF p.1, Summary and Interpretation; PDF p.5, Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • About 37% for brief ictal central apnoeaictal central apnoeaPercentage · Temporal lobe seizures in the cited prior literature · ictalPDF p.9, Discussion
  • >17 seconds ictalprolonged peri-ictal central apnoeaDuration · Source-authored interpretation based on the primary cohort’s peri-ictal apnoea analyses · Proposed study-derived threshold · ictal and postictalPDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion
  • >14 seconds postictalprolonged peri-ictal central apnoeaDuration · Source-authored interpretation based on the primary cohort’s peri-ictal apnoea analyses · Proposed study-derived threshold · ictal and postictalPDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion
  • ≥15 seconds postictalprolonged peri-ictal central apnoeaOther reported value · Source-authored interpretation based on the primary cohort’s peri-ictal apnoea analyses · Discussion definition of prolonged postictal central apnoea · ictal and postictalPDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Jamais vuReported: Non-dominant hemisphereNo single reliable side5 manuscripts · 5 findings · 2 reported values
Weighted evidence supportevidence weight 9.01 across 5 manuscripts · 1 independent primary study · 3 narrative, educational, or cited context · 1 case report or observation

The cited table describes déjà vu/jamais vu aura as non-lateralising. The case lists déjà vu, jamais vu, and abdominal aura terms without a side or lateralization direction. The review table labels both fear and déjà vu/jamais vu as nonlateralizing, while noting an often-nondominant tendency only for déjà vu/jamais vu. The review describes dysmnesic manifestations as characteristic of MTLE and reports déjà vu more often with nondominant MTLE. No hemisphere or body-side direction is reported.

Evidence by contributing manuscript 5

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 13 déjà/jamais/abdominal auraDéjà vu, jamais vu, and abdominal aura terms were listed for patient 13.PDF p.4, Figure 3
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • fear and déjà vu or jamais vu auras in Table 1Table 1 lists fear as arising from the amygdala, hippocampus, and mesial frontal lobe and as nonlateralizing; it lists déjà vu or jamais vu as arising from the uncus, entorhinal cortex, and temporal neocortex and as nonlateralizing, often nondominant.PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • dysmnesic manifestations, déjà vu, jamais vu, prescience, and “dreamy state”Dysmnesic manifestations are characteristic of MTLE; déjà vu has been reported as predominant in nondominant MTLE, prescience is rarely described, and the “dreamy state” may include déjà vu, strangeness or unreality, and complex auditory or visual hallucinations.PDF p.7, Focal cognitive seizures
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal cognitive (deja vu/jamais vu)Focal cognitive (deja vu/jamais vu) semiology occurred in 6/61 individuals (10%) both as initial semiology and in the combined set-of-semiology.PDF p.3, Results; PDF p.5, Table 2
Reported values
  • Initial 6/61 (10%)Focal cognitive (deja vu/jamais vu)Percentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
  • Combined 6/61 (10%)Focal cognitive (deja vu/jamais vu)Percentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.3, Results; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Deja vu/jamais vu auraTable 2 associates deja vu/jamais vu aura with uncus, entorhinal/perirhinal cortex, and temporal neocortex and describes it as non-lateralising.PDF p.3, Table 2

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Unilateral ictal eye blinkingReported: ContralateralAlso reported: Ipsilateral8 manuscripts · 13 findings · 11 reported values
Weighted evidence supportevidence weight 9 across 8 manuscripts · 1 manuscript weight pending · 1 structured design not resolved · 6 narrative, educational, or cited context · 1 systematic review or meta-analysis

Unilateral eye blinking was more frequent ipsilateral than contralateral to the ictal EEG focus, with both patient-level and seizure-level observations reported. The cited discussion restates that unilateral blinking has been described as ipsilateral to the seizure focus. The review restates three source-relative relations: hemifield visual aura contralateral to occipital onset, unilateral eye blinking ipsilateral to the blinking eye, and epileptic-nystagmus fast component contralateral to the seizure-onset hemisphere. The cited source describes unilateral ictal blinking or winking as a rare automatism that usually indicates an ipsilateral seizure focus. The cited table restates ipsilateral lateralisation for unilateral eye blinking. The review restates unilateral eye blinking as an infrequent but reported ipsilateral lateralizing sign and separately states that it has no localizing value. The cited review restates that unilateral eye blinking is ipsilateral to the EZ in about 80% of cases. The review states that unilateral ictal eye blinking generally lateralizes ipsilateral to the epileptogenic zone, with 83% ipsilateral in the reported subgroup. The cited Wada series is restated as five patients with unilateral blinking ipsilateral to the ictal discharge. A cited study found unilateral blinking ipsilateral in 10/12 patients with a unilateral EEG focus. The cited series is restated as reporting ipsilateral ictal blinking in 2 of 239 cases. The handbook lists ictal unilateral blinking as ipsilateral but does not state the reference side or viewpoint. The handbook lists unilateral eye blinking as ipsilateral but does not state the reference side or viewpoint.

Source-defined result groups 4
Lateralization: Contralateral / IpsilateralObserved proportion 10.3%ipsilateral to ictal EEG focus · 2 contralateral seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 1.7%contralateral to ictal EEG focus · 12 ipsilateral seizures · seizures1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 5.3%contralateral eye blinking · 5 ipsilateral-side patients · patients1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 26.3%ipsilateral eye blinking · 1 contralateral-side patient · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 8

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Unilateral ictal blinkingUnilateral ictal blinking or winking is described as a rare automatism that usually indicates an ipsilateral seizure focus.PDF p.4, Table 2; PDF p.4, section 4; PDF p.5, section 5
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • hemifield visual aura; unilateral eye blinking; epileptic nystagmusHemifield visual aura has good lateralising value to the contralateral occipital lobe; unilateral eye blinking lateralises to the hemisphere ipsilateral to the blinking eye; and in epileptic nystagmus the fast component is contralateral to the seizure-onset hemisphere.PDF p.10, Lateralising signs; PDF p.8, Parieto-occipital junction
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 2 findings
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Ictal unilateral blinkingBoth tables list Ictal unilateral blinking as Ipsilateral.PDF p.2, Lateralizing signs/Localization table row "Ictal unilateral blinking" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Ictal unilateral blinking" (printed p.5)
  • Unilateral eye blinkingBoth tables list Unilateral eye blinking as Ipsilateral; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Unilateral eye blinking*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Unilateral eye blinking" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • unilateral eye blinkingUnilateral eye blinking is observed ipsilateral to the epileptogenic zone in about 80% of cases and often suggests activation of the amygdala or mesial temporal structures.PDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • About 80% ipsilateral to EZunilateral eye blinkingPercentage · patients with focal seizures · ictalPDF p.5, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Unilateral eye blinkingTable 3 associates unilateral eye blinking with mesial temporal involvement and ipsilateral lateralisation.PDF p.4, Table 3
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 4 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral ictal eye blinkingUnilateral ictal eye blinking generally lateralizes ipsilateral to the epileptogenic zone.PDF p.8, section 3.14; PDF p.12, Table 1
  • unilateral eye blinkingWada described five patients whose unilateral blinking was ipsilateral to the ictal discharge.PDF p.8, section 3.14
  • unilateral blinking unassociated with facial clonic activityBenbadis et al. found unilateral blinking ipsilateral in 10 of 12 patients with a unilateral EEG focus.PDF p.8, section 3.14; PDF p.12, Table 1
  • ipsilateral ictal blinkingAnother series found ipsilateral ictal blinking in two patients.PDF p.8, section 3.14
Reported values
  • Unilateral ictal eye blinking ipsilateral in 83%unilateral ictal eye blinkingPercentage · epilepsy monitoring unit patients with unilateral blinking unassociated with facial clonus · Patients with unilateral blinking · ictalPDF p.8, section 3.14; PDF p.12, Table 1
  • Unilateral ictal eye blinking in 1.5% of EMU patientsunilateral ictal eye blinkingPercentage · epilepsy monitoring unit patients with unilateral blinking unassociated with facial clonus · Epilepsy monitoring unit · ictalPDF p.8, section 3.14; PDF p.12, Table 1
  • 5 patients, all ipsilateralunilateral eye blinkingCount · n/N 5/5 · five patients with unilateral ictal blinking · ictalPDF p.8, section 3.14
  • 10/12 (83%) were ipsilateralunilateral blinking unassociated with facial clonic activityPercentage · n/N 10/12 · 914 monitored patients, including 14 with unilateral blinking · unilateral EEG focus · ictalPDF p.8, section 3.14; PDF p.12, Table 1
  • 14/914 (1.5%) had the signunilateral blinking unassociated with facial clonic activityPercentage · n/N 14/914 · 914 monitored patients, including 14 with unilateral blinking · all monitored patients · ictalPDF p.8, section 3.14; PDF p.12, Table 1
  • 2/239 (0.8%)ipsilateral ictal blinkingPercentage · n/N 2/239 · 239 reviewed patients · ictalPDF p.8, section 3.14
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 2 findings · 4 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • unilateral eye blinkingUnilateral eye blinking was observed more often ipsilateral than contralateral to the ictal EEG focus.PDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • unilateral blinkingThe discussion reports that unilateral blinking has been described as ipsilateral to the seizure focus.PDF p.6, Discussion
Reported values
  • 2 contralateral seizures (2% of all 116 seizures)unilateral eye blinkingPercentage · n/N 2/116 · 19 patients with unilateral TLE; eye blinking occurred in 5 ipsilateral-side patients and 1 contralateral-side patient · contralateral to ictal EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • 1 contralateral-side patientunilateral eye blinkingCount · n/N 1/19 · 19 patients with unilateral TLE; eye blinking occurred in 5 ipsilateral-side patients and 1 contralateral-side patient · contralateral eye blinking · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • 12 ipsilateral seizures (11% of all 116 seizures)unilateral eye blinkingPercentage · n/N 12/116 · 19 patients with unilateral TLE; eye blinking occurred in 5 ipsilateral-side patients and 1 contralateral-side patient · ipsilateral to ictal EEG focus · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
  • 5 ipsilateral-side patientsunilateral eye blinkingCount · n/N 5/19 · 19 patients with unilateral TLE; eye blinking occurred in 5 ipsilateral-side patients and 1 contralateral-side patient · ipsilateral eye blinking · ictalPDF p.1, Abstract; PDF p.3, Results and Table 1; PDF p.4, Figure 1; PDF p.6, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • unilateral eye blinkingThe review states that unilateral eye blinking is infrequent but has been reported as a good lateralizing sign to the ipsilateral hemisphere and has no localizing value; its mechanism has not been elucidated.PDF p.6, Unilateral eye blinking

8 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal hypersalivationReported: BilateralAlso reported: ContralateralAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere5 manuscripts · 10 findings · 5 reported values
Weighted evidence supportevidence weight 9 across 5 manuscripts · 1 independent primary study · 1 systematic review or meta-analysis · 3 narrative, educational, or cited context

The educational opercular-seizure description associates oral symptoms and speech difficulty with focal clonic movements of the contralateral face. The cited Chassoux series restatement includes bilateral tonic-clonic seizures alongside oro-alimentary, salivation, dystonic, and head-deviation phenomena. The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. The review says ictal hypersalivation is reported more often with nondominant-hemisphere mesial temporal epilepsy. No source-supported hemispheric lateralization is reported. This record provides no seizure lateralization. No seizure lateralization is reported.

Source-defined result groups 1
Localization: FrontalObserved proportion 19.0%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 5

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • sialorrheaSialorrhea was reported at similar relative frequencies in TL and T+ seizures; the table provides no row-specific P value.PDF p.6, Table 2
Reported values
  • T+ 21.7%sialorrheaPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.6, Table 2
  • TL 25.4%sialorrheaPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.6, Table 2
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 6 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • oral symptoms; sialorrhea; speech difficulties; focal clonic movements of the contralateral faceThe source's introductory clinical description associates opercular seizures with oral symptoms such as sialorrhea and speech difficulties, together with focal clonic movements of the contralateral face.PDF p.2, Introduction
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • SalivationTable 2 reports 4/21 (19%) for Salivation; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • SalivationTable 2 reports 2/12 patients with Salivation in the prefrontal operculum group.PDF p.7, Table 2
  • SalivationTable 2 reports 2/9 patients with Salivation in the precentral Rolandic operculum group.PDF p.7, Table 2
  • SalivationFisher's exact comparison of Salivation between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 4/21 (19%)SalivationPercentage · n/N 4/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 2/12 patientsSalivationProportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 2/9 patientsSalivationProportion · n/N 2/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • salivationSalivation was one of the viscero-vegetative signs elicited by insular stimulation.PDF p.5, Visceral Symptoms
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • Chassoux cohort; oro-alimentary automatisms; salivation; dystonic signs; head deviation; bilateral tonic-clonic seizuresThe review restates that Chassoux et al. described 33 patients with oro-alimentary automatisms, salivation, motor signs including dystonia and head deviation, and bilateral tonic-clonic seizures in the medio-lateral context.PDF p.4, Medio-lateral temporal origin
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal hypersalivationThe review states that ictal hypersalivation is an uncommon sign found more frequently in mesial temporal lobe epilepsy, particularly in the non-dominant hemisphere.PDF p.3, Autonomic seizures

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal amnesiaReported: IpsilateralAlso reported: Right hemisphere2 manuscripts · 3 findings · 4 reported values
Weighted evidence supportevidence weight 8.86 across 2 manuscripts · 2 independent primary study

No hemisphere or body-side relationship is reported. The TL-versus-T+ post-ictal amnesia comparison reports no hemisphere direction. M, ML, and L are temporal onset subtypes, not hemisphere directions.

Source-defined result groups 2
Localization: T+ group / TL groupSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 4 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.86 · 2 × 1.5 × 1.952
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • post-ictal amnesiaPatients were frequently amnesic of the ictal phase, reported in 76.2% of analyzed seizures, although the aura was usually remembered.PDF p.5, Seizure clinical semiology; PDF p.9, Post-ictal signs
  • post-ictal amnesiaPost-ictal amnesia was more frequent in TL than T+ seizures.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Post-ictal signs
Reported values
  • post-ictal amnesia 76.2%post-ictal amnesiaPercentage · 80 analyzed seizures, one typical seizure per patient · post-ictalPDF p.5, Seizure clinical semiology; PDF p.9, Post-ictal signs
  • TL 81.4%post-ictal amnesiaPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · post-ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Post-ictal signs
  • T+ 56.5%post-ictal amnesiaPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · post-ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Post-ictal signs
  • P=0.02post-ictal amnesiaP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · post-ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.7, Table 3; PDF p.8, Post-ictal signs
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • postictal amnesiaThe distribution of postictal amnesia did not differ statistically between M, ML, and L groups, but the source does not provide the corresponding values in the displayed table.PDF p.7, Postictal behavior

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal speech disturbanceReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side6 manuscripts · 6 findings · 10 reported values
Weighted evidence supportevidence weight 8.5 across 6 manuscripts · 1 manuscript weight pending · 1 structured design not resolved · 3 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 independent primary study

Mumbling was observed in both dominant- and nondominant-origin groups without a statistically significant directional association. The review is subtype-dependent: ictal speech arrest is not reliably lateralizing, whereas selected ictal language and postictal aphasia patterns are associated with dominant, usually right nondominant, or left dominant temporal language networks. The six lesion cases included three left temporal lesions with aphasic fits, central lesions in two speech-arrest cases, and temporal/SMA lesion contexts for other signs. The educational statement gives no hemisphere or lateralizing direction for language disturbances in insular seizures. No hemisphere or body-side direction is reported. The cited anterior-versus-posterior insular comparison provides no lateralizing information.

Source-defined result groups 12
Lateralization: Does not lateralizeSource-defined values retained separatelyNondominant-hemisphere seizures (NHS) · Dominant-hemisphere seizures (DHS) · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphereObserved proportion 16.7%Speech automatism · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalObserved proportion 33.3%Speech arrest · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphereObserved proportion 33.3%Speech arrest · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphereSource-defined values retained separatelySpeech arrest · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalObserved proportion 16.7%Speech automatism · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelyDominant-hemisphere seizures (DHS) · Nondominant-hemisphere seizures (NHS) · patient1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeObserved proportion 2.6%Dominant-hemisphere seizures (DHS) · Nondominant-hemisphere seizures (NHS) · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphereObserved proportion 50.0%Aphasic fit · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalObserved proportion 50.0%Aphasic fit · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelySpeech arrest · Lesion location across speech-disturbance types · case1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeObserved proportion 0.9%Nondominant-hemisphere seizures (NHS) · Dominant-hemisphere seizures (DHS) · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • language disturbances and motor phenomenaThe abstract characterizes basal temporal seizures as frequently presenting with language disturbances and motor phenomena, with less pronounced emotional and sensory signs than other temporal lobe epilepsy forms.PDF p.1, Abstract; PDF p.2, Key points
ictal-speech-disturbance-cerebral-dominance.pdfIndependent primary study · 1 finding · 4 reported values
ictal-speech-disturbance-cerebral-dominance.pdf
Independent primary study · Class II · Evidence weight 2.50 · 2 × 0.9 × 1.389
The authors collected about 43 cases with ictal speech disturbances over 8 years. Interictal EEG was examined at least twice per case; laterality was defined by a spike or sharp-wave focus, unilateral dominant spike or sharp wave, or unilateral slow wave corresponding to same-region brain damage or tumor. Laterality was confirmed in 36 cases; 7 cases with independent foci, no laterality, or normal findings were excluded. The statistical report concerns 34 right-handed epileptics because 2 left-handed patients could not be tested statistically. A control pool comprised 243 right-handed patients with unilateral abnormal EEG findings, 136 left and 117 right, and was assessed by t test.
Findings
  • lesions associated with ictal speech disturbancesLesions were clearly observed by history in 6 cases: 3 aphasic-fit cases had left temporal lesions, 2 speech-arrest cases had central lesions, and 1 speech-automatism case had a temporal lesion; the discussion additionally identifies a speech-arrest patient with a meningioma in the supplementary motor area.PDF p.4, Results paragraph beginning “The lesions were clearly observed”; PDF p.4, Discussion paragraph beginning “It seems that the side of focus”
Reported values
  • Speech-automatism cases with temporal lesion 1/6lesions associated with ictal speech disturbancesPercentage · n/N 1/6 · 6 cases with head injury, meningioma, or vascular lesion by history · Speech automatism · ictalPDF p.4, Results paragraph beginning “The lesions were clearly observed”; PDF p.4, Discussion paragraph beginning “It seems that the side of focus”
  • Aphasic-fit cases with left temporal lesions 3/6lesions associated with ictal speech disturbancesPercentage · n/N 3/6 · 6 cases with head injury, meningioma, or vascular lesion by history · Aphasic fit · ictalPDF p.4, Results paragraph beginning “The lesions were clearly observed”; PDF p.4, Discussion paragraph beginning “It seems that the side of focus”
  • Speech-arrest cases with central lesions 2/6lesions associated with ictal speech disturbancesPercentage · n/N 2/6 · 6 cases with head injury, meningioma, or vascular lesion by history · Speech arrest · ictalPDF p.4, Results paragraph beginning “The lesions were clearly observed”; PDF p.4, Discussion paragraph beginning “It seems that the side of focus”
  • Speech-arrest patient with SMA meningioma n=1lesions associated with ictal speech disturbancesCount · 6 cases with head injury, meningioma, or vascular lesion by history · Speech arrest · ictalPDF p.4, Results paragraph beginning “The lesions were clearly observed”; PDF p.4, Discussion paragraph beginning “It seems that the side of focus”
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • language disturbanceLanguage disturbances are among the clinical manifestations reported with insular seizures.PDF p.2, Clinical Features
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No systematic-search method or unified study cohort is reported. The review focuses mainly on spontaneous focal seizures in patients undergoing presurgical evaluation for intractable focal epilepsy and discusses SEEG recordings, signal analysis, cortical stimulation, and complementary imaging. Tables 1 and 2 retain the study-specific numbers of subjects and seizures, controls or comparators, brain regions, and analysis approaches; the review does not pool their results.
Findings
  • hyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsIn the summarized Peltola et al. study of pure insular epilepsies, hyperkinetic signs, speech modifications, and viscerosensory symptoms were related to an anterior insular seizure-onset zone, whereas pain, asymmetric tonic, focal clonic, and tonic symptoms were more frequent in patients with a posterior insular seizure onset.PDF p.7, Table 2 (continued), Peltola et al. 2020 row
Reported values
  • 79 seizureshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
  • 11 subjectshyperkinetic signs; speech modifications; viscerosensory symptoms; pain; asymmetric tonic; focal clonic; tonic symptomsCount · 11 subjects with pure insular epilepsy; 79 seizures · Peltola et al. pure insular epilepsy study · ictal onset and semiologic expressionPDF p.7, Table 2 (continued), Peltola et al. 2020 row
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • ictal language and postictal aphasiaIctal speech arrest is not reliably lateralizing; focal aware speech arrest may represent dominant temporal aphasia, well-formed ictal language strongly suggests a nondominant, usually right, temporal lobe, ictal jargon is associated with dominant temporal involvement, and postictal aphasia strongly supports left dominant temporal localization.PDF p.50; PDF p.51; PDF p.52
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 1 finding · 4 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • mumbling or nonidentifiable speechMumbling was observed in both dominant- and nondominant-hemisphere seizure-onset groups without a statistically significant difference.PDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
Reported values
  • 1 NHS patientmumbling or nonidentifiable speechCount · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Nondominant-hemisphere seizures (NHS) · ictal language manifestation as classified by the studyPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • DHS 3/116 seizures (3%)mumbling or nonidentifiable speechPercentage · n/N 3/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Dominant-hemisphere seizures (DHS) · ictal language manifestation as classified by the studyPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • NHS 1/116 seizure (1%)mumbling or nonidentifiable speechPercentage · n/N 1/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Nondominant-hemisphere seizures (NHS) · ictal language manifestation as classified by the studyPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2
  • 3 DHS patientsmumbling or nonidentifiable speechCount · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Dominant-hemisphere seizures (DHS) · ictal language manifestation as classified by the studyPDF p.3, Methods/Results; PDF p.4, Results and Table 2; PDF p.5, Figure 2

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Visual illusionsReported: ContralateralAlso reported: Right hemisphere4 manuscripts · 6 findings · 3 reported values
Weighted evidence supportevidence weight 8.28 across 4 manuscripts · 3 narrative, educational, or cited context · 1 independent primary study

The review restates stimulation findings of contralateral visual fields for elementary/intermediary hallucinations, central calcarine responses, and right-predominant associative visual effects with posterior exceptions. The primary result reports visual illusions in 9/82 patients (11%) without an aggregated side or localization axis. The primary table lists 11 visual-illusion aura entries without an aggregated side or lateralization direction. No hemisphere or body-side direction is reported. No lateralizing direction is reported for the complex visual phenomena. The visual hallucination review synthesis reports no hemisphere or lateralizing direction.

Source-defined result groups 1
Localization: Occipital / Parietal / TemporalSource-defined values retained separatelyAll reported · elementary/intermediary versus complex hallucinations; right versus left hemisphere; calcarine versus noncalcarine visual field · visual hallucination responses among 22 patients; exact response denominator not reported1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 4

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • complex visual phenomena and visual illusionsComplex visual phenomena such as dyschromatopsia or metamorphopsia are described as implying temporal or occipito-temporal seizure organization with discharge in visual associative areas rather than primary visual onset; the review distinguishes hallucination at the cortical entry from distortion or illusion at downstream interpreter sites.PDF p.3, section 4
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Complex visual hallucinations and illusionsThe review associates complex visual hallucinations with visual association cortex, including medial limbic, lateral temporal, posterior parietal, and temporo-parietal-occipital regions, and describes well-formed scenery, people, animals, faces, and distortions or illusions of object size, shape, colour, and motion.PDF p.6, section 1.12
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 3 findings · 2 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 5.28 · 2 × 1.35 × 1.957
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • visual illusionsVisual illusions were reported by nine patients and corresponded to 11% of the cohort.PDF p.3, Results, Aurae; PDF p.9, Discussion
  • visual illusion entries in Table 1Table 1 lists 11 visual-illusion aura entries.PDF p.4, Table 1
  • visual illusion formsThe source describes visual illusions in which figures looked larger, were maloriented in space, or perceived images or objects were moving.PDF p.9, Discussion
Reported values
  • 9/82 (11%) patientsvisual illusionsPercentage · n/N 9/82 · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae; PDF p.9, Discussion
  • 11 source-reported aura entriesvisual illusion entries in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • elementary, intermediary, and complex visual hallucinations; visual illusionsIn a cited depth-electrode study of 22 patients with epilepsy, the source reports that 85% of elementary and intermediary visual hallucination responses were induced from calcarine sulcus, lingual gyrus, lateral occipital cortex, fusiform gyrus, or cuneus/parieto-occipital sulcus; elementary and intermediary hallucinations were in the contralateral visual hemifield except after calcarine stimulation, when they were central. Complex meaningful hallucinations were associated with cuneus/parieto-occipital sulcus, precuneus, and fusiform gyrus, while color or spatial-background illusions were elicited from right rhinal, parahippocampal, collateral-sulcus, and fusiform regions; visual phenomena were more probable in the right than left hemisphere except at the most posterior sites.PDF p.14-15, Visual; PDF p.15, visual lateralization paragraph
Reported values
  • 85% of elementary/intermediary visual hallucination responses attributed to the listed occipital, fusiform, and cuneus/parieto-occipital siteselementary, intermediary, and complex visual hallucinations; visual illusionsPercentage · 22 patients with epilepsy in the cited depth-electrode study; exact response denominator not reported · stimulation-induced visual phenomenonPDF p.14-15, Visual; PDF p.15, visual lateralization paragraph

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal central apneaReported: Right hemisphere3 manuscripts · 10 findings · 22 reported values
Weighted evidence supportevidence weight 8.2 across 3 manuscripts · 1 narrative, educational, or cited context · 2 independent primary study

Right frontotemporal seizure indexed by Fp2-F8 No source lateralization is reported. The postictal central-apnoea risk result gives no hemisphere or body-side direction. No lateralizing direction is reported for ictal versus postictal central apnoea. No lateralization evidence is reported.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • postictal cardiorespiratory arrest in 10-year-old caseOne 10-year-old female MORTEMUS case had cardiorespiratory arrest in the postictal period.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
Reported values
  • 1 case with postictal cardiorespiratory arrestpostictal cardiorespiratory arrest in 10-year-old caseCount · one MORTEMUS insular near-SUDEP case · postictal periodPDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 4 findings · 11 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 2.40 · 2 × 1.2 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • prolonged postictal apnea in case MO#11In the illustrated MO#11 right frontotemporal seizure, an ictal apnea was followed by several postictal apnea episodes extending for several minutes after seizure termination, with oxygen saturation remaining between approximately 85% and 80% until minute 8 of the postictal period.PDF p.8, Figure 3 caption
  • postictal central apnea (PICA)PICA occurred only in seizures with concomitant ICA, in 24 seizures from 12 patients; it occurred in 33.8% of ICA seizures and 5.9% of all analyzed focal seizures.PDF p.1, Abstract Results and Discussion; PDF p.5, PICA in Focal Seizures; PDF p.7, Discussion; PDF p.11, final paragraph
  • PICA event patternPICA appeared either as one apneic event extending from the ictal into the postictal period or as multiple postictal apneic events after breathing had resumed.PDF p.1, Abstract Results; PDF p.5, PICA in Focal Seizures; PDF p.9, Discussion
  • awareness of PICAThe surrounding text reports no awareness of apnea in the actively interrogated PICA seizures and no air hunger or subjective dyspnea in the untested PICA seizures, but the sentence itself contains contradictory wording about awareness.PDF p.6, Awareness of Apnea in the Postictal Period and the Role of External Interventions; PDF p.10, Discussion of unawareness
Reported values
  • SpO2 approximately 85% to 80%prolonged postictal apnea in case MO#11Range · Individual patient MO#11 with a right frontotemporal lobe seizure · MO#11 illustrated seizure · ictal-to-postictal and postictalPDF p.8, Figure 3 caption
  • until minute 8 of the postictal periodprolonged postictal apnea in case MO#11Duration · Individual patient MO#11 with a right frontotemporal lobe seizure · MO#11 illustrated seizure · ictal-to-postictal and postictalPDF p.8, Figure 3 caption
  • PICA among all analyzed focal seizures 24/406 (5.9%)postictal central apnea (PICA)Percentage · n/N 24/406 · 69 patients and 406 analyzed focal-onset seizures; 71 seizures had ICA · All analyzed focal-onset seizures · postictal, including ictal apnea extending into the postictal periodPDF p.1, Abstract Results and Discussion; PDF p.5, PICA in Focal Seizures; PDF p.7, Discussion; PDF p.11, final paragraph
  • PICA among ICA seizures 24/71 (33.8%)postictal central apnea (PICA)Percentage · n/N 24/71 · 69 patients and 406 analyzed focal-onset seizures; 71 seizures had ICA · ICA seizures · postictal, including ictal apnea extending into the postictal periodPDF p.1, Abstract Results and Discussion; PDF p.5, PICA in Focal Seizures; PDF p.7, Discussion; PDF p.11, final paragraph
  • PICA seizures n=24postictal central apnea (PICA)Count · 69 patients and 406 analyzed focal-onset seizures; 71 seizures had ICA · postictal, including ictal apnea extending into the postictal periodPDF p.1, Abstract Results and Discussion; PDF p.5, PICA in Focal Seizures; PDF p.7, Discussion; PDF p.11, final paragraph
  • Patients with PICA n=12postictal central apnea (PICA)Count · 69 patients and 406 analyzed focal-onset seizures; 71 seizures had ICA · postictal, including ictal apnea extending into the postictal periodPDF p.1, Abstract Results and Discussion; PDF p.5, PICA in Focal Seizures; PDF p.7, Discussion; PDF p.11, final paragraph
  • 2–8 eventsPICA event patternRange · 24 seizures with PICA · multiple-event seizures · ictal-to-postictal or postictalPDF p.1, Abstract Results; PDF p.5, PICA in Focal Seizures; PDF p.9, Discussion
  • single ictal-to-postictal event in 11/24 seizuresPICA event patternPercentage · n/N 11/24 · 24 seizures with PICA · single event · ictal-to-postictal or postictalPDF p.1, Abstract Results; PDF p.5, PICA in Focal Seizures; PDF p.9, Discussion
  • multiple postictal events in 13/24 seizuresPICA event patternPercentage · n/N 13/24 · 24 seizures with PICA · multiple events · ictal-to-postictal or postictalPDF p.1, Abstract Results; PDF p.5, PICA in Focal Seizures; PDF p.9, Discussion
  • 0 reported awareness among 15 actively interrogated seizuresawareness of PICACount · 24 seizures with PICA · actively interrogated · postictalPDF p.6, Awareness of Apnea in the Postictal Period and the Role of External Interventions; PDF p.10, Discussion of unawareness
  • no sign of air hunger or subjective dyspnea in 8 seizures not actively questionedawareness of PICACount · 24 seizures with PICA · not actively questioned · postictalPDF p.6, Awareness of Apnea in the Postictal Period and the Role of External Interventions; PDF p.10, Discussion of unawareness
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdfIndependent primary study · 5 findings · 10 reported values
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf
Independent primary study · Class II · Evidence weight 4.80 · 2 × 1.2 × 2
The study enrolled 2632 children and adults with epilepsy at nine epilepsy-monitoring centres in the USA and UK between 2011 and 2021; 164 were lost to follow-up and 2468 participants were included in the primary follow-up analyses. There were 38 SUDEP outcomes and two near-SUDEP events. During admission, 1660 participants had seizures captured, 1432 had analysable seizures, and the report describes 1091 analysable generalised convulsive seizures and 2117 non-convulsive seizures. The primary endpoint was time to SUDEP or censoring due to other causes. Cox proportional hazards models assessed clinical and electroclinical predictors; repeated seizure predictors were aggregated to the most severe feature per patient, using the maximum for continuous features or presence for categorical features. Analyses used prolonged video-EEG, ECG, pulse oximetry, and chest/abdominal inductance plethysmography. Statistical significance in primary analyses required two-sided p<0.05 after Bonferroni correction; the report states that secondary-analysis confidence intervals were not intended for hypothesis testing. Main-text results include varying denominators and missing data, which are retained below.
Findings
  • postictal central apnoeaPostictal central apnoea was present in 13/30 (43%) of SUDEP-or-near-SUDEP participants with available data versus 198/1001 (20%) of non-SUDEP participants, and median duration was 21 seconds (IQR 14-50) versus 13 seconds (9-24); each 10-second increase was associated with higher SUDEP risk in the primary Cox model, HR 1.32 (95% CI 1.14-1.54; p=0.0002), while the 5-year risk was 13.4% (0-24.9) for median duration >14 seconds versus 3.6% (1.8-5.3) for <=14 seconds. The association did not reach significance in the adjusted multivariable model or after excluding possible and near-SUDEP cases, when the reported HR was 1.25 (1.00-1.56).PDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • postictal central apnoeaThe Discussion restates that postictal central apnoea occurs in 18% of generalised convulsive seizures.PDF p.9, Discussion
  • ictal central apnoea; postictal central apnoeaThe Discussion restates that ictal central apnoea is associated with postictal central apnoea, suggesting that individuals with ictal central apnoea are more likely to develop postictal breathing cessation.PDF p.9, Discussion
  • terminal postictal central apnoea; terminal asystoleThe Discussion reports that the retrospective MORTEMUS study of epilepsy-monitoring-unit SUDEP cases with video-EEG longer than 24 hours showed terminal postictal central apnoea preceding terminal asystole.PDF p.9, Discussion
  • postictal central apnoea; cardiorespiratory brainstem nucleiThe authors hypothesise that postictal central apnoea may reflect brainstem depression through spreading depolarisation, seizure propagation, or impaired CO2 detection, leading to ventilatory and arousal failure; they note cited imaging and neuropathological evidence of changes in the ventrolateral medulla and raphe nuclei but state that whether these findings directly predispose to or relate to premortem postictal central apnoea is unknown.PDF p.9, Discussion
Reported values
  • HR 1.25 (95% CI 1.00–1.56)postictal central apnoeaHazard ratio · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · excluding possible and near-SUDEP cases · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 13.4% (95% CI 0–24.9) at 5 yearspostictal central apnoeaPercentage · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · median duration >14 seconds · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 21 seconds (IQR 14–50)postictal central apnoeaMedian · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · median duration >14 seconds · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 401/1432 missing postictal-apnoea datapostictal central apnoeaCount · n/N 401/1432 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · missing-data population · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 3.6% (95% CI 1.8–5.3) at 5 yearspostictal central apnoeaPercentage · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · median duration ≤14 seconds · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 198/1001 (20%)postictal central apnoeaPercentage · n/N 198/1001 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · non-SUDEP · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • HR 1.32 per 10-second increasepostictal central apnoeaHazard ratio · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · primary model · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 13/30 (43%)postictal central apnoeaPercentage · n/N 13/30 · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · SUDEP or near-SUDEP · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 13 seconds (IQR 9–24)postictal central apnoeaMedian · Primary follow-up cohort; electroclinical subgroup with analysable admission seizures and available postictal central-apnoea data · median duration >14 seconds · postictalPDF p.1, Summary and Interpretation; PDF p.5, Results and Table 2; PDF p.6, Results and Figure 2; PDF p.8, Table 3; PDF p.9, Table 4 and Discussion
  • 18% occurrencepostictal central apnoeaPercentage · Generalised convulsive seizures in the cited prior literature · postictalPDF p.9, Discussion

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal body deviationReported: Right hemisphere2 manuscripts · 2 findings · 2 reported values
Weighted evidence supportevidence weight 8.11 across 2 manuscripts · 2 independent primary study

Table 2 records rightward head, eye, and body deviation in a case with source-reported right occipital onset. No hemisphere or body-side direction is reported.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Head/Body turnHead/Body turn semiology occurred in 3/61 individuals (5%) as initial semiology and 6/61 (10%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Combined 6/61 (10%)Head/Body turnPercentage · n/N 6/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Initial 3/61 (5%)Head/Body turnPercentage · n/N 3/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • head-eye-body deviation to the rightTable 2 records head, eye, and body deviation to the right in Case 5.PDF p.6, Table 2 Case 5

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Epileptic spasmsReported: Bilateral6 manuscripts · 7 findings · 4 reported values
Weighted evidence supportevidence weight 8 across 6 manuscripts · 5 narrative, educational, or cited context · 1 systematic review or meta-analysis

The illustrative boy's profile remained generalized across 3 months, 9 months, and age 6, with age-specific syndrome labels and bilateral cortical-development malformation; seizure-frequency ranges are retained as educational context. No seizure lateralization is reported; the source only describes usually bilateral arm abduction. No seizure lateralization is reported. No seizure lateralization is reported for the 3-case, 4% epileptic-spasm entry. No seizure lateralization is reported for the 3/60 (5%) epileptic-spasm entry. No source-supported hemispheric or body-side lateralization is reported.

Evidence by contributing manuscript 6

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Epileptic spasms (Table 3)Table 3 reports epileptic spasms in 3 cases (4%), more during propagation.PDF p.6, Table 3
  • Epileptic spasms (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports epileptic spasms in 3 cases (5%).PDF p.7, Table 4
Reported values
  • 3 cases (4%)Epileptic spasms (Table 3)Percentage · Table 3 basal temporal seizure cases · propagationPDF p.6, Table 3
  • 3/60 (5%)Epileptic spasms (Table 4)Percentage · n/N 3/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • epileptic spasms in insulo-opercular epilepsyThe review reports that insulo-opercular epilepsy can also present with epileptic spasms.PDF p.2, Clinical Features
loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a proposal and narrative synthesis, not a primary empirical study. The authors review prior classification approaches, define the five dimensions, provide tables and conceptual figures, and demonstrate the proposed format with illustrative profiles. The framework is stated to apply to patients with epilepsy, defined here as at least two spontaneous epileptic seizures; for patients with unclear epileptic or nonepileptic events, the source recommends the term paroxysmal event. Clinical history, seizure semiology, EEG, MRI, other diagnostic studies, and etiologic information are translated into a best available working classification that can be refined as information accrues. No formal study cohort, sampling method, reference standard, comparator cohort, or statistical analysis is reported.
Findings
  • Example 1: a 3-month-old boy with epileptic spasmsIn an illustrative longitudinal profile, a boy with epileptic spasms is classified at 3 months as generalized EZ with epileptic spasms, unknown etiology, daily frequency, and developmental-delay epileptic encephalopathy; at 9 months the profile remains generalized with epileptic spasms but is labeled West syndrome and bilateral cortical-development malformation; at age 6 the generalized profile is labeled Lennox-Gastaut and includes atonic seizures, tonic seizures, and epileptic spasms, with bilateral cortical-development malformation and daily frequency.PDF p.5, Example 1 and its three five-dimensional profiles
Reported values
  • 3–15 clusters of epileptic spasms per dayExample 1: a 3-month-old boy with epileptic spasmsRange · One illustrative boy followed at approximately 3 months, 9 months, and 6 years; not a study cohort · Illustrative patient · Longitudinal developmental and seizure-course examplesPDF p.5, Example 1 and its three five-dimensional profiles
  • 2–4 seizures per dayExample 1: a 3-month-old boy with epileptic spasmsRange · One illustrative boy followed at approximately 3 months, 9 months, and 6 years; not a study cohort · Illustrative patient · Longitudinal developmental and seizure-course examplesPDF p.5, Example 1 and its three five-dimensional profiles
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Epileptic spasmEpileptic spasms are variable-duration contractions affecting predominantly axial muscles, frequently occurring in clusters whose contractions may range from a short myoclonic jerk to sustained tonic posturing; the source describes bilateral arm abduction in a “salaam” posture as usual.PDF p.4, Simple motor seizures, Epileptic spasms; PDF p.2, Table 1
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • epileptic spasms; “leading spike”; widespread fast-wave burstsThe chapter restates two ictal electrocorticographic patterns described for epileptic spasms: a “leading spike” followed by fast-wave bursts and a pattern without the leading spike consisting of widespread fast-wave bursts; fast-wave bursts in noncontiguous cortical regions at the time of the spasm are said to suggest a cortico-subcortical pathway possibly involving basal ganglia, thalamus, and brainstem, while some authors regard focal-epilepsy spasms as secondary generalization.PDF p.5, pediatric epileptic spasms
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • epileptic spasmsThe review describes epileptic spasms as relatively symmetric tonic or myoclonic contractions affecting proximal axial muscles, usually with trunk flexion and arm extension/abduction in a “salaam position”; they commonly occur in clusters as the patient goes to sleep and have predominantly generalized EEG patterns. They are usually seen with generalized epilepsies, but well-documented focal cases, particularly parieto-occipital, have undergone successful resective surgery; the mechanism is not clearly determined.PDF p.4, Epileptic spasms

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal bradycardia / asystoleReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side6 manuscripts · 11 findings · 15 reported values
Weighted evidence supportevidence weight 8 across 6 manuscripts · 1 systematic review or meta-analysis · 4 narrative, educational, or cited context · 1 case report or observation

The cited series reports tachycardia or bradycardia with bilateral insular stimulation, with posterior-versus-anterior subregional differences and mild left-right asymmetry. Five EMU seizures had independent bitemporal onsets: 3 right temporal and 2 left temporal; one left temporal seizure had slumping after bradycardia and 9 seconds of asystole. The cited review reports tachycardia above 100 bpm in more than 50% of seizures, greater early tachycardia in temporal than extratemporal epilepsy with right MTLE emphasis, and no localizing or lateralizing value for bradycardia below 60 bpm. The review describes ictal tachycardia/bradycardia as more frequent in temporal impaired-awareness seizures, particularly left-hemisphere cases, with slight MTLE predominance in some studies. No lateralizing direction is reported for the vegetative-sign result. No lateralizing direction is reported for bradycardia. No hemisphere or body-side direction is reported for bradycardia. No source-supported hemispheric or body-side lateralization is reported. No seizure lateralization is reported.

Source-defined result groups 8
Lateralization: bitemporal / Left hemisphere / Right hemisphereObserved proportion 40.0%Left temporal onset · seizure1 manuscript · 1 reported value · not pooled
Lateralization: bitemporal / Left hemisphere / Right hemisphereObserved proportion 60.0%Right temporal onset · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLeft temporal onset · temporal seizure onset with versus without bradycardia/asystole and slumping · seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 0.0%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 4.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 60.0%Right temporal onset · seizure1 manuscript · 1 reported value · not pooled
Lateralization: bitemporal / Left hemisphere / Right hemisphereSource-defined values retained separatelyLeft temporal onset · temporal seizure onset with versus without bradycardia/asystole and slumping · seizure1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 40.0%Left temporal onset · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal tachycardia, bradycardia, asystole, and arrhythmiaIctal tachycardia, defined in the review as heart rate above 100 bpm, is reported in more than 50% of seizures and early significant tachycardia is more common in temporal than extratemporal epilepsy, particularly right MTLE. Ictal bradycardia below 60 bpm is less common and has not shown localizing or lateralizing value; ictal asystole and arrhythmia are rare and are implicated in SUDEP pathogenesis.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
Reported values
  • Ictal tachycardia in more than 50% of seizuresictal tachycardia, bradycardia, asystole, and arrhythmiaPercentage · patients with focal epilepsy and otherwise subclinical seizures · Ictal tachycardia · ictal autonomicPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • Ictal tachycardia defined as heart rate >100 bpmictal tachycardia, bradycardia, asystole, and arrhythmiaThreshold · patients with focal epilepsy and otherwise subclinical seizures · Ictal tachycardia · ictal autonomicPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • Ictal bradycardia defined as heart rate <60 bpmictal tachycardia, bradycardia, asystole, and arrhythmiaThreshold · patients with focal epilepsy and otherwise subclinical seizures · Ictal bradycardia · ictal autonomicPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal tachycardia, bradycardia, and asystoleIctal tachycardia and bradycardia, which may lead to ictal asystole, are described as more frequent in temporal focal seizures with impaired awareness than in extratemporal seizures, particularly when seizures originate from the left hemisphere; some studies report a slight MTLE predominance.PDF p.8, Focal autonomic seizures
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • vegetative signs; tachycardia; bradycardia; rubefactionThe source reports vegetative signs including tachycardia, bradycardia, and rubefaction in 5 of 21 patients (25%).PDF p.6, Anatomical and clinical correlations
  • BradycardiaTable 2 reports 1/21 (5%) for Bradycardia; timing is late, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • BradycardiaTable 2 reports 0/12 patients with Bradycardia in the prefrontal operculum group.PDF p.7, Table 2
  • BradycardiaTable 2 reports 1/9 patients with Bradycardia in the precentral Rolandic operculum group.PDF p.7, Table 2
  • BradycardiaFisher's exact comparison of Bradycardia between the prefrontal and precentral Rolandic operculum groups has p=0.429.PDF p.7, Table 2
Reported values
  • 5/21 (25%)vegetative signs; tachycardia; bradycardia; rubefactionPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
  • 1/21 (5%)BradycardiaPercentage · n/N 1/21 · 21 included fronto-opercular epilepsy patients · LatePDF p.7, Table 2
  • 0/12 patientsBradycardiaProportion · n/N 0/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · LatePDF p.7, Table 2
  • 1/9 patientsBradycardiaProportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · LatePDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • ictal asystole in 54-year-old caseThe second MORTEMUS insular near-SUDEP case, a 54-year-old female, had ictal asystole.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
  • insular seizure or spread bradycardiaCase reports have suggested that seizures of insular origin or seizures spreading to the insula might provoke bradycardia.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
Reported values
  • 1 case with ictal asystoleictal asystole in 54-year-old caseCount · one MORTEMUS insular near-SUDEP case · ictal periodPDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding · 7 reported values
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • bitemporal seizures with ictal bradycardia and asystoleIn the illustrated case, five EMU seizures had independent bitemporal ictal onsets, three right temporal and two left temporal, with independent bitemporal interictal discharges; one left temporal seizure produced slumping after ictal bradycardia and 9 seconds of asystole, and bradycardia occurred in four of five recorded seizures while asystole occurred in three.PDF p.386; PDF p.387; PDF p.388; PDF p.389
Reported values
  • 2 left temporal onsetsbitemporal seizures with ictal bradycardia and asystoleCount · n/N 2/5 · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Left temporal onset · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
  • Bradycardia in 4/5 recorded seizuresbitemporal seizures with ictal bradycardia and asystoleCount · n/N 4/5 · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Illustrated case · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
  • one left temporal seizure produced slumpingbitemporal seizures with ictal bradycardia and asystoleCount · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Left temporal onset · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
  • 3 right temporal onsetsbitemporal seizures with ictal bradycardia and asystoleCount · n/N 3/5 · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Right temporal onset · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
  • 5 recorded EMU seizuresbitemporal seizures with ictal bradycardia and asystoleCount · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Illustrated case · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
  • 9 seconds of asystolebitemporal seizures with ictal bradycardia and asystoleDuration · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Left temporal seizure with slumping · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
  • Asystole in 3/5 recorded seizuresbitemporal seizures with ictal bradycardia and asystoleCount · n/N 3/5 · 70-year-old woman with habitual impaired-awareness seizures and additional slumping events · Illustrated case · ictal and cardiocirculatory post-onset sequencePDF p.386; PDF p.387; PDF p.388; PDF p.389
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • tachycardia and bradycardia; insular stimulationThe source reports that right and left insular stimulation can induce tachycardia or bradycardia; tachycardia predominated in posterior insula sites, whereas bradycardia sites were more anterior in the median insula, with mild left-right asymmetry. Tachycardia was accompanied by increased LF/HF ratio and bradycardia tended to be accompanied by increased HF.PDF p.14, Cardiorespiratory response

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal hyperventilationReported: Right hemisphereNo single reliable side4 manuscripts · 9 findings · 8 reported values
Weighted evidence supportevidence weight 8 across 4 manuscripts · 2 systematic review or meta-analysis · 2 narrative, educational, or cited context

The cited table describes tachycardia/hyperventilation as non-lateralising and often right. No lateralizing information is present. No lateralizing direction is reported. No fixed cerebral side or body-side direction is reported.

Source-defined result groups 4
Localization: FrontalObserved proportion 0.0%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 4.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: fronto-opercular epilepsy cohortObserved proportion 28.6%All reported · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 8.3%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 4

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Hyperventilation (Table 3)Table 3 reports hyperventilation in 2 cases (2%), more at seizure onset.PDF p.6, Table 3
  • Hyperventilation (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports hyperventilation in 1 case (2%).PDF p.7, Table 4
Reported values
  • 2 cases (2%)Hyperventilation (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 1/60 (2%)Hyperventilation (Table 4)Percentage · n/N 1/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal hyperventilation, apnea, dyspnea, and stridorIctal hyperventilation, defined as at least a 10% increase in respiratory rate from baseline, was observed in seizures of more than 50% of children in one series and was more common in temporal than frontal lobe epilepsy. In adults with TLE it is more common with mesial than neocortical onset; ictal apnea is most common in infants and neonates, while ictal dyspnea and stridor are rare and occur primarily during the tonic phase of GTCSs.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
Reported values
  • at least a 10% increaseictal hyperventilation, apnea, dyspnea, and stridorThreshold · children with focal seizures; adults with TLE; infants and neonates · ictal hyperventilation definition · ictal, with dyspnea and stridor primarily tonic phase of GTCSPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • more than 50%ictal hyperventilation, apnea, dyspnea, and stridorOther reported value · children with focal seizures; adults with TLE; infants and neonates · children in one cited series · ictal, with dyspnea and stridor primarily tonic phase of GTCSPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • respiratory symptoms; dyspnea; hyperventilationThe source reports respiratory symptoms such as dyspnea and hyperventilation in 6 of 21 patients (29%).PDF p.6, Anatomical and clinical correlations
  • HyperventilationTable 2 reports 1/21 (5%) for Hyperventilation; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • HyperventilationTable 2 reports 1/12 patients with Hyperventilation in the prefrontal operculum group.PDF p.7, Table 2
  • HyperventilationTable 2 reports 0/9 patients with Hyperventilation in the precentral Rolandic operculum group.PDF p.7, Table 2
  • HyperventilationFisher's exact comparison of Hyperventilation between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 6/21 (29%)respiratory symptoms; dyspnea; hyperventilationPercentage · n/N 6/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
  • 1/21 (5%)HyperventilationPercentage · n/N 1/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 1/12 patientsHyperventilationProportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 0/9 patientsHyperventilationProportion · n/N 0/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Tachycardia/hyperventilationTable 2 associates autonomic tachycardia/hyperventilation with amygdala, insula, anterior cingulum, ventro-medial prefrontal cortex, and hippocampus and describes it as non-lateralising, often right.PDF p.3, Table 2

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Colored visual elementary hallucinations (yellow, red, blue, multicolored)Reported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere4 manuscripts · 5 findings · 1 reported value
Weighted evidence supportevidence weight 7.9 across 4 manuscripts · 1 independent primary study · 1 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 case report or observation

No source lateralization is reported. The case records yellow-green spots in the right visual field; this is a visual-field frame, not an inferred cerebral side. The review restates that a left visual-field elementary hallucination indicates right infra-calcarine discharge and is contralateral to the relevant visual cortex. left occipital pole

Evidence by contributing manuscript 4

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • elementary visual hallucinationsThe review reports that an elementary visual hallucination such as colored circles, twinkling stars, or moving flies in the left superior visual-field quadrant indicates discharge in the right infra-calcarine cortex, and that elementary hallucinations do not arise in spontaneous seizures beginning in structures distant from visual cortex.PDF p.2, section 4; PDF p.3, section 4
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • primary visual cortex; elementary visual auraSeizures arising from primary visual (calcarine) cortex cause elementary visual aura and tend to be brief, usually less than 2 minutes; flashing coloured or bright white lights are described, and lateral occipital cortex is said to probably produce pulsating visual features.PDF p.8, Primary visual cortex; PDF p.3, Figure 1
Reported values
  • duration usually <2 minprimary visual cortex; elementary visual auraDuration Threshold · occipital lobe seizure literature · ictal auraPDF p.8, Primary visual cortex; PDF p.3, Figure 1
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfCase report or observation · 1 finding
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • coloured lights elicited from left occipital poleIn patient 4, cortical stimulation of the left occipital pole elicited the habitual aura of coloured lights that whirled as usual.PDF p.18, Fig. 4
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 2 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • elementary visual hallucination color progressionTable 2 records elementary visual hallucinations progressing from black/white spots to enlarging spots and colored spots, followed by headache.PDF p.6, Table 2 Case 3
  • yellow-green visual hallucinations in right visual fieldTable 2 records elementary visual hallucinations of yellow-green spots in the right visual field in Case 6 Sz1.PDF p.6, Table 2 Case 6 Sz1

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Dacrystic seizures (ictal crying)Source terms: Dacrystic seizuresReported: Ipsilateral4 manuscripts · 5 findings · 4 reported values
Weighted evidence supportevidence weight 7.9 across 4 manuscripts · 1 independent primary study · 2 narrative, educational, or cited context · 1 systematic review or meta-analysis

Laughing or crying did not differ significantly between TL and T+ groups; no hemisphere or body-side direction is reported. No lateralization information is reported. No source-supported hemispheric or body-side lateralization is reported. No lateralizing direction is reported for the other-automatisms subset.

Evidence by contributing manuscript 4

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • other automatisms; gelastic and dacrystic seizuresAmong the 108 cases categorized as other automatisms, 62 were gelastic or dacrystic seizures.PDF p.8, Seizure semiology localizing values
  • other automatisms; gelastic and dacrystic seizuresThe denominator for the reported gelastic/dacrystic subset was 108 other-automatisms cases.PDF p.8, Seizure semiology localizing values
Reported values
  • 62/108 other-automatisms casesother automatisms; gelastic and dacrystic seizuresProportion · n/N 62/108 · other automatisms category · gelastic or dacrystic seizuresPDF p.8, Seizure semiology localizing values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • laughing or cryingLaughing or crying did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 8.5%laughing or cryingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 4.3%laughing or cryingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Dacrystic seizuresDacrystic seizures are listed as localizing to temporal or hypothalamic regions.PDF p.4, Table 2; PDF p.3, section 2.5 Automatisms
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • laughter and crying; mimic automatismsOne restricted-OFC case with mimic automatisms displayed a combination of laughter and crying.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 1 patientlaughter and crying; mimic automatismsCount · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Kinesthetic hallucination (movement without movement)Source terms: Kinesthetic aura; Kinesthetic hallucinationReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Non-dominant hemisphere3 manuscripts · 9 findings · 8 reported values
Weighted evidence supportevidence weight 7.89 across 3 manuscripts · 2 independent primary study · 1 narrative, educational, or cited context

One stimulation-evoked body-image case included a twisting sensation in the contralateral extremity. MCC stimulation produced qualitative ipsilateral-limb or whole-body effects, with contralateral shift for whole-body effects and backward direction for limb-only effects. The stimulation report contains conflicting source-side descriptions: Table 2 labels S14 bilateral and S17 ipsilateral, while the prose and patient identifiers do not reconcile cleanly. MCC stimulation elicited a left-hemibody floating sensation contralateral to the stimulation side. The stimulation-induced vestibular record provides no lateralizing information. No hemisphere or body-side direction is reported. Three patients reported a movement sensation in the extremity contralateral to stimulation near the post-central gyrus. All three patients with a reported movement sensation had a contralateral extremity sensation, without observed actual movement. The case describes a stimulation-evoked swaying sensation from the non-dominant inferior parietal lobule.

Source-defined result groups 6
Lateralization: Bilateral / IpsilateralSource-defined values retained separatelyprose: Patient 14; Table 2 identity unresolved · stimulation observation1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%All reported · observed motor movement · patients with movement sensation1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / IpsilateralSource-defined values retained separatelyprose: Patient 11; Table 2 identity unresolved · stimulation observation1 manuscript · 1 reported value · not pooled
Lateralization: Non-dominant hemisphereObserved proportion 50.0%All reported · other body-image response · patients with body-image disturbance1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 50.0%All reported · other body-image response · patients with body-image disturbance1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 23.5%All reported · stimulation trial1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 3 findings · 3 reported values
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 2.91 · 2 × 0.9 × 1.615
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • sensation of being pushed/pulled upwards/backwardFour MCC stimulations (S3, S8, S9, and S10) produced sensations of being pushed, pulled, or pushed backwards; the source describes effects involving an ipsilateral limb or the entire body, with a contralateral shift when the entire body was affected and a backward direction when only a limb was involved.PDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
  • illusory sensation of movementThe Results prose describes two movement illusions: Patient 11 felt the upper body move to the ceiling during right MCC stimulation, and Patient 14 felt the right upper limb move to the left during right PCC stimulation; Table 2 instead lists S14 under Patient 9 as a bilateral trunk effect and S17 under Patient 12 as an ipsilateral upper-limb effect.PDF p.5, Section 3.1 Clinical effects; PDF p.6, continuation of Section 3.1; PDF p.7, Table 2
  • sensation of floating of the left hemibodyMCC stimulation S1 in Patient 1 elicited the sensation that the left hemibody floated; Table 2 labels the distribution contralateral to the stimulation.PDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
Reported values
  • Four qualitative push/pull/backward effectssensation of being pushed/pulled upwards/backwardCount · n/N 4/17 · Four MCC stimulation trials S3, S8, S9, and S10 · HFS-evoked body-perception responsePDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
  • one prose-described upper-body movement illusionillusory sensation of movementCount · Two prose-described movement observations and the related Table 2 rows S14 and S17 · prose: Patient 11; Table 2 identity unresolved · HFS-evoked body-perception responsePDF p.5, Section 3.1 Clinical effects; PDF p.6, continuation of Section 3.1; PDF p.7, Table 2
  • one prose-described right-upper-limb movement illusionillusory sensation of movementCount · Two prose-described movement observations and the related Table 2 rows S14 and S17 · prose: Patient 14; Table 2 identity unresolved · HFS-evoked body-perception responsePDF p.5, Section 3.1 Clinical effects; PDF p.6, continuation of Section 3.1; PDF p.7, Table 2
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 5 findings · 5 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 3.99 · 2 × 1.35 × 1.477
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • twisting sensation in contralateral extremity after stimulationOne patient with stimulation-evoked body-image disturbance felt a twisting sensation in the contralateral extremity.PDF p.5, Electrical cortical stimulation
  • movement sensation in one extremityThree patients with body-image disturbance described a sensation of movement in one extremity.PDF p.3, Results, Aurae
  • sensation of movement in contralateral extremity after stimulationThree patients reported a sensation of movement in the contralateral extremity after stimulation near the post-central gyrus.PDF p.5, Electrical cortical stimulation
  • no observed movement after movement sensationNo actual movement was observed by the surgeon in the three patients who reported a movement sensation after stimulation.PDF p.5, Electrical cortical stimulation
  • swaying sensation after non-dominant inferior parietal stimulationOne patient stated “I just swayed” after stimulation of the non-dominant inferior parietal lobule.PDF p.5, Electrical cortical stimulation
Reported values
  • 1 patienttwisting sensation in contralateral extremity after stimulationCount · n/N 1/2 · two patients with stimulation-evoked body-image disturbance · stimulation responsePDF p.5, Electrical cortical stimulation
  • 3 patientsmovement sensation in one extremityCount · n/N 3/9 · nine narrative patients with body-image disturbance · aura or seizure evolutionPDF p.3, Results, Aurae
  • 3 patientssensation of movement in contralateral extremity after stimulationCount · n/N 3/80 · 80 stimulated patients · stimulation responsePDF p.5, Electrical cortical stimulation
  • 3/3 patientsno observed movement after movement sensationProportion · n/N 3/3 · three patients with stimulation-evoked movement sensation · stimulation responsePDF p.5, Electrical cortical stimulation
  • 1 patientswaying sensation after non-dominant inferior parietal stimulationCount · n/N 1/2 · two patients with stimulation-evoked body-image disturbance · stimulation responsePDF p.5, Electrical cortical stimulation
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • illusions of rotation, translations, and body motion; temporo-peri-sylvian vestibular cortexThe source reports that parietal stimulation induced vestibular symptoms including illusions of rotation, translations, and indefinable body motion; a lateral temporo-peri-sylvian vestibular cortex extending above and below the sylvian fissure was described, with parietal operculum stimulation particularly sensitive for pitch-plane illusions and mid or posterior first and second temporal gyri stimulation preferentially causing yaw-plane illusions. A separate review found vertigo significantly associated with 50-Hz versus 1-Hz stimulation of posterior cingulum.PDF p.12, Vestibular Symptoms; PDF p.14, cingulate topography

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Out-of-body experience (OBE / autoscopy / heautoscopy)Source terms: Out-of-body experienceReported: BilateralAlso reported: IpsilateralAlso reported: Right hemisphereNo single reliable side5 manuscripts · 5 findings · 0 reported values
Weighted evidence supportevidence weight 7.8 across 5 manuscripts · 1 independent primary study · 3 narrative, educational, or cited context · 1 systematic review or meta-analysis

MCC stimulation elicited ipsilateral rightward head turning within a composite experience whose table distribution was labeled bilateral. The review explicitly states that autoscopic phenomena have no lateralizing value. Review synthesis describes possible right-hemispheric lateralization for ictal autoscopy. No hemisphere or side-relative direction is reported. No lateralization axis information is reported for the pleasant, multisensorial, and out-of-body auras.

Evidence by contributing manuscript 5

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • visual association area; complex visual hallucination; kinetopsia; macropsia; micropsia; autoscopyComplex visual hallucinations in occipital epilepsy are linked to prestriate cortex or propagation to adjacent temporoparietal areas; formed hallucinations and visual distortions such as kinetopsia, macropsia, micropsia, and rarely autoscopy are described.PDF p.8, Visual association areas; PDF p.3, Figure 1
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • pleasant emotional, multisensorial, and out-of-body aurasPleasant emotional auras such as euphoria or satisfaction are associated with the mesiobasal temporal area; multisensorial hallucinations require mesiobasal temporal, lateral temporal, or TPO activation; and out-of-body experiences are produced by stimulation near the temporoparietal junction.PDF p.3, section 3.1 Auras; PDF p.2, Table 1
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal autoscopyIctal autoscopy has been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • head turns to the right, detaches from the neck, and sees himself from outsideMCC stimulation S12 in Patient 7 elicited a composite body-perception experience in which the head turned to the right, was felt likely to detach from the neck after a sensation that it would explode, and was followed by a visual hallucination of seeing himself from outside from all angles without a secondary body.PDF p.5, Section 3.1 Clinical effects; PDF p.6, continuation of Section 3.1; PDF p.7, Table 2
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • psychic and autoscopic aurasThe review states that psychic auras include complex hallucinations or illusions such as autoscopy, fear, elation, déjà vu, and jamais vu. The temporal lobe is usually involved in autoscopic phenomena, but they have no lateralizing value; stimulation has elicited related sensations from the temporal convexity or posterior temporal-occipital/parietal junction, with mesial temporal structures concurrently involved in most cited cases.PDF p.2, Psychic auras; PDF p.3, Psychic auras (continued)

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Body-image disturbanceReported: BilateralAlso reported: ContralateralAlso reported: Dominant hemisphereAlso reported: IpsilateralAlso reported: Non-dominant hemisphere3 manuscripts · 8 findings · 4 reported values
Weighted evidence supportevidence weight 7.5 across 3 manuscripts · 2 independent primary study · 1 systematic review or meta-analysis

MCC stimulation elicited a contralateral left-lower-limb decomposition sensation. MCC stimulation elicited ipsilateral rightward head turning within a composite experience whose table distribution was labeled bilateral. The review assigns non-dominant context to body-image distortion and dominant parietotemporal context to the distinct manifestation of reading and writing impairment; no direction is stated for kinetopsia, macropsia, or micropsia. No source-supported hemispheric lateralization is reported. No seizure lateralization is reported.

Source-defined result groups 2
Localization: ParietalObserved proportion 2.5%All reported · no body-image disturbance · patients with cortical stimulation1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · other visual or body-image sensations · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • parietal association seizure; macrosomatognosis; microsomatagnosis; epileptic kinetopsia; macropsia; micropsiaThe review relates non-dominant parietal association seizures to distortions of body image, superior parietal lobule and precuneus seizures to enlarged or shrunken body-part perception, epileptic kinetopsia to superior parietal lobule/intraparietal sulcus, and macropsia or micropsia to precuneus involvement; dominant parietotemporal seizures may cause reading and writing impairment.PDF p.7, Parietal association areas; PDF p.3, Figure 1
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 2 findings
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • decomposition and disconnection of one body part from the bodyMCC stimulation S2 in Patient 2 elicited a sensation of decomposition in which the left lower limb detached from the body and “looses it”; Table 2 records the lower-limb distribution as contralateral.PDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
  • head turns to the right, detaches from the neck, and sees himself from outsideMCC stimulation S12 in Patient 7 elicited a composite body-perception experience in which the head turned to the right, was felt likely to detach from the neck after a sensation that it would explode, and was followed by a visual hallucination of seeing himself from outside from all angles without a secondary body.PDF p.5, Section 3.1 Clinical effects; PDF p.6, continuation of Section 3.1; PDF p.7, Table 2
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 5 findings · 4 reported values
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • disturbance of body imageDisturbances of body image were reported in nine patients in the narrative results.PDF p.3, Results, Aurae
  • disturbances of body image in Table 1Table 1 lists 11 disturbance-of-body-image aura entries.PDF p.4, Table 1
  • body-image disturbance after stimulationTwo patients developed a disturbance of body image after stimulation.PDF p.5, Electrical cortical stimulation
  • far-away and distant-small sensation after area 5b stimulationA previously described patient reported a “far away sensation” and that things seemed distant and small after stimulation of area 5b.PDF p.5, Electrical cortical stimulation
  • body-image illusion termsThe the source's own body-image phenomena included distorted posture or limb position, a feeling of movement, and a feeling that an extremity was alien or absent.PDF p.9, Discussion
Reported values
  • 9 patientsdisturbance of body imageCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.3, Results, Aurae
  • 11 source-reported aura entriesdisturbances of body image in Table 1Count · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
  • 2 patientsbody-image disturbance after stimulationCount · n/N 2/80 · 80 stimulated patients · stimulation responsePDF p.5, Electrical cortical stimulation
  • 1 patientfar-away and distant-small sensation after area 5b stimulationCount · one cited stimulation case · stimulation responsePDF p.5, Electrical cortical stimulation

3 contributing manuscripts; source-reported values remain separate and are not pooled.

PalinacousisReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side3 manuscripts · 13 findings · 14 reported values
Weighted evidence supportevidence weight 7.42 across 3 manuscripts · 1 independent primary study · 1 systematic review or meta-analysis · 1 case report or observation

During right superior temporal gyrus stimulation, palinacousis was perceived in the contralateral left ear. The fan-hum and phone-ring palinacousis did not seem to lateralize to one side. The palinacousis itself was not assigned to one auditory side; right temporal AVM and left-sided typical-seizure symptoms are context only. Palinacousis was perceived in the right ear after a left temporal hemorrhagic lesion. The synthesis reports a right-hemisphere stimulation predominance for verbal hallucinations, with no general hemisphere rule for all auditory percept types. Right-sided hemorrhage/encephalomalacia is lesion context; no auditory laterality or ictal hemisphere was established for the episodes. Echoed sounds were perceived in the right ear while current conversation could be followed with the left ear. No aggregate lateralizing direction is reported. No lateralization information is reported.

Source-defined result groups 1
Localization: TemporalObserved proportion 14.3%Stimulation-associated · case1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 3 findings · 3 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)In the cortical-stimulation synthesis, SH were mainly induced by posterior insula and Heschl’s gyrus (HG); CH by STG, STS, mesiotemporal structures, and insula; I by STG, HG, STS, and temporal plane with about one-third from extratemporal structures; VH included 60% produced by right-hemisphere stimulation, mostly STG; MH involved STG, HG, temporal plane, and SMG; HD involved temporal structures and insula, especially PLST, posterior STG, and HG; and few PAL reports were identified.PDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • palinacousis (PAL)A large proportion of PAL cases (42%) involved extratemporal areas, mostly the parietal lobe; the review discusses the IPL as a possible substrate for auditory-memory and temporal-integration mechanisms.PDF p.9, section 6.2.2; PDF p.7, Table 2; PDF p.9, Conclusion
  • parietal/inferior-parietal-lobule contribution to palinacousisThe review states that several cited lesion case studies suggested that the parietal lobe, particularly the IPL, may play a role in PAL.PDF p.9, section 6.2.2
Reported values
  • Verbal hallucinations from right-hemisphere stimulation 60%simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Verbal hallucinations · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • Auditory illusions from extratemporal stimulation about one-thirdsimple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Auditory illusions · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • 42% of PAL cases involved extratemporal areas, mostly parietalpalinacousis (PAL)Percentage · PAL cases in the review’s AS localization synthesis · Ictal/postictal auditory perseveration as described by the sourcePDF p.9, section 6.2.2; PDF p.7, Table 2; PDF p.9, Conclusion
e236615-full.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
e236615-full.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • palinacousisThe index patient was a 24-year-old right-handed woman with a ruptured left temporal cavernous malformation causing subarachnoid and intraparenchymal haemorrhage over the left Heschl's gyrus and Wernicke area; after aphasia improved, she heard recently heard words and sounds in her right ear.PDF p.1, Summary/Case presentation; PDF p.2, Figure 1 caption; PDF p.2, Investigations
  • palinacousis episodesIn the index case, the patient usually heard one repeated word, sometimes paraphrases; the maximum stimulus-to-echo delay was 1 hour, the echo was usually immediate, episodes lasted 30 seconds to 5 minutes, episodes were more frequent before bedtime or during conversation, and palinacousis disappeared spontaneously in approximately 48 hours.PDF p.1, Case presentation; PDF p.3, Patient's perspective
  • perseverating auditory soundAcross the reviewed cases, most patients heard the perseverating sound immediately after cessation of the original auditory stimulus; some heard their own voice as an echo, and some reported perseveration of inner speech, termed palinendophonia.PDF p.3, Discussion
Reported values
  • Maximum stimulus-to-echo delay 1 hourpalinacousis episodesDuration · Same index patient · Symptomatic period before surgery, beginning three days after admissionPDF p.1, Case presentation; PDF p.3, Patient's perspective
  • Spontaneous resolution in approximately 48 hourspalinacousis episodesDuration · Same index patient · Symptomatic period before surgery, beginning three days after admissionPDF p.1, Case presentation; PDF p.3, Patient's perspective
  • Episode duration 30 seconds to 5 minutespalinacousis episodesRange · Same index patient · Symptomatic period before surgery, beginning three days after admissionPDF p.1, Case presentation; PDF p.3, Patient's perspective
palinacousis-seven-new-cases.pdfIndependent primary study · 7 findings · 8 reported values
palinacousis-seven-new-cases.pdf
Independent primary study · Class II · Evidence weight 3.42 · 2 × 1.2 × 1.423
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • palinacousis elicited by superior temporal gyrus stimulationDuring brain mapping in a 26-year-old man, superior temporal gyrus stimulation elicited echoes of spoken words and of internally thought words, stopped when stimulation stopped, and was perceived as coming from the contralateral ear.PDF p.1, Results case 1; PDF p.2, Table 1 case 1; PDF p.4, Discussion
  • peri-ictal fan hum and phone-ring palinacousisA woman with Sturge-Weber syndrome reported hearing a fan hum after leaving the room and a phone ring after picking it up for minutes while an ambulatory EEG captured numerous right occipital seizures, but the source could not determine whether the palinacousis coincided with an electrographic seizure.PDF p.1, Results case 4; PDF p.2, Table 1 case 4 and caption; PDF p.3, case 4; PDF p.4, Discussion
  • post-seizure echo after right temporal AVMA woman with a right temporal arteriovenous malformation experienced palinacousis after a typical seizure with left hemianopsia and left arm tingling or numbness, without sound lateralization or apparent speech impairment; the narrative says episodes lasted days, whereas a Table 1 quotation describes a 20-minute episode.PDF p.2, Table 1 case 5 and caption; PDF p.3, case 5
  • repeating voices during altered responsiveness without electrographic seizureA man with a right intracranial hemorrhage in childhood had brief episodes of altered responsiveness off anti-seizure medication, repeatedly said shh, and later described surrounding people's voices repeating, although EEG showed no electrographic seizures; tachycardia accompanied the episodes.PDF p.2, Table 1 case 7 and caption; PDF p.3, case 7
  • seven new cases of palinacousisIn the seven-patient series, one case occurred with superior temporal gyrus stimulation, two occurred during video-EEG-captured seizures, and four occurred in peri- or post-ictal periods.PDF p.1, Abstract Results; PDF p.1, Results opening
  • prior reported palinacousis casesBefore the current report, the authors state that approximately 32 palinacousis cases had been reported, most in the setting of recent seizures, with none clearly ictal.PDF p.1, Introduction
  • Penfield-Perot stimulation-associated repeated phraseAs restated by the source, a patient with epilepsy had an epigastric sensation followed by a recently heard phrase repeating, and stimulation of three superior temporal gyrus contacts during surgery reproduced the examiner's voice even when no one was speaking and resembled the patient's usual seizure.PDF p.3, Discussion
Reported values
  • 20-minute episodepost-seizure echo after right temporal AVMDuration · 37-year-old woman with right temporal arteriovenous malformation and post-resection status in Table 1 · Table 1 quotation · Post-ictal after a typical seizurePDF p.2, Table 1 case 5 and caption; PDF p.3, case 5
  • Palinacousis after stimulation 1/7seven new cases of palinacousisPercentage · n/N 1/7 · Seven patients with epilepsy and palinacousis seen in the epilepsy clinic or EMU · Stimulation-associated · Direct cortical stimulation, ictal, peri-ictal, or post-ictalPDF p.1, Abstract Results; PDF p.1, Results opening
  • Ictal palinacousis 2/7seven new cases of palinacousisPercentage · n/N 2/7 · Seven patients with epilepsy and palinacousis seen in the epilepsy clinic or EMU · Ictal · Direct cortical stimulation, ictal, peri-ictal, or post-ictalPDF p.1, Abstract Results; PDF p.1, Results opening
  • Peri- or postictal palinacousis 4/7seven new cases of palinacousisPercentage · n/N 4/7 · Seven patients with epilepsy and palinacousis seen in the epilepsy clinic or EMU · Peri- or postictal · Direct cortical stimulation, ictal, peri-ictal, or post-ictalPDF p.1, Abstract Results; PDF p.1, Results opening
  • none clearly ictalprior reported palinacousis casesCount · Published palinacousis cases preceding the current seven-case series · prior reported cases · Mostly recent-seizure setting; none clearly ictal according to the sourcePDF p.1, Introduction
  • approximately 32 reported casesprior reported palinacousis casesCount · Published palinacousis cases preceding the current seven-case series · Mostly recent-seizure setting; none clearly ictal according to the sourcePDF p.1, Introduction
  • three superior temporal gyrus contactsPenfield-Perot stimulation-associated repeated phraseCount · One patient with epilepsy as described in the current source · superior temporal gyrus · Seizure aura and intraoperative cortical stimulationPDF p.3, Discussion
  • one patientPenfield-Perot stimulation-associated repeated phraseCount · One patient with epilepsy as described in the current source · Penfield-Perot cited case · Seizure aura and intraoperative cortical stimulationPDF p.3, Discussion

3 contributing manuscripts; source-reported values remain separate and are not pooled.

M2E automatism (mouth-to-hand: ipsilateral hand moves to mouth)Source terms: M2E automatismReported: ContralateralAlso reported: Ipsilateral6 manuscripts · 9 findings · 45 reported values
Weighted evidence supportevidence weight 7.22 across 6 manuscripts · 2 manuscript weight pending · 3 narrative, educational, or cited context · 2 structured design not resolved · 1 independent primary study

The review table lists fencing (M2E) as contralateral. M2e posturing was contralateral to the source-reported focus in all 3 patients, across 8 seizures from 3 of 26 patients. The cited study reports M2e contralateral to seizure onset in 96% of cases and present in 45% of metrazol-induced seizures. The study reports sign-specific epileptogenic-zone direction, predominantly contralateral, with ipsilateral direction for asymmetric clonic ending. Version-first and version-plus-tonic sequence counts are reported, with correct EZ lateralization in 3/4 tonic-start/asymmetric-clonic sequences and 1/1 M2e-to-clonic sequence, but no direction is stated. The cited restatement attributes excellent or very strong contralateral lateralizing value to M2e under the Ajmone-Marsan definition. The educational tables list M2e as contralateral without specifying the reference side or viewpoint. No lateralization axis information is reported for the anterior-cingulate stimulation response. The arm was on the side of contraversion, but no relation to seizure-onset side is supplied.

Source-defined result groups 10
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyasymmetric clonic ending · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 75.0%Correct EZ lateralization among tonic-start/asymmetric-clonic sequences · Version-first versus non-version-first order; variable sequence patterns · representative seizure (source also uses patient labels)1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 100.0%Correct EZ lateralization in M2e-to-clonic sequence · Version-first versus non-version-first order; variable sequence patterns · representative seizure (source also uses patient labels)1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral tonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyunilateral clonic · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyM2e · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyFig of 4 · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelydystonia · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyversion · representative seizure with sign1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyTodd's paralysis · representative seizure with sign1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Fencing (M2E)The fencing (M2E) posture is listed as contralateral and associated with a supplementary motor localization.PDF p.4, Table 2
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfNarrative, educational, or cited context · 1 finding
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Consecutive presurgical SEEG series from Timone Hospital, Marseille, February 2000-November 2010: 54 patients in whom SEEG-defined EZ was within the frontal lobe, selected from 180 SEEG explorations; patients with inconclusive intracranial recording (n=1) or a nonpredominantly frontal EZ were excluded. All patients had noninvasive presurgical assessment and video-SEEG after complete or partial antiepileptic-drug withdrawal; 374 seizures were recorded and analyzed. The cohort included 22 male and 32 female patients, mean age 24.9 +/- 9.5 years, mean epilepsy duration 16.9 +/- 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed VEEG and electrical data; 31 ictal signs and 24 brain-area variables were scored 0-1-2 per patient, with rank-based PCA, hierarchical clustering, correlation matrices, and Kendall tests at p < 0.05. The source describes sampling 20 cortical regions in one methods passage and distinguishes the SEEG-defined EZ from the source-defined early spread network.
Findings
  • Anterior cingulate stimulation; grasping and hand-to-mouth movementsThe Discussion states that a previous stimulation study of the anterior cingulate gyrus provoked grasping and hand-to-mouth movements, citing Talairach et al., 1973.PDF p.11, discussion of Group 3 behavior; PDF p.14, reference list
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • M2e signBoth tables list M2e sign as Contralateral.PDF p.2, Lateralizing signs/Localization table row "M2e sign" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "M2e sign" (printed p.5)
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 2 findings · 5 reported values
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • M2e posturingIn Group II, M2e posturing occurred in 8 seizures from 3 of 26 patients (11.5%); it evolved into ATLP, and M2e was contralateral to the focus in all 3 patients.PDF p.3, Other characteristics of ATLP—item 1
  • M2e posturingThe article reports that Ajmone-Marsan and Ralston found M2e posturing contralateral to seizure onset in 96% of their cases and present in 45% of metrazol-induced seizures.PDF p.6, Discussion—M2e posturing
Reported values
  • contralateral in 3/3 patientsM2e posturingPercentage · n/N 3/3 · Group II patients undergoing EEG-video monitoring · patients with M2e · M2e before the tonic phase, followed by ATLP and then clonic movementsPDF p.3, Other characteristics of ATLP—item 1
  • 8 seizuresM2e posturingCount · Group II patients undergoing EEG-video monitoring · M2e before the tonic phase, followed by ATLP and then clonic movementsPDF p.3, Other characteristics of ATLP—item 1
  • 3/26 patients (11.5%)M2e posturingPercentage · n/N 3/26 · Group II patients undergoing EEG-video monitoring · M2e before the tonic phase, followed by ATLP and then clonic movementsPDF p.3, Other characteristics of ATLP—item 1
  • 96%M2e posturingPercentage · Metrazol-induced seizures in the cited report · M2e posturing · Before the tonic phase of GTC seizuresPDF p.6, Discussion—M2e posturing
  • 45%M2e posturingPercentage · Metrazol-induced seizures in the cited report · M2e posturing · Before the tonic phase of GTC seizuresPDF p.6, Discussion—M2e posturing
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 3 findings · 37 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisIn the 47 representative seizures, Table 1 reports the following prevalence counts, PPVs, and Fleiss Kappa indices: version 36, 97%, 0.6961; unilateral tonic 24, 96%, 0.2594; M2e 21, 100%, 0.7364; unilateral clonic 10, 90%, 0.3643; Fig of 4 23, 74%, 0.4873; dystonia 6, 67%, 0.2620; asymmetric clonic ending 28, 89%, 0.6761; Todd's paralysis 6, 83%, 0.4360.PDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • version-first ictal motor sequence; version plus tonic and/or M2e progressionAmong the 38 sequence seizures, version was the first motor sign in 29/38; among those 29 version-first seizures, M2e followed in 15/29 and tonic posturing in 7/29, which the authors combine as version followed by a tonic seizure in 22/29 because they treat M2e as a special tonic form. One seizure had simultaneous version and tonic posturing as the first sign followed by secondary generalization and asymmetric clonic ending; three of the remaining non-version-first seizures showed version plus tonic activity in a different order; in total 33/38 showed version plus tonic activity in variable order. Version was absent in 5/38, four seizures started with tonic activity and ended with asymmetric clonic ending, three of those lateralized the EZ correctly, and one M2e-to-clonic sequence lateralized the EZ correctly.PDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2eThe current paper attributes an excellent or very strong contralateral lateralizing value for M2e to the definition described by Ajmone-Marsan, in which one arm is elevated with no or late involvement of the opposite arm.PDF p.7, M2e definition and cited value; PDF p.13, discussion of the cited M2e result
Reported values
  • 0.262version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 28/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 28/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 89%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 67%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 96%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 10/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 10/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 23/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 23/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 36/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 36/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.2594version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.3643version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 90%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral clonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 21/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 21/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 83%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6961version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 100%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 97%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · version · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 6/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 6/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · dystonia · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 74%version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPositive predictive value · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.6761version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · asymmetric clonic ending · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.7364version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · M2e · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.4873version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Fig of 4 · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 24/47version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisPercentage · n/N 24/47 · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · unilateral tonic · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • 0.436version; unilateral tonic; M2e; unilateral clonic; Fig of 4; dystonia; asymmetric clonic ending; Todd's paralysisKappa · 47 patients with one representative secondarily generalized motor seizure each; Table 1 labels prevalence n=47 · Todd's paralysis · ictal motor signs before or through secondary generalization; Todd's paralysis is postictalPDF p.18, Table 1; PDF p.9, Results statement on low PPV and exclusion of Fig of 4 and ictal dystonia; PDF p.13, discussion of M2e PPV and inter-rater reliability
  • Correct EZ lateralization in M2e-to-clonic sequence 1/1version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/1 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Correct EZ lateralization in M2e-to-clonic sequence · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2e-to-clonic sequence 1/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · M2e-to-clonic sequence · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version absent 5/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 5/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version absent · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version as second sign in non-version-first seizures 4/9version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 4/9 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version as second sign in non-version-first seizures · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Non-version-first with version plus tonic in different order 3/9version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 3/9 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Non-version-first with version plus tonic in different order · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version plus tonic in variable order 33/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 33/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version plus tonic in variable order · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Tonic start with asymmetric clonic ending 4/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 4/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Tonic start with asymmetric clonic ending · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Tonic posturing second after version 7/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 7/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Tonic posturing second after version · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version followed by tonic including M2e 22/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 22/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version followed by tonic including M2e · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Version first 29/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 29/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Version first · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • M2e second after version 15/29version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 15/29 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · M2e second after version · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Simultaneous version and tonic as first sign 1/38version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 1/38 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Simultaneous version and tonic as first sign · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
  • Correct EZ lateralization among tonic-start/asymmetric-clonic sequences 3/4version-first ictal motor sequence; version plus tonic and/or M2e progressionPercentage · n/N 3/4 · 38 representative sequence seizures from the 47-patient cohort; the source also uses “patients” for some of these counts · Correct EZ lateralization among tonic-start/asymmetric-clonic sequences · pre-secondary-generalization ictal motor sequencePDF p.2, Summary; PDF p.9, Results; PDF p.10, Discussion; PDF p.11, Discussion; PDF p.21, Fig. 1 captioned prevalence of individual signs as first sign
wyllie1986.pdfStructured design not resolved · 1 finding · 3 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • fencing position and M2e postureIn 23 versive seizures from 14 patients, arm posturing included the “fencing position” with elbow flexion followed by approximately 90-degree shoulder abduction; the authors state that M2e posturing was common in temporal and extratemporal onset versive seizures without ictal activity localized to the supplementary motor areas and probably reflected widespread ictal involvement of precentral contraversive and arm/face motor areas rather than localized supplementary motor activation.PDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization
Reported values
  • Versive seizures with fencing posturing n=23fencing position and M2e postureCount · 23 versive seizures from 14 patients; temporal and extratemporal onset versive seizures in the authors’ discussion · During contraversionPDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization
  • Shoulder abduction approximately 90 degreesfencing position and M2e postureOther reported value · 23 versive seizures from 14 patients; temporal and extratemporal onset versive seizures in the authors’ discussion · During contraversionPDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization
  • Patients with fencing posturing n=14fencing position and M2e postureCount · 23 versive seizures from 14 patients; temporal and extratemporal onset versive seizures in the authors’ discussion · During contraversionPDF p.3, Table 3 paragraph describing fencing position; PDF p.4, discussion of M2e posturing and supplementary motor area localization

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal hypersalivation / droolingReported: Non-dominant hemisphere3 manuscripts · 10 findings · 4 reported values
Weighted evidence supportevidence weight 7 across 3 manuscripts · 2 systematic review or meta-analysis · 1 narrative, educational, or cited context

The review says ictal hypersalivation is reported more often with nondominant-hemisphere mesial temporal epilepsy. The onset/propagation synthesis provides no lateralization information. The cited propagation finding provides no lateralization information. This finding provides no hemispheric lateralization information. This finding provides no lateralization information.

Source-defined result groups 3
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Drooling · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Drooling · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 7 findings · 3 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • DroolingTable 3 reports 1 studies assessing Drooling.PDF p.6, Table 3
  • DroolingTable 3 reports 17 patients assessed for Drooling.PDF p.6, Table 3
  • DroolingTable 3 reports 5.9% as the percentage range or value for Drooling; the overall association grade is Low.PDF p.6, Table 3
  • Drooling; lateral versus mesial comparisonTable 5 reports 1 studies comparing Drooling in lateral and mesial TLE.PDF p.9, Table 5
  • Drooling; lateral TLE patient denominatorTable 5 reports 17 lateral-TLE patients assessed for Drooling.PDF p.9, Table 5
  • Drooling; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 5.9% for Drooling.PDF p.9, Table 5
  • Drooling; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 20% for Drooling.PDF p.9, Table 5
Reported values
  • 5.9%DroolingPercentage · Lateral temporal epilepsy patients assessed for Drooling · ictalPDF p.6, Table 3
  • 5.9%Drooling; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Drooling · Lateral TLE patients assessed for Drooling · ictalPDF p.9, Table 5
  • 20%Drooling; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Drooling · Mesial TLE patients assessed for Drooling · ictalPDF p.9, Table 5
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • hypersalivation; respiratory disorders; opercular involvementThe source states that hypersalivation and respiratory disorders can occur when an ictal discharge involves the operculum, including after insular onset with peri-Sylvian spread.PDF p.8–9, Discussion
  • hypersalivation; respiratory disorders; peri-Sylvian spreadThe cited Peltola series reported hypersalivation and respiratory disorders in 5 of 11 patients (45%) when the ictal discharge spread outside the insular cortex and remained peri-Sylvian.PDF p.9, Discussion
Reported values
  • 5/11 (45%)hypersalivation; respiratory disorders; peri-Sylvian spreadPercentage · n/N 5/11 · 11 patients in the cited Peltola series · ictal propagationPDF p.9, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal hypersalivationThe review states that ictal hypersalivation is an uncommon sign found more frequently in mesial temporal lobe epilepsy, particularly in the non-dominant hemisphere.PDF p.3, Autonomic seizures

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal scotoma / contralateral hemianopiaSource terms: Postictal scotoma/hemianopia; Postictal hemianopiaReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere3 manuscripts · 3 findings · 2 reported values
Weighted evidence supportevidence weight 6.89 across 3 manuscripts · 2 narrative, educational, or cited context · 1 independent primary study

The review gives right occipital seizure with left homonymous hemianopia as an example and reports 100% predictive value for contralateral onset. Reported transient postictal hemianopia was contralateral to suspected seizure onset. The finding reports no cerebral lateralization.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Visual field defect and homonymous hemianopiaThe review states that clear identification of a visual-field defect establishes involvement of symptomatogenic cortex; a right occipital seizure could produce left homonymous hemianopia, and the deficit had a reported 100% predictive value for contralateral onset in reported series.PDF p.6, section 1.12
Reported values
  • Reported 100% predictive value for contralateral onsetVisual field defect and homonymous hemianopiaPercentage · Reported occipital-lobe seizure series; exact population not reported · ictal or postictalPDF p.6, section 1.12
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • transient postictal hemianopiaReported transient postictal hemianopia lateralized contralateral to suspected seizure onset.PDF p.10, section 5.2
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • post-ictal hemianopiaPost-ictal hemianopia occurred in two of 42 patients.PDF p.6, Results, Non-visual manifestations
Reported values
  • 2/42 (5%) patientspost-ictal hemianopiaPercentage · n/N 2/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · post-ictalPDF p.6, Results, Non-visual manifestations

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal cardiovascular autonomic changeReported: Ipsilateral2 manuscripts · 3 findings · 9 reported values
Weighted evidence supportevidence weight 6.86 across 2 manuscripts · 1 independent primary study · 1 narrative, educational, or cited context

No lateralizing direction is reported. No lateralization evidence is reported.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 2 findings · 9 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.86 · 2 × 1.5 × 1.952
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • cardiovascular autonomic signsAutonomic changes were frequent and most often consisted of cardiovascular signs, reported in 60% of analyzed seizures.PDF p.5, Seizure clinical semiology
  • cardiovascular autonomic changesCardiovascular autonomic changes did not differ significantly between TL and T+ groups across tachycardia, bradycardia, and pallor or flushing.PDF p.6, Table 2
Reported values
  • cardiovascular signs 60%cardiovascular autonomic signsPercentage · 80 analyzed seizures, one typical seizure per patient · ictalPDF p.5, Seizure clinical semiology
  • T+ 52.2%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • T+ 13%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 0%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 0%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • T+ 26.1%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 61%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • TL 15.3%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • TL 27.1%cardiovascular autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • heart-rate changes as autonomic symptomHeart-rate changes are among the autonomic symptoms reported with insular seizures.PDF p.2, Clinical Features

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Focal-to-bilateral tonic-clonic evolutionReported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere6 manuscripts · 13 findings · 28 reported values
Weighted evidence supportevidence weight 6.48 across 6 manuscripts · 4 manuscript weight pending · 4 structured design not resolved · 1 independent primary study · 1 narrative, educational, or cited context

Correct lateralization was reported for 28/28 patients with recorded secondary generalization versus 29/45 without it, p=0.0001. The primary result reports secondary generalization in 4/54 RTL seizures (6%) versus 19/73 LTL seizures (24%), with the shared comparison p=0.01. Secondary generalization is reported after contraversive movement, with focal arm/face activity on the side of contraversion; no independent cerebral reference frame is added. No lateralization is reported. No lateralizing direction is reported for secondary generalization in the temporal-versus-frontal differential. No lateralizing direction is reported for the atypical anterior profile. No lateralizing direction is reported for the secondary-generalization observation. No lateralization relationship is reported. No lateralizing direction is reported for the atypical-anterior secondary-generalization result. No lateralizing direction is reported for the frequent-secondary-generalization result. No lateralizing direction is reported for the posterior-cingulate secondary-generalization result. No lateralizing direction is reported for the frequent posterior-cingulate secondary-generalization result.

Source-defined result groups 4
Lateralization: Left hemisphere / Right hemisphereObserved proportion 26.0%LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 7.4%RTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 64.4%without recorded secondarily generalized seizures · Patients with recorded secondarily generalized seizures versus patients without them. · Patient1 manuscript · 1 reported value · not pooled
Lateralization: unspecifiedObserved proportion 100.0%recorded secondarily generalized seizures · Patients with recorded secondarily generalized seizures versus patients without them. · Patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 7 findings · 7 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • atypical group simple-motor/generalization patternThe abstract characterizes the atypical anterior group by simple motor seizures and more frequent generalization.PDF p.1, Abstract
  • typical anterior video-EEG secondary generalizationOne typical anterior patient had a single secondarily generalized seizure during video EEG while not taking antiseizure medication.PDF p.5, Clinical Presentation
  • typical anterior repeated secondary generalizationOne typical anterior patient had five secondarily generalized seizures within three years while experiencing frequent habitual partial seizures daily.PDF p.5, Clinical Presentation
  • atypical anterior secondary generalizationAll four atypical anterior patients had experienced secondarily generalized seizures.PDF p.5, Clinical Presentation
  • atypical anterior frequent secondary generalizationSecondary generalization was frequent in three of four atypical anterior patients.PDF p.5, Clinical Presentation
  • posterior cingulate secondary generalizationSecondary generalization was seen in all four posterior cingulate patients.PDF p.5, Clinical Presentation
  • posterior cingulate frequent secondary generalizationSecondary generalization was frequent in three of four posterior cingulate patients.PDF p.5, Clinical Presentation
Reported values
  • 1/6 with one video-EEG secondary generalized seizure off medicationtypical anterior video-EEG secondary generalizationProportion · n/N 1/6 · 6 typical anterior cingulate cases · seizure evolutionPDF p.5, Clinical Presentation
  • 5 secondarily generalized seizures within 3 yearstypical anterior repeated secondary generalizationCount · one typical anterior patient · seizure evolutionPDF p.5, Clinical Presentation
  • 7 habitual partial seizures/daytypical anterior repeated secondary generalizationRate · one typical anterior patient · seizure evolutionPDF p.5, Clinical Presentation
  • 4/4 with secondary generalizationatypical anterior secondary generalizationProportion · n/N 4/4 · 4 atypical anterior cingulate cases · seizure evolutionPDF p.5, Clinical Presentation
  • 3/4 with frequent secondary generalizationatypical anterior frequent secondary generalizationProportion · n/N 3/4 · 4 atypical anterior cingulate cases · seizure evolutionPDF p.5, Clinical Presentation
  • 4/4 secondary generalizationposterior cingulate secondary generalizationProportion · n/N 4/4 · 4 posterior cingulate cases · seizure evolutionPDF p.5, Clinical Presentation
  • 3/4 with frequent secondary generalizationposterior cingulate frequent secondary generalizationProportion · n/N 3/4 · 4 posterior cingulate cases · seizure evolutionPDF p.5, Clinical Presentation
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 2 findings
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Secondary generalization in temporal-versus-frontal differentialTable 1 reports secondary generalization as less common in temporal lobe seizures and common in frontal lobe seizures.PDF p.2, Table 1
  • Secondary generalization in childhood TLESecondary generalization of temporal-lobe seizures is described as uncommon in childhood.PDF p.5, section 6; PDF p.6, childhood-semiology continuation
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 3 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 5.48 · 2 × 1.5 × 1.827
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Secondary generalization and lateralization yieldAll 28 patients with recorded secondarily generalized seizures were correctly lateralized by semiology, compared with 29/45 patients without secondarily generalized seizures, with p=0.0001.PDF p.1, Abstract; PDF p.3, §5.2; PDF p.5, §7
Reported values
  • p=0.0001Secondary generalization and lateralization yieldP value · Patients in the 73-patient surgical cohort stratified by recorded secondarily generalized seizures. · Seizures with or without secondary generalization.PDF p.1, Abstract; PDF p.3, §5.2; PDF p.5, §7
  • 28/28 correctly lateralizedSecondary generalization and lateralization yieldPercentage · n/N 28/28 · Patients in the 73-patient surgical cohort stratified by recorded secondarily generalized seizures. · recorded secondarily generalized seizures · Seizures with or without secondary generalization.PDF p.1, Abstract; PDF p.3, §5.2; PDF p.5, §7
  • 29/45 correctly lateralizedSecondary generalization and lateralization yieldPercentage · n/N 29/45 · Patients in the 73-patient surgical cohort stratified by recorded secondarily generalized seizures. · without recorded secondarily generalized seizures · Seizures with or without secondary generalization.PDF p.1, Abstract; PDF p.3, §5.2; PDF p.5, §7
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Seizures secondarily generalizedSeizures secondarily generalized were more common in LTL than RTL seizures.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
Reported values
  • RTL secondarily generalized seizures 4/54 (6%)Seizures secondarily generalizedPercentage · n/N 4/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · Ictal progression to secondary generalizationPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • LTL secondarily generalized seizures 19/73 (24%)Seizures secondarily generalizedPercentage · n/N 19/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · Ictal progression to secondary generalizationPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 1 finding · 1 reported value
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.452
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • secondary generalizationFive of eight patients reported secondary generalization at least on rare occasions.PDF p.2, Results
Reported values
  • 5/8 patients with secondary generalizationsecondary generalizationProportion · n/N 5/8 · 8-patient temporal pole lesion cohort · seizure evolutionPDF p.2, Results
wyllie1986.pdfStructured design not resolved · 1 finding · 15 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • secondary generalization after contraversionNone of 13 complex partial seizures without contraversion generalized; among versive seizures, 27 (44%) secondarily generalized 2-34 seconds (mean 15) after contraversive movement, with generalized tonic-clonic activity lasting 27-82 seconds (mean 54), and generalization frequency and duration did not differ by focal arm/face involvement or temporal versus extratemporal onset.PDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
Reported values
  • none of 13secondary generalization after contraversionCount · n/N 0/13 · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · complex partial seizures without contraversion · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 54 secondssecondary generalization after contraversionMean · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · secondarily generalized versive seizures · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 2secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · parietal onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 15 secondssecondary generalization after contraversionMean · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · secondarily generalized versive seizures · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 25secondary generalization after contraversionCount · n/N 25/27 patients · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · versive-seizure cohort · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 27–82 secondssecondary generalization after contraversionRange · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · secondarily generalized versive seizures · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 15secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · frontal onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 0secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · occipital onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 8secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · temporal onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 27 (44%)secondary generalization after contraversionPercentage · n/N 27/61 · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · versive seizures · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 9secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · temporal onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 2secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · parietal onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 16secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · frontal onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 0secondary generalization after contraversionCount · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · occipital onset · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”
  • 2–34 secondssecondary generalization after contraversionRange · 13 complex partial seizures without contraversion and 61 versive seizures from 27 patients · secondarily generalized versive seizures · Secondary generalization after onset of contraversionPDF p.3, Table 3; PDF p.3, paragraphs beginning “Of the 13 complex partial seizures” and “Among the versive seizures”

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal ocular movementReported: Contralateral2 manuscripts · 3 findings · 4 reported values
Weighted evidence supportevidence weight 6.11 across 2 manuscripts · 1 independent primary study · 1 case report or observation

The cited stimulation report elicited contralateral eye movement and eye closure in two patients. One depth-recorded case reports eye movements contralateral to the seizure discharge. No cerebral hemisphere or body-side direction is reported.

Source-defined result groups 5
Localization: FrontalObserved proportion 3.3%All reported · 1/61 (2%) initial · individuals1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%All reported · ipsilateral eye movement · case1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · no contralateral eye response · patients1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyAll reported · no contralateral eye response · patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 1.6%All reported · 2/61 (3%) combined · individuals1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Eye movementsEye-movement semiology occurred in 1/61 individuals (2%) as initial semiology and 2/61 (3%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • 1/61 (2%) initialEye movementsPercentage · n/N 1/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • 2/61 (3%) combinedEye movementsPercentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfCase report or observation · 2 findings · 2 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • contralateral eye movement and eye closure after stimulationContralateral eye movement and eye closure were elicited in two patients after stimulation of the lateral occipital cortex.PDF p.15, Cortical stimulation
  • contralateral eye movement in depth-recorded caseIn one patient studied with depth electrodes, eye movements were contralateral to the seizure discharge.PDF p.6, Results, Non-visual manifestations
Reported values
  • 2 patientscontralateral eye movement and eye closure after stimulationCount · two cited patients · stimulation responsePDF p.15, Cortical stimulation
  • 1 casecontralateral eye movement in depth-recorded caseCount · n/N 1/1 · one depth-recorded cohort patient · ictal manifestationPDF p.6, Results, Non-visual manifestations

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Visual hallucinationReported: Right hemisphere2 manuscripts · 2 findings · 4 reported values
Weighted evidence supportevidence weight 6.07 across 2 manuscripts · 1 narrative, educational, or cited context · 1 independent primary study

The cited subset frequency contains no lateralization information. The primary comparison is among medial, medial-lateral, and lateral temporal onset subtypes and reports no hemisphere-level lateralization.

Source-defined result groups 3
Localization: TemporalObserved proportion 8.3%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 16.7%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 30.8%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • visual hallucination (Duchowny study)The review reports visual hallucinations in 2 of 10 cases in the cited Duchowny series.PDF p.7, cited-study discussion
Reported values
  • 2/10 cases (percentage not reported)visual hallucination (Duchowny study)Proportion · n/N 2/10 · cited Duchowny semiology subset · ictal; timing not otherwise reportedPDF p.7, cited-study discussion
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • visual hallucination or illusionVisual hallucination or illusion was numerically more frequent in L than M or ML patients, but the group difference was not statistically significant.PDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
Reported values
  • ML 3/18 (16.7%)visual hallucination or illusionPercentage · n/N 3/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • L 4/13 (30.8%)visual hallucination or illusionPercentage · n/N 4/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations
  • M 2/24 (8.3%)visual hallucination or illusionPercentage · n/N 2/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · initial ictal subjective symptomPDF p.5, Table 2; PDF p.8, Initial sensory illusions and hallucinations

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Tonic limb posturingReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral7 manuscripts · 11 findings · 19 reported values
Weighted evidence supportevidence weight 6 across 7 manuscripts · 1 manuscript weight pending · 6 narrative, educational, or cited context · 1 structured design not resolved

The review restates unilateral tonic limb posturing as associated with a contralateral seizure focus. The cited review passage reports correct side-of-onset prediction in 40% of temporal and 67% of extratemporal tonic-seizure cases but does not state the directional rule used. The cited table associates asymmetric tonic limb posturing during secondary generalized tonic-clonic seizures with contralateral direction. The extended elbow was contralateral to the source-reported ictal-onset side in 35 of 39 patients with ATLP. The review defines the initial figure-of-4 posture as extension of the limb contralateral to the epileptogenic hemisphere with flexion of the ipsilateral limb and reports 90% correct lateralization. The cited rule lateralizes seizure onset contralateral to the initially extended tonic arm in the figure-of-4 sign. The review describes the extended limb in the figure-of-four posture as contralateral to the seizure focus. The review reports that the extended elbow in asymmetric tonic limb posturing is predominantly contralateral to seizure onset, with ipsilateral and bilateral exceptions. The cited series predominantly associated the extended elbow component with the hemisphere contralateral to seizure onset. The cited study reported asymmetric tonic limb posturing as contralateral in 70%, ipsilateral in 17%, and bilateral in 13% of affected patients. No seizure lateralization is reported.

Source-defined result groups 4
Localization: TemporalSource-defined values retained separatelytemporal-lobe epilepsy · Temporal versus extratemporal lobe epilepsy · patient; case1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 89.7%All reported · ictal-onset side · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 89.7%asymmetric tonic limb posturing · non-contralateral · case1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyextratemporal-lobe epilepsy · Temporal versus extratemporal lobe epilepsy · patient; case1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Tonic limb posturingUnilateral tonic limb posturing is associated with a contralateral seizure focus.PDF p.4, Table 2; PDF p.5, tonic limb posturing paragraph
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • asymmetric tonic limb posturing or figure-4 signAsymmetric tonic limb posturing is a figure-4 posture in which the elbow contralateral to the epileptogenic hemisphere is extended and the ipsilateral limb flexes over the chest during the tonic phase of an SGTCS. The sign provides correct lateralization in 90% of cases, is most common in temporal-lobe seizures, and can change sides, so only its initial appearance should be used for lateralization.PDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
Reported values
  • Correct lateralization in 90% of casesasymmetric tonic limb posturing or figure-4 signPercentage · patients with secondarily generalized tonic-clonic seizures · initial tonic phase of SGTCSPDF p.6, section 7 Lateralizing signs of secondarily generalized tonic–clonic seizures; PDF p.5, Table 2
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • asymmetric tonic limb posturing (“figure-of-4” sign)During the tonic phase of a focal to bilateral tonic-clonic seizure, asymmetric tonic limb posturing, also called the “figure-of-4” sign, is described as contralateral to the seizure focus.PDF p.9, Focal to bilateral tonic-clonic seizures
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Asymmetric tonic limb posturingTable 3 associates asymmetric tonic limb posturing during secondary generalized tonic-clonic seizures with SSMA and precentral area and lists contralateral lateralisation.PDF p.4, Table 3
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdfStructured design not resolved · 2 findings · 1 reported value
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.796
Group I comprised 54 patients with partial epilepsy successfully treated by temporal-lobe resection (n=34) or extratemporal resection (n=20: 14 frontal, 3 parietal, 3 occipital); 238 seizures were recorded, including 59 secondarily generalized seizures from 31 patients. Surgical success was complete seizure freedom or >90% seizure reduction at 1 year. Group II comprised 28 prospectively collected patients with 70 GTC or generalized clonic seizures over 7 months; 6 seizures and 2 patients were excluded for inadequate video visualization of both upper limbs, leaving 64 seizures from 26 patients, including 23 with focal epilepsy and 3 with symptomatic generalized epilepsy. Three observers reviewed seizures independently while blinded to ictal EEG side and other clinical data. Version was defined as forced, sustained, unnatural eye and/or head deviation to one side; ATLP was assessed against version using interobserver kappa, and Wilcoxon rank-sum tests compared ATLP timing and duration between temporal-lobe epilepsy (TLE) and extratemporal epilepsy (XTLE).
Findings
  • asymmetric tonic limb posturing (ATLP) / “Figure 4 Sign”The article summary reports that the extended elbow was contralateral to the side of ictal onset in 35 of 39 patients who had ATLP during their seizures.PDF p.1, Summary—Results
  • asymmetric tonic limb posturing and supplementary motor area seizuresThe article states that asymmetric tonic posturing of the limbs is typically observed in supplementary motor area seizures.PDF p.6, Discussion
Reported values
  • 35 of 39 patientsasymmetric tonic limb posturing (ATLP) / “Figure 4 Sign”Count · n/N 35/39 · Patients with ATLP across the two analyzed groups; aggregate construction Not reported · Tonic phase of a secondarily generalized GTC seizurePDF p.1, Summary—Results
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 4 findings · 16 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Tonic limb posturing and tonic seizureBleasel et al. observed tonic limb posturing in 17.7% of temporal lobe epilepsy cases and 15% of extratemporal lobe epilepsy cases; tonic seizures correctly predicted side of onset in 40% of temporal lobe cases and 67% of extratemporal lobe cases.PDF p.5, section 3.5 Unilateral tonic activity
  • Asymmetric tonic limb posturing (figure-of-4 sign)The review describes asymmetric tonic limb posturing before bilateral tonic arm posturing as a lateralizing sign in which the extended elbow is usually contralateral to seizure onset; Table 1 summarizes 17.7% in temporal and 15% in extratemporal lobe epilepsy and 89% contralateral.PDF p.5, section 3.6 Asymmetric tonic limb posturing; PDF p.5, section 3.6.1 Mechanism; PDF p.12, Table 1
  • Asymmetric tonic limb posturing (figure-of-4 sign)Kotagal et al. retrospectively reviewed 59 secondary generalized tonic-clonic seizures in 31 patients seizure free after surgery and prospectively analyzed 64 seizures in 26 patients; the extended elbow was contralateral to seizure onset in 35 of 39 cases.PDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Asymmetric tonic limb posturingTrinka et al. noted asymmetric tonic limb posturing in 23 of 57 retrospectively and prospectively reviewed patients; it was contralateral in 70%, ipsilateral in 17%, and bilateral in 13%, with P < 0.001.PDF p.5, section 3.6 Asymmetric tonic limb posturing
Reported values
  • tonic limb posturing 15% extratemporalTonic limb posturing and tonic seizurePercentage · Temporal and extratemporal lobe epilepsy cases · extratemporal-lobe epilepsy · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • side prediction 67% extratemporalTonic limb posturing and tonic seizurePercentage · Temporal and extratemporal lobe epilepsy cases · extratemporal-lobe epilepsy · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • tonic limb posturing 17.7% temporalTonic limb posturing and tonic seizurePercentage · Temporal and extratemporal lobe epilepsy cases · temporal-lobe epilepsy · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • side prediction 40% temporalTonic limb posturing and tonic seizurePercentage · Temporal and extratemporal lobe epilepsy cases · temporal-lobe epilepsy · Ictal tonic phasePDF p.5, section 3.5 Unilateral tonic activity
  • 15%Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · extratemporal lobe epilepsy · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.12, Table 1
  • 17.7%Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · temporal lobe epilepsy · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.12, Table 1
  • 35 of 39 (89%)Asymmetric tonic limb posturing (figure-of-4 sign)Percentage · n/N 35/39 · Patients with secondary generalized tonic-clonic seizures and temporal or extratemporal lobe epilepsy · asymmetric tonic limb posturing · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing; PDF p.5, section 3.6.1 Mechanism; PDF p.12, Table 1
  • 26 prospective patientsAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · prospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 64 prospective seizuresAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · prospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • extended elbow contralateral in 35/39 casesAsymmetric tonic limb posturing (figure-of-4 sign)Percentage · n/N 35/39 · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 59 retrospective seizuresAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · retrospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • 31 retrospective patientsAsymmetric tonic limb posturing (figure-of-4 sign)Count · 31 patients seizure free after epilepsy surgery and 26 prospectively analyzed patients; 59 retrospective and 64 prospective secondary generalized tonic-clonic seizures · retrospective series · Early tonic phase of secondary generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • ATLP bilateral 13% of affected patientsAsymmetric tonic limb posturingPercentage · 57 patients with temporal lobe epilepsy · Bilateral · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • ATLP ipsilateral 17% of affected patientsAsymmetric tonic limb posturingPercentage · 57 patients with temporal lobe epilepsy · Ipsilateral · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • ATLP contralateral 70% of affected patientsAsymmetric tonic limb posturingPercentage · 57 patients with temporal lobe epilepsy · Contralateral · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
  • Patients with ATLP 23/57Asymmetric tonic limb posturingPercentage · n/N 23/57 · 57 patients with temporal lobe epilepsy · Early tonic phase of generalized tonic-clonic seizurePDF p.5, section 3.6 Asymmetric tonic limb posturing
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • figure of 4 sign; asymmetric tonic limb posturingThe current paper reports that figure of 4 has been described as having approximately 90% contralateral lateralizing value and attributes to the original Kotagal report the rule that the initial tonic arm extension is the component to use because a later figure of 4 may appear on the opposite side.PDF p.7, figure of 4 definition and cited value; PDF p.8, cited initial-component rule; PDF p.12, discussion of the source definition
Reported values
  • Approximately 90% contralateral lateralizing valuefigure of 4 sign; asymmetric tonic limb posturingPercentage · Cited source population as summarized in the current paper; Not reported · Beginning of the tonic phase of a secondary generalized tonic-clonic seizurePDF p.7, figure of 4 definition and cited value; PDF p.8, cited initial-component rule; PDF p.12, discussion of the source definition

7 contributing manuscripts; source-reported values remain separate and are not pooled.

GTCSReported: Contralateral2 manuscripts · 17 findings · 5 reported values
Weighted evidence supportevidence weight 6 across 2 manuscripts · 1 independent primary study · 1 systematic review or meta-analysis

Source reports contralateral limb posturing in a sequential occipital-onset phenotype. This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. No lateralization is reported for the behavioral-arrest phenotype. No source-supported hemispheric or body-side lateralization is reported. Lateral-temporal versus mesial-temporal is a localization comparison, not a cerebral hemisphere direction.

Source-defined result groups 4
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for (sudden) GTCS · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for (sudden) GTCS · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 13 findings · 5 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • (sudden) GTCSTable 3 reports 3 studies assessing (sudden) GTCS.PDF p.6, Table 3
  • (sudden) GTCSTable 3 reports 54 patients assessed for (sudden) GTCS.PDF p.6, Table 3
  • (sudden) GTCSTable 3 reports 5.3–33.3% as the percentage range or value for (sudden) GTCS; the overall association grade is Low.PDF p.6, Table 3
  • (sudden) GTCSTable 3 reports 1 study with onset timing for (sudden) GTCS.PDF p.6, Table 3
  • (sudden) GTCSTable 3 reports an onset latency of 12 s for (sudden) GTCS.PDF p.6, Table 3
  • odds of occurrence; (sudden) GTCSTable 4 reports overall odds of 0.22 for occurrence of (sudden) GTCS in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; (sudden) GTCSTable 4 reports a 95% confidence interval of 0.07–0.70 for the overall odds of (sudden) GTCS.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; (sudden) GTCSThe heterogeneity test for the Table 4 odds estimate for (sudden) GTCS has p=0.1184.PDF p.7, Table 4
  • (sudden) GTCS; lateral versus mesial comparisonTable 5 reports 2 studies comparing (sudden) GTCS in lateral and mesial TLE.PDF p.9, Table 5
  • (sudden) GTCS; lateral TLE patient denominatorTable 5 reports 32 lateral-TLE patients assessed for (sudden) GTCS.PDF p.9, Table 5
  • (sudden) GTCS; mesial TLE patient denominatorTable 5 reports 51 mesial-TLE patients assessed for (sudden) GTCS.PDF p.9, Table 5
  • (sudden) GTCS; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 17.6–33.3% for (sudden) GTCS.PDF p.9, Table 5
  • (sudden) GTCS; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 10–41.9% for (sudden) GTCS.PDF p.9, Table 5
Reported values
  • 5.3–33.3%(sudden) GTCSPercentage Range · Lateral temporal epilepsy patients assessed for (sudden) GTCS · ictalPDF p.6, Table 3
  • median onset latency 12 s(sudden) GTCSMedian · Lateral temporal epilepsy study reporting onset timing for (sudden) GTCS · ictal onsetPDF p.6, Table 3
  • odds 0.22odds of occurrence; (sudden) GTCSOdds · Lateral temporal epilepsy patients assessed for (sudden) GTCS · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 17.6–33.3%(sudden) GTCS; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for (sudden) GTCS · Lateral TLE patients assessed for (sudden) GTCS · ictalPDF p.9, Table 5
  • 10–41.9%(sudden) GTCS; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for (sudden) GTCS · Mesial TLE patients assessed for (sudden) GTCS · ictalPDF p.9, Table 5
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 4 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • behavioral-arrest onset phenotypePhenotype V begins with behavioral arrest and progresses to oculomotor or motor signs, including limb tonic or hypermotor activity, with a tendency to evolve into GTCS.PDF p.9, Phenotype V
  • GTCS evolutionSome Phenotype III seizures evolved to GTCS.PDF p.9, Phenotype III

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal flushingReported: Right hemisphere2 manuscripts · 7 findings · 6 reported values
Weighted evidence supportevidence weight 6 across 2 manuscripts · 2 systematic review or meta-analysis

No lateralizing direction is reported for the vegetative-sign result. Rubefaction/flushing occurred in 2/21 patients; no hemisphere or body-side direction is reported. Rubefaction/flushing occurred in 1/12 prefrontal-operculum patients; no hemisphere or body-side direction is reported. Rubefaction/flushing occurred in 1/9 precentral Rolandic-operculum patients; no hemisphere or body-side direction is reported. No seizure lateralization is reported. No lateralizing direction is reported for the restricted high/very-high-confidence subset.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • Rubefaction (Table 3)Table 3 reports rubefaction in 16 cases (19%), more at seizure onset.PDF p.6, Table 3
  • Rubefaction (Table 4)In the 60 high/very-high-confidence cases, Table 4 reports rubefaction in 7 cases (12%).PDF p.7, Table 4
Reported values
  • 16 cases (19%)Rubefaction (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 7/60 (12%)Rubefaction (Table 4)Percentage · n/N 7/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictalPDF p.7, Table 4
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • vegetative signs; tachycardia; bradycardia; rubefactionThe source reports vegetative signs including tachycardia, bradycardia, and rubefaction in 5 of 21 patients (25%).PDF p.6, Anatomical and clinical correlations
  • Rubefaction/flushingTable 2 reports 2/21 (10%) for Rubefaction/flushing; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Rubefaction/flushingTable 2 reports 1/12 patients with Rubefaction/flushing in the prefrontal operculum group.PDF p.7, Table 2
  • Rubefaction/flushingTable 2 reports 1/9 patients with Rubefaction/flushing in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Rubefaction/flushingFisher's exact comparison of Rubefaction/flushing between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 5/21 (25%)vegetative signs; tachycardia; bradycardia; rubefactionPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
  • 2/21 (10%)Rubefaction/flushingPercentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 1/12 patientsRubefaction/flushingProportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 1/9 patientsRubefaction/flushingProportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Rhythmic ictal non-clonic hand movementReported: ContralateralAlso reported: Dominant hemisphereAlso reported: Non-dominant hemisphereNo single reliable side2 manuscripts · 3 findings · 0 reported values
Weighted evidence supportevidence weight 6 across 2 manuscripts · 2 systematic review or meta-analysis

The review states that rhythmic non-clonic hand motion may be contralateral and that rare unilateral simple auditory aura is contralateral. RINCH is described with contralateral frontal propagation from a temporal-lobe seizure source. The review distinguishes dominant-hemisphere dysphasia, nondominant ictal speech or preserved awareness, contralateral RINCH motions, and nonlateralizing speech arrest.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • rhythmic ictal non-clonic hand motion; unilateral elementary auditory auraRhythmic ictal non-clonic hand motions may be a contralateral sign in temporal lobe epilepsy, and a simple unilateral auditory aura, described as rare, is also a contralateral sign.PDF p.10, Lateralising signs; PDF p.6, Lateral/neocortical temporal lobe
  • ictal/postictal dysphasia; ictal speech; preserved awareness; RINCH motionsIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value and must be distinguished from non-lateralising speech arrest; formed nonsensical ictal speech and preserved awareness during ictal automatisms point to the nondominant hemisphere, while rhythmic ictal non-clonic hand motions may be contralateral in temporal lobe epilepsy and peri-ictal drinking, spitting, vomiting, or urge to urinate point to a nondominant focus.PDF p.10, Lateralising signs
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • rhythmic ictal non-clonic hand motion (RINCH)The source describes rhythmic ictal non-clonic hand motion (RINCH) as a sign of temporal-lobe seizure spread to regions of the contralateral frontal lobe, mainly orbitofrontal cortex and anterior cingulate gyrus.PDF p.12, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Scalp interictal EEG absence and false localizationReported: Ipsilateral1 manuscript · 1 finding · 8 reported values
Weighted evidence supportevidence weight 5.8 across 1 manuscript · 1 independent primary study

The interictal EEG report contains ipsilateral false-localization labels but no source-supported semiologic lateralizing direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 8 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 5.80 · 2 × 1.5 × 1.932
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Scalp interictal EEG absence and false localizationScalp interictal EEG had no interictal discharges in 17/73 patients, and the source reports false ipsilateral temporal or central localization in three occipital/parietal cases.PDF p.4, §5.4
Reported values
  • 9/27 frontal patientsScalp interictal EEG absence and false localizationCount · n/N 9/27 · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · frontal · InterictalPDF p.4, §5.4
  • 17/73 (23%) had no interictal dischargesScalp interictal EEG absence and false localizationPercentage · n/N 17/73 · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · entire cohort · InterictalPDF p.4, §5.4
  • 1 parietal patient falsely localized to ipsilateral temporal lobeScalp interictal EEG absence and false localizationCount · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · parietal epilepsy · InterictalPDF p.4, §5.4
  • 5/8 parietal patientsScalp interictal EEG absence and false localizationCount · n/N 5/8 · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · parietal · InterictalPDF p.4, §5.4
  • 1 occipital patient falsely localized to ipsilateral central regionScalp interictal EEG absence and false localizationCount · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · occipital · InterictalPDF p.4, §5.4
  • 1/8 occipital patientsScalp interictal EEG absence and false localizationCount · n/N 1/8 · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · occipital · InterictalPDF p.4, §5.4
  • 2/30 temporal patientsScalp interictal EEG absence and false localizationCount · n/N 2/30 · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · temporal · InterictalPDF p.4, §5.4
  • 2 occipital patients falsely localized to ipsilateral temporal lobeScalp interictal EEG absence and false localizationCount · Entire cohort of 73 patients during scalp EEG monitoring; no-discharge subgroup included 9 frontal, 5 parietal, 2 temporal, and 1 occipital patient. · occipital epilepsy · InterictalPDF p.4, §5.4

1 contributing manuscript; source-reported values remain separate and are not pooled.

cluster 2Reported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 20 reported values
Weighted evidence supportevidence weight 5.65 across 1 manuscript · 1 independent primary study

Cluster 2 contained separate ipsilateral, contralateral, and bilateral motor subtypes rather than one uniform lateralizing direction.

Source-defined result groups 8
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 47.8% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 39.1% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 25.4% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 0% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 52.2% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyTL · T+ 4.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 25.4% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyT+ · TL 37.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 20 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • cluster 2In cluster 2, rotatory vertigo and ipsilateral tonic motor signs were significantly associated with the T+ group, while visual illusions, visual hallucinations, anger, distortion of reality, contralateral giration, bilateral tonic motor signs, and contralateral tonic motor signs were more frequent in T+ but not significant; the source associates this cluster with the TPO subgroup.PDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
Reported values
  • TL 25.4%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 25.4%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 3.4%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • P=0.02cluster 2P value · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 8.7%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 5.1%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 0%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 37.3%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 4.3%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 1.7%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 13%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • P=0.05cluster 2P value · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 3.4%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 4.3%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 52.2%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 47.8%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • TL 0%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 4.3%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 39.1%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras
  • T+ 4.3%cluster 2Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3 and Auras

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal respiratory changeReported: Ipsilateral1 manuscript · 1 finding · 11 reported values
Weighted evidence supportevidence weight 5.65 across 1 manuscript · 1 independent primary study

No lateralization information is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 11 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • respiratory autonomic changesRespiratory autonomic changes did not differ significantly between TL and T+ groups across apnoea, bradypnoea, polypnoea, and cough.PDF p.6, Table 2
Reported values
  • TL 15.3%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • P=0.29respiratory autonomic changesP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • TL 3.4%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 4.3%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 28.8%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 0%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 1.7%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 8.7%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 10.2%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 17.4%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • T+ 0%respiratory autonomic changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal motor deficitReported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 5.65 across 1 manuscript · 1 independent primary study

This record provides no seizure lateralization.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyTL · T+ 4.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 11.9% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • post-ictal motor deficitPost-ictal motor deficit did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • P=0.3post-ictal motor deficitP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · post-ictalPDF p.6, Table 2
  • T+ 4.3%post-ictal motor deficitPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · post-ictalPDF p.6, Table 2
  • TL 11.9%post-ictal motor deficitPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · post-ictalPDF p.6, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

left temporal lobe epilepsyReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 5 reported values
Weighted evidence supportevidence weight 5.61 across 1 manuscript · 1 independent primary study

The selected unilateral-TLE cohort was predominantly left-sided overall, with side distribution differing by M, ML, and L subtype.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 5 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.61 · 2 × 1.5 × 1.87
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • left temporal lobe epilepsyThe cohort contained 16/55 patients with right temporal lobe epilepsy (29.1%) and 39/55 with left temporal lobe epilepsy (70.9%); left temporal epilepsy was reported in M=20/24 (83.3%), ML=13/18 (72.2%), and L=6/13, with the prose giving 46.2% for L while Table 1 displays 42.6%, and the group comparison was not significant.PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
Reported values
  • M subgroup with left TLE 20/24 (83.3%)left temporal lobe epilepsyPercentage · n/N 20/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • ML subgroup with left TLE 13/18 (72.2%)left temporal lobe epilepsyPercentage · n/N 13/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • Right temporal-lobe epilepsy 16/55 (29.1%)left temporal lobe epilepsyPercentage · n/N 16/55 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · Overall right TLEPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • Left temporal-lobe epilepsy 39/55 (70.9%)left temporal lobe epilepsyPercentage · n/N 39/55 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · Overall left TLEPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • L subgroup with left TLE 6/13 (46.2% prose; 42.6% Table 1)left temporal lobe epilepsyPercentage · n/N 6/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal autonomic signsReported: Right hemisphere3 manuscripts · 3 findings · 10 reported values
Weighted evidence supportevidence weight 5.54 across 3 manuscripts · 1 systematic review or meta-analysis · 2 narrative, educational, or cited context

No lateralizing direction is reported for the vegetative-sign result. The stimulation-site count contains no lateralization information. The stimulation-response counts contain no lateralization information.

Source-defined result groups 8
Localization: insulaSource-defined values retained separatelyAll reported · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelynausea · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelydyspnea · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelyurge to urinate · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelyfainting fit · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelysweaty hands · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelyfacial blush · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Localization: insulaSource-defined values retained separatelysalivation · viscero-vegetative symptom subtypes · evoked viscero-vegetative response1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • vegetative signs; tachycardia; bradycardia; rubefactionThe source reports vegetative signs including tachycardia, bradycardia, and rubefaction in 5 of 21 patients (25%).PDF p.6, Anatomical and clinical correlations
Reported values
  • 5/21 (25%)vegetative signs; tachycardia; bradycardia; rubefactionPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • viscero-vegetative responsesViscero-vegetative signs were elicited from 27 insular stimulation sites.PDF p.5, Visceral Symptoms
Reported values
  • 27 stimulation sites with viscero-vegetative signsviscero-vegetative responsesCount · visceral responses in the cited insular stimulation series · stimulation-evoked autonomic semiologyPDF p.5, Visceral Symptoms
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 8 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.716
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • viscero-vegetative sensationsThe 27 viscero-vegetative responses comprised nausea (10), salivation (5), facial blush (5), fainting fit (3), dyspnea (2), urge to urinate (1), and sweaty hands (1).PDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
Reported values
  • 27 viscero-vegetative responsesviscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • sweaty hands n=1viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · sweaty hands · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • fainting fit n=3viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · fainting fit · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • facial blush n=5viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · facial blush · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • dyspnea n=2viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · dyspnea · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • urge to urinate n=1viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · urge to urinate · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • nausea n=10viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · nausea · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B
  • salivation n=5viscero-vegetative sensationsCount · 27 viscero-vegetative responses within the 82 visceral responses · salivation · stimulation-evoked visceral sensationPDF p.3, Results; PDF p.5, Visceral Sensations and Fig. 4B

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Gestural motor behaviorReported: Bilateral4 manuscripts · 31 findings · 29 reported values
Weighted evidence supportevidence weight 5.54 across 4 manuscripts · 1 manuscript weight pending · 2 narrative, educational, or cited context · 1 systematic review or meta-analysis · 1 structured design not resolved

Group 2 is described with symmetric axial tonic posture and bilateral facial contraction; no left/right hemisphere direction is reported. The EZN-extension association provides no lateralizing information. No lateralizing direction is reported. No lateralization axis information is reported for mimic automatisms in the restricted-OFC cases. No lateralization information is reported. No lateralization axis information is reported for the HkB mimic-automatism comparison. No lateralization axis information is reported for non-HkB mimic automatisms. No lateralization axis information is reported for mimic automatisms in the entire OFC-involving group. No lateralization axis information is reported for mimic automatisms in the restricted-OFC EZN group. No hemisphere or body-side direction is reported. The mimetic-automatism definition contains no lateralization evidence. The row reports an all-data panel sample size, not lateralization evidence. The row reports a non-topological panel sample size, not lateralization evidence. No lateralization axis information is reported for mimetic automatisms in the cingulate context. The cited frontal rostrocaudal gradient is not lateralizing. Group 3 included 10 patients with integrated gestural and stereotyped motor behavior, and an early spread network involving rostral prefrontal and rostral cingulate regions. No left/right or dominance-based lateralizing direction is reported. The rostrocaudal cluster gradient is not lateralizing.

Source-defined result groups 2
Localization: FrontalSource-defined values retained separatelyfrontal localization given mimetic automatisms · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelytemporal localization given mimetic automatisms · localizing data point1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 4

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 12 findings · 5 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • mimetic automatismsTable 1 defines or exemplifies the the source's own semiology category “mimetic automatisms” as Grimacing, raising eyebrows, or facial expressions such as a fearful expression.PDF p.7, Table 1 Semiology descriptions and frequencies
  • mimetic automatismsMimetic automatisms comprised 3.1% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • mimetic automatisms; Figure 3 all-data subsetFigure 3 reports N = 229 for the all-data mimetic automatisms panel.PDF p.9, Figure 3 and caption
  • mimetic automatisms; Figure 3 non-topological subsetFigure 3 reports N = 108 for the non-topological mimetic automatisms panel.PDF p.9, Figure 3 and caption
  • mimetic automatisms; frontal lobeMimetic automatisms mainly involved the frontal lobe in 40%.PDF p.8, Seizure semiology localizing values
  • mimetic automatisms; frontal lobeThe 95% CI for mimetic automatisms; frontal lobe was 29%–52%.PDF p.8, Seizure semiology localizing values
  • mimetic automatisms; cingulateMimetic automatisms mainly involved the cingulate in 26%.PDF p.8, Seizure semiology localizing values
  • mimetic automatisms; cingulateThe 95% CI for mimetic automatisms; cingulate was 18%–33%.PDF p.8, Seizure semiology localizing values
  • mimetic automatisms; temporal lobeMimetic automatisms mainly involved the temporal lobe in 20%.PDF p.8, Seizure semiology localizing values
  • mimetic automatisms; temporal lobeThe 95% CI for mimetic automatisms; temporal lobe was 13%–30%.PDF p.8, Seizure semiology localizing values
  • mimetic automatisms; cingulateMimetic automatisms had an intrinsic localizing OR of 5.6 for cingulate localization.PDF p.8, Relative localizing values of semiologies
  • mimetic automatisms; cingulateThe 95% CI for mimetic automatisms; cingulate was 3.6–8.7.PDF p.8, Relative localizing values of semiologies
Reported values
  • mimetic automatisms 3.1%mimetic automatismsPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • mimetic automatisms; frontal lobe 40%mimetic automatisms; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • mimetic automatisms; cingulate 26%mimetic automatisms; cingulatePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • mimetic automatisms; temporal lobe 20%mimetic automatisms; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 5.6mimetic automatisms; cingulateOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfStructured design not resolved · 4 findings · 8 reported values
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.349
This single-center presurgical series included 54 patients whose SEEG-defined epileptogenic zone (EZ) predominantly involved the frontal lobe, selected from 180 SEEG explorations performed from February 2000 through November 2010; one inconclusive exploration and nonpredominantly frontal cases were excluded. The cohort included 22 male and 32 female patients, mean age 24.9 ± 9.5 years, mean epilepsy duration 16.9 ± 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed all seizures and scored presence/absence of 31 ictal signs; each patient's sign was assigned 0, 1, or 2 according to reproducibility. The “early spread network” was the cortical tissue involved from electrical onset through completion of clinical semiology and was explicitly distinguished from the EZ. SEEG sampling is described as 20 frontal cortical regions, while the later matrices are described as containing 24 brain-area variables. Analyses used correlation matrices, Kendall tests with p < 0.05, PCA on rank-transformed sign scores, hierarchical clustering, and value-test ≥ 2 to identify characteristic variables.
Findings
  • Group 2 nonintegrated gestural motor behaviorGroup 2 comprised 23 patients and was characterized by co-occurring elementary motor signs, typically symmetric axial tonic posture and facial contraction such as “chapeau de gendarme,” with nonintegrated gestural motor behavior. Nonlocalized aura and complex nonverbal vocalization were also frequent; integrated gestural behavior, distal stereotypies, early clonic signs, and fixed facial expression never occurred. Both premotor and lateral prefrontal regions were frequently co-involved; lateral-to-medial propagation was more frequent, although medial premotor onset could propagate laterally.PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 2
  • Group 3 integrated gestural motor behavior with distal stereotypiesGroup 3 comprised 10 patients and typically showed integrated gestural motor behavior with distal stereotypies, fixed facial expression or positive emotional expression, proximal stereotypies, and speech production; absence of any elementary motor sign was characteristic. The early spread network involved rostral ventrolateral prefrontal regions (BA 47/12, BA 10, BA 11, BA 46) and rostral cingulate regions (BA 32 and rostral BA 24), with systematic co-involvement either simultaneously at onset or through lateromedial propagation.PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 3
  • Group 4 fearful integrated gestural behaviorGroup 4 comprised five patients with integrated gestural behavior of fear, sometimes hyperkinetic, including attempts to fight or escape, frightened facial expression, occasional screaming or swearing, and autonomic signs; elementary motor signs never occurred. Its involved network corresponded to orbital/medial prefrontal regions (BA 14, BA 32, BA 24r, BA 10) with propagation to amygdala and anterior temporal regions, but not to lateral frontal cortex.PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 4
  • Hyperkinetic versus normokinetic gestural behaviorHyperkinetic and normokinetic gestural motor behavior could both occur within the same patient group and in the same patient from one seizure to another; the authors therefore judged hyperkinetic character per se not to be a useful indicator of seizure localization.PDF p.10, Electroclinical subgroups; PDF p.11, Electroclinical spectrum following a rostrocaudal gradient
Reported values
  • p < 0.05Group 2 nonintegrated gestural motor behaviorP value · Group 2, 23 patients · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 2
  • qualitative semiologic and propagation profileGroup 2 nonintegrated gestural motor behaviorCount · Group 2, 23 patients · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 2
  • p < 0.01Group 2 nonintegrated gestural motor behaviorP value · Group 2, 23 patients · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 2
  • Group size 23 patientsGroup 2 nonintegrated gestural motor behaviorCount · Group 2, 23 patients · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 2
  • qualitative semiologic and early spread-network profileGroup 3 integrated gestural motor behavior with distal stereotypiesCount · Group 3, 10 patients · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 3
  • Group size 10 patientsGroup 3 integrated gestural motor behavior with distal stereotypiesCount · Group 3, 10 patients · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 3
  • never occurredGroup 4 fearful integrated gestural behaviorPercentage · n/N 0/5 · Group 4, 5 patients · Group 4 · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 4
  • five patientsGroup 4 fearful integrated gestural behaviorCount · Group 4, 5 patients · Group 4 · Ictal; early spread networkPDF p.5, Figure 2; PDF p.8, Table 1; PDF p.10, Group 4
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 13 findings · 11 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • frontal and insular EZN extension; hyperkinetic behavior; mimic automatisms; gestural automatismsFrontal and insular extensions are described as more likely to show hyperkinetic behavior, mimic automatisms, and gestural automatisms.PDF p.7, Conclusion
  • mimic automatismsThe source states that mimic automatisms may suggest EZN extension beyond the OFC into the insular or frontal lobe rather than the temporal lobe.PDF p.4, Complex motor phenomena—automatisms
  • mimic automatismsMimic automatisms were reported in three of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • pouting; mimic automatismsTwo restricted-OFC cases with mimic automatisms displayed pouting.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • laughter and crying; mimic automatismsOne restricted-OFC case with mimic automatisms displayed a combination of laughter and crying.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • mimic automatisms; HkB subgroupOne HkB case had mimic automatisms, compared with two in the non-HkB group.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • mimic automatisms; non-HkB subgroupTwo non-HkB cases had mimic automatisms.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • mimic automatisms; entire groupThe source reports 17% for mimic automatisms in the entire ofc-involving group.PDF p.4, Complex motor phenomena—automatisms
  • mimic automatisms; OFC-restricted EZNThe source reports 12% for mimic automatisms in the ofc-restricted ezn group.PDF p.4, Complex motor phenomena—automatisms
  • mimic automatisms; OFC-extended EZNThe source reports 24% for mimic automatisms in the ofc-extended ezn group.PDF p.4, Complex motor phenomena—automatisms
  • mimic automatisms; temporal subgroupThe source reports 0% for mimic automatisms in the temporal subgroup of ofc-extended ezn.PDF p.4, Complex motor phenomena—automatisms
  • mimic automatisms; insular subgroupThe source reports 40% for mimic automatisms in the insular subgroup of ofc-extended ezn.PDF p.4, Complex motor phenomena—automatisms
  • mimic automatisms; frontal subgroupThe source reports 36% for mimic automatisms in the frontal subgroup of ofc-extended ezn.PDF p.4, Complex motor phenomena—automatisms
Reported values
  • 3/26 (11.5%)mimic automatismsPercentage · n/N 3/26 · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 2 patientspouting; mimic automatismsCount · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 1 patientlaughter and crying; mimic automatismsCount · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 1 patientmimic automatisms; HkB subgroupCount · n/N 1/14 · HkB subgroup within OFC-restricted EZN · HkB subgroup within OFC-restricted EZN · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 2 patientsmimic automatisms; non-HkB subgroupCount · n/N 2/12 · Non-HkB subgroup within OFC-restricted EZN · Non-HkB subgroup within OFC-restricted EZN · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 17%mimic automatisms; entire groupPercentage · Entire OFC-involving group · Entire OFC-involving group · ictalPDF p.4, Complex motor phenomena—automatisms
  • 12%mimic automatisms; OFC-restricted EZNPercentage · OFC-restricted EZN group · OFC-restricted EZN group · ictalPDF p.4, Complex motor phenomena—automatisms
  • 24%mimic automatisms; OFC-extended EZNPercentage · OFC-extended EZN group · OFC-extended EZN group · ictalPDF p.4, Complex motor phenomena—automatisms
  • 0%mimic automatisms; temporal subgroupPercentage · Temporal subgroup of OFC-extended EZN · Temporal subgroup of OFC-extended EZN · ictalPDF p.4, Complex motor phenomena—automatisms
  • 40%mimic automatisms; insular subgroupPercentage · Insular subgroup of OFC-extended EZN · Insular subgroup of OFC-extended EZN · ictalPDF p.4, Complex motor phenomena—automatisms
  • 36%mimic automatisms; frontal subgroupPercentage · Frontal subgroup of OFC-extended EZN · Frontal subgroup of OFC-extended EZN · ictalPDF p.4, Complex motor phenomena—automatisms
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 5 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • elementary motor signs; gestural motor behavior; emotional expressionThe review reports that Bonini, McGonigal et al. (2014) identified four frontal-lobe semiologic groups along a rostro-caudal gradient: Group 1 had elementary motor signs without gestural motor behavior; Group 2 combined elementary and gestural motor signs, often with mainly proximal tonic signs and facial contraction; Group 3 had no elementary motor signs and often distal, integrated gestural behavior; and Group 4 had no elementary motor signs with integrated gestural behavior in an emotional, usually fearful, context.PDF p.6, Table 2, Frontal lobe row
  • elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresIn the summarized Bonini, McGonigal et al. study, automated clustering of clinical signs and brain areas involved in seizure onset and early propagation found a rostrocaudal frontal gradient with four groups: elementary motor signs without gestural behavior; elementary plus gestural signs with mainly proximal tonic signs and facial contraction; gestural behavior without elementary signs and often distal or integrated; and gestural behavior in an emotional, often fearful, context with an integrated appearance.PDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
Reported values
  • 374 seizureselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • 54 subjectselementary motor signs; gestural motor behavior; emotional expressionCount · 54 subjects with frontal-lobe epilepsy and 374 seizures · Seizure onset and early propagationPDF p.6, Table 2, Frontal lobe row
  • Semiology clusters n=4elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Patients in semiology series n=54elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row
  • Seizures in semiology series n=374elementary motor signs; gestural motor behavior; emotional expression; frontal lobe seizuresCount · 54 subjects with frontal-lobe epilepsy; 374 seizures · seizure onset and early propagation; ictal semiologic expressionPDF p.6, Table 2, Bonini, McGonigal et al. 2014 row

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Bilateral tonic posturingReported: Bilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 5.11 across 1 manuscript · 1 independent primary study

The frontal surgical cohort reports bilateral tonic signs at the stated frequencies, without a cerebral-side interpretation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • Focal motor (tonic - bilateral)Focal motor (tonic - bilateral) semiology occurred in 3/61 individuals (5%) as initial semiology and 23/61 (38%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • 23/61 (38%) combinedFocal motor (tonic - bilateral)Percentage · n/N 23/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • 3/61 (5%) initialFocal motor (tonic - bilateral)Percentage · n/N 3/61 · 61 individuals undergoing frontal lobe epilepsy surgery · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

combined set-of-semiology lateralization direction and 12-month outcomeReported: ContralateralNo single reliable side1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight 5.11 across 1 manuscript · 1 independent primary study

Combined semiology correctly lateralized the presumed EZ in 47/61 (77%), predicted the opposite hemisphere in 8/61 (13%), and was non-lateralizing in 6/61 (10%); correct means same side as resection.

Source-defined result groups 3
Lateralization: Contralateral / Does not lateralize / unspecifiedObserved proportion 77.0%same side · Congruent/same-side versus opposite-side versus non-lateralizing SVT prediction · individual1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Does not lateralize / unspecifiedObserved proportion 13.1%opposite side · Congruent/same-side versus opposite-side versus non-lateralizing SVT prediction · individual1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / Does not lateralize / unspecifiedObserved proportion 9.8%non-lateralizing · Congruent/same-side versus opposite-side versus non-lateralizing SVT prediction · individual1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 6 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • combined set-of-semiology lateralization direction and 12-month outcomeCombined set-of-semiology correctly lateralized the presumed EZ in 47/61 individuals (77%), lateralized to the opposite hemisphere in 8/61 (13%), and was non-lateralizing in 6/61 (10%); seizure freedom at one year occurred in 24/47 (51%) with congruent predictions, 3/8 (38%) with opposite-side predictions, and 1/6 (17%) with non-lateralizing predictions.PDF p.4, Results; PDF p.6, Discussion
Reported values
  • 47/61 (77%) same-side predictioncombined set-of-semiology lateralization direction and 12-month outcomePercentage · n/N 47/61 · 61 individuals after frontal lobe epilepsy surgery · same side · Ictal semiology prediction and 12-month postsurgical outcomePDF p.4, Results; PDF p.6, Discussion
  • 8/61 (13%) opposite-side predictioncombined set-of-semiology lateralization direction and 12-month outcomePercentage · n/N 8/61 · 61 individuals after frontal lobe epilepsy surgery · opposite side · Ictal semiology prediction and 12-month postsurgical outcomePDF p.4, Results; PDF p.6, Discussion
  • 3/8 (38%) seizure freecombined set-of-semiology lateralization direction and 12-month outcomePercentage · n/N 3/8 · 61 individuals after frontal lobe epilepsy surgery · opposite-side prediction · Ictal semiology prediction and 12-month postsurgical outcomePDF p.4, Results; PDF p.6, Discussion
  • 6/61 (10%) non-lateralizing predictioncombined set-of-semiology lateralization direction and 12-month outcomePercentage · n/N 6/61 · 61 individuals after frontal lobe epilepsy surgery · non-lateralizing · Ictal semiology prediction and 12-month postsurgical outcomePDF p.4, Results; PDF p.6, Discussion
  • 24/47 (51%) seizure freecombined set-of-semiology lateralization direction and 12-month outcomePercentage · n/N 24/47 · 61 individuals after frontal lobe epilepsy surgery · same-side prediction · Ictal semiology prediction and 12-month postsurgical outcomePDF p.4, Results; PDF p.6, Discussion
  • 1/6 (17%) seizure freecombined set-of-semiology lateralization direction and 12-month outcomePercentage · n/N 1/6 · 61 individuals after frontal lobe epilepsy surgery · non-lateralizing prediction · Ictal semiology prediction and 12-month postsurgical outcomePDF p.4, Results; PDF p.6, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

incorrect frontal-lobe localization destinationsReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 5.11 across 1 manuscript · 1 independent primary study

Among incorrect semiology-based localization outputs, ipsilateral mesial temporal destinations predominated over contralateral mesial temporal destinations relative to the resection.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 4 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • incorrect frontal-lobe localization destinationsAmong the 26/61 individuals (43%) whose combined set-of-semiology did not correctly localize to the frontal lobe, the most common incorrect localization was ipsilateral mesial temporal (n=19), followed by contralateral mesial temporal (n=4) and other extrafrontal areas (n=3).PDF p.4, Results
Reported values
  • n=3 other extrafrontal incorrect localizationsincorrect frontal-lobe localization destinationsCount · n/N 3/26 · 61 individuals with combined set-of-semiology SVT predictions · Incorrect localization destination · Ictal semiology prediction compared with resectionPDF p.4, Results
  • 26/61 (43%) incorrect frontal-lobe localizationsincorrect frontal-lobe localization destinationsPercentage · n/N 26/61 · 61 individuals with combined set-of-semiology SVT predictions · Combined set-of-semiology predictions · Ictal semiology prediction compared with resectionPDF p.4, Results
  • n=19 ipsilateral mesial temporal incorrect localizationsincorrect frontal-lobe localization destinationsCount · n/N 19/26 · 61 individuals with combined set-of-semiology SVT predictions · Incorrect localization destination · Ictal semiology prediction compared with resectionPDF p.4, Results
  • n=4 contralateral mesial temporal incorrect localizationsincorrect frontal-lobe localization destinationsCount · n/N 4/26 · 61 individuals with combined set-of-semiology SVT predictions · Incorrect localization destination · Ictal semiology prediction compared with resectionPDF p.4, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

tonic upper-limb posturingReported: Right hemisphere1 manuscript · 2 findings · 6 reported values
Weighted evidence supportevidence weight 5.07 across 1 manuscript · 1 independent primary study

Early upper-limb tonic-posturing rates across temporal onset subtypes provide no hemisphere direction. Late upper-limb tonic-posturing rates across temporal onset subtypes provide no hemisphere direction.

Source-defined result groups 6
Localization: TemporalObserved proportion 8.3%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 7.7%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 27.8%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 25.0%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 7.7%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 2 findings · 6 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • early upper-limb tonic posturingEarly upper-limb tonic posturing did not differ significantly across M, ML, and L groups.PDF p.6, Table 4; PDF p.6, Early features
  • late upper-limb tonic posturingLate upper-limb tonic posturing did not differ significantly across M, ML, and L groups.PDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
Reported values
  • L 1/13 (7.7%)early upper-limb tonic posturingPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • M 2/24 (8.3%)early upper-limb tonic posturingPercentage · n/N 2/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • ML 0/18 (0%)early upper-limb tonic posturingPercentage · n/N 0/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · early ictal, first half of seizurePDF p.6, Table 4; PDF p.6, Early features
  • M 6/24 (25%)late upper-limb tonic posturingPercentage · n/N 6/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
  • L 1/13 (7.7%)late upper-limb tonic posturingPercentage · n/N 1/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics
  • ML 5/18 (27.8%)late upper-limb tonic posturingPercentage · n/N 5/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · late ictal, second half of seizurePDF p.7, Table 5; PDF p.7, Later features; PDF p.9, Nondifferentiating ictal characteristics

1 contributing manuscript; source-reported values remain separate and are not pooled.

frequent secondary generalizationsReported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 5.07 across 1 manuscript · 1 independent primary study

The primary comparison reports no hemisphere-level lateralization; it compares lateral temporal onset with M and ML onset.

Source-defined result groups 3
Localization: TemporalObserved proportion 16.7%ML · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 16.7%M · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 61.5%L · other M/ML/L subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • frequent secondary generalizationsRecurring secondary generalizations, defined by the source as at least two per year, were more frequent in L than M or ML patients.PDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Secondary generalizations
Reported values
  • 3/18 (16.7%)frequent secondary generalizationsPercentage · n/N 3/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · seizure history/frequency; secondary generalization during the epilepsy coursePDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Secondary generalizations
  • 4/24 (16.7%)frequent secondary generalizationsPercentage · n/N 4/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · seizure history/frequency; secondary generalization during the epilepsy coursePDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Secondary generalizations
  • 8/13 (61.5%)frequent secondary generalizationsPercentage · n/N 8/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · seizure history/frequency; secondary generalization during the epilepsy coursePDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.8, Secondary generalizations

1 contributing manuscript; source-reported values remain separate and are not pooled.

hippocampal sclerosisReported: Right hemisphere1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight 5.07 across 1 manuscript · 1 independent primary study

No cerebral hemisphere or body-side direction is reported.

Source-defined result groups 6
Localization: TemporalObserved proportion 0.0%Pathology; L · Other onset subtypes within Pathology · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 79.2%Pathology; M · Other onset subtypes within Pathology · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 66.7%MRI; M · Other onset subtypes within MRI · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%MRI; L · Other onset subtypes within MRI · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 44.4%Pathology; ML · Other onset subtypes within Pathology · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 22.2%MRI; ML · Other onset subtypes within MRI · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 6 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • hippocampal sclerosisHippocampal sclerosis was more frequent in M than ML patients and was absent in L patients by both MRI and pathology measures.PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
Reported values
  • Pathology hippocampal sclerosis, M 19/24 (79.2%)hippocampal sclerosisPercentage · n/N 19/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · Pathology; MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • MRI hippocampal sclerosis, L 0/13 (0%)hippocampal sclerosisPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRI; LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • MRI hippocampal sclerosis, M 16/24 (66.7%)hippocampal sclerosisPercentage · n/N 16/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRI; MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • Pathology hippocampal sclerosis, ML 8/18 (44.4%)hippocampal sclerosisPercentage · n/N 8/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · Pathology; MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • Pathology hippocampal sclerosis, L 0/13 (0%)hippocampal sclerosisPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · Pathology; LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • MRI hippocampal sclerosis, ML 4/18 (22.2%)hippocampal sclerosisPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRI; MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

long seizure durationReported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 5.07 across 1 manuscript · 1 independent primary study

No hemisphere direction is reported.

Source-defined result groups 3
Localization: TemporalObserved proportion 83.3%ML · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 38.5%L · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 95.8%M · Other onset subtypes · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • long seizure durationSeizure duration longer than 60 seconds was more frequent in M and ML than L patients.PDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.9, Synthesis and perspectives
Reported values
  • ML 15/18 (83.3%)long seizure durationPercentage · n/N 15/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · ML · whole ictal seizure durationPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.9, Synthesis and perspectives
  • M 23/24 (95.8%)long seizure durationPercentage · n/N 23/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · M · whole ictal seizure durationPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.9, Synthesis and perspectives
  • L 5/13 (38.5%)long seizure durationPercentage · n/N 5/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · L · whole ictal seizure durationPDF p.6, Table 3; PDF p.6, General ictal characteristics; PDF p.9, Synthesis and perspectives

1 contributing manuscript; source-reported values remain separate and are not pooled.

medial temporal lesionReported: Right hemisphere1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight 5.07 across 1 manuscript · 1 independent primary study

No lateralization axis information is reported for the medial temporal lesion comparison.

Source-defined result groups 6
Localization: TemporalObserved proportion 0.0%MRI; L · other M/ML/L subtypes within MRI · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 22.2%MRI; ML · other M/ML/L subtypes within MRI · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%MRI; M · other M/ML/L subtypes within MRI · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%pathology; L · other M/ML/L subtypes within pathology · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 0.0%pathology; M · other M/ML/L subtypes within pathology · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 22.2%pathology; ML · other M/ML/L subtypes within pathology · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 6 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • medial temporal lesionA medial temporal lesion, with or without hippocampal sclerosis, was reported only in the ML group in this cohort.PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
Reported values
  • 0/13 (0%)medial temporal lesionPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRI; LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 0/24 (0%)medial temporal lesionPercentage · n/N 0/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRI; MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 0/13 (0%)medial temporal lesionPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · pathology; LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 0/24 (0%)medial temporal lesionPercentage · n/N 0/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · pathology; MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 4/18 (22.2%)medial temporal lesionPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRI; MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 4/18 (22.2%)medial temporal lesionPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · pathology; MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

neocortical temporal lesionReported: Right hemisphere1 manuscript · 1 finding · 8 reported values
Weighted evidence supportevidence weight 5.07 across 1 manuscript · 1 independent primary study

No lateralization evidence is reported for the neocortical temporal lesion finding.

Source-defined result groups 6
Localization: TemporalObserved proportion 61.5%L · M versus ML versus L; MRI versus pathology ascertainment · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 33.3%ML · M versus ML versus L; MRI versus pathology ascertainment · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 8.3%M · M versus ML versus L; MRI versus pathology ascertainment · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 44.4%ML · M versus ML versus L; MRI versus pathology ascertainment · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 4.2%M · M versus ML versus L; MRI versus pathology ascertainment · patients1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 61.5%L · M versus ML versus L; MRI versus pathology ascertainment · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 8 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 5.07 · 2 × 1.5 × 1.69
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • neocortical temporal lesionNeocortical temporal lesions were more frequent in L and ML than M patients by MRI and pathology, with the highest proportion in L.PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
Reported values
  • MRI L=8/13 (61.5%)neocortical temporal lesionPercentage · n/N 8/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • pathology M=1/24 (4.2%)neocortical temporal lesionPercentage · n/N 1/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • pathology L=8/13 (61.5%)neocortical temporal lesionPercentage · n/N 8/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • MRI M=2/24 (8.3%)neocortical temporal lesionPercentage · n/N 2/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • p=0.002neocortical temporal lesionP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MRIPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • pathology ML=6/18 (33.3%)neocortical temporal lesionPercentage · n/N 6/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • p=0.001neocortical temporal lesionP value · 55 patients with unilateral TLE; M=24, ML=18, L=13 · pathologyPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • MRI ML=8/18 (44.4%)neocortical temporal lesionPercentage · n/N 8/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

extensive ictal scalp-EEG distributionReported: Ipsilateral1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 5.01 across 1 manuscript · 1 independent primary study

The primary abstract context says interictal and ictal discharges were mostly ipsilateral perisylvian, while the regional counts have no side-specific breakdown.

Source-defined result groups 4
Localization: Insular / TemporalObserved proportion 17.6%Extensive ictal scalp-EEG distribution · patient with extensive distribution1 manuscript · 1 reported value · not pooled
Localization: Insular / TemporalObserved proportion 76.5%Extensive ictal scalp-EEG distribution · patient with extensive distribution1 manuscript · 1 reported value · not pooled
Localization: Insular / TemporalObserved proportion 5.9%Extensive ictal scalp-EEG distribution · patient with extensive distribution1 manuscript · 1 reported value · not pooled
Localization: Insular / TemporalObserved proportion 77.3%Extensive ictal scalp-EEG distribution · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 4 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • extensive ictal scalp-EEG distributionExtensive ictal scalp-EEG distribution was observed in 17 patients, involving the suprasylvian region in 3, the infrasylvian region in 1, and the perisylvian region including temporal regions in 13.PDF p.1, Abstract—Results; PDF p.4, Scalp-EEG data analysis
Reported values
  • Suprasylvian 3/17 (18%)extensive ictal scalp-EEG distributionPercentage · n/N 3/17 · 22 patients with insulo-opercular epilepsy; ictal scalp-EEG distribution reported for 17 patients · Extensive ictal scalp-EEG distribution · ictalPDF p.1, Abstract—Results; PDF p.4, Scalp-EEG data analysis
  • Infrasylvian 1/17 (6%)extensive ictal scalp-EEG distributionPercentage · n/N 1/17 · 22 patients with insulo-opercular epilepsy; ictal scalp-EEG distribution reported for 17 patients · Extensive ictal scalp-EEG distribution · ictalPDF p.1, Abstract—Results; PDF p.4, Scalp-EEG data analysis
  • Extensive ictal scalp-EEG distribution in 17/22 patientsextensive ictal scalp-EEG distributionCount · n/N 17/22 · 22 patients with insulo-opercular epilepsy; ictal scalp-EEG distribution reported for 17 patients · Extensive ictal scalp-EEG distribution · ictalPDF p.1, Abstract—Results; PDF p.4, Scalp-EEG data analysis
  • Perisylvian including temporal 13/17 (76%)extensive ictal scalp-EEG distributionPercentage · n/N 13/17 · 22 patients with insulo-opercular epilepsy; ictal scalp-EEG distribution reported for 17 patients · Extensive ictal scalp-EEG distribution · ictalPDF p.1, Abstract—Results; PDF p.4, Scalp-EEG data analysis

1 contributing manuscript; source-reported values remain separate and are not pooled.

tonic facial posturingReported: BilateralAlso reported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 5.01 across 1 manuscript · 1 independent primary study

The source supports unilateral/asymmetric-bilateral perioral activity and reports three ipsilateral cases, but the ipsilateral reference side is not defined at the result locus.

Source-defined result groups 1
Lateralization: Bilateral / IpsilateralObserved proportion 50.0%unilateral or asymmetric bilateral perioral focal tonic seizures · symmetric facial tonic contraction · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 3 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • focal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionFocal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas occurred in 11 patients, with ipsilateral involvement reported in three, while four patients had symmetric facial tonic contraction including pouting, grimace, or bilateral eyelid tonic closure.PDF p.3, Results—Seizure semiology; PDF p.5, Table 1
Reported values
  • four (18%)focal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionPercentage · n/N 4/22 · 22 patients with insulo-opercular epilepsy · symmetric facial tonic contraction · early ictal motor signPDF p.3, Results—Seizure semiology; PDF p.5, Table 1
  • 11/22 (50%)focal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionPercentage · n/N 11/22 · 22 patients with insulo-opercular epilepsy · unilateral or asymmetric bilateral perioral focal tonic seizures · early ictal motor signPDF p.3, Results—Seizure semiology; PDF p.5, Table 1
  • three patientsfocal tonic seizures restricted to unilateral or asymmetric bilateral perioral areas; symmetric facial tonic contractionCount · 22 patients with insulo-opercular epilepsy · ipsilateral involvement within the perioral group · early ictal motor signPDF p.3, Results—Seizure semiology; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal spittingReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphereNo single reliable side6 manuscripts · 10 findings · 10 reported values
Weighted evidence supportevidence weight 5 across 6 manuscripts · 1 manuscript weight pending · 4 narrative, educational, or cited context · 1 structured design not resolved · 1 case report or observation

The review lists ictal spitting or drinking as localizing to a right temporal-lobe focus. Ictal spitting is restated as non-lateralizing. Cited-study restatement places ictal spitting most often in nondominant temporal seizures, with less common dominant temporal, insular, and frontal contexts. Ictal spitting was reported in 11/54 RTL seizures and 0/73 LTL seizures. The review states that ictal spitting is rare and most often associated with the nondominant hemisphere. The cited series is reported as five right temporal lobe cases with the the source's own facial finding. A case observation reports ictal spitting in left temporal, nondominant temporal-lobe epilepsy. The cited series restates right temporal, nondominant seizure onset in 9 of 12 ictal-spitting patients and summarizes right, nondominant onset in 14 of 20 literature cases. The cited review reports ictal spitting predominantly in right or nondominant cases (14/20). The handbook lists ictal spitting as a nondominant-hemisphere sign with an explicit low-reliability qualifier on one rendering.

Source-defined result groups 4
Lateralization: Right hemisphereObserved proportion 0.0%LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Non-dominant hemisphereObserved proportion 100.0%All reported · right temporal cases · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalObserved proportion 100.0%All reported · right temporal cases · patient1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 20.4%RTL · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 6

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal spitting or drinkingIctal spitting or drinking is listed as localizing to a right temporal-lobe focus.PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Ictal spittingBoth tables list Ictal spitting as Nondominant hemisphere; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Ictal spitting*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Ictal spitting" (printed p.5)
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal spittingIctal spitting was reported in the RTL group and not in the LTL group.PDF p.4, Table 5; PDF p.5, Discussion
Reported values
  • 0/73Ictal spittingPercentage · n/N 0/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.4, Table 5; PDF p.5, Discussion
  • 11/54 (21%)Ictal spittingPercentage · n/N 11/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.4, Table 5; PDF p.5, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal spitting and Table 2 ictal splittingThe narrative calls the phenomenon ictal spitting and says it is most often observed in nondominant TLE, less commonly in dominant temporal, insular, or frontal seizures; Table 2 labels the row "ictal splitting" and associates it with complex automatisms, excessive salivation, or bad mouth sensations and nondominant TLE.PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfCase report or observation · 5 findings · 8 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal spittingIctal spitting is rare and most often lateralizes to the nondominant hemisphere.PDF p.7, section 3.12; PDF p.12, Table 1
  • ictal spittingVoss et al. found ictal spitting in five patients, all with right temporal lobe epilepsy.PDF p.7, section 3.12
  • ictal spittingIctal spitting was reported in left temporal, nondominant temporal lobe epilepsy.PDF p.7, section 3.12
  • ictal spittingKellinghaus et al. found right temporal, nondominant onset in 9 of 12 patients with ictal spitting.PDF p.7, section 3.12
  • ictal spitting in published casesA literature review found right, nondominant seizure onset in 14 of 20 reported ictal-spitting cases.PDF p.7, section 3.12
Reported values
  • 75%ictal spittingPercentage · epilepsy monitoring unit patients · patients with ictal spitting · ictalPDF p.7, section 3.12; PDF p.12, Table 1
  • approximately 0.3%ictal spittingPercentage · epilepsy monitoring unit patients · epilepsy monitoring unit patients · ictalPDF p.7, section 3.12; PDF p.12, Table 1
  • 5/2500 patients had ictal spitting and right TLEictal spittingCount · n/N 5/2500 · 2500 reviewed patients · ictalPDF p.7, section 3.12
  • 1 caseictal spittingCount · n/N 1/1 · one patient with left temporal lobe epilepsy · ictalPDF p.7, section 3.12
  • remaining 9ictal spittingCount · n/N 9/12 · 12 patients with ictal spitting · ictal spitting · ictalPDF p.7, section 3.12
  • 9 of 12ictal spittingPercentage · n/N 9/12 · 12 patients with ictal spitting · ictal spitting · ictalPDF p.7, section 3.12
  • 3/12ictal spittingPercentage · n/N 3/12 · 12 patients with ictal spitting · ictal spitting · ictalPDF p.7, section 3.12
  • 14/20 casesictal spitting in published casesCount · n/N 14/20 · 20 literature cases of ictal spitting · ictalPDF p.7, section 3.12
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal spittingThe review describes ictal spitting as a rare sign that also occurs in temporal lobe epilepsy and has no lateralizing value.PDF p.3, Autonomic seizures

6 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal urinary urgeReported: Non-dominant hemisphereAlso reported: Right hemisphere5 manuscripts · 7 findings · 2 reported values
Weighted evidence supportevidence weight 5 across 5 manuscripts · 5 narrative, educational, or cited context

The review lists ictal emeticus and ictal urinary urge as localizing to a right temporal focus. The educational tables associate peri-ictal urinary urge with the nondominant hemisphere. The review states that ictal urinary urge usually arises from the nondominant hemisphere. The review associates ictal urinary urge with nondominant temporal-lobe or nondominant-hemisphere epilepsy. The review reports ictal urinary urge in six patients classified with nondominant temporal-lobe epilepsy. A cited video-EEG study found ictal urinary urge in six additional patients with nondominant-hemisphere epilepsy. The finding reports no cerebral lateralization.

Evidence by contributing manuscript 5

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal emeticus and ictal urinary urgeIctal emeticus and ictal urinary urge are each listed as localizing to a right temporal-lobe focus.PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Peri-ictal urinary urgeBoth tables list Peri-ictal urinary urge as Nondominant hemisphere; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Peri-ictal urinary urge*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Peri-ictal urinary urge" (printed p.5)
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal urinary urgeIctal urinary urge is usually seen in seizures arising from the nondominant hemisphere, often the temporal lobe, and the table attributes it to activation of central bladder control.PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • urge to urinateUrge to urinate was one of the viscero-vegetative signs elicited by insular stimulation.PDF p.5, Visceral Symptoms
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Ictal urinary urgeThe review associates ictal urinary urge with non-dominant temporal or hemispheric epilepsy and describes the symptomatogenic zone as involving the mesial frontal region, medial temporal gyrus, or operculum.PDF p.3, section 2.7 Ictal urinary urge; PDF p.3, section 2.7.1 Mechanism
  • Ictal urinary urgeBaumgartner et al. found urinary urge in 6 of 227 patients with temporal lobe epilepsy confirmed by video/EEG and neuroimaging, and classified these patients as having non-dominant temporal lobe epilepsy.PDF p.3, section 2.7 Ictal urinary urge
  • Ictal urinary urgeA second study found urinary urge in 6 additional patients with non-dominant hemisphere epilepsy among 3446 patients undergoing video/EEG monitoring.PDF p.3, section 2.7 Ictal urinary urge
Reported values
  • 6 of 227 patientsIctal urinary urgeCount · n/N 6/227 · 227 patients with temporal lobe epilepsy · IctalPDF p.3, section 2.7 Ictal urinary urge
  • 6 additional patients among 3446Ictal urinary urgeCount · n/N 6/3446 · 3446 patients undergoing video/EEG monitoring · IctalPDF p.3, section 2.7 Ictal urinary urge

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal dysarthriaReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphere4 manuscripts · 6 findings · 1 reported value
Weighted evidence supportevidence weight 5 across 4 manuscripts · 1 manuscript weight pending · 1 systematic review or meta-analysis · 2 narrative, educational, or cited context · 1 structured design not resolved

The review states that anarthria alone is insufficient for hemispheric lateralization. The cited stimulation series describes left superior temporal stimulation effects that vary by task and subregion, including auditory phenomena, phonological errors, and naming or reading deficits. One isolated-dysarthria seizure arose from the dominant temporal lobe. No sign-specific lateralizing direction can be assigned to stimulation-evoked slurred speech. No sign-specific lateralizing direction can be assigned to stimulation-evoked lowering of voice intensity. No hemisphere or body-side direction is reported.

Source-defined result groups 2
Localization: TemporalObserved proportion 100.0%All reported · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphereObserved proportion 100.0%All reported · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 4

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 1 reported value
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • isolated dysarthriaIsolated dysarthria without dysphasia occurred in 1 seizure of dominant temporal-lobe onset and was associated with otherwise normal ictal speech.PDF p.3, Table 3 and Results
Reported values
  • 1 isolated-dysarthria seizure with dominant onsetisolated dysarthriaCount · n/N 1/1 · 1 seizure in the 35-patient temporal-lobe epilepsy cohort · ictalPDF p.3, Table 3 and Results
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 2 findings
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • speech arrest; anarthria; dysarthria; dysphasiaThe source states that speech arrest, including anarthria or dysarthria, can be the first sign of seizures starting from the frontal operculum, while anarthria alone is not sufficient to assign hemispheric lateralization.PDF p.9, Discussion
  • speech arrest; motor aphasia; dysprosody; dysarthriaThe discussion reports that language disorders in the cited Peltola series combined motor aphasia, dysprosody, or dysarthria early in seizure semiology but not at initial onset, suggesting opercular spread.PDF p.9, Discussion
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • slurred speech from insular stimulationSlurred speech was one of the speech impairments evoked by insular stimulation.PDF p.5, Other Insular Responses
  • lowering of voice intensity from insular stimulationLowering of voice intensity was one of the speech impairments evoked by insular stimulation.PDF p.5, Other Insular Responses
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • hallucinations or illusions; auditory symptoms; articulatory or phonological errors; naming or reading deficitsIn the posterior left superior temporal region, the source reports task- and subregion-specific effects: word-repetition stimulation of Heschl’s gyrus induced hallucinations or illusions without language deficit; planum temporale stimulation induced auditory symptoms with comprehension deficit; left planum temporale or Spt stimulation during word or pseudoword repetition elicited articulatory or phonological errors and difficulty maintaining the phonological loop; and posterior left STS stimulation during naming or reading produced naming or reading deficits without positive auditory symptoms, including the source’s reported “graphene” decoding, comprehension, and “graphene to phoneme” deficits.PDF p.7, posterior left superior temporal gyrus paragraph; PDF p.8, Fig. 10.3 caption

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Dyspnea / ictal respiratory distress sensationSource terms: Dyspnea/ictal respiratory distressReported: Right hemisphere3 manuscripts · 8 findings · 6 reported values
Weighted evidence supportevidence weight 5 across 3 manuscripts · 1 systematic review or meta-analysis · 2 narrative, educational, or cited context

No lateralization axis information is reported for choking, dyspnea, apnea, or throat constriction. No lateralization axis information is reported for the prefrontal-operculum choking/dyspnea/apnea/throat-constriction result. No lateralization axis information is reported for the precentral Rolandic-operculum choking/dyspnea/apnea/throat-constriction result. The primary choking/dyspnea/apnea/throat-constriction comparison reports no hemisphere or lateralization direction. No lateralizing information is present. No lateralization axis information is reported for suffocation and breathlessness. No lateralization axis information is reported for stimulation-evoked dyspnea. No fixed cerebral side or body-side direction is reported.

Source-defined result groups 4
Localization: FrontalObserved proportion 23.8%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 16.7%12 patients with EZ in the prefrontal operculum · precentral Rolandic operculum group (N=9) · patients in the prefrontal operculum group1 manuscript · 1 reported value · not pooled
Localization: fronto-opercular epilepsy cohortObserved proportion 28.6%All reported · all included patients1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 33.3%9 patients with EZ in the precentral Rolandic operculum · prefrontal operculum group (N=12) · patients in the precentral Rolandic operculum group1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal hyperventilation, apnea, dyspnea, and stridorIctal hyperventilation, defined as at least a 10% increase in respiratory rate from baseline, was observed in seizures of more than 50% of children in one series and was more common in temporal than frontal lobe epilepsy. In adults with TLE it is more common with mesial than neocortical onset; ictal apnea is most common in infants and neonates, while ictal dyspnea and stridor are rare and occur primarily during the tonic phase of GTCSs.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
Reported values
  • at least a 10% increaseictal hyperventilation, apnea, dyspnea, and stridorThreshold · children with focal seizures; adults with TLE; infants and neonates · ictal hyperventilation definition · ictal, with dyspnea and stridor primarily tonic phase of GTCSPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
  • more than 50%ictal hyperventilation, apnea, dyspnea, and stridorOther reported value · children with focal seizures; adults with TLE; infants and neonates · children in one cited series · ictal, with dyspnea and stridor primarily tonic phase of GTCSPDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 5 findings · 4 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Choking, dyspnea, apnea, throat constrictionTable 2 reports 5/21 (24%) for Choking, dyspnea, apnea, throat constriction; timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded High.PDF p.7, Table 2
  • Choking, dyspnea, apnea, throat constrictionTable 2 reports 2/12 patients with Choking, dyspnea, apnea, throat constriction in the prefrontal operculum group.PDF p.7, Table 2
  • Choking, dyspnea, apnea, throat constrictionTable 2 reports 3/9 patients with Choking, dyspnea, apnea, throat constriction in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Choking, dyspnea, apnea, throat constrictionFisher's exact comparison of Choking, dyspnea, apnea, throat constriction between the prefrontal and precentral Rolandic operculum groups has p=0.611.PDF p.7, Table 2
  • respiratory symptoms; dyspnea; hyperventilationThe source reports respiratory symptoms such as dyspnea and hyperventilation in 6 of 21 patients (29%).PDF p.6, Anatomical and clinical correlations
Reported values
  • 5/21 (24%)Choking, dyspnea, apnea, throat constrictionPercentage · n/N 5/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 2/12 patientsChoking, dyspnea, apnea, throat constrictionProportion · n/N 2/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 3/9 patientsChoking, dyspnea, apnea, throat constrictionProportion · n/N 3/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
  • 6/21 (29%)respiratory symptoms; dyspnea; hyperventilationPercentage · n/N 6/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 2 findings
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • suffocation and breathlessnessSuffocation and breathlessness are described as clinical features that can be highly suggestive of insular or insulo-opercular seizures.PDF p.2, Clinical Features
  • dyspneaDyspnea was one of the viscero-vegetative signs elicited by insular stimulation.PDF p.5, Visceral Symptoms

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal facial flushing / blushReported: IpsilateralAlso reported: Left hemisphere3 manuscripts · 6 findings · 3 reported values
Weighted evidence supportevidence weight 5 across 3 manuscripts · 1 systematic review or meta-analysis · 2 narrative, educational, or cited context

The review assigns ipsilateral direction to marching piloerection, left-temporal onset context to pallor in one pediatric series, and no lateralizing value to flushing. Rubefaction/flushing occurred in 2/21 patients; no hemisphere or body-side direction is reported. Rubefaction/flushing occurred in 1/12 prefrontal-operculum patients; no hemisphere or body-side direction is reported. Rubefaction/flushing occurred in 1/9 precentral Rolandic-operculum patients; no hemisphere or body-side direction is reported. No seizure lateralization is reported. No lateralizing direction is reported.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal piloerection, pallor, and flushingIctal piloerection presents as marching goose bumps involving a limb ipsilateral to seizure onset and is most common in TLE. Ictal pallor, usually occurring with other cutaneous signs, was associated with left temporal onset in one pediatric series, whereas ictal flushing involving mainly the face has no localizing value.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Rubefaction/flushingTable 2 reports 2/21 (10%) for Rubefaction/flushing; timing is onset or propagation, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Rubefaction/flushingTable 2 reports 1/12 patients with Rubefaction/flushing in the prefrontal operculum group.PDF p.7, Table 2
  • Rubefaction/flushingTable 2 reports 1/9 patients with Rubefaction/flushing in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Rubefaction/flushingFisher's exact comparison of Rubefaction/flushing between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 2/21 (10%)Rubefaction/flushingPercentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · BothPDF p.7, Table 2
  • 1/12 patientsRubefaction/flushingProportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · BothPDF p.7, Table 2
  • 1/9 patientsRubefaction/flushingProportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · BothPDF p.7, Table 2
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • facial blushFacial blush was one of the viscero-vegetative signs elicited by insular stimulation.PDF p.5, Visceral Symptoms

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Visual phenomenon (unspecified type)Reported: Contralateral3 manuscripts · 3 findings · 4 reported values
Weighted evidence supportevidence weight 5 across 3 manuscripts · 1 systematic review or meta-analysis · 2 narrative, educational, or cited context

Visual phenomena in occipital seizures are described as usually lateralized and contralateral to the seizure-onset hemisphere, with diffuse visual changes in up to 30%. In the cited series, 6 of 11 patients located the visual sensation in the contralateral eye or contralateral visual field relative to the occipital source. The cited series restatement reports visual manifestations in the contralateral hemifield in 12 of 42 patients with occipital-lobe epilepsy.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding · 1 reported value
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • visual phenomenon; occipital seizureVisual phenomena in occipital seizures are described as lateralised and contralateral to the hemisphere of seizure onset in most patients, but up to 30% may have more diffuse visual changes; true ictal visual-field loss or amaurosis is rare and may be postictal, especially when long lasting.PDF p.8, Primary visual cortex; PDF p.10, Lateralising signs
Reported values
  • diffuse visual changes up to 30%visual phenomenon; occipital seizureUpper-bound percentage · patients with occipital lobe seizures · ictal and postictal visual manifestationPDF p.8, Primary visual cortex; PDF p.10, Lateralising signs
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Visual manifestation in contralateral hemifieldSalanova et al. described visual manifestations in the contralateral hemifield in 12 of 42 patients with occipital lobe epilepsy; seizure freedom after resection was confirmed in 46% of patients.PDF p.3, section 2.5 Visual auras; PDF p.12, Table 1
Reported values
  • 12 of 42Visual manifestation in contralateral hemifieldPercentage · n/N 12/42 · 42 patients with occipital lobe epilepsy treated between 1930 and 1991 as summarized by the review · occipital lobe epilepsy · Ictal visual manifestationPDF p.3, section 2.5 Visual auras; PDF p.12, Table 1
  • 46%Visual manifestation in contralateral hemifieldPercentage · 42 patients with occipital lobe epilepsy treated between 1930 and 1991 as summarized by the review · resected occipital lobe epilepsy cohort · Ictal visual manifestationPDF p.3, section 2.5 Visual auras; PDF p.12, Table 1
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • contralateral visual sensationIn the cited Penfield and Kristiansen series, six of the 11 patients described the visual sensation in the contralateral eye or contralateral visual field.PDF p.2, Introduction
Reported values
  • 6/11 cited patientscontralateral visual sensationProportion · n/N 6/11 · 11 cited patients with visual sensations · seizure onsetPDF p.2, Introduction

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal eye pursuitReported: Contralateral1 manuscript · 6 findings · 1 reported value
Weighted evidence supportevidence weight 4.92 across 1 manuscript · 1 independent primary study

Source reports contralateral limb posturing in a sequential occipital-onset phenotype. This phenotype includes contralateral upper-limb tonic or asymmetric posturing after eye and oral/hand manifestations. Case 6 records repetitive head/eye pursuit to the right after a visual aura. Case 8 records eyes pursuing to the left after motor arrest. No lateralization axis information is reported for eye pursuit. No lateralizing direction is reported for the visual-aura sequence.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 6 findings · 1 reported value
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 4.92 · 2 × 1.5 × 1.639
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • oculomotor-onset evolving motor phenotypePhenotype IV begins with eye blinking or eye pursuit without a clear visual aura, followed by oral/hand automatisms and contralateral upper-limb tonic or asymmetric posturing, sometimes progressing to GTCS.PDF p.9, Phenotype IV
  • repetitive head-eye pursuit to the rightTable 2 records repetitive head/eye pursuit to the right after the Case 6 Sz1 visual aura.PDF p.6, Table 2 Case 6 Sz1
  • left eye pursuitTable 2 records eyes pursuing to the left in Case 8 after motor arrest.PDF p.7, Table 2 Case 8
  • eye pursuitEye pursuit occurred in five of 19 patients (26.3%).PDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1
  • visual aura to head-eye deviation or pursuitIn Phenotype III, a visual aura rapidly progresses to head-eye deviation or eye pursuit.PDF p.9, Phenotype III; PDF p.13, Phenotype III discussion
Reported values
  • 5/19 (26.3%) eye pursuiteye pursuitPercentage · n/N 5/19 · 19 patients monitored with SEEG · ictal oculomotor semiologyPDF p.5, Ictal Semiology and Seizure Capture During SEEG Monitoring; PDF p.9, Figure 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

tonic hand posturingReported: Contralateral2 manuscripts · 2 findings · 1 reported value
Weighted evidence supportevidence weight 4.91 across 2 manuscripts · 1 narrative, educational, or cited context · 1 independent primary study

One of 18 parietal-epilepsy patients had a hand tonic posture contralateral to the resected side. This finding provides no hemispheric lateralization information.

Source-defined result groups 2
Localization: ParietalObserved proportion 5.6%All reported · ipsilateral resected side · patients1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 5.6%All reported · ipsilateral resected side · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • contralateral hand tonic postureOne patient had a contralateral hand tonic posture.PDF p.2, Results
Reported values
  • 1/18 contralateral hand tonic posturecontralateral hand tonic postureProportion · n/N 1/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfNarrative, educational, or cited context · 1 finding
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • psychomotor semiology: hand posturingTypical temporal psychomotor semiology included hand posturing.PDF p.4, Seizure semiology on video-EEG recording

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Adversive/versive seizureReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 4.89 across 1 manuscript · 1 independent primary study

Conscious adversion was contralateral to the seizure focus in five patients.

Source-defined result groups 1
Lateralization: ContralateralObserved proportion 11.9%All reported · no conscious adversion · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfIndependent primary study · 1 finding · 1 reported value
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Independent primary study · Class II · Evidence weight 4.89 · 2 × 1.35 × 1.812
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • conscious adversionFive patients had conscious adversion contralateral to the focus.PDF p.6, Results, Non-visual manifestations
Reported values
  • 5/42 (11%) patientsconscious adversionPercentage · n/N 5/42 · 42 medically refractory patients with source-defined occipital lobe epilepsy · ictal manifestationPDF p.6, Results, Non-visual manifestations

1 contributing manuscript; source-reported values remain separate and are not pooled.

Paroxysmal dysphasiaReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere2 manuscripts · 10 findings · 23 reported values
Weighted evidence supportevidence weight 4.6 across 2 manuscripts · 1 independent primary study · 1 narrative, educational, or cited context

The dysphasia cohort was predominantly left-sided: 16 of 17 resections were left-sided, with one right-sided exception; the source also uses dominant/recessive temporal terminology. Among 17 dysphasia patients, temporal interictal discharges were exclusively left-sided in 10, bilateral in 7, with left predominance in 6 bilateral cases and right predominance in 1. The primary study reports relatively frequent slight left hemicranial diminution in paroxysmal dysphasia and speculates about left posterior temporal speech mechanisms; hemicranial-side context for speech automatisms remained mixed. The cited Hecaen and Piercy results restate dysphasia counts for left- versus right-sided foci across handedness strata. The cited study restates more paroxysmal dysphasia in patients with left-sided foci (31/63) than right-sided discharges (4/34). The cited 17-case dysphasia series is restated as predominantly left-sided, with bilateral discharges and no exclusively right-sided discharge. The primary result distinguishes paroxysmal dysphasia from ictal speech automatism without reporting a hemisphere or lateralization direction. No seizure lateralization is reported. No hemisphere or body-side direction is reported. No lateralization axis information is reported for the cited paroxysmal dysphasia and ictal speech-automatism frequency.

Source-defined result groups 7
Lateralization: Dominant hemisphere / Left hemisphere / Non-dominant hemisphere / Right hemisphereObserved proportion 94.1%left-sided resection; interpreted dominant temporal lobe · right-sided resection · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Left hemisphere / Non-dominant hemisphere / Right hemisphereObserved proportion 5.9%right-sided resection; interpreted recessive temporal lobe · left-sided resection · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 0.0%exclusively right-sided temporal discharges · exclusive left and bilateral · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 58.8%exclusively left-sided temporal discharges · bilateral and exclusively right-sided · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 41.2%bilateral temporal discharges · exclusive left and exclusive right · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 85.7%left-predominant among bilateral discharges · right-predominant bilateral · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Left hemisphere / Right hemisphereObserved proportion 14.3%right-predominant among bilateral discharges · left-predominant bilateral · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfNarrative, educational, or cited context · 3 findings · 6 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • paroxysmal dysphasiaThe source reports that Hecaen and Piercy found paroxysmal dysphasia in 31 of 63 right-handed patients with left-sided foci versus 4 of 34 patients with right-sided discharges.PDF p.5, Discussion
  • paroxysmal dysphasiaThe source reports that, in Serafetinides and Falconer’s 17 cases with paroxysmal dysphasia, 10 had exclusively left-sided discharges, 7 had bilateral discharges, and none had exclusively right-sided discharges.PDF p.5, Discussion
  • paroxysmal dysphasia and ictal speech automatismsThe source reports that, after excluding speech arrest and vocalization, Serafetinides and Falconer found paroxysmal dysphasia and ictal speech automatisms in 67% of their patients.PDF p.5, Discussion
Reported values
  • 4/34 patients with right-sided dischargesparoxysmal dysphasiaPercentage · n/N 4/34 · Right-handed patients in the cited Hecaen and Piercy report · right-sided discharges · paroxysmal; exact ictal/postictal phase not reported in this restatementPDF p.5, Discussion
  • 31/63 patients with left-sided fociparoxysmal dysphasiaPercentage · n/N 31/63 · Right-handed patients in the cited Hecaen and Piercy report · left-sided foci · paroxysmal; exact ictal/postictal phase not reported in this restatementPDF p.5, Discussion
  • none ... exclusively right-sidedparoxysmal dysphasiaPercentage · n/N 0/17 · 17 cases with paroxysmal dysphasia in the cited series · exclusively right-sided discharges · paroxysmal; exact ictal/postictal phase not reported in this restatementPDF p.5, Discussion
  • 7/17paroxysmal dysphasiaPercentage · n/N 7/17 · 17 cases with paroxysmal dysphasia in the cited series · bilateral discharges · paroxysmal; exact ictal/postictal phase not reported in this restatementPDF p.5, Discussion
  • 10/17paroxysmal dysphasiaPercentage · n/N 10/17 · 17 cases with paroxysmal dysphasia in the cited series · exclusively left-sided discharges · paroxysmal; exact ictal/postictal phase not reported in this restatementPDF p.5, Discussion
  • 67% of patients with paroxysmal dysphasia and/or ictal speech automatismsparoxysmal dysphasia and ictal speech automatismsPercentage · Patients in the cited Serafetinides and Falconer series; exact denominator not reported in this passage · paroxysmal/ictal according to the cited phenomenon namesPDF p.5, Discussion
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfIndependent primary study · 7 findings · 17 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Independent primary study · Class II · Evidence weight 3.60 · 2 × 0.9 × 2
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • paroxysmal dysphasiaWithin Group A, 16 of 17 patients with paroxysmal dysphasia had left-sided resections and 1 had a right-sided resection; the authors interpreted these as 16 cases related to the dominant temporal lobe and 1 to the recessive temporal lobe, noting that the right-handed exception occasionally showed left temporal spike discharges.PDF p.5, Table II and adjacent text; PDF p.6, discussion of Group A dysphasia; PDF p.7, discussion of Group A dysphasia
  • paroxysmal dysphasia; pre-operative interictal spike dischargesAmong 17 Group A patients with paroxysmal dysphasia, pre-operative interictal EEG showed exclusively left-sided temporal discharges in 10 and bilateral discharges in 7; the bilateral discharges were left-predominant in 6 and right-predominant in 1, and none were exclusively right-sided.PDF p.7, EEG discussion; PDF p.12, Table IV, Group A dysphasia row
  • paroxysmal dysphasia; ictal speech automatism; hemicranial diminutionPre-operative radiology showed a relatively high incidence of slight diminution of left hemicranial size among patients with paroxysmal dysphasia compared with the remainder, whereas similar diminution of either hemicranium was uncommon in patients with ictal speech automatisms; the authors speculated that dysphasia might involve wider-ranging discharges reaching vulnerable left posterior temporal speech mechanisms.PDF p.11, discussion of radiological studies
  • paroxysmal dysphasiaThe current article reports that Hecaen and Piercy selected 126 epileptic patients from 3,000 who met lateralization criteria and found dysphasia in 31/63 right-handed patients with left-sided foci, 4/34 right-sided-foci patients, 17/18 left-handed patients with left-hemisphere foci, and 9/11 left-handed patients with right-hemisphere foci.PDF p.10, discussion of prior dysphasia reports
  • paroxysmal dysphasia versus ictal speech automatismThe authors treated paroxysmal dysphasia and ictal speech automatism as different aspects of ictal speech disorder: in the few patients with both phenomena they occurred at separate times and never together in the same seizure.PDF p.9, discussion points (1); PDF p.12, Summary
  • persistent nominal dysphasia; persistent paroxysmal dysphasiaAmong 17 Group A patients with pre-operative paroxysmal dysphasia, 3 were left with relatively mild persistent nominal dysphasia; in the full 100-patient series, 5 had persistent nominal dysphasia, and no patient had persistent paroxysmal dysphasia post-operatively.PDF p.11, prognostic discussion
  • paroxysmal dysphasia; ictal speech automatism; grand mal attacksThe authors report that more than three-quarters of the 34 patients with paroxysmal dysphasia also had grand mal attacks, whereas slightly less than half of the patients with ictal speech automatism had these major seizures.PDF p.11, discussion of seizure severity
Reported values
  • 16/17paroxysmal dysphasiaPercentage · n/N 16/17 · Group A; 17 patients with pre-operative paroxysmal dysphasia · left-sided resection; interpreted dominant temporal lobe · Pre-operative; dysphasia at seizure onset or immediately after recoveryPDF p.5, Table II and adjacent text; PDF p.6, discussion of Group A dysphasia; PDF p.7, discussion of Group A dysphasia
  • 1/17paroxysmal dysphasiaPercentage · n/N 1/17 · Group A; 17 patients with pre-operative paroxysmal dysphasia · right-sided resection; interpreted recessive temporal lobe · Pre-operative; dysphasia at seizure onset or immediately after recoveryPDF p.5, Table II and adjacent text; PDF p.6, discussion of Group A dysphasia; PDF p.7, discussion of Group A dysphasia
  • 10/17paroxysmal dysphasia; pre-operative interictal spike dischargesPercentage · n/N 10/17 · Group A; 17 patients with paroxysmal dysphasia · exclusively left-sided temporal discharges · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A dysphasia row
  • 7/17paroxysmal dysphasia; pre-operative interictal spike dischargesPercentage · n/N 7/17 · Group A; 17 patients with paroxysmal dysphasia · bilateral temporal discharges · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A dysphasia row
  • none were exclusively right-sidedparoxysmal dysphasia; pre-operative interictal spike dischargesPercentage · n/N 0/17 · Group A; 17 patients with paroxysmal dysphasia · exclusively right-sided temporal discharges · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A dysphasia row
  • 6/7paroxysmal dysphasia; pre-operative interictal spike dischargesPercentage · n/N 6/7 · Group A; 17 patients with paroxysmal dysphasia · left-predominant among bilateral discharges · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A dysphasia row
  • 1/7paroxysmal dysphasia; pre-operative interictal spike dischargesPercentage · n/N 1/7 · Group A; 17 patients with paroxysmal dysphasia · right-predominant among bilateral discharges · Pre-operative interictal EEGPDF p.7, EEG discussion; PDF p.12, Table IV, Group A dysphasia row
  • 17/18paroxysmal dysphasiaPercentage · n/N 17/18 · Hecaen and Piercy’s cited cohort of 126 selected from 3,000 epileptic patients; handedness and EEG-focus subgroups as reported by the current article · left-handed; left-hemisphere foci · Paroxysmal dysphasia associated with epileptic focusPDF p.10, discussion of prior dysphasia reports
  • 9/11paroxysmal dysphasiaPercentage · n/N 9/11 · Hecaen and Piercy’s cited cohort of 126 selected from 3,000 epileptic patients; handedness and EEG-focus subgroups as reported by the current article · left-handed; right-hemisphere foci · Paroxysmal dysphasia associated with epileptic focusPDF p.10, discussion of prior dysphasia reports
  • 4/34paroxysmal dysphasiaPercentage · n/N 4/34 · Hecaen and Piercy’s cited cohort of 126 selected from 3,000 epileptic patients; handedness and EEG-focus subgroups as reported by the current article · right-handed; right-sided foci · Paroxysmal dysphasia associated with epileptic focusPDF p.10, discussion of prior dysphasia reports
  • 126 ... from 3,000paroxysmal dysphasiaPercentage · n/N 126/3,000 · Hecaen and Piercy’s cited cohort of 126 selected from 3,000 epileptic patients; handedness and EEG-focus subgroups as reported by the current article · patients meeting lateralization criteria · Paroxysmal dysphasia associated with epileptic focusPDF p.10, discussion of prior dysphasia reports
  • 31/63paroxysmal dysphasiaPercentage · n/N 31/63 · Hecaen and Piercy’s cited cohort of 126 selected from 3,000 epileptic patients; handedness and EEG-focus subgroups as reported by the current article · right-handed; left-sided foci · Paroxysmal dysphasia associated with epileptic focusPDF p.10, discussion of prior dysphasia reports
  • Persistent nominal dysphasia 3/17 in Group A dysphasia subgrouppersistent nominal dysphasia; persistent paroxysmal dysphasiaCount · n/N 3/17 · Group A dysphasia subgroup and the full 100-patient surgical series · Group A patients with pre-operative dysphasia · Post-operative follow-upPDF p.11, prognostic discussion
  • Persistent nominal dysphasia 5/100 overallpersistent nominal dysphasia; persistent paroxysmal dysphasiaCount · n/N 5/100 · Group A dysphasia subgroup and the full 100-patient surgical series · Full surgical series · Post-operative follow-upPDF p.11, prognostic discussion
  • Persistent paroxysmal dysphasia 0/100persistent nominal dysphasia; persistent paroxysmal dysphasiaCount · n/N 0/100 · Group A dysphasia subgroup and the full 100-patient surgical series · Full surgical series · Post-operative follow-upPDF p.11, prognostic discussion
  • slightly less than half of 38 speech-automatism patientsparoxysmal dysphasia; ictal speech automatism; grand mal attacksPercentage · Patients with pre-operative paroxysmal dysphasia and patients with pre-operative ictal speech automatisms · ictal speech automatism · Pre-operative seizure historyPDF p.11, discussion of seizure severity
  • more than three-quarters of 34 dysphasia patientsparoxysmal dysphasia; ictal speech automatism; grand mal attacksPercentage · Patients with pre-operative paroxysmal dysphasia and patients with pre-operative ictal speech automatisms · paroxysmal dysphasia · Pre-operative seizure historyPDF p.11, discussion of seizure severity

2 contributing manuscripts; source-reported values remain separate and are not pooled.

hemisphere of seizure onsetReported: Left hemisphereAlso reported: Right hemisphereNo single reliable side1 manuscript · 1 finding · 5 reported values
Weighted evidence supportevidence weight 4.35 across 1 manuscript · 1 independent primary study

ICA was not associated with onset hemisphere: ICA 15/27 left and 12/27 right versus no-apnea 18/42 left and 24/42 right; chi-square 0.61, p=0.43.

Source-defined result groups 5
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereSource-defined values retained separatelyAll reported · Patients without seizure-related apnea · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 57.1%no apnea; right onset · Patients without seizure-related apnea · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 42.9%no apnea; left onset · Patients without seizure-related apnea · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 44.4%ICA; right onset · Patients without seizure-related apnea · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 55.6%ICA; left onset · Patients without seizure-related apnea · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 1 finding · 5 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 4.35 · 2 × 1.2 × 1.812
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • hemisphere of seizure onsetThe distribution of right- versus left-hemisphere seizure onset did not differ significantly between patients with ICA and patients without seizure-related apnea.PDF p.4, Results, ICA in Focal Seizures; PDF p.5, Table 1, Hemisphere of seizure onset
Reported values
  • right onset 24/42 (57%) without apneahemisphere of seizure onsetPercentage · n/N 24/42 · ICA group 27 patients versus no-seizure-related-apnea group 42 patients · no apnea; right onset · ictal onset localizationPDF p.4, Results, ICA in Focal Seizures; PDF p.5, Table 1, Hemisphere of seizure onset
  • left onset 15/27 (56%) with ICAhemisphere of seizure onsetPercentage · n/N 15/27 · ICA group 27 patients versus no-seizure-related-apnea group 42 patients · ICA; left onset · ictal onset localizationPDF p.4, Results, ICA in Focal Seizures; PDF p.5, Table 1, Hemisphere of seizure onset
  • right onset 12/27 (44%) with ICAhemisphere of seizure onsetPercentage · n/N 12/27 · ICA group 27 patients versus no-seizure-related-apnea group 42 patients · ICA; right onset · ictal onset localizationPDF p.4, Results, ICA in Focal Seizures; PDF p.5, Table 1, Hemisphere of seizure onset
  • chi-square=0.61hemisphere of seizure onsetOther reported value · ICA group 27 patients versus no-seizure-related-apnea group 42 patients · ictal onset localizationPDF p.4, Results, ICA in Focal Seizures; PDF p.5, Table 1, Hemisphere of seizure onset
  • left onset 18/42 (43%) without apneahemisphere of seizure onsetPercentage · n/N 18/42 · ICA group 27 patients versus no-seizure-related-apnea group 42 patients · no apnea; left onset · ictal onset localizationPDF p.4, Results, ICA in Focal Seizures; PDF p.5, Table 1, Hemisphere of seizure onset

1 contributing manuscript; source-reported values remain separate and are not pooled.

“reliable” motor signs; PPV threshold for sequence analysisReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight 4.22 across 1 manuscript · 1 independent primary study

The source retained 38/47 representative seizures with at least two reliable motor signs and described primarily contralateral reliable directions, with asymmetric clonic ending ipsilateral.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 1 finding · 6 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.22 · 2 × 1.15 × 1.836
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • “reliable” motor signs; PPV threshold for sequence analysisThe source excluded figure of 4 and hand dystonia (ictal dystonia) from sequence analysis because their PPVs were below the source-defined reliability threshold, retained 38 of the 47 representative seizures with at least two reliable motor signs, and identified version, unilateral tonic posturing, M2e, unilateral clonic seizure, asymmetric clonic ending, and Todd's paralysis as reliable signs.PDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results
Reported values
  • PPV >80%; PPV ≤80% excluded“reliable” motor signs; PPV threshold for sequence analysisThreshold · 47 patients with one representative seizure each; the retained sequence subset is described as 38 seizures in Results and 38 patients in the Summary · motor-sign sequence leading to secondary generalization, with Todd's paralysis as a postictal sign when includedPDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results
  • 38/47 retained for sequence analysis“reliable” motor signs; PPV threshold for sequence analysisPercentage · n/N 38/47 · 47 patients with one representative seizure each; the retained sequence subset is described as 38 seizures in Results and 38 patients in the Summary · retained · motor-sign sequence leading to secondary generalization, with Todd's paralysis as a postictal sign when includedPDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results
  • 9/47 excluded“reliable” motor signs; PPV threshold for sequence analysisPercentage · n/N 9/47 · 47 patients with one representative seizure each; the retained sequence subset is described as 38 seizures in Results and 38 patients in the Summary · excluded; only one reliable motor sign · motor-sign sequence leading to secondary generalization, with Todd's paralysis as a postictal sign when includedPDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results
  • six reliable signs“reliable” motor signs; PPV threshold for sequence analysisCount · 47 patients with one representative seizure each; the retained sequence subset is described as 38 seizures in Results and 38 patients in the Summary · source-defined reliable · motor-sign sequence leading to secondary generalization, with Todd's paralysis as a postictal sign when includedPDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results
  • PPV ≥80%“reliable” motor signs; PPV threshold for sequence analysisThreshold · 47 patients with one representative seizure each; the retained sequence subset is described as 38 seizures in Results and 38 patients in the Summary · motor-sign sequence leading to secondary generalization, with Todd's paralysis as a postictal sign when includedPDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results
  • two lower-PPV signs“reliable” motor signs; PPV threshold for sequence analysisCount · 47 patients with one representative seizure each; the retained sequence subset is described as 38 seizures in Results and 38 patients in the Summary · excluded lower-PPV · motor-sign sequence leading to secondary generalization, with Todd's paralysis as a postictal sign when includedPDF p.2, Summary; PDF p.3, Key Point Box; PDF p.6, Methods; PDF p.9, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

combination of two or more reliable motor signs pointing to the same sideReported: Contralateral1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight 4.12 across 1 manuscript · 1 independent primary study

Among seizures with reliable combinations of signs, agreeing versions, clonic, tonic, M2e, asymmetric clonic, or Todd signs lateralized the EZ to the contralateral hemisphere, with mixed and contradictory exceptions described.

Source-defined result groups 6
Lateralization: ContralateralObserved proportion 2.6%two contradictory signs · other consistency patterns · representative seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyat least two reliable motor signs · Consistent versus mixed or contradictory sign directions · representative seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 84.2%wholly consistent signs · mixed signs · representative seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 100.0%agreeing combination · Consistent versus mixed or contradictory sign directions · seizure with at least two consistent reliable signs1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 83.3%at least two consistent signs and one contradictory sign · two contradictory signs · representative seizure with mixed signs1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralObserved proportion 15.8%mixed sign directions · wholly consistent signs · representative seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfIndependent primary study · 1 finding · 6 reported values
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Independent primary study · Class II · Evidence weight 4.12 · 2 × 1.15 × 1.79
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • combination of two or more reliable motor signs pointing to the same sideOf the 38 seizures with at least two reliable signs, 32 had signs consistently lateralizing the EZ, six had a mixture of signs pointing to either hemisphere, five of those six still had at least two consistent signs and only one contradictory sign, and one seizure had two contradictory signs. In all 37 seizures with at least two consistent signs, a combination of two or more of version, clonic, tonic, M2e, asymmetric clonic, or Todd's signs, when in agreement, had a PPV of 100% and lateralized the EZ to the contralateral hemisphere.PDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions
Reported values
  • 6/38combination of two or more reliable motor signs pointing to the same sidePercentage · n/N 6/38 · 38 representative sequence seizures with at least two reliable motor signs · mixed sign directions · motor sequence before or through secondary generalization; Todd's paralysis is postictal when presentPDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions
  • 32/38combination of two or more reliable motor signs pointing to the same sidePercentage · n/N 32/38 · 38 representative sequence seizures with at least two reliable motor signs · wholly consistent signs · motor sequence before or through secondary generalization; Todd's paralysis is postictal when presentPDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions
  • 1/38combination of two or more reliable motor signs pointing to the same sidePercentage · n/N 1/38 · 38 representative sequence seizures with at least two reliable motor signs · two contradictory signs · motor sequence before or through secondary generalization; Todd's paralysis is postictal when presentPDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions
  • 38 seizurescombination of two or more reliable motor signs pointing to the same sideCount · 38 representative sequence seizures with at least two reliable motor signs · at least two reliable motor signs · motor sequence before or through secondary generalization; Todd's paralysis is postictal when presentPDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions
  • 5/6combination of two or more reliable motor signs pointing to the same sidePercentage · n/N 5/6 · 38 representative sequence seizures with at least two reliable motor signs · at least two consistent signs and one contradictory sign · motor sequence before or through secondary generalization; Todd's paralysis is postictal when presentPDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions
  • 100%combination of two or more reliable motor signs pointing to the same sidePositive predictive value · n/N 37/37 · 38 representative sequence seizures with at least two reliable motor signs · agreeing combination · motor sequence before or through secondary generalization; Todd's paralysis is postictal when presentPDF p.2, Results in Summary; PDF p.3, Key Point Box; PDF p.10, Results; PDF p.11, Discussion; PDF p.14, Conclusions

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal paraphasia / word substitution errorsSource terms: Ictal paraphasiaReported: Dominant hemisphereAlso reported: Left hemisphereNo single reliable side4 manuscripts · 8 findings · 2 reported values
Weighted evidence supportevidence weight 4 across 4 manuscripts · 1 case report or observation · 3 narrative, educational, or cited context

The review states that paraphasia had not been identified as a clear lateralizing sign in epilepsy before the reported case. The review synthesis restates an association between paraphasic seizures and left or dominant-hemisphere onset. The review associates paraphasic errors and alexia with seizures originating in the dominant hemisphere. The cited-study restatement says phonemic paraphasic errors are more clinically useful than semantic errors for lateralising information in temporal-lobe epilepsy, without specifying a side. No hemisphere or body-side direction is reported. Ictal-paraphasia duration has no hemisphere or body-side information. This single case had left temporal onset and supports the authors' interpretation of ictal paraphasia as a dominant-temporal lateralizing sign. The source attributes to Hecaen the statement that ictal paraphasia/Jargon aphasia is present in the dominant hemisphere.

Evidence by contributing manuscript 4

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Paraphasic errors and alexiaParaphasic errors and alexia are reported as clearly associated with CPSs originating in the dominant hemisphere.PDF p.5, language-disturbances paragraph
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 5 findings · 2 reported values
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • paraphasia; fluent and non-fluent paraphasiaThe authors characterize ictal paraphasia as rarely described, state that non-fluent paraphasia is relatively known while fluent paraphasia has few reported cases, and state that paraphasia had not been identified as a clear lateralizing sign in epilepsy.PDF p.2, Introduction; PDF p.3, Discussion
  • paraphasic seizuresThe article states that more recent series and case reports have associated paraphasic seizures with left/dominant hemisphere onset.PDF p.3, Discussion
  • semantic/verbal and phonemic paraphasias; ictal paraphasiaIn this case, focal-onset unaware episodes were characterized by loss of awareness, confusion, and semantic/verbal and phonemic paraphasias, including using “cielo” for “hielo” and “placo” for “plato.”PDF p.2, Abstract and Materials and Methods; PDF p.3, Discussion
  • ictal paraphasia durationThe reported episodes lasted about 1 minute by history, while paraphasias during video-EEG-recorded events lasted 30–50 seconds.PDF p.2, Materials and Methods
  • ictal paraphasia as a dominant temporal lateralizing signOn the basis of the reported left temporal anatomo-electro-clinical correlation, the authors state that this case reinforces interpreting ictal paraphasia as a dominant temporal lateralizing sign.PDF p.3, Discussion
Reported values
  • 30-50 secondsictal paraphasia durationRange · One 73-year-old right-handed woman · Video-EEG observation · IctalPDF p.2, Materials and Methods
  • about 1 minuteictal paraphasia durationDuration · One 73-year-old right-handed woman · Clinical history · IctalPDF p.2, Materials and Methods
ictal-speech-disturbance-cerebral-dominance.pdfNarrative, educational, or cited context · 1 finding
ictal-speech-disturbance-cerebral-dominance.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors collected about 43 cases with ictal speech disturbances over 8 years. Interictal EEG was examined at least twice per case; laterality was defined by a spike or sharp-wave focus, unilateral dominant spike or sharp wave, or unilateral slow wave corresponding to same-region brain damage or tumor. Laterality was confirmed in 36 cases; 7 cases with independent foci, no laterality, or normal findings were excluded. The statistical report concerns 34 right-handed epileptics because 2 left-handed patients could not be tested statistically. A control pool comprised 243 right-handed patients with unilateral abnormal EEG findings, 136 left and 117 right, and was assessed by t test.
Findings
  • ictal paraphasia or Jargon aphasiaThe authors state that ictal paraphasia or Jargon aphasia has occasionally been mistaken for speech automatism and attribute to Hecaen the statement that ictal paraphasia is present in the dominant hemisphere.PDF p.5, Discussion paragraph beginning “The question of why”
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Phonemic and semantic paraphasic errorsThe review reports that phonemic paraphasic errors are more clinically useful than semantic paraphasic errors for lateralising information in temporal-lobe epilepsy.PDF p.6, section 1.9

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Myoclonic jerkingReported: Contralateral4 manuscripts · 5 findings · 5 reported values
Weighted evidence supportevidence weight 4 across 4 manuscripts · 4 narrative, educational, or cited context

The cited table labels myoclonic/negative myoclonus contralateral when unilateral. Myoclonic seizures are usually generalized or bilateral, while unilateral myoclonus is described as contralateral to primary motor or premotor cortex. The generalized-epilepsy association does not report lateralization. No lateralization is reported.

Evidence by contributing manuscript 4

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • myoclonic and negative myoclonus seizuresMyoclonic seizures are usually generalized or bilateral but can be focal; unilateral myoclonic seizures are generated from the primary motor or premotor cortex contralateral to the seizure. Negative myoclonus is brief muscle atonia during contraction, and negative epileptic myoclonus is rarely observed in perirolandic epilepsy.PDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
Reported values
  • Myoclonic duration shorter than 400 msmyoclonic and negative myoclonus seizuresDuration · patients with focal or generalized epilepsy · Myoclonic seizure · ictal motorPDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
  • Negative myoclonus duration 20–400 msmyoclonic and negative myoclonus seizuresRange · patients with focal or generalized epilepsy · Negative myoclonus · ictal motorPDF p.3, section 3.2 Simple motor seizures; PDF p.2, Table 1
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Myoclonic/negative myoclonusTable 2 associates myoclonic/negative myoclonus with primary motor cortex (BA 4), premotor cortex (BA 6), and primary somatosensory area and lists contralateral lateralisation if unilateral.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • myoclonic seizureThe source defines myoclonic seizures as short muscle contractions lasting less than 400 ms.PDF p.4, Simple motor seizures
  • Myoclonic seizureMyoclonic seizures consist of short muscle contractions lasting less than 400 milliseconds.PDF p.4, Simple motor seizures, Myoclonic seizures; PDF p.2, Table 1
Reported values
  • muscle-contraction duration <400 msmyoclonic seizureDuration Threshold · ictalPDF p.4, Simple motor seizures
  • <400 ms muscle-contraction durationMyoclonic seizureCount · IctalPDF p.4, Simple motor seizures, Myoclonic seizures; PDF p.2, Table 1
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • myoclonic seizuresThe review defines myoclonic seizures as short muscle contractions lasting less than 200 msec and states that they are most often seen in generalized epilepsies.PDF p.3, Simple motor seizures/Myoclonic seizures
Reported values
  • Muscle contractions lasting <200 msecmyoclonic seizuresCount · Patients with myoclonic seizures; no cohort reported · IctalPDF p.3, Simple motor seizures/Myoclonic seizures

4 contributing manuscripts; source-reported values remain separate and are not pooled.

motor phenomenon (unspecified type)Reported: Contralateral2 manuscripts · 2 findings · 0 reported values
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 narrative, educational, or cited context · 1 systematic review or meta-analysis

Focal motor seizures are described as contralateral to the involved primary motor cortex. No cerebral lateralization is reported.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • focal motor seizure; automotor seizureThe review describes focal motor seizures arising from contralateral primary motor cortex as highly specific or pathognomonic for that region, while automotor seizures are less localising because they can arise from different brain regions.PDF p.2, Introduction
jobst-insula-and-its-epilepsies-2019.pdfNarrative, educational, or cited context · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • unilateral motor symptoms in perisylvian spreadUnilateral motor symptoms occur later in the source-described perisylvian propagation sequence.PDF p.1, Abstract

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Genital / perineal somatosensory auraSource terms: Genital/perineal somatosensory auraReported: Bilateral2 manuscripts · 2 findings · 2 reported values
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 independent primary study · 1 narrative, educational, or cited context

The cited source places genital aura in the postcentral parasagittal region and notes that bilateral symptoms can arise from SII activation. No seizure lateralization is reported.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • uro-genital auraUro-genital auras did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • T+ 4.3%uro-genital auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 1.7%uro-genital auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • genital aurasGenital auras are often painful or unpleasant and associated with fear; the symptomatogenic zone is the postcentral parasagittal region, but bilateral symptoms can arise from SII activation.PDF p.3, section 3.1 Auras

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal autonomic changeReported: Left hemisphereAlso reported: Right hemisphere2 manuscripts · 2 findings · 10 reported values
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 independent primary study · 1 case report or observation

Right facial pain, right-ear ringing, right hemibody and foot manifestations predominated in the early sequence, while left-sided stiffening occurred in half of seizures. No hemisphere or body-side direction is reported.

Source-defined result groups 6
Localization: Frontal / TemporalSource-defined values retained separatelyFrontal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyTemporal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyOperculoinsular SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyTemporal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyFrontal SOZ · frontal, temporal, operculoinsular, and posterior SOZ subgroups · patient1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyleft-sided stiffening · Early diurnal versus later nocturnal/postoperative semiology · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 5 reported values
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • epigastric and autonomic manifestationsTable 2 lists epigastric manifestations as n=8 frontal, n=3 temporal, and n=2 operculoinsular, with no posterior entry; it lists autonomic manifestations as n=6 frontal and n=2 temporal, with no operculoinsular or posterior entry. The narrative states that epigastric and autonomic features were present in all but the posterior subgroup.PDF p.6, Table 2; PDF p.7, section 3.3
Reported values
  • Autonomic manifestations, temporal n=2epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Temporal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Epigastric manifestations, temporal n=3epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Temporal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Epigastric manifestations, operculoinsular n=2epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Operculoinsular SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Epigastric manifestations, frontal n=8epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Frontal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
  • Autonomic manifestations, frontal n=6epigastric and autonomic manifestationsCount · 115 SHE patients in the early nonmotor semiology table and SOZ subgroups · Frontal SOZ · early nonmotor seizure onsetPDF p.6, Table 2; PDF p.7, section 3.3
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding · 5 reported values
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyCase 2 was a 46-year-old right-handed man whose seizures began with lancinating right facial pain followed within 2 seconds by high-pitched right-ear ringing descending along the right hemibody to the foot, sometimes with right-foot tremor, witnessed erratic right-sided and truncal movements, and left-sided stiffening in half the seizures; he was usually conscious without postictal paresis, had 10–15-second events up to 100 times per day triggered by sounds, and could develop hypersalivation, speech difficulty, later nocturnal hypermotor seizures, and urinary incontinence.PDF p.11, Case 2; PDF p.13, continuation of Case 2
Reported values
  • within 2 secondsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyDuration · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · early sensory sequence · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 10–15-second eventsCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · habitual events · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • 2–3 per monthCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyRange · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · youth · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • in half the seizuresCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyOther reported value · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · left-sided stiffening · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2
  • up to 100 times per dayCase 2 painful somatosensory, auditory-reflex, hypermotor, and autonomic/speech semiologyFrequency · Individual Case 2; 46-year-old right-handed man, seizure onset age 16 · later high-frequency period · Ictal; longitudinal diurnal, nocturnal, and postoperative descriptionsPDF p.11, Case 2; PDF p.13, continuation of Case 2

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal pupillary changeReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral2 manuscripts · 2 findings · 2 reported values
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 independent primary study · 1 narrative, educational, or cited context

The cited report describes usually bilateral pupillary dilation in GTCSs, focal unilateral mydriasis, temporo-occipital ipsilateral mydriasis, and benign-childhood frontal contralateral mydriasis. No seizure lateralization is reported.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • pupillary changesPupillary changes did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 16.9%pupillary changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 26.1%pupillary changesPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • pupillary changes and mydriasisPupillary dilation is typically bilateral in GTCSs but may be unilateral in focal epilepsy. Unilateral mydriasis was ipsilateral to the epileptogenic zone in temporo-occipital seizures but contralateral to the frontal focus in benign childhood epilepsy; bilateral and unilateral miosis are rarely described in temporal and occipital seizures.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal speech manifestation (unspecified subtype)Reported: ContralateralAlso reported: Dominant hemisphereAlso reported: Non-dominant hemisphere2 manuscripts · 3 findings · 1 reported value
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 case report or observation · 1 systematic review or meta-analysis

The review associates mesial-temporal automatisms with hand or mouth movements, ictal speech with nondominant seizures, and unilateral dystonic posturing with a contralateral seizure-onset relation. The review links ictal or postictal dysphasia to the dominant hemisphere, formed nonsensical ictal speech to the nondominant hemisphere, and explicitly describes speech arrest as non-lateralising. No source lateralization is reported.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • mesial temporal automatisms; ictal speech; unilateral dystonic posturingMesial temporal automatisms often involve the hands or mouth; less common vocalisations and ictal speech are associated with non-dominant seizures; unilateral dystonic posturing can occur and is described as a contralateral sign.PDF p.5, Mesial temporal lobe including hippocampus
  • ictal/postictal dysphasia; speech arrest; ictal speechIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value; speech arrest is described as non-lateralising, whereas ictal speech consisting of formed nonsensical phrases is a non-dominant sign.PDF p.10, Lateralising signs
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding · 1 reported value
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • ictal speech manifestationsThe article reports that Yen et al. evaluated 68 patients and 261 seizures and found ictal speech manifestations in 47.1% of patients.PDF p.3, Discussion
Reported values
  • Ictal speech manifestations in 47.1% of patientsictal speech manifestationsPercentage · Yen et al. (1996) series of 68 patients with 261 seizures · IctalPDF p.3, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal verbalizationReported: Non-dominant hemisphere2 manuscripts · 35 findings · 34 reported values
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 case report or observation · 1 systematic review or meta-analysis

The review restates that 9 of 10 patients with ictal verbalization had a non-dominant temporal origin. No seizure lateralization is reported. No source-supported hemispheric or body-side lateralization is reported. No cerebral hemisphere or body-side direction is reported. No lateralizing direction is reported. No hemisphere or body-side direction is reported. The source reports OR 0.5 for motor gestural automatisms relative to vocalization/verbalization; no hemisphere direction is reported. No lateralization evidence is reported. This finding provides no lateralization information. The source reports OR <0.1 for laughter relative to vocalization/verbalization; no hemisphere direction is reported. No lateralizing semiology is reported for the tonic-clonic versus vocalization/verbalization odds comparison. No lateralization axis information is reported for vocalization/verbalization versus autonomic signs. No lateralizing semiology is reported for the reciprocal vocalization/verbalization versus tonic-clonic odds comparison.

Source-defined result groups 11
Localization: anterior cingulate cortex/cingulate seizure casesSource-defined values retained separatelypatient-level frequency synthesized across eligible studies1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyF to BTC · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyFacial expression change · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: anterior cingulate cortex/cingulate seizure casesSource-defined values retained separatelypatient1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyVocalization/verbalization · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyHead-eye deviation · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 34 findings · 32 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • verbalizationThe source reports a frequency of 5% for verbalization.PDF p.13, Table 3
  • verbalization; reported frequency rangeThe source reports a frequency range of 0–50% for verbalization.PDF p.13, Table 3
  • vocalization/verbalization; Figure 4 rateFigure 4 displays a 61.3% rate for vocalization/verbalization.PDF p.10, Figure 4
  • verbalizationVerbalizations occurred in five patients across five studies.PDF p.7, Objective symptomatology
  • vocalization/verbalization typicalityVocalization/verbalization met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • vocalization/verbalization; pairwise odds-ratio significanceVocalization/verbalization occurred significantly more often than nine of the other 15 symptoms in pairwise Holm-corrected comparisons.PDF p.10, Statistical analysis of ictal semiology
  • pairwise OR: Hypermotor-complex motor behavior relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.9 for Hypermotor-complex motor behavior relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.8 for Affective/autonomic aura relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.6 for Autonomic signs relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.5 for Facial expression change relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.5 for Motor (gestural) automatisms relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.3 for Loss of consciousness relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Laughter relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Vocalization/verbalizationFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 1.1 for Vocalization/verbalization relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Affective/autonomic auraFigure 6 reports an odds ratio of 1.2 for Vocalization/verbalization relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Autonomic signsFigure 6 reports an odds ratio of 1.7 for Vocalization/verbalization relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Facial expression changeFigure 6 reports an odds ratio of 1.8 for Vocalization/verbalization relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 2.1 for Vocalization/verbalization relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.9 for Vocalization/verbalization relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 3.6 for Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 6.1 for Vocalization/verbalization relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Dystonic posturingFigure 6 reports an odds ratio of 6.5 for Vocalization/verbalization relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Head-eye deviationFigure 6 reports an odds ratio of 9.6 for Vocalization/verbalization relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to LaughterFigure 6 reports an odds ratio of 14.5 for Vocalization/verbalization relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 16.5 for Vocalization/verbalization relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Tonic-clonicFigure 6 reports an odds ratio of 27.3 for Vocalization/verbalization relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to F to BTCFigure 6 reports an odds ratio of 27.3 for Vocalization/verbalization relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 5% (frequency range 0–50%)verbalizationPercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.13, Table 3
  • 61.3%vocalization/verbalization; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.10, Figure 4
  • 5 patientsverbalizationCount · Reviewed ACC seizure cases with reported semiology · Reviewed ACC seizure casesPDF p.7, Objective symptomatology
  • 9/15 significant pairwise comparisonsvocalization/verbalization; pairwise odds-ratio significanceProportion · n/N 9/15 · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.10, Statistical analysis of ictal semiology
  • OR 0.9pairwise OR: Hypermotor-complex motor behavior relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Affective/autonomic aura relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Autonomic signs relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Facial expression change relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Motor (gestural) automatisms relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Loss of consciousness relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Dystonic posturing relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Laughter relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Vocalization/verbalization relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Vocalization/verbalization relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Vocalization/verbalization relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.8pairwise OR: Vocalization/verbalization relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Vocalization/verbalization relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Vocalization/verbalization relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Vocalization/verbalization relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.1pairwise OR: Vocalization/verbalization relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 6.5pairwise OR: Vocalization/verbalization relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.6pairwise OR: Vocalization/verbalization relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 14.5pairwise OR: Vocalization/verbalization relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 16.5pairwise OR: Vocalization/verbalization relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 27.3pairwise OR: Vocalization/verbalization relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 27.3pairwise OR: Vocalization/verbalization relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding · 2 reported values
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • ictal verbalizationIn the Yen et al. series, ictal verbalization occurred in 10 patients (14.7%), and 9 of those patients had a non-dominant temporal origin.PDF p.3, Discussion
Reported values
  • 10/68 patients (14.7%) with ictal verbalizationictal verbalizationPercentage · n/N 10/68 · Yen et al. (1996) series of 68 patients with 261 seizures · patients with ictal verbalization · IctalPDF p.3, Discussion
  • 9/10 with non-dominant temporal originictal verbalizationPercentage · n/N 9/10 · Yen et al. (1996) series of 68 patients with 261 seizures · patients with ictal verbalization · IctalPDF p.3, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Jacksonian march (sequential somatomotor spread)Source terms: Jacksonian marchReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere2 manuscripts · 4 findings · 0 reported values
Weighted evidence supportevidence weight 4 across 2 manuscripts · 1 narrative, educational, or cited context · 1 systematic review or meta-analysis

The review describes unilateral clonic, tonic, or myoclonic activity as contralateral to primary motor cortex onset. Primary motor cortex seizures are described as producing contralateral unilateral clonic, tonic, or myoclonic activity. In this single case, left face and arm clonic spread and subsequent left-arm extension were contralateral to the right frontocentral ictal EEG onset. The finding reports no cerebral lateralization.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfNarrative, educational, or cited context · 1 finding
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • motor marchProgressive somatotopic engagement of limb musculature is presented as the classical motor “march,” but it is rarely observed; the form of motor semiology is also related to discharge frequency, with high-frequency tonic discharges tending toward tonic seizures and lower-frequency spike discharges toward clonic jerks.PDF p.4, section 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 3 findings
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf; chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • primary motor cortex; Jacksonian marchSeizures from primary motor cortex comprise contralateral unilateral clonic, and sometimes tonic or myoclonic, activity that can spread along the motor homunculus as a Jacksonian march; lateral versus medial precentral onset can be distinguished by initial face, upper-limb, or lower-limb involvement.PDF p.2, Primary motor cortex; PDF p.3, Figure 1
  • primary motor cortex; Jacksonian marchSeizures from primary motor cortex comprise contralateral unilateral clonic, and sometimes tonic or myoclonic, activity that can spread to adjacent body parts in a Jacksonian march along the motor homunculus; the starting face, upper limb, or lower limb can distinguish lateral from medial precentral onset.PDF p.2, Primary motor cortex; PDF p.3, Figure 1
  • fencing posture; Jacksonian spreadIn the review’s video case 1, a 50-year-old man with a cystic lesion in the right middle frontal gyrus had an aura followed by behavioural arrest, left-face clonic movements spreading over the left arm, then left-arm extension in a fencing posture before secondary generalisation; the semiology and ictal EEG pointed to right frontocentral/right hemispheric onset.PDF p.3, Video case 1; PDF p.4, Figure 2 and Video case 1 description

2 contributing manuscripts; source-reported values remain separate and are not pooled.

hand/finger clonic jerks (precentral knob)Source terms: Focal hand/finger clonic jerksReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 3.91 across 1 manuscript · 1 independent primary study

One patient had hand clonic jerks contralateral to the resected side.

Source-defined result groups 1
Lateralization: ContralateralObserved proportion 5.6%All reported · ipsilateral resected side · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdfIndependent primary study · 1 finding · 1 reported value
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
Independent primary study · Class II · Evidence weight 3.91 · 2 × 1.2 × 1.628
The authors reviewed patients with drug-resistant parietal lobe epilepsy evaluated for surgery at Jefferson Comprehensive Epilepsy Center from 1986 through 2015. The diagnosis was based on ictal semiology, MRI lesion, and EEG findings; presurgical evaluation included brain MRI and prolonged video-EEG, and all patients underwent resective surgery. Sufficient data were available for 18 patients in the present cohort; denominator-specific EEG and MRI analyses are represented only when source-explicit.
Findings
  • contralateral hand clonic jerksOne patient had contralateral hand clonic jerks.PDF p.2, Results
Reported values
  • 1/18 contralateral hand clonic jerkscontralateral hand clonic jerksProportion · n/N 1/18 · 18-patient drug-resistant parietal lobe epilepsy cohort · auraPDF p.2, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal coughReported: Left hemisphereAlso reported: Right hemisphere5 manuscripts · 6 findings · 4 reported values
Weighted evidence supportevidence weight 3.9 across 5 manuscripts · 1 manuscript weight pending · 3 narrative, educational, or cited context · 1 case report or observation · 1 structured design not resolved

Ictal coughing was reported in the RTL group (6/54; 11%) and not in the LTL group (0/73). The review associates ictal coughing with possible right-hemispheric lateralization. The ictal-coughing network restatement reports no side. No lateralization axis information is reported for ictal coughing. The case lists heavy coughing during the hypermotor phase without a side or lateralization direction. The cited review says ictal or postictal cough occurs more often in temporal than extratemporal seizures and reports no hemisphere direction.

Evidence by contributing manuscript 5

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfCase report or observation · 1 finding
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • patient 5 heavy coughingHeavy coughing was listed in the hypermotor phase for patient 5.PDF p.4, Figure 3
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal coughingIctal coughing was reported in the RTL group and not in the LTL group.PDF p.4, Table 5; PDF p.5, Discussion
Reported values
  • RTL ictal coughing 6/54 (11%)Ictal coughingPercentage · n/N 6/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · IctalPDF p.4, Table 5; PDF p.5, Discussion
  • LTL ictal coughing 0/73Ictal coughingPercentage · n/N 0/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · IctalPDF p.4, Table 5; PDF p.5, Discussion
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal and postictal coughIctal or postictal cough can occur with temporal or extratemporal seizures but occurs more often in temporal seizures; the table attributes it to increased secretions or direct activation of the central autonomic system.PDF p.4, section 3.5 Autonomic seizures; PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal coughingIctal coughing has been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • ictal coughingThe review reports that Roux et al. (2019) found a cortical and subcortical network during ictal coughing, particularly involving perisylvian cortices and the caudate nucleus, in a temporal-lobe seizure.PDF p.5, Table 1, Ictal coughing row
  • ictal coughingIn the summarized Roux et al. case, functional connectivity during ictal coughing implicated a network of cortical and subcortical regions, particularly perisylvian cortices and the caudate nucleus.PDF p.5, Table 1 (continued), Roux et al. 2019 row
Reported values
  • n=1 subjectictal coughingCount · 1 subject with temporal-lobe epilepsy · During coughingPDF p.5, Table 1, Ictal coughing row
  • single subjectictal coughingCount · 1 subject with temporal-lobe epilepsy; number of seizures Not reported · ictal, during coughingPDF p.5, Table 1 (continued), Roux et al. 2019 row

5 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal head deviationReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphereNo single reliable side4 manuscripts · 5 findings · 5 reported values
Weighted evidence supportevidence weight 3.9 across 4 manuscripts · 2 narrative, educational, or cited context · 2 case report or observation

The cited discussion does not establish a reliable lateralizing direction for forceful head turning. The review distinguishes right-temporal tendencies for selected automatisms or well-formed ictal language, contralateral nonmanipulative movements and dystonia, ipsilateral early head turning with dystonia, and predominantly contralateral late or versive turning. Two recorded bilateral tonic-clonic seizures began with left head deviation despite generalized bifrontally predominant EEG activity; an earlier event reportedly turned right, so head direction was not proof of focal epilepsy. Cited evidence is conflicting: some reports found no lateralizing value, whereas Wyllie et al. reported contralateral onset when deviation was forced, involuntary, and sustained. Rightward head deviation is a the source's own behavioral direction; no cerebral hemisphere relation is supplied.

Evidence by contributing manuscript 4

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Ictal head deviation in cited studiesThe current paper reports conflicting cited evidence on ictal head deviation: Robillard et al. (1983) and Ochs et al. (1984) indicated no lateralizing value, whereas Wyllie et al. (1986) found seizure onset lateralized to the contralateral hemisphere when head and eye deviation was defined as unquestionably forced, involuntary, and sustained.PDF p.6, Discussion, tonic-head-deviation paragraph
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 2 findings · 4 reported values
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • temporal automatisms, dystonic posturing, and head turningOroalimentary automatisms suggest temporal involvement but are not specific; spitting, drinking, and preserved responsiveness during automatisms favor right temporal localization; manipulative automatisms alone do not lateralize, whereas nonmanipulative distal or proximal movements tend to be contralateral and may precede contralateral dystonic posturing; dystonic posturing is usually contralateral, early head turning with dystonia tends ipsilateral, late head turning is more often contralateral, and versive head turning is almost always contralateral.PDF p.50; PDF p.51
  • generalized epilepsy with ictal head deviationIn the illustrated adult case, two recorded bilateral tonic-clonic seizures began with head deviation to the left, but the EEG began with generalized bifrontally predominant rhythmic 12 Hz activity and 4-4.5 Hz spike-and-wave activity; an earlier witnessed event reportedly turned to the right, and the case was diagnosed as adult-onset idiopathic generalized epilepsy, illustrating that head direction at onset is not by itself proof of focal epilepsy.PDF p.380; PDF p.381; PDF p.386
Reported values
  • 4–4.5 Hz spike-and-wave activitygeneralized epilepsy with ictal head deviationRange · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
  • two recorded bilateral tonic-clonic seizuresgeneralized epilepsy with ictal head deviationCount · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · illustrated adult case · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
  • up to 60% of primary generalized seizures may have head deviationgeneralized epilepsy with ictal head deviationPercentage · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · primary generalized seizures · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
  • generalized bifrontally predominant rhythmic 12 Hz activitygeneralized epilepsy with ictal head deviationFrequency · 36-year-old right-handed woman with two recorded bilateral tonic-clonic seizures and prior witnessed events · ictal onset and transition to bilateral tonic-clonic activityPDF p.380; PDF p.381; PDF p.386
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfNarrative, educational, or cited context · 1 finding
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • severity of head turning and eye movementThe discussion reports that Ochs et al. (1984) and Robillard et al. (1983) found no localizing or lateralizing value for forceful head turning at clinical seizure onset, while Wyllie et al. (1986) found lateralizing significance only for very severe head and eye movements with marked sustained unnatural positioning.PDF p.5, Discussion; PDF p.6, Discussion
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfCase report or observation · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • rightward head deviation in Fig. 1In Figure 1, the right-fingertip aura was followed by head deviation to the right.PDF p.4, Fig. 1
Reported values
  • 1 caserightward head deviation in Fig. 1Count · n/N 1/1 · patient 7 (M.B.) · ictal evolutionPDF p.4, Fig. 1

4 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal cursing / coprolalia (involuntary obscene vocalizations)Source terms: Ictal cursing / coprolaliaReported: Non-dominant hemisphere3 manuscripts · 3 findings · 2 reported values
Weighted evidence supportevidence weight 3.9 across 3 manuscripts · 1 manuscript weight pending · 1 narrative, educational, or cited context · 1 structured design not resolved · 1 systematic review or meta-analysis

Coprolalia and related verbal automatisms have limited lateralizing value toward the nondominant hemisphere and can arise from either hemisphere. This finding provides no lateralization information.

Source-defined result groups 2
Localization: TemporalObserved proportion 25.0%All reported · other hypermotor semiology features · patients1 manuscript · 1 reported value · not pooled
Localization: OFC-involving seizure casesSource-defined values retained separatelyAll reported · patients with coprolalia1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • coprolalia; verbal automatismsCoprolalia was documented in one patient in the reviewed OFC-involving literature.PDF p.5, Vocal automatisms
Reported values
  • 1 patientcoprolalia; verbal automatismsCount · OFC-involving seizure cases · ictalPDF p.5, Vocal automatisms
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 1 finding
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • verbal automatisms; coprolaliaThe source states that verbal automatisms, particularly coprolalia, occur in temporal or orbitofrontal epilepsy, have limited lateralizing value toward the non-dominant hemisphere, and can be triggered by seizures from either hemisphere.PDF p.12, Discussion
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdfStructured design not resolved · 1 finding · 1 reported value
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.301
The authors retrospectively reviewed consecutive epilepsy-surgery patients with MRI and pathology evidence of temporal pole lesions. Eight patients with intractable complex partial seizures were identified; long-term scalp-sphenoidal video-EEG was obtained, and two patients also underwent subdural-grid monitoring. MRI was performed in all patients; FDG PET was available for seven and ictal SPECT for three. The study classified recorded seizures as hypermotor or typical psychomotor under the source-described semiologic scheme.
Findings
  • vocal expletivesAmong the four hypermotor patients, the source reports 1 patient with vocal expletives.PDF p.4, Seizure semiology on video-EEG recording
Reported values
  • 1/4 vocal expletivesvocal expletivesProportion · n/N 1/4 · 4 patients with hypermotor seizure semiology · ictal semiologyPDF p.4, Seizure semiology on video-EEG recording

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Auditory palinacousis / echoReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphere2 manuscripts · 3 findings · 1 reported value
Weighted evidence supportevidence weight 3.9 across 2 manuscripts · 1 case report or observation · 1 systematic review or meta-analysis

The case describes a right temporal seizure/right-hemisphere evolution with a subjective auditory percept on the left or contralateral side. The case records a right-sided lesion context and an echo perceived in the left ear. The review restates contralateral auditory-echo perception as typical, with bilateral/indeterminate reports and an ipsilateral lesion-specific exception.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

e236615-full.pdfSystematic review or meta-analysis · 1 finding
e236615-full.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • ear of the auditory echoIn lesional cases, the echo was heard most of the time in the ear contralateral to the lesion; some patients heard it bilaterally, some could not distinguish the perceiving ear, and one cited right medial geniculate nucleus infarct produced echoes exclusively in the right ear ipsilateral to the lesion.PDF p.4, Discussion
palinacousis-seven-new-cases.pdfCase report or observation · 2 findings · 1 reported value
palinacousis-seven-new-cases.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • ictal auditory echoIn a 40-year-old man with nonlesional right or lateral temporal epilepsy, typical seizures included a voice or song repeating for 10 to 15 seconds; during a video-EEG-captured right temporal seizure he heard his own voice echo on the left or over the contralateral shoulder, and the seizure secondarily generalized.PDF p.1, Results case 2; PDF p.2, Table 1 case 2 and caption
  • left-ear echo of son's voice after lesion resection and statusOne week after resection complicated by a right epidural hematoma and convulsive status epilepticus, a man had several episodes in which his son's voice echoed in his left ear for seconds after the son entered the room.PDF p.2, Table 1 case 6; PDF p.3, case 6
Reported values
  • Repeated voice or song lasted 10-15 seconds in the patient's typical seizuresictal auditory echoCount · 40-year-old man with nonlesional lateral/right temporal epilepsy · IctalPDF p.1, Results case 2; PDF p.2, Table 1 case 2 and caption

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal dysprosodyReported: Non-dominant hemisphereAlso reported: Right hemisphere2 manuscripts · 3 findings · 1 reported value
Weighted evidence supportevidence weight 3.9 across 2 manuscripts · 1 case report or observation · 1 systematic review or meta-analysis

Ictal dysprosodic speech began after discharge invaded posterior temporal and opercular sites in the source-described right, non-dominant hemisphere. Stimulation of the right precentral operculum in the non-dominant hemisphere reproduced dysprosodic features after a post-discharge. No hemisphere or body-side direction is reported.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 1 finding
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • speech arrest; motor aphasia; dysprosody; dysarthriaThe discussion reports that language disorders in the cited Peltola series combined motor aphasia, dysprosody, or dysarthria early in seizure semiology but not at initial onset, suggesting opercular spread.PDF p.9, Discussion
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 2 findings · 1 reported value
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • ictal dysprosodic speech; non-dominant opercular involvementSpeech utterances began after ictal discharge invaded the posterior first temporal gyrus and the precentral and post-central opercula of the non-dominant hemisphere; they were monotonous, hypophonic, emotionally neutral repetitions of stereotyped sentences despite their semantic content and persisted until the EEG discharge ended.PDF p.1, abstract; PDF p.3, left column, paragraph beginning “Speech utterances started thereafter”; PDF p.4, Figure 3 caption
  • stimulation-induced dysprosody; right precentral operculumHigh-frequency stimulation of the right precentral operculum induced a 20-second post-discharge restricted to the stimulated electrode and disrupted prosody during counting from 1 to 20; counting became faster, higher-pitched, and hypophonic, reproducing some features of the spontaneous ictal dysprosodic utterances.PDF p.1, abstract; PDF p.3, right column, paragraph beginning “Similar high frequency stimulation”; PDF p.4, Figure 3 caption
Reported values
  • 20-second post-discharge with faster rate, higher pitch, and hypophoniastimulation-induced dysprosody; right precentral operculumCount · one patient undergoing intracranial stimulation · stimulation-induced post-dischargePDF p.1, abstract; PDF p.3, right column, paragraph beginning “Similar high frequency stimulation”; PDF p.4, Figure 3 caption

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal restlessnessReported: Left hemisphere2 manuscripts · 11 findings · 5 reported values
Weighted evidence supportevidence weight 3.9 across 2 manuscripts · 1 systematic review or meta-analysis · 1 case report or observation

A single case caption reports left temporal rhythmic 4–6/sec EEG activity during a focal seizure with restlessness, aphasia, and eye blinking. This record provides no hemispheric lateralization. This lateral-versus-mesial temporal statistic provides no hemispheric lateralization.

Source-defined result groups 3
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Restlessness · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Restlessness · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 10 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • RestlessnessTable 3 reports 1 studies assessing Restlessness.PDF p.6, Table 3
  • RestlessnessTable 3 reports 15 patients assessed for Restlessness.PDF p.6, Table 3
  • RestlessnessTable 3 reports 46.77% as the percentage range or value for Restlessness; the overall association grade is Low.PDF p.6, Table 3
  • RestlessnessTable 3 reports 1 study with onset timing for Restlessness.PDF p.6, Table 3
  • RestlessnessTable 3 reports an onset latency of 8 s for Restlessness.PDF p.6, Table 3
  • Restlessness; lateral versus mesial comparisonTable 5 reports 1 studies comparing Restlessness in lateral and mesial TLE.PDF p.9, Table 5
  • Restlessness; lateral TLE patient denominatorTable 5 reports 15 lateral-TLE patients assessed for Restlessness.PDF p.9, Table 5
  • Restlessness; mesial TLE patient denominatorTable 5 reports 31 mesial-TLE patients assessed for Restlessness.PDF p.9, Table 5
  • Restlessness; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 46.7% for Restlessness.PDF p.9, Table 5
  • Restlessness; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 45.2% for Restlessness.PDF p.9, Table 5
Reported values
  • 46.77%RestlessnessPercentage · Lateral temporal epilepsy patients assessed for Restlessness · ictalPDF p.6, Table 3
  • median onset latency 8 sRestlessnessMedian · Lateral temporal epilepsy study reporting onset timing for Restlessness · ictal onsetPDF p.6, Table 3
  • 46.7%Restlessness; lateral TLE prevalencePercentage · Lateral TLE patients assessed for Restlessness · Lateral TLE patients assessed for Restlessness · ictalPDF p.9, Table 5
  • 45.2%Restlessness; mesial TLE prevalencePercentage · Mesial TLE patients assessed for Restlessness · Mesial TLE patients assessed for Restlessness · ictalPDF p.9, Table 5
unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 1 finding · 1 reported value
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • focal seizure with restlessness, aphasia, and eye blinkingFigure 2 depicts a 59-year-old female with a focal seizure involving restlessness, aphasia, and eye blinking, with a seizure pattern showing left temporal rhythmic 4–6/sec activity.PDF p.3, Fig.2 caption and EEG rendering
Reported values
  • Rhythmic 4–6/sec EEG activityfocal seizure with restlessness, aphasia, and eye blinkingCount · Female, 59 years; focal seizure · ictalPDF p.3, Fig.2 caption and EEG rendering

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Paroxysmal speech disturbanceReported: Left hemisphereAlso reported: Right hemisphereNo single reliable side1 manuscript · 3 findings · 16 reported values
Weighted evidence supportevidence weight 3.35 across 1 manuscript · 1 independent primary study

The cited 49-case report is summarized as 38 left-sided EEG abnormalities, 2 right-sided, and 9 with no clear lateralization. The Group A left/right counts are cohort context only; no speech-sign lateralization is reported. The source supports unilateral/asymmetric-bilateral perioral activity and reports three ipsilateral cases, but the ipsilateral reference side is not defined at the result locus.

Source-defined result groups 3
Lateralization: Left hemisphere / Right hemisphere / unclearObserved proportion 18.4%no clear lateralization · Left-sided versus right-sided versus unclear EEG lateralization · case1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / unclearObserved proportion 77.6%left-sided EEG abnormality · Left-sided versus right-sided versus unclear EEG lateralization · case1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphere / unclearObserved proportion 4.1%right-sided EEG abnormality · Left-sided versus right-sided versus unclear EEG lateralization · case1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfIndependent primary study · 3 findings · 16 reported values
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Independent primary study · Class II · Evidence weight 3.35 · 2 × 0.9 × 1.862
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • paroxysmal speech disturbanceThe current article reports that Alajouanine and Sabouraud studied 49 cases with paroxysmal speech disturbances, including speech arrest and dysarthria, and found a left-sided EEG abnormality in 38, a right-sided abnormality in 2, and no clear lateralization in 9.PDF p.10, discussion of prior paroxysmal speech-disturbance reports
  • paroxysmal speech disturbance in Group AAmong 53 Group A patients who became seizure-free or almost so and were presumed correctly diagnosed, 38 (72%) exhibited a pre-operative paroxysmal speech disturbance: 17 had dysphasia and 23 had speech automatisms; 15 had no recorded speech disturbance and 2 had both types.PDF p.5, Table II; PDF p.5, discussion of Group A
  • paroxysmal speech disturbance in Group BIn Group B, 29 of 47 patients with continuing fits had a recorded speech disturbance and 18 did not; the whole-group Table III comparison reports dysphasia in 17 patients, 14 after left-sided resection and 3 after right-sided resection, and speech automatisms in 15 patients, 6 after left-sided and 9 after right-sided resection.PDF p.6, Table III; PDF p.7, comparison of Group B with Group A
Reported values
  • left 38/49paroxysmal speech disturbancePercentage · n/N 38/49 · Alajouanine and Sabouraud’s cited 49 cases with paroxysmal speech disturbances, including speech arrest and dysarthria · left-sided EEG abnormality · Paroxysmal speech disturbancePDF p.10, discussion of prior paroxysmal speech-disturbance reports
  • no clear lateralization 9/49paroxysmal speech disturbancePercentage · n/N 9/49 · Alajouanine and Sabouraud’s cited 49 cases with paroxysmal speech disturbances, including speech arrest and dysarthria · no clear lateralization · Paroxysmal speech disturbancePDF p.10, discussion of prior paroxysmal speech-disturbance reports
  • right 2/49paroxysmal speech disturbancePercentage · n/N 2/49 · Alajouanine and Sabouraud’s cited 49 cases with paroxysmal speech disturbances, including speech arrest and dysarthria · right-sided EEG abnormality · Paroxysmal speech disturbancePDF p.10, discussion of prior paroxysmal speech-disturbance reports
  • Speech automatisms 23/53 (43%)paroxysmal speech disturbance in Group APercentage · n/N 23/53 · Group A; 53 patients seizure-free or almost so after operation and presumed to have been correctly diagnosed · Group A · Pre-operative; connected with seizuresPDF p.5, Table II; PDF p.5, discussion of Group A
  • Any paroxysmal speech disturbance 38/53 (72%)paroxysmal speech disturbance in Group APercentage · n/N 38/53 · Group A; 53 patients seizure-free or almost so after operation and presumed to have been correctly diagnosed · Group A · Pre-operative; connected with seizuresPDF p.5, Table II; PDF p.5, discussion of Group A
  • Dysphasia 17/53 (32%)paroxysmal speech disturbance in Group APercentage · n/N 17/53 · Group A; 53 patients seizure-free or almost so after operation and presumed to have been correctly diagnosed · Group A · Pre-operative; connected with seizuresPDF p.5, Table II; PDF p.5, discussion of Group A
  • Both disturbance types in 2/53 patientsparoxysmal speech disturbance in Group ACount · n/N 2/53 · Group A; 53 patients seizure-free or almost so after operation and presumed to have been correctly diagnosed · Group A · Pre-operative; connected with seizuresPDF p.5, Table II; PDF p.5, discussion of Group A
  • No recorded speech disturbance 15/53paroxysmal speech disturbance in Group ACount · n/N 15/53 · Group A; 53 patients seizure-free or almost so after operation and presumed to have been correctly diagnosed · Group A · Pre-operative; connected with seizuresPDF p.5, Table II; PDF p.5, discussion of Group A
  • Dysphasia after right-sided resection in 3/17paroxysmal speech disturbance in Group BCount · n/N 3/17 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Right-sided resection · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • Speech automatisms in 15/47 patientsparoxysmal speech disturbance in Group BCount · n/N 15/47 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Group B · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • Any recorded speech disturbance 29/47paroxysmal speech disturbance in Group BCount · n/N 29/47 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Group B · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • Dysphasia in 17/47 patientsparoxysmal speech disturbance in Group BCount · n/N 17/47 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Group B · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • Speech automatisms after right-sided resection in 9/15paroxysmal speech disturbance in Group BCount · n/N 9/15 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Right-sided resection · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • Speech automatisms after left-sided resection in 6/15paroxysmal speech disturbance in Group BCount · n/N 6/15 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Left-sided resection · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • Dysphasia after left-sided resection in 14/17paroxysmal speech disturbance in Group BCount · n/N 14/17 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Left-sided resection · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A
  • No recorded speech disturbance 18/47paroxysmal speech disturbance in Group BCount · n/N 18/47 · Group B; 47 patients with continuing fits, including 30 improved and 17 slightly benefited or unchanged · Group B · Pre-operative; connected with seizuresPDF p.6, Table III; PDF p.7, comparison of Group B with Group A

1 contributing manuscript; source-reported values remain separate and are not pooled.

Epileptic spasmReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral3 manuscripts · 5 findings · 5 reported values
Weighted evidence supportevidence weight 3 across 3 manuscripts · 2 narrative, educational, or cited context · 1 case report or observation

The review reports bilateral spasms in three patients with DNET. The cited study reported asymmetric infantile spasms contralateral to the epileptogenic zone. One infant had bilateral asymmetric spasms whose asymmetry could be contralateral or ipsilateral to the epileptogenic zone. No seizure lateralization is reported; the source only describes usually bilateral arm abduction. No lateralizing direction is reported for the cited asymmetric infantile-spasm frequency.

Source-defined result groups 1
Lateralization: Contralateral / IpsilateralSource-defined values retained separatelyAll reported · infant and observer ratings1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 3

Alphabetical by manuscript.

bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • bilateral spasmsThe review reports bilateral spasms in three patients with DNET.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
Reported values
  • 3 patients with bilateral spasmsbilateral spasmsCount · basal temporal seizure cases; three-patient DNET subset for spasms · ictal; propagation for gelastic behavior in Table 3PDF p.4, Semiology and clinical features; PDF p.6, Table 3
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfCase report or observation · 3 findings · 4 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • asymmetry of infantile spasmsAsymmetric infantile spasms were reported in 12 of 60 infants, with multimodal testing also indicating a contralateral epileptogenic zone.PDF p.6, section 3.7
  • bilateral asymmetric spasmsOne additional infant had bilateral asymmetric spasms that could be contralateral or ipsilateral to the epileptogenic zone.PDF p.6, section 3.7
  • asymmetric infantile spasms during vigabatrin-response assessmentA later study by the same authors reported asymmetric spasms in 3 of 44 patients.PDF p.6, section 3.7
Reported values
  • 12/60 (20%) had asymmetric spasmsasymmetry of infantile spasmsPercentage · n/N 12/60 · 60 patients younger than 12 months · ictalPDF p.6, section 3.7
  • 80% reliabilitybilateral asymmetric spasmsPercentage · one infant with bilateral asymmetric spasms · observer ratings · ictalPDF p.6, section 3.7
  • 1 additional infantbilateral asymmetric spasmsCount · one infant with bilateral asymmetric spasms · ictalPDF p.6, section 3.7
  • 3/44 (6.8%) had asymmetric spasmsasymmetric infantile spasms during vigabatrin-response assessmentPercentage · n/N 3/44 · 44 patients with infantile spasms assessed for vigabatrin treatment response · ictalPDF p.6, section 3.7
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Epileptic spasmEpileptic spasms are variable-duration contractions affecting predominantly axial muscles, frequently occurring in clusters whose contractions may range from a short myoclonic jerk to sustained tonic posturing; the source describes bilateral arm abduction in a “salaam” posture as usual.PDF p.4, Simple motor seizures, Epileptic spasms; PDF p.2, Table 1

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Facial asymmetryReported: ContralateralAlso reported: Non-dominant hemisphere3 manuscripts · 5 findings · 9 reported values
Weighted evidence supportevidence weight 3 across 3 manuscripts · 3 narrative, educational, or cited context

The review restates predominantly contralateral lower facial weakness relative to a unilateral temporal-lobe focus, reported in 3/4 of the cited sample. Cited-study restatement combines nondominant ictal smile, contralateral lower facial asymmetry, and qualitative frontal associations. The cited series reported facial asymmetry contralateral to MRI hippocampal atrophy in 31/36 cases. No seizure lateralization is reported.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Lower facial weakness or facial asymmetryLower facial weakness was reported contralateral to a unilateral temporal-lobe focus in 3/4 of a sample of 50 patients and was more prominent with mimetic movements.PDF p.5, facial weakness paragraph
Reported values
  • weakness more prominent with mimetic movementsLower facial weakness or facial asymmetryCount · n/N 3/4 · 50-patient sample with unilateral temporal-lobe focus as reported by the review. · Ictal facial manifestationPDF p.5, facial weakness paragraph
  • 3/4 of a sample of 50 patientsLower facial weakness or facial asymmetryCount · n/N 3/4 · 50-patient sample with unilateral temporal-lobe focus as reported by the review. · Ictal facial manifestationPDF p.5, facial weakness paragraph
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • emotional facial expression and facial asymmetryIctal smile suggests nondominant-hemisphere onset in children with parieto-occipital epilepsy and FLE; lower facial asymmetry occurs in 70% of patients with TLE and is usually contralateral to the epileptogenic zone. Ictal crying is rare in temporal or mesial frontal epilepsy, and facial expressions of fear or anger suggest frontal-lobe origin.PDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
Reported values
  • Lower facial asymmetry in 70% of TLE patientsemotional facial expression and facial asymmetryPercentage · children with parieto-occipital epilepsy or FLE; patients with TLE; patients with temporal or mesial frontal epilepsy · ictalPDF p.4, section 4 Lateralizing motor signs in complex motor seizures; PDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • emotional facial asymmetryJacob et al. found unilateral facial asymmetry usually contralateral to hippocampal atrophy on MRI.PDF p.7, section 3.11
  • emotional facial asymmetryLower facial weakness that is more pronounced with emotional movement may lateralize a temporal epileptogenic focus to the contralateral side.PDF p.7, section 3.11
  • facial asymmetry with mesial temporal sclerosisA selected case series was reported as confirming the association between facial asymmetry and temporal lobe epilepsy.PDF p.7, section 3.11
Reported values
  • Facial asymmetry contralateral to MRI hippocampal atrophy 31/36 (86%)emotional facial asymmetryPercentage · n/N 31/36 · 50 patients with hippocampal atrophy and seizure freedom or 90% seizure reduction after surgery · Patients with unilateral asymmetry · interictal examinationPDF p.7, section 3.11
  • Unilateral facial asymmetry 36/50 (72%)emotional facial asymmetryPercentage · n/N 36/50 · 50 patients with hippocampal atrophy and seizure freedom or 90% seizure reduction after surgery · interictal examinationPDF p.7, section 3.11
  • 10/12 became seizure freefacial asymmetry with mesial temporal sclerosisPercentage · n/N 10/12 · 13 selected patients with facial asymmetry; 12 underwent surgery · surgical subgroup · interictal examinationPDF p.7, section 3.11
  • 12 underwent surgeryfacial asymmetry with mesial temporal sclerosisCount · 13 selected patients with facial asymmetry; 12 underwent surgery · surgical subgroup · interictal examinationPDF p.7, section 3.11
  • 13 selected patientsfacial asymmetry with mesial temporal sclerosisCount · 13 selected patients with facial asymmetry; 12 underwent surgery · interictal examinationPDF p.7, section 3.11
  • mesial temporal sclerosis in all surgical patientsfacial asymmetry with mesial temporal sclerosisPercentage · 13 selected patients with facial asymmetry; 12 underwent surgery · surgical subgroup · interictal examinationPDF p.7, section 3.11

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Orgasmic auraReported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere3 manuscripts · 6 findings · 5 reported values
Weighted evidence supportevidence weight 3 across 3 manuscripts · 3 narrative, educational, or cited context

The cited review restates right- or nondominant-hemisphere ictal onset as the most frequent association for initial orgasmic aura. The cited review restates a right-TLE group association for orgasmic auras. The review associates orgasmic auras mainly with right non-dominant mesiotemporal and right frontal areas while explicitly reporting left-hemisphere cases. The cited review reports right hemispheric epilepsy in 13/15 cases with unilateral EEG findings and in all 9 cases meeting stricter focus-definition criteria, within 22 reviewed orgasmic-aura cases. The cited series is restated as six right-temporal and one left-temporal epileptogenic zones among seven patients with orgasmic auras. The cited review reports cases of orgasmic auras with seizures arising from the left hemisphere.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Orgasmic auraOrgasmic auras most frequently represent right-hemispheric or nondominant-hemispheric ictal onset and are described as having good lateralizing and localizing value when they are the initial seizure manifestation.PDF p.6, section 8 Orgasmic Aura’s Lateralizing and Localizing Semiological Features in TLE
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • orgasmic aurasOrgasmic auras, defined as erotic thoughts or feelings, sexual arousal, and orgasm sometimes accompanied by a viscerosensory phenomenon, were observed more often in women with right TLE.PDF p.3, section 3.1 Auras
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 4 findings · 5 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Orgasmic auraThe review describes orgasmic auras as usually associated with the right non-dominant mesiotemporal and right frontal areas, while explicitly noting left-hemisphere cases.PDF p.4, section 2.8 Orgasmic auras; PDF p.4, section 2.8.1 Mechanism
  • Orgasmic auraJanszky et al. reviewed 22 cases of orgasmic aura; 15 had unilateral EEG findings and 13 of those 15 had right hemispheric epilepsy. Under stricter criteria requiring seizure freedom after surgery or a confirmed epileptogenic lesion, all 9 included patients had right hemispheric epilepsy.PDF p.4, section 2.8 Orgasmic auras
  • Orgasmic auraIn a separate study, Janszky et al. reported 7 patients with orgasmic auras; clinical means, EEG, and MRI localized the epileptogenic zone to the right temporal lobe in 6 and the left in 1.PDF p.4, section 2.8 Orgasmic auras
  • Orgasmic auraThe review also cites cases of orgasmic auras with seizures arising from the left hemisphere.PDF p.4, section 2.8 Orgasmic auras
Reported values
  • all 9Orgasmic auraPercentage · n/N 9/9 · 22 reviewed cases; 15 with unilateral EEG findings; 9 meeting stricter focus criteria · stricter focus-definition criteria · Ictal auraPDF p.4, section 2.8 Orgasmic auras
  • 15 of 22Orgasmic auraPercentage · n/N 15/22 · 22 reviewed cases; 15 with unilateral EEG findings; 9 meeting stricter focus criteria · reviewed orgasmic-aura cases · Ictal auraPDF p.4, section 2.8 Orgasmic auras
  • 13 of 15Orgasmic auraPercentage · n/N 13/15 · 22 reviewed cases; 15 with unilateral EEG findings; 9 meeting stricter focus criteria · cases with unilateral EEG findings · Ictal auraPDF p.4, section 2.8 Orgasmic auras
  • 1 left temporal among 7 patientsOrgasmic auraPercentage · n/N 1/7 · 7 patients with orgasmic auras · left temporal · Ictal auraPDF p.4, section 2.8 Orgasmic auras
  • 6 right temporal among 7 patientsOrgasmic auraPercentage · n/N 6/7 · 7 patients with orgasmic auras · right temporal · Ictal auraPDF p.4, section 2.8 Orgasmic auras

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Peri-ictal water drinkingReported: Non-dominant hemisphere3 manuscripts · 3 findings · 7 reported values
Weighted evidence supportevidence weight 3 across 3 manuscripts · 3 narrative, educational, or cited context

Peri-ictal water drinking has been reported to lateralize seizure onset to the non-dominant temporal side. Peri-ictal water drinking is described as usually arising from the nondominant hemisphere. The review restates peri-ictal water drinking in a nondominant temporal-lobe epilepsy cohort.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • peri-ictal water drinkingPeri-ictal water drinking, defined as drinking during or within 2 minutes of termination of an automotor seizure, is usually seen in seizures arising from the nondominant hemisphere, often the temporal lobe.PDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
Reported values
  • during or within 2 minutes of terminationperi-ictal water drinkingOther reported value · patients with automotor seizures · ictal or within 2 minutes postictalPDF p.5, section 5 Nondominant temporal signs; PDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 6 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • peri-ictal water drinkingTrinka et al. reported peri-ictal water drinking in nondominant temporal lobe epilepsy.PDF p.11, section 5.8
Reported values
  • Patients excluded for pending/refused surgery 3/10peri-ictal water drinkingPercentage · n/N 3/10 · 68 consecutive patients with nondominant temporal lobe epilepsy · Water-drinking cases · ictal or up to 2 minutes postictalPDF p.11, section 5.8
  • Wieser class I at 1 year in all reported surgical patientsperi-ictal water drinkingPercentage · 68 consecutive patients with nondominant temporal lobe epilepsy · Reported surgical patients · ictal or up to 2 minutes postictalPDF p.11, section 5.8
  • Astrocytoma pathology n=1peri-ictal water drinkingCount · 68 consecutive patients with nondominant temporal lobe epilepsy · Astrocytoma · ictal or up to 2 minutes postictalPDF p.11, section 5.8
  • Peri-ictal water drinking 10/68 (15.3%)peri-ictal water drinkingPercentage · n/N 10/68 · 68 consecutive patients with nondominant temporal lobe epilepsy · ictal or up to 2 minutes postictalPDF p.11, section 5.8
  • Hippocampal sclerosis pathology n=5peri-ictal water drinkingCount · 68 consecutive patients with nondominant temporal lobe epilepsy · Hippocampal sclerosis · ictal or up to 2 minutes postictalPDF p.11, section 5.8
  • Ganglioglioma pathology n=1peri-ictal water drinkingCount · 68 consecutive patients with nondominant temporal lobe epilepsy · Ganglioglioma · ictal or up to 2 minutes postictalPDF p.11, section 5.8
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • peri-ictal water drinkingThe review reports peri-ictal water drinking as a sign reported to lateralize seizure onset to the non-dominant temporal lobe, but states that its validity has been contested.PDF p.6, Peri-ictal water drinking

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal unilateral limb flaccidity / hemiparesisSource terms: Postictal unilateral weaknessReported: ContralateralAlso reported: Ipsilateral3 manuscripts · 5 findings · 7 reported values
Weighted evidence supportevidence weight 3 across 3 manuscripts · 3 narrative, educational, or cited context

The educational tables label postictal hemiparesis as contralateral. The chapter restates that postictal hemiparesis is contralateral, whereas the nose-wiping hand is ipsilateral to the seizure focus. Postictal paresis is restated as predominantly contralateral to the seizure-onset hemisphere, with 93% contralateral in the cited patient subgroup. In the cited evaluable subgroup, postictal palsy was always contralateral to seizure onset. In the cited 44-patient postictal-paresis subgroup, paresis was always contralateral to the suspected epilepsy focus.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Postictal hemiparesisBoth tables list Postictal hemiparesis as Contralateral.PDF p.2, Lateralizing signs/Localization table row "Postictal hemiparesis" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Postictal hemiparesis" (printed p.5)
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal hemiparesis and nose wipingPostictal hemiparesis reflects a contralateral seizure focus, whereas postictal nose wiping affects the hand ipsilateral to the seizure focus.PDF p.9, Postictal state
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 3 findings · 7 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal paresisPostictal paresis generally lateralizes contralateral to the seizure-onset hemisphere.PDF p.10, section 5.1; PDF p.12, Table 1
  • postictal palsyKellinghaus et al. found postictal paresis always contralateral among patients whose suspected epileptogenic zone could be lateralized.PDF p.10, section 5.1
  • postictal paresisGallmetzer et al. observed postictal paresis in 44 of 328 patients and reported it as always contralateral to the suspected focus.PDF p.10, section 5.1
Reported values
  • Postictal paresis in 0.6% of EMU patientspostictal paresisPercentage · epilepsy monitoring unit patients with postictal paresis · Epilepsy monitoring unit · postictalPDF p.10, section 5.1; PDF p.12, Table 1
  • Postictal paresis contralateral in 93%postictal paresisPercentage · epilepsy monitoring unit patients with postictal paresis · Patients with postictal paresis · postictalPDF p.10, section 5.1; PDF p.12, Table 1
  • 29/4500postictal palsyPercentage · n/N 29/4500 · 4500 monitored epilepsy patients, including 29 with postictal palsy and 27 with a lateralized suspected zone · monitored epilepsy patients · postictalPDF p.10, section 5.1
  • 27postictal palsyCount · n/N 27/29 · 4500 monitored epilepsy patients, including 29 with postictal palsy and 27 with a lateralized suspected zone · patients with postictal palsy · postictalPDF p.10, section 5.1
  • always contralateralpostictal palsyOther reported value · 4500 monitored epilepsy patients, including 29 with postictal palsy and 27 with a lateralized suspected zone · postictal palsy with lateralized suspected zone · postictalPDF p.10, section 5.1
  • always contralateralpostictal paresisPercentage · 328 patients with concordant EEG and MRI findings · patients with postictal paresis · postictalPDF p.10, section 5.1
  • 44/328 (13.4%) had postictal paresispostictal paresisPercentage · n/N 44/328 · 328 patients with concordant EEG and MRI findings · postictalPDF p.10, section 5.1

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal urinationReported: Ipsilateral2 manuscripts · 5 findings · 5 reported values
Weighted evidence supportevidence weight 3 across 2 manuscripts · 1 manuscript weight pending · 1 independent primary study · 1 structured design not resolved

The zero-occurrence row provides no hemispheric direction. This record provides no seizure lateralization.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 4 findings · 3 reported values
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.5
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • anterior cingulate ictal urination aggregateInvoluntary ictal urination during seizures without secondary generalization was observed in two anterior-group patients.PDF p.6, Discussion
  • typical anterior ictal urinationOne typical anterior patient had frequent ictal urination without generalization.PDF p.5, Clinical Presentation
  • atypical anterior ictal urinationOne atypical anterior patient had ictal urination during partial seizures without generalization.PDF p.5, Clinical Presentation
  • patient 2 ictal urination and personality changesIctal urination and personality changes were listed among patient 2’s other clinical features.PDF p.4, Figure 3
Reported values
  • 2/10 ictal urination without secondary generalizationanterior cingulate ictal urination aggregateProportion · n/N 2/10 · 10 anterior cingulate cases · ictal autonomic sign and evolutionPDF p.6, Discussion
  • 1/6 frequent ictal urination without generalizationtypical anterior ictal urinationProportion · n/N 1/6 · 6 typical anterior cingulate cases · ictal autonomic sign and evolutionPDF p.5, Clinical Presentation
  • 1/4 ictal urination without generalizationatypical anterior ictal urinationProportion · n/N 1/4 · 4 atypical anterior cingulate cases · ictal autonomic sign and evolutionPDF p.5, Clinical Presentation
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • urinationUrination was reported at 0% in both TL and T+ seizures; the table provides no row-specific P value.PDF p.6, Table 2
Reported values
  • TL 0%urinationPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 0%urinationPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2

2 contributing manuscripts; source-reported values remain separate and are not pooled.

age at onset of epilepsyReported: Right hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

No hemisphere or body-side direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 4 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • age at onset of epilepsyMean age at epilepsy onset was younger in M patients than in ML or L patients.PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
Reported values
  • M=7.9 yearsage at onset of epilepsyMean · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • p=0.021age at onset of epilepsyP value · 55 patients with unilateral TLE; M=24, ML=18, L=13PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • L=11.2 yearsage at onset of epilepsyMean · 55 patients with unilateral TLE; M=24, ML=18, L=13 · LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • ML=12.8 yearsage at onset of epilepsyMean · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

anterior versus posterior insula; insular sensory territoryReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

Insular sensory responses may be ipsilateral or bilateral rather than strictly contralateral.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • anterior versus posterior insula; insular sensory territoryViscerosensory symptoms such as abdominal aura and laryngeal constriction and autonomic signs such as nausea, hypersalivation, and sweating are suggested to arise from anterior insula, whereas painful burning, electric-shock, or tingling sensations are more likely posterior insular; insular sensory responses may involve a larger skin territory including perioral regions, be bilateral or ipsilateral, and more often evolve to complex motor phenomena than primary or secondary somatosensory responses.PDF p.8, Insular seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

Axial tonic posturing (trunk extension or flexion)Source terms: Axial tonic posturingReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Case 2 has a right occipital lesion and source side right in the seizure pathway accompanying head and neck hyperextension.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • head and neck hyperextensionTable 2 records head and neck hyperextension after vocalization and eye blinking in Case 2.PDF p.6, Table 2 Case 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

bilateral and precentral interictal spikes and/or slow wavesReported: Bilateral1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

The source reports bilateral interictal EEG abnormalities as an electrophysiologic comparator finding.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 4 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • bilateral and precentral interictal spikes and/or slow wavesT+ patients more frequently exhibited bilateral interictal spikes and/or slow waves and precentral spike-and-wave complexes than TL patients.PDF p.1, abstract; PDF p.4, Table 1; PDF p.5, Scalp-EEG findings; PDF p.9, Scalp-EEG findings
Reported values
  • TL 1.7%bilateral and precentral interictal spikes and/or slow wavesPercentage · TL group (n=58) versus T+ group (n=22) · TL · interictalPDF p.1, abstract; PDF p.4, Table 1; PDF p.5, Scalp-EEG findings; PDF p.9, Scalp-EEG findings
  • T+ 43.5%bilateral and precentral interictal spikes and/or slow wavesPercentage · TL group (n=58) versus T+ group (n=22) · T+ · interictalPDF p.1, abstract; PDF p.4, Table 1; PDF p.5, Scalp-EEG findings; PDF p.9, Scalp-EEG findings
  • T+ 43.5%bilateral and precentral interictal spikes and/or slow wavesPercentage · TL group (n=58) versus T+ group (n=22) · T+ · interictalPDF p.1, abstract; PDF p.4, Table 1; PDF p.5, Scalp-EEG findings; PDF p.9, Scalp-EEG findings
  • TL 8.5%bilateral and precentral interictal spikes and/or slow wavesPercentage · TL group (n=58) versus T+ group (n=22) · TL · interictalPDF p.1, abstract; PDF p.4, Table 1; PDF p.5, Scalp-EEG findings; PDF p.9, Scalp-EEG findings

1 contributing manuscript; source-reported values remain separate and are not pooled.

cluster 9Reported: Contralateral1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Cluster 9's versive manifestation is described as contralateral to seizure onset.

Source-defined result groups 6
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 4 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • cluster 9In cluster 9, contralateral versive manifestations were significantly associated with the T+ group, anxiety was not, and no T+ subgroup predominance was found.PDF p.5, cluster-analysis discussion; PDF p.7, Table 3; PDF p.8, Motor signs
Reported values
  • TL 11.9%cluster 9Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ 43.5%cluster 9Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3; PDF p.8, Motor signs
  • TL 10.2%cluster 9Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · TL · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3; PDF p.8, Motor signs
  • T+ 21.7%cluster 9Percentage · TL group (n=58) versus T+ group (n=22); cluster analysis of ictal events · T+ · ictalPDF p.5, cluster-analysis discussion; PDF p.7, Table 3; PDF p.8, Motor signs

1 contributing manuscript; source-reported values remain separate and are not pooled.

to bilateral tonic-clonicReported: Bilateral1 manuscript · 2 findings · 1 reported value
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

Focal-to-bilateral tonic-clonic evolution is described as an infrequent secondary propagation manifestation and does not lateralize onset. Figure 4 repeats a 5.4% focal-to-bilateral tonic-clonic rate; bilateral spread does not lateralize the onset hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 1 reported value
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • ACC seizure; focal to bilateral tonic-clonicFocal to bilateral tonic-clonic and versive manifestations are described as infrequent and secondary during ictal propagation.PDF p.12, Discussion
  • focal to bilateral tonic-clonic; Figure 4 rateFigure 4 displays a 5.4% rate for focal to bilateral tonic-clonic.PDF p.10, Figure 4
Reported values
  • 5.4%focal to bilateral tonic-clonic; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.10, Figure 4

1 contributing manuscript; source-reported values remain separate and are not pooled.

to bilateral tonic-clonic manifestationsReported: Bilateral1 manuscript · 3 findings · 1 reported value
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The source reports a frequency of 5% for focal to bilateral tonic-clonic manifestations. The source reports a frequency range of 0–40% for focal to bilateral tonic-clonic manifestations. Table 3 assigns the source's Low overall association grade to focal to bilateral tonic-clonic manifestations.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 1 reported value
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • focal to bilateral tonic-clonic manifestationsThe source reports a frequency of 5% for focal to bilateral tonic-clonic manifestations.PDF p.13, Table 3
  • focal to bilateral tonic-clonic manifestations; reported frequency rangeThe source reports a frequency range of 0–40% for focal to bilateral tonic-clonic manifestations.PDF p.13, Table 3
  • focal to bilateral tonic-clonic manifestations; ACC association gradeTable 3 assigns the source's Low overall association grade to focal to bilateral tonic-clonic manifestations.PDF p.13, Table 3
Reported values
  • 5% (frequency range 0–40%)focal to bilateral tonic-clonic manifestationsPercentage · Reviewed ACC seizure cases with reported semiology · ictal propagationPDF p.13, Table 3

1 contributing manuscript; source-reported values remain separate and are not pooled.

to bilateral tonic-clonic seizureReported: Bilateral1 manuscript · 4 findings · 3 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

Focal-to-bilateral tonic-clonic evolution was late in 4 of 21 fronto-opercular patients. The prefrontal operculum subgroup contributed 3 of the 4 focal-to-bilateral tonic-clonic cases. The precentral Rolandic operculum subgroup contributed 1 of the 4 focal-to-bilateral tonic-clonic cases. Focal-to-bilateral seizure evolution is not a cerebral lateralization result.

Source-defined result groups 1
Localization: FrontalObserved proportion 19.0%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Focal to bilateral tonic-clonic seizureTable 2 reports 4/21 (19%) for Focal to bilateral tonic-clonic seizure; timing is late, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Focal to bilateral tonic-clonic seizureTable 2 reports 3/12 patients with Focal to bilateral tonic-clonic seizure in the prefrontal operculum group.PDF p.7, Table 2
  • Focal to bilateral tonic-clonic seizureTable 2 reports 1/9 patients with Focal to bilateral tonic-clonic seizure in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Focal to bilateral tonic-clonic seizureFisher's exact comparison of Focal to bilateral tonic-clonic seizure between the prefrontal and precentral Rolandic operculum groups has p=0.603.PDF p.7, Table 2
Reported values
  • 4/21 (19%)Focal to bilateral tonic-clonic seizurePercentage · n/N 4/21 · 21 included fronto-opercular epilepsy patients · LatePDF p.7, Table 2
  • 3/12 patientsFocal to bilateral tonic-clonic seizureProportion · n/N 3/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · LatePDF p.7, Table 2
  • 1/9 patientsFocal to bilateral tonic-clonic seizureProportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · LatePDF p.7, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

tonic limb posturingReported: Contralateral1 manuscript · 3 findings · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Source reports contralateral limb posturing in a sequential occipital-onset phenotype. Phenotype III includes progression to contralateral limb tonic posturing after an occipital-onset sequence. No lateralization is reported for the behavioral-arrest phenotype.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 3 findings
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • visual aura to oculomotor to evolving motor phenotypePhenotype III progresses from visual aura to head-eye deviation or eye pursuit, then to contralateral limb tonic or asymmetric tonic posturing, with some seizures evolving to GTCS.PDF p.9, Phenotype III
  • contralateral limb tonic posturingPhenotype III includes progression to contralateral limb tonic posturing.PDF p.9, Phenotype III
  • behavioral-arrest onset phenotypePhenotype V begins with behavioral arrest and progresses to oculomotor or motor signs, including limb tonic or hypermotor activity, with a tendency to evolve into GTCS.PDF p.9, Phenotype V

1 contributing manuscript; source-reported values remain separate and are not pooled.

frontal lobe seizures versus temporal lobe seizuresReported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

Only ictal speech is linked to the nondominant hemisphere; the broader frontal-versus-temporal comparison carries no general side direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • frontal lobe seizures versus temporal lobe seizuresTable 2 contrasts frontal seizures as often daily, sleep-typical, abrupt, usually brief, rapidly evolving, less often automatistic, early and prominently complex-motor, commonly hypermotor, loud and nonspeech in vocalization, more often secondarily generalized, and followed by shorter or less prominent postictal confusion, versus temporal seizures as less frequent, less sleep-associated, gradual, usually longer, gradually evolving, more often and longer automatistic, later and less frequent complex-motor, rarely hypermotor, sometimes ictal speech in the nondominant hemisphere, less often secondarily generalized, and followed by longer or more prominent postictal confusion.PDF p.2, Frontal lobe seizures; PDF p.4, Temporal lobe seizures; PDF p.5, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

hemispheric dominance for language; preferential unilateral exploration; symmetric contralateral electrodesReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 society guideline or consensus

The guideline discusses hemispheric language dominance and preferred unilateral or symmetric contralateral exploration; no patient-specific direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

isnard-french-guidelines-stereoelectroencephalography-2018.pdfSociety guideline or consensus · 1 finding
isnard-french-guidelines-stereoelectroencephalography-2018.pdf
Society guideline or consensus · Class I · Evidence weight 3.00 · 3 × 1 × 1
The document reports a French expert workgroup drawn from centers performing more than 10 SEEG explorations per year for at least 5 years; six subgroups of 4–6 experts developed topics, and the complete workgroup graded recommendations by the RAND/UCLA 1–9 method through four rounds, with at most one deviating grade discarded. Scores of 1–3, 4–6, and 7–9 represented disagreement, unresolved, and agreement areas; overlap produced weak status, and items without consensus were labeled “non-consensual agreement.” The subgroup literature searches covered French- and English-language medical articles in PubMed and Web of Science through June 2017, with topic-specific keywords. The intended population is adults and children with drug-resistant focal epilepsy being considered for invasive presurgical SEEG, with recommendations addressing temporal, frontal, posterior, perisylvian, lesional, focal cortical dysplasia, polymicrogyria, and hypothalamic-hamartoma contexts. The guideline does not report one analyzed patient cohort, a single reference standard, or patient-level denominators for its recommendations; where relevant, non-invasive anatomo-electroclinical data, subdural exploration, conventional surgery, and the epileptogenic zone are the source's comparators or decision references.
Findings
  • hemispheric dominance for language; preferential unilateral exploration; symmetric contralateral electrodesDetermination of language hemispheric dominance before implantation is appropriate when evaluable for the patient’s age and cooperation; one hemisphere should be preferentially explored, contralateral electrodes should be placed symmetrically when indicated if possible, and bilateral symmetric exploration with equal electrode numbers is not recommended.PDF p.5, Planning and management of SEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

history of childhood febrile seizuresReported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

No source lateralization is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfIndependent primary study · 1 finding · 3 reported values
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • history of childhood febrile seizuresA history of childhood febrile seizures was more frequent in M than ML patients and was absent in the L group.PDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
Reported values
  • 14/24 (58.3%)history of childhood febrile seizuresPercentage · n/N 14/24 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 4/18 (22.2%)history of childhood febrile seizuresPercentage · n/N 4/18 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · MLPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1
  • 0/13 (0%)history of childhood febrile seizuresPercentage · n/N 0/13 · 55 patients with unilateral TLE; M=24, ML=18, L=13 · LPDF p.4, Medical history, morphologic data, and general characteristics; PDF p.5, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal emotional facial expressionReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review lists multiple bilateral/symmetrical facial descriptors but explicitly warns that the labels do not always refer to the same feature.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • semiologic synonym setThe review records non-identical descriptions including “pouting,” “bilateral tonic facial contraction,” “symmetrical down-turned mouth,” “grimacing,” “inverted smile with a tearful expression,” “mouth turning down with symmetric puckering,” and “labial corners lowered with chin contraction.”PDF p.2, Introduction; PDF p.4, Study characteristics

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal facial motor signReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review lists multiple bilateral/symmetrical facial descriptors but explicitly warns that the labels do not always refer to the same feature.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • semiologic synonym setThe review records non-identical descriptions including “pouting,” “bilateral tonic facial contraction,” “symmetrical down-turned mouth,” “grimacing,” “inverted smile with a tearful expression,” “mouth turning down with symmetric puckering,” and “labial corners lowered with chin contraction.”PDF p.2, Introduction; PDF p.4, Study characteristics

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal nose rubbingReported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

No source-supported hemispheric or body-side lateralization is reported.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyTL · T+ 4.3% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · TL 5% · seizures (one analyzed seizure per patient)1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • nose rubbingNose rubbing did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • P=0.8nose rubbingP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.6, Table 2
  • T+ 4.3%nose rubbingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2
  • TL 5%nose rubbingPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal respiratory symptomsReported: Right hemisphere1 manuscript · 4 findings · 2 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The source text does not provide a hemisphere direction, but the prefilled lateralization value says right. No lateralizing information is present. The onset/propagation synthesis provides no lateralization information. The cited propagation finding provides no lateralization information.

Source-defined result groups 1
Localization: fronto-opercular epilepsy cohortObserved proportion 28.6%All reported · all included patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 2 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • elementary motor symptoms; speech dysfunction; complex motor behavior; respiratory symptoms; salivation; laughter; preserved consciousnessThe source's abstract identifies elementary motor symptoms, speech dysfunction, complex motor behavior, respiratory symptoms, salivation, and laughter as ictal signs with preserved consciousness in fronto-opercular epilepsy.PDF p.1, Abstract; PDF p.2, Key points
  • respiratory symptoms; dyspnea; hyperventilationThe source reports respiratory symptoms such as dyspnea and hyperventilation in 6 of 21 patients (29%).PDF p.6, Anatomical and clinical correlations
  • hypersalivation; respiratory disorders; opercular involvementThe source states that hypersalivation and respiratory disorders can occur when an ictal discharge involves the operculum, including after insular onset with peri-Sylvian spread.PDF p.8–9, Discussion
  • hypersalivation; respiratory disorders; peri-Sylvian spreadThe cited Peltola series reported hypersalivation and respiratory disorders in 5 of 11 patients (45%) when the ictal discharge spread outside the insular cortex and remained peri-Sylvian.PDF p.9, Discussion
Reported values
  • 6/21 (29%)respiratory symptoms; dyspnea; hyperventilationPercentage · n/N 6/21 · 21 included fronto-opercular epilepsy patients · ictal onset and early propagationPDF p.6, Anatomical and clinical correlations
  • 5/11 (45%)hypersalivation; respiratory disorders; peri-Sylvian spreadPercentage · n/N 5/11 · 11 patients in the cited Peltola series · ictal propagationPDF p.9, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal thermoregulatory changeReported: Ipsilateral1 manuscript · 1 finding · 10 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Thermoregulatory change and piloerection provide no lateralizing information in this record.

Source-defined result groups 2
Localization: T+ group / TL groupSource-defined values retained separatelyT+ group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Localization: T+ group / TL groupSource-defined values retained separatelyTL group · TL group versus T+ group · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 10 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • thermoregulatory change and piloerectionThermoregulatory changes did not differ overall between TL and T+ groups, but piloerection was more frequent in T+ seizures.PDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
Reported values
  • TL thermoregulatory 20.3%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ pilo-erection 13%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ sensation of heat or cold 13%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • TL sweat 3.4%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ sweat 4.3%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • P=0.03thermoregulatory change and piloerectionP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • TL sensation of heat or cold 15.3%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • T+ thermoregulatory 30.4%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • TL pilo-erection 1.7%thermoregulatory change and piloerectionPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL group · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms
  • P=0.33thermoregulatory change and piloerectionP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictalPDF p.1, abstract; PDF p.5, Seizure clinical semiology; PDF p.6, Table 2; PDF p.8, Autonomic symptoms

1 contributing manuscript; source-reported values remain separate and are not pooled.

interictal PET statistical hypometabolic networkReported: BilateralAlso reported: IpsilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

The PET network includes ipsilateral and bilateral findings, but the imaging side labels are cohort/network context rather than a semiologic hemisphere rule.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 1 reported value
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • interictal PET statistical hypometabolic networkCompared with healthy controls, the 17-patient PET group showed significant hypometabolism in the insular lobe, ipsilateral central operculum, ipsilateral supplementary motor area, ipsilateral middle cingulate cortex, bilateral caudate nuclei, and putamen.PDF p.2, 18FDG-PET scans and analysis; PDF p.4, Neuroimaging and PET statistical analysis; PDF p.7, Figure 2 caption
Reported values
  • P < 0.05interictal PET statistical hypometabolic networkP value · 17 patients after exclusion of three with previous epilepsy surgery and two younger than 7 years; 18 healthy controls · interictal PETPDF p.2, 18FDG-PET scans and analysis; PDF p.4, Neuroimaging and PET statistical analysis; PDF p.7, Figure 2 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

lateral/neocortical temporal lobe seizureReported: ContralateralAlso reported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review restates subtype-dependent associations: unilateral elementary auditory aura may accompany contralateral onset, while ictal dysphasia is associated with the dominant hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • lateral/neocortical temporal lobe seizureAuras are less common in lateral temporal seizures and may be auditory or vertiginous; elementary sounds suggest primary auditory cortex, complex sounds or distortions auditory association areas, unilateral elementary auditory aura contralateral onset, and early ictal dysphasia dominant-hemisphere involvement. Compared with mesial temporal seizures, lateral temporal seizures are shorter, have earlier loss of awareness, more frontal propagation with complex motor features, and more frequent bilateral tonic-clonic evolution, although reciprocal connections create overlap.PDF p.6, Lateral/neocortical temporal lobe

1 contributing manuscript; source-reported values remain separate and are not pooled.

Lateralization comparison with interictal EEG, ictal EEG, and MRIReported: BilateralNo single reliable side1 manuscript · 1 finding · 22 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Aggregate comparisons report no statistically significant lateralization differences between semiology and interictal EEG, ictal EEG, or MRI, with bilateral MRI cases noted in the source.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdfIndependent primary study · 1 finding · 22 reported values
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The cohort comprised consecutive patients operated between 1999 and 2007: temporal lobe epilepsy (30 patients, 63 seizures), frontal lobe epilepsy (27 patients, 51 seizures), parietal lobe epilepsy (8 patients, 14 seizures), and occipital lobe epilepsy (8 patients, 18 seizures). Patients were at least 12 years old, had one focal resection without hemispherectomy or multilobar resection, and had Engel class Ia outcome for at least 1 year; the study population was 73 patients and 145 seizures. Three investigators independently reviewed one or two best video examples of each seizure type while blinded to clinical details, with charted auras supplied by an unblinded investigator. A positive result required agreement of at least two of three raters; the same rule defined presence of a sign, correct lateralization, and correct lobar or sublobar localization. The surgical resection and lasting seizure freedom were used as the reference for the epileptogenic zone. Free Marginal Kappa and positive predictive value were calculated. Noninvasive EEG, MRI, and PET had been reviewed in the presurgical conference; PET was available for 40/73 patients and ictal SPECT for 20/73.
Findings
  • Lateralization comparison with interictal EEG, ictal EEG, and MRIThe source reports no statistically significant lateralization differences between seizure semiology and interictal EEG, ictal EEG, or MRI, although interictal EEG appeared least informative.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
Reported values
  • Interictal EEG Total 44/73 (60%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 44/73 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Total lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • MRI lateralization PPV Occipital 75%Lateralization comparison with interictal EEG, ictal EEG, and MRIPositive predictive value · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Occipital lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Ictal EEG Frontal 22/27 (81%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 22/27 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Frontal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • MRI lateralization PPV Frontal 78%Lateralization comparison with interictal EEG, ictal EEG, and MRIPositive predictive value · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Frontal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Figure 1 correct-patient label 55 for MRILateralization comparison with interictal EEG, ictal EEG, and MRICount · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Overall cohort · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • MRI lateralization PPV Total 78%Lateralization comparison with interictal EEG, ictal EEG, and MRIPositive predictive value · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Total lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • 6/8 MRI lesional cases in Parietal groupLateralization comparison with interictal EEG, ictal EEG, and MRICount · n/N 6/8 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Parietal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • MRI lateralization PPV Parietal 75%Lateralization comparison with interictal EEG, ictal EEG, and MRIPositive predictive value · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Parietal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • 6/8 MRI lesional cases in Occipital groupLateralization comparison with interictal EEG, ictal EEG, and MRICount · n/N 6/8 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Occipital lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Figure 1 correct-patient label 53 for semiologyLateralization comparison with interictal EEG, ictal EEG, and MRICount · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Overall cohort · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Ictal EEG Temporal 28/30 (93%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 28/30 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Temporal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Interictal EEG Occipital 6/8 (75%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 6/8 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Occipital lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • 24/30 MRI lesional cases in Temporal groupLateralization comparison with interictal EEG, ictal EEG, and MRICount · n/N 24/30 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Temporal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Ictal EEG Total 64/73 (87.5%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 64/73 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Total lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Ictal EEG Occipital 7/8 (87.5%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 7/8 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Occipital lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • 59/73 MRI lesional cases in Total groupLateralization comparison with interictal EEG, ictal EEG, and MRICount · n/N 59/73 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Total lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Interictal EEG Parietal 2/8 (25%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 2/8 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Parietal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Interictal EEG Frontal 12/27 (44%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 12/27 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Frontal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • 21/27 MRI lesional cases in Frontal groupLateralization comparison with interictal EEG, ictal EEG, and MRICount · n/N 21/27 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Frontal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • MRI lateralization PPV Temporal 73%Lateralization comparison with interictal EEG, ictal EEG, and MRIPositive predictive value · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Temporal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Interictal EEG Temporal 24/30 (80%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 24/30 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Temporal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1
  • Ictal EEG Parietal 7/8 (87.5%)Lateralization comparison with interictal EEG, ictal EEG, and MRIPercentage · n/N 7/8 · The 73-patient cohort; MRI values are reported for lesional cases and PET is not part of Table 4. · Parietal lobe epilepsy · Aggregate seizure semiology versus interictal or ictal presurgical tests.PDF p.4, §5.4/Fig. 1/Table 4; PDF p.5, §6.1

1 contributing manuscript; source-reported values remain separate and are not pooled.

lesion lateralisationReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review table restates lesion-lateralisation categories of right hemisphere 14/36 (38.9%), left hemisphere 14/36 (38.9%), bilateral 3/36 (8.3%), and other non-lesional contexts 5/36 (13.9%).

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfSystematic review or meta-analysis · 1 finding · 4 reported values
e236615-full.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • lesion lateralisationTable 2 reports lesions in the right hemisphere 14 (38.9%), left hemisphere 14 (38.9%), bilateral 3 (8.3%), and other non-lesional contexts such as alcohol or antipsychotic cessation 5 (13.9%).PDF p.3, Table 2
Reported values
  • 14 (38.9%)lesion lateralisationPercentage · n/N 14/36 · Review population stated as 36 total cases · left hemispherePDF p.3, Table 2
  • 3 (8.3%)lesion lateralisationPercentage · n/N 3/36 · Review population stated as 36 total cases · bilateralPDF p.3, Table 2
  • 5 (13.9%)lesion lateralisationPercentage · n/N 5/36 · Review population stated as 36 total cases · other non-lesional contextsPDF p.3, Table 2
  • 14 (38.9%)lesion lateralisationPercentage · n/N 14/36 · Review population stated as 36 total cases · right hemispherePDF p.3, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

lesion lateralisation by hemispheric dominanceReported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

When lesion dominance was specified, lesions were equally distributed between dominant and nondominant hemispheres.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfSystematic review or meta-analysis · 1 finding
e236615-full.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • lesion lateralisation by hemispheric dominanceWhen specified, lesions were lateralised equally in dominant and non-dominant hemispheres.PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

mesial temporal lobe including hippocampusReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review describes unilateral dystonic posturing as contralateral to the mesial temporal focus.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • mesial temporal lobe including hippocampusMesial temporal seizures may have experiential or abdominal auras and early autonomic phenomena, then behavioural arrest, manual or oral automatisms, and impaired awareness; unilateral dystonic posturing is described as contralateral, and mesial seizures tend to be longer than lateral temporal seizures and less often evolve to bilateral tonic-clonic seizures.PDF p.5, Mesial temporal lobe including hippocampus; PDF p.6, Mesial temporal lobe including hippocampus

1 contributing manuscript; source-reported values remain separate and are not pooled.

Micropsia / macropsia (visual size illusion)Source terms: Micropsia / macropsiaReported: Dominant hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 2 findings · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review assigns non-dominant context to body-image distortion and dominant parietotemporal context to the distinct manifestation of reading and writing impairment; no direction is stated for kinetopsia, macropsia, or micropsia. No hemisphere or side-relative direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 2 findings
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • parietal association seizure; macrosomatognosis; microsomatagnosis; epileptic kinetopsia; macropsia; micropsiaThe review relates non-dominant parietal association seizures to distortions of body image, superior parietal lobule and precuneus seizures to enlarged or shrunken body-part perception, epileptic kinetopsia to superior parietal lobule/intraparietal sulcus, and macropsia or micropsia to precuneus involvement; dominant parietotemporal seizures may cause reading and writing impairment.PDF p.7, Parietal association areas; PDF p.3, Figure 1
  • visual association area; complex visual hallucination; kinetopsia; macropsia; micropsia; autoscopyComplex visual hallucinations in occipital epilepsy are linked to prestriate cortex or propagation to adjacent temporoparietal areas; formed hallucinations and visual distortions such as kinetopsia, macropsia, micropsia, and rarely autoscopy are described.PDF p.8, Visual association areas; PDF p.3, Figure 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

Neck hyperextensionReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Case 2 has a right occipital lesion and source side right in the seizure pathway accompanying head and neck hyperextension.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdfIndependent primary study · 1 finding
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
This single-center retrospective case series included 19 patients with SEEG-confirmed occipital lobe seizure onset. The authors reviewed video-EEG/clinical descriptions and SEEG-anchored temporal evolution, used MRI/CT-fused electrode localization, and assigned a predominant propagation pattern through electroclinical concordance. The source’s occipital parcellation and phenotype labels are preserved without imposing a Lüders or ILAE crosswalk.
Findings
  • head and neck hyperextensionTable 2 records head and neck hyperextension after vocalization and eye blinking in Case 2.PDF p.6, Table 2 Case 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

network dysfunctionReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review's network hypothesis is based on palinacousis being predominantly contralateral, with bilateral or indeterminate reports and an ipsilateral right medial-geniculate-nucleus lesion exception.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfSystematic review or meta-analysis · 1 finding
e236615-full.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • network dysfunctionBased on the contralateral pattern, the ipsilateral right medial geniculate nucleus exception, and auditory redundancy observations, the authors propose that palinacousis may reflect network dysfunction rather than only a local lesion; they suggest network reorganisation could explain failed intraoperative reproduction.PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

No auraReported: Ipsilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

No hemisphere or body-side direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • no auraThe source reports no significant group difference for the absence of an aura.PDF p.6, Table 2
Reported values
  • T+ 8.7%no auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 15.3%no auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

other frontal regionsReported: ContralateralAlso reported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review describes early head and eye version as contralateral to frontal-eye-field seizure onset and dysphasia as associated with dominant-hemisphere frontal or Broca-region seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • other frontal regionsThe review associates orbitofrontal seizures with impaired awareness, automatisms, occasional olfactory aura, ictal tachycardia, and complex motor evolution; frontopolar seizures with impaired awareness followed by motor features; ventromedial prefrontal/anterior cingulate seizures with forced thinking, fear, and hypermotor features; contralateral dorsolateral frontal seizures involving frontal eye fields with early head and eye version; dominant frontal or Broca-region seizures with dysphasia; and frontal operculum seizures with unilateral face clonus, laryngeal symptoms, hypersalivation, and articulation difficulty.PDF p.3, Figure 1; PDF p.4, Other frontal regions

1 contributing manuscript; source-reported values remain separate and are not pooled.

posterior epilepsies; multilobar sampling; pathways of propagationReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 society guideline or consensus

Unilateral versus bilateral describes the SEEG sampling plan, not a lateralizing semiologic direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

isnard-french-guidelines-stereoelectroencephalography-2018.pdfSociety guideline or consensus · 1 finding
isnard-french-guidelines-stereoelectroencephalography-2018.pdf
Society guideline or consensus · Class I · Evidence weight 3.00 · 3 × 1 × 1
The document reports a French expert workgroup drawn from centers performing more than 10 SEEG explorations per year for at least 5 years; six subgroups of 4–6 experts developed topics, and the complete workgroup graded recommendations by the RAND/UCLA 1–9 method through four rounds, with at most one deviating grade discarded. Scores of 1–3, 4–6, and 7–9 represented disagreement, unresolved, and agreement areas; overlap produced weak status, and items without consensus were labeled “non-consensual agreement.” The subgroup literature searches covered French- and English-language medical articles in PubMed and Web of Science through June 2017, with topic-specific keywords. The intended population is adults and children with drug-resistant focal epilepsy being considered for invasive presurgical SEEG, with recommendations addressing temporal, frontal, posterior, perisylvian, lesional, focal cortical dysplasia, polymicrogyria, and hypothalamic-hamartoma contexts. The guideline does not report one analyzed patient cohort, a single reference standard, or patient-level denominators for its recommendations; where relevant, non-invasive anatomo-electroclinical data, subdural exploration, conventional surgery, and the epileptogenic zone are the source's comparators or decision references.
Findings
  • posterior epilepsies; multilobar sampling; pathways of propagationPosterior epilepsies most often require multilobar sampling, which may be unilateral or bilateral, with particular attention to propagation pathways and involvement of functional structures.PDF p.5, Planning and management of SEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal automatismsReported: Ipsilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

The TL-versus-T+ comparison provides no lateralization information.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • post-ictal automatismsPost-ictal automatisms did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 42.4%post-ictal automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · post-ictalPDF p.6, Table 2
  • T+ 47.8%post-ictal automatismsPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · post-ictalPDF p.6, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

primary sensory cortex; parietal association areasReported: ContralateralAlso reported: Dominant hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review restates contralateral primary-sensory tingling/numbness and dominant/nondominant parietal association symptom contexts.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • primary sensory cortex; parietal association areasPrimary sensory cortex seizures tend to begin with contralateral tingling or numbness that may spread through the sensory homunculus, sometimes with pain or altered thermal sensation; non-dominant parietal association seizures may distort body image, superior parietal/precuneus seizures may produce macrosomatognosis or microsomatognosis, superior parietal/intraparietal seizures may produce kinetopsia, precuneus seizures macropsia or micropsia, and dominant parietotemporal seizures language impairment.PDF p.7, Primary sensory cortex; PDF p.7, Parietal association areas

1 contributing manuscript; source-reported values remain separate and are not pooled.

RINCH movementsReported: ContralateralAlso reported: Dominant hemisphereAlso reported: Non-dominant hemisphereNo single reliable side1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review distinguishes dominant-hemisphere dysphasia, nondominant ictal speech or preserved awareness, contralateral RINCH motions, and nonlateralizing speech arrest.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
Narrative review; the authors summarize literature on focal seizures and present illustrative cases from their centre using clinical history, videotelemetry, scalp or intracranial stereo-EEG, MRI/PET, and surgical outcome where stated. No single review cohort, systematic eligibility set, pooled analysis, or uniform endpoint denominator is reported. Populations, analysis units, and reference standards are therefore retained at finding level; source-reported reference standards include ictal EEG, imaging, lesion location, clinical semiology, and seizure freedom after resection.
Findings
  • ictal/postictal dysphasia; ictal speech; preserved awareness; RINCH motionsIctal or postictal dysphasia lateralises to the dominant hemisphere but has poor localising value and must be distinguished from non-lateralising speech arrest; formed nonsensical ictal speech and preserved awareness during ictal automatisms point to the nondominant hemisphere, while rhythmic ictal non-clonic hand motions may be contralateral in temporal lobe epilepsy and peri-ictal drinking, spitting, vomiting, or urge to urinate point to a nondominant focus.PDF p.10, Lateralising signs

1 contributing manuscript; source-reported values remain separate and are not pooled.

seizure duration greater than one minuteReported: Ipsilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

Seizure duration greater than one minute provides no hemispheric direction.

Source-defined result groups 2
Localization: TemporalSource-defined values retained separatelyT+ · seizures1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyTL · T+ · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 2 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • seizure duration greater than one minuteThe proportion of analyzed ictal events lasting longer than one minute did not differ between TL and T+ groups.PDF p.6, Table 2
Reported values
  • TL 78%seizure duration greater than one minutePercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictalPDF p.6, Table 2
  • T+ 73.9%seizure duration greater than one minutePercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictalPDF p.6, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

seizure lateralizationReported: Left hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 independent primary study

The source reports a significant left-side predominance in the narrative, but Table 1 displays conflicting left-lateralized cells and does not reconcile them.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 3.00 · 2 × 1.5 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • seizure lateralizationThe Results text describes a significant left-side predominance of seizures in the TL group compared with the T+ group (P<0.0001), while the rendered Table 1 cells read “4 L” for TL and “20 L” for T+; the source does not resolve this directional discrepancy.PDF p.4, Results and Table 1; PDF p.5, discussion of non-operated T+ cases and hemisphere
Reported values
  • Table 1 cell “4 L” for TLseizure lateralizationCount · TL group (n=58) versus T+ group (n=22) · TL group · seizure onset/lateralizationPDF p.4, Results and Table 1; PDF p.5, discussion of non-operated T+ cases and hemisphere
  • Table 1 cell “20 L” for T+ groupseizure lateralizationCount · TL group (n=58) versus T+ group (n=22) · T+ group · seizure onset/lateralizationPDF p.4, Results and Table 1; PDF p.5, discussion of non-operated T+ cases and hemisphere
  • P<0.0001seizure lateralizationP value · TL group (n=58) versus T+ group (n=22) · seizure onset/lateralizationPDF p.4, Results and Table 1; PDF p.5, discussion of non-operated T+ cases and hemisphere

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal lobe epilepsy sampling; mesial temporal structures; contralateral mesial temporal structuresReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 society guideline or consensus

The guideline recommendation includes contralateral mesial-temporal sampling targets but provides no lateralizing seizure-sign rule.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

isnard-french-guidelines-stereoelectroencephalography-2018.pdfSociety guideline or consensus · 1 finding
isnard-french-guidelines-stereoelectroencephalography-2018.pdf
Society guideline or consensus · Class I · Evidence weight 3.00 · 3 × 1 × 1
The document reports a French expert workgroup drawn from centers performing more than 10 SEEG explorations per year for at least 5 years; six subgroups of 4–6 experts developed topics, and the complete workgroup graded recommendations by the RAND/UCLA 1–9 method through four rounds, with at most one deviating grade discarded. Scores of 1–3, 4–6, and 7–9 represented disagreement, unresolved, and agreement areas; overlap produced weak status, and items without consensus were labeled “non-consensual agreement.” The subgroup literature searches covered French- and English-language medical articles in PubMed and Web of Science through June 2017, with topic-specific keywords. The intended population is adults and children with drug-resistant focal epilepsy being considered for invasive presurgical SEEG, with recommendations addressing temporal, frontal, posterior, perisylvian, lesional, focal cortical dysplasia, polymicrogyria, and hypothalamic-hamartoma contexts. The guideline does not report one analyzed patient cohort, a single reference standard, or patient-level denominators for its recommendations; where relevant, non-invasive anatomo-electroclinical data, subdural exploration, conventional surgery, and the epileptogenic zone are the source's comparators or decision references.
Findings
  • temporal lobe epilepsy sampling; mesial temporal structures; contralateral mesial temporal structuresIn temporal lobe epilepsy, sampling usually includes the hippocampus, amygdala, entorhinal cortex, middle temporal gyrus and basal cortex, superior temporal gyrus, temporal pole, and insular cortex floor; when extra-temporal or contralateral structures are involved, orbitofrontal cortex, perisylvian region, temporoparietal junction, and contralateral mesial temporal structures can also be sampled.PDF p.5, Planning and management of SEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal semiology; mesial symptomatology or lesion; extra-temporal or contralateral involvementReported: BilateralAlso reported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 society guideline or consensus

Contralateral temporal involvement and a bilateral EZ are alternative presurgical hypotheses that can support SEEG, not lateralizing directions of a specific semiologic sign.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

isnard-french-guidelines-stereoelectroencephalography-2018.pdfSociety guideline or consensus · 1 finding
isnard-french-guidelines-stereoelectroencephalography-2018.pdf
Society guideline or consensus · Class I · Evidence weight 3.00 · 3 × 1 × 1
The document reports a French expert workgroup drawn from centers performing more than 10 SEEG explorations per year for at least 5 years; six subgroups of 4–6 experts developed topics, and the complete workgroup graded recommendations by the RAND/UCLA 1–9 method through four rounds, with at most one deviating grade discarded. Scores of 1–3, 4–6, and 7–9 represented disagreement, unresolved, and agreement areas; overlap produced weak status, and items without consensus were labeled “non-consensual agreement.” The subgroup literature searches covered French- and English-language medical articles in PubMed and Web of Science through June 2017, with topic-specific keywords. The intended population is adults and children with drug-resistant focal epilepsy being considered for invasive presurgical SEEG, with recommendations addressing temporal, frontal, posterior, perisylvian, lesional, focal cortical dysplasia, polymicrogyria, and hypothalamic-hamartoma contexts. The guideline does not report one analyzed patient cohort, a single reference standard, or patient-level denominators for its recommendations; where relevant, non-invasive anatomo-electroclinical data, subdural exploration, conventional surgery, and the epileptogenic zone are the source's comparators or decision references.
Findings
  • temporal semiology; mesial symptomatology or lesion; extra-temporal or contralateral involvementIn temporal lobe epilepsy with mesial symptomatology or a mesial lesion, SEEG is indicated when non-invasive data suggest early involvement of extra-limbic or extra-temporal cortex or the contralateral temporal lobe; more generally, in epilepsy with temporal semiology it is indicated when extra-temporal origin or extension, or a bilateral EZ, is suggested.PDF p.4, Indications and limits of SEEG; PDF p.5, Indications and limits of SEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Tonic facial contractionReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 systematic review or meta-analysis

The review lists multiple bilateral/symmetrical facial descriptors but explicitly warns that the labels do not always refer to the same feature.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • semiologic synonym setThe review records non-identical descriptions including “pouting,” “bilateral tonic facial contraction,” “symmetrical down-turned mouth,” “grimacing,” “inverted smile with a tearful expression,” “mouth turning down with symmetric puckering,” and “labial corners lowered with chin contraction.”PDF p.2, Introduction; PDF p.4, Study characteristics

1 contributing manuscript; source-reported values remain separate and are not pooled.

unilateral polymicrogyria (PMG); bilateral PMGReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 3 across 1 manuscript · 1 society guideline or consensus

The guideline recommends SEEG to determine PMG involvement and notes that bilateral PMG may still have a unilateral EZ; no left/right direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

isnard-french-guidelines-stereoelectroencephalography-2018.pdfSociety guideline or consensus · 1 finding
isnard-french-guidelines-stereoelectroencephalography-2018.pdf
Society guideline or consensus · Class I · Evidence weight 3.00 · 3 × 1 × 1
The document reports a French expert workgroup drawn from centers performing more than 10 SEEG explorations per year for at least 5 years; six subgroups of 4–6 experts developed topics, and the complete workgroup graded recommendations by the RAND/UCLA 1–9 method through four rounds, with at most one deviating grade discarded. Scores of 1–3, 4–6, and 7–9 represented disagreement, unresolved, and agreement areas; overlap produced weak status, and items without consensus were labeled “non-consensual agreement.” The subgroup literature searches covered French- and English-language medical articles in PubMed and Web of Science through June 2017, with topic-specific keywords. The intended population is adults and children with drug-resistant focal epilepsy being considered for invasive presurgical SEEG, with recommendations addressing temporal, frontal, posterior, perisylvian, lesional, focal cortical dysplasia, polymicrogyria, and hypothalamic-hamartoma contexts. The guideline does not report one analyzed patient cohort, a single reference standard, or patient-level denominators for its recommendations; where relevant, non-invasive anatomo-electroclinical data, subdural exploration, conventional surgery, and the epileptogenic zone are the source's comparators or decision references.
Findings
  • unilateral polymicrogyria (PMG); bilateral PMGIn unilateral PMG-associated epilepsy, SEEG is the method of choice for determining PMG involvement in the EZ; in bilateral PMG, SEEG can be proposed when non-invasive data suggest a unilateral EZ.PDF p.5, Indications and limits of SEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Body-part heaviness/lightness sensationReported: Contralateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 2.91 across 1 manuscript · 1 independent primary study

Five MCC stimulations produced heavier or lighter body-part sensations described as contralateral to the stimulated MCC.

Source-defined result groups 2
Localization: MCCObserved proportion 29.4%All reported · stimulation trial1 manuscript · 2 reported values · not pooled
Lateralization: ContralateralObserved proportion 29.4%All reported · stimulation trial1 manuscript · 2 reported values · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding · 2 reported values
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 2.91 · 2 × 0.9 × 1.615
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • body part becomes heavier/lighterFive stimulations (S5, S7, S13, S15, and S16) produced a weight-change illusion without an associated motor deficit; the Results text describes right or left upper-limb effects contralateral to the stimulated MCC, while Table 2 records S15 as right hemibody and head heaviness and S16 as upper-right-limb heaviness associated with pain.PDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
Reported values
  • Five qualitative heavier/lighter effectsbody part becomes heavier/lighterCount · n/N 5/17 · Five stimulation trials S5, S7, S13, S15, and S16 in the included cohort · HFS-evoked body-perception responsePDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
  • no associated motor deficit reported in Section 3.1body part becomes heavier/lighterCount · n/N 5/17 · Five stimulation trials S5, S7, S13, S15, and S16 in the included cohort · HFS-evoked body-perception responsePDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

contralateral, ipsilateral, bilateral, or axial clinical effectReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 2.91 across 1 manuscript · 1 independent primary study

Among 17 cingulate stimulations evoking body-perception changes, 9 effects were contralateral, 4 ipsilateral, and 4 bilateral or axial.

Source-defined result groups 6
Localization: cingulate cortexObserved proportion 23.5%bilateral or axial · stimulation trial1 manuscript · 1 reported value · not pooled
Lateralization: axial / Bilateral / Contralateral / IpsilateralObserved proportion 52.9%contralateral · stimulation trial1 manuscript · 1 reported value · not pooled
Localization: cingulate cortexObserved proportion 52.9%contralateral · stimulation trial1 manuscript · 1 reported value · not pooled
Localization: cingulate cortexObserved proportion 23.5%ipsilateral · stimulation trial1 manuscript · 1 reported value · not pooled
Lateralization: axial / Bilateral / Contralateral / IpsilateralObserved proportion 23.5%ipsilateral · stimulation trial1 manuscript · 1 reported value · not pooled
Lateralization: axial / Bilateral / Contralateral / IpsilateralObserved proportion 23.5%bilateral or axial · stimulation trial1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding · 3 reported values
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 2.91 · 2 × 0.9 × 1.615
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • contralateral, ipsilateral, bilateral, or axial clinical effectOf the 17 cingulate stimulations that evoked body-perception changes, 9 effects were contralateral to the stimulated side, 4 were ipsilateral, and 4 were bilateral or involved the axial body, defined here by the source as the head or trunk.PDF p.6, Section 3.1 Clinical effects; PDF p.7, Table 2
Reported values
  • 4 bilateral/axial effects among 17 stimulationscontralateral, ipsilateral, bilateral, or axial clinical effectCount · n/N 4/17 · 17 body-perception-evoking cingulate stimulation trials in 12 patients · bilateral or axial · Stimulation-evoked body-perception responsePDF p.6, Section 3.1 Clinical effects; PDF p.7, Table 2
  • 4 ipsilateral effects among 17 stimulationscontralateral, ipsilateral, bilateral, or axial clinical effectCount · n/N 4/17 · 17 body-perception-evoking cingulate stimulation trials in 12 patients · ipsilateral · Stimulation-evoked body-perception responsePDF p.6, Section 3.1 Clinical effects; PDF p.7, Table 2
  • 9 contralateral effects among 17 stimulationscontralateral, ipsilateral, bilateral, or axial clinical effectCount · n/N 9/17 · 17 body-perception-evoking cingulate stimulation trials in 12 patients · contralateral · Stimulation-evoked body-perception responsePDF p.6, Section 3.1 Clinical effects; PDF p.7, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

Pressure sensationReported: Bilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 2.91 across 1 manuscript · 1 independent primary study

Both ACC stimulation pressure responses were described as bilateral/axial, involving head, face, trunk, or whole-body distributions.

Source-defined result groups 2
Lateralization: axial / BilateralObserved proportion 11.8%All reported · stimulation trial1 manuscript · 1 reported value · not pooled
Localization: ACCObserved proportion 11.8%All reported · stimulation trial1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding · 1 reported value
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 2.91 · 2 × 0.9 × 1.615
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • sensation of pressureTwo ACC stimulations produced pressure phenomena: S4 was recorded in Table 2 as pressure at the top of the head, and S11 as pressure beginning at the face and descending through the body; fear was reported when the S11 sensation reached the heart region, which the authors attributed to the chest pressure rather than to stimulation per se.PDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2
Reported values
  • Two qualitative pressure effects, with fear associated with the S11 chest/heart-level sensationsensation of pressureCount · n/N 2/17 · Two ACC stimulation trials S4 and S11 · HFS-evoked body-perception responsePDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

ipsilateral amygdala volumeReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight 2.4 across 1 manuscript · 1 independent primary study

Whole amygdala and several subnuclei had larger volume ipsilateral to the epileptogenic zone in the ICA/PICA comparison with controls and no-ICA patients.

Source-defined result groups 2
Lateralization: IpsilateralSource-defined values retained separatelyipsilateral amygdala-volume analysis · study groups · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyipsilateral amygdala-volume analysis · study groups · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 1 finding · 6 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 2.40 · 2 × 1.2 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • ipsilateral amygdala volumeWhole amygdala volume and several amygdala subnuclei were increased ipsilateral to the epileptogenic zone in patients with ICA or PICA compared with healthy controls and patients without seizure-related apnea.PDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion
Reported values
  • 10 PICAipsilateral amygdala volumeCount · MRI subset of 22 ICA/PICA patients (12 ICA, 10 PICA), 31 no-ICA patients, and 30 healthy controls · PICA · peri-ictal breathing-disorder phenotypePDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion
  • 22 ICA/PICA patientsipsilateral amygdala volumeCount · MRI subset of 22 ICA/PICA patients (12 ICA, 10 PICA), 31 no-ICA patients, and 30 healthy controls · ICA/PICA MRI subset · peri-ictal breathing-disorder phenotypePDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion
  • 30 healthy controlsipsilateral amygdala volumeCount · MRI subset of 22 ICA/PICA patients (12 ICA, 10 PICA), 31 no-ICA patients, and 30 healthy controls · healthy controls · peri-ictal breathing-disorder phenotypePDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion
  • 31 no-ICA patientsipsilateral amygdala volumeCount · MRI subset of 22 ICA/PICA patients (12 ICA, 10 PICA), 31 no-ICA patients, and 30 healthy controls · no-ICA · peri-ictal breathing-disorder phenotypePDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion
  • F(1,75) = 5.478ipsilateral amygdala volumeOther reported value · MRI subset of 22 ICA/PICA patients (12 ICA, 10 PICA), 31 no-ICA patients, and 30 healthy controls · ipsilateral amygdala-volume analysis · peri-ictal breathing-disorder phenotypePDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion
  • 12 ICAipsilateral amygdala volumeCount · MRI subset of 22 ICA/PICA patients (12 ICA, 10 PICA), 31 no-ICA patients, and 30 healthy controls · ICA · peri-ictal breathing-disorder phenotypePDF p.1, Abstract Results and Discussion; PDF p.7, Subcortical Structures and Amygdala Volumes; PDF p.9, Figure 5; PDF p.10, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

ipsilateral hippocampal thickness in the no-ICA groupReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 2.4 across 1 manuscript · 1 independent primary study

Ipsilateral hippocampus, particularly head and body, relative to the epileptogenic zone

Evidence by contributing manuscript 1

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 1 finding
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 2.40 · 2 × 1.2 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • ipsilateral hippocampal thickness in the no-ICA groupThe no-ICA group had a thinner ipsilateral hippocampus, particularly the head and body, than healthy controls.PDF p.7, Subcortical Structures and Amygdala Volumes

1 contributing manuscript; source-reported values remain separate and are not pooled.

ipsilateral hippocampus and thalamus in ICA/PICAReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 2.4 across 1 manuscript · 1 independent primary study

The source measured ipsilateral hippocampal and thalamic volumes relative to the epileptogenic zone.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 1 finding
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 2.40 · 2 × 1.2 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • ipsilateral hippocampus and thalamus in ICA/PICAPatients with ICA/PICA did not differ from healthy controls in ipsilateral hippocampal volume or ipsilateral thalamus volume.PDF p.7, Subcortical Structures and Amygdala Volumes, ipsilateral hippocampus; PDF p.7, final thalamus paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

non-amygdala and contralateral subcortical morphometryReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 2.4 across 1 manuscript · 1 independent primary study

No lateralization relationship is reported; contralateral is retained only as the source's comparison-side qualifier.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfIndependent primary study · 1 finding
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Independent primary study · Class II · Evidence weight 2.40 · 2 × 1.2 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • non-amygdala and contralateral subcortical morphometryNo group differences were observed in the brainstem or cerebellum, and no differences were found in the amygdala, hippocampus, or thalamic nuclei contralateral to the epileptogenic zone.PDF p.7, Subcortical Structures and Amygdala Volumes

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal lesions and absent event-time EEG in cases 5-7Reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 2.23 across 1 manuscript · 1 independent primary study

Right temporal or right superior temporal lesions occurred in some of cases 5-7, without event-time EEG confirmation.

Source-defined result groups 1
Localization: TemporalObserved proportion 100.0%cases 5–7 · Cases with versus without event-time electrographic support · case1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

palinacousis-seven-new-cases.pdfIndependent primary study · 1 finding · 2 reported values
palinacousis-seven-new-cases.pdf
Independent primary study · Class II · Evidence weight 2.23 · 2 × 0.9 × 1.239
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • temporal lesions and absent event-time EEG in cases 5-7In cases 5, 6, and 7, the authors state that the lesions involved the temporal lobes and that no supporting electrographic data were available at the time of palinacousis.PDF p.3, cases 5-6; PDF p.3, case 7; PDF p.4, Discussion
Reported values
  • 3/3temporal lesions and absent event-time EEG in cases 5-7Percentage · n/N 3/3 · Current case-series cases 5-7 · cases 5–7 · Peri- or post-event palinacousis without event-time EEG supportPDF p.3, cases 5-6; PDF p.3, case 7; PDF p.4, Discussion
  • 0/3temporal lesions and absent event-time EEG in cases 5-7Percentage · n/N 0/3 · Current case-series cases 5-7 · cases 5–7 · Peri- or post-event palinacousis without event-time EEG supportPDF p.3, cases 5-6; PDF p.3, case 7; PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal speech disturbance (unspecified subtype)Reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 2.07 across 1 manuscript · 1 independent primary study

The two speech-automatism plus speech-arrest cases split evenly by EEG abnormality side: one left and one right.

Source-defined result groups 3
Lateralization: Left hemisphere / Right hemisphereObserved proportion 50.0%Right EEG abnormality · Symptom-combination categories · case1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 50.0%Left EEG abnormality · Symptom-combination categories · case1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelySpeech automatism + speech arrest · Symptom-combination categories · case1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

ictal-speech-disturbance-cerebral-dominance.pdfIndependent primary study · 1 finding · 4 reported values
ictal-speech-disturbance-cerebral-dominance.pdf
Independent primary study · Class II · Evidence weight 2.07 · 2 × 0.9 × 1.151
The authors collected about 43 cases with ictal speech disturbances over 8 years. Interictal EEG was examined at least twice per case; laterality was defined by a spike or sharp-wave focus, unilateral dominant spike or sharp wave, or unilateral slow wave corresponding to same-region brain damage or tumor. Laterality was confirmed in 36 cases; 7 cases with independent foci, no laterality, or normal findings were excluded. The statistical report concerns 34 right-handed epileptics because 2 left-handed patients could not be tested statistically. A control pool comprised 243 right-handed patients with unilateral abnormal EEG findings, 136 left and 117 right, and was assessed by t test.
Findings
  • combined ictal speech disturbancesThe authors found no case combining aphasic fit with speech automatism, found two cases combining speech automatism with speech arrest with one left and one right EEG abnormality, and could not confirm whether aphasic fit combined with speech arrest exists.PDF p.3, Results, paragraph preceding Table I; PDF p.4, Results
Reported values
  • Combined speech-automatism/speech-arrest cases with left EEG abnormality n=1combined ictal speech disturbancesCount · n/N 1/2 · Reported ictal speech-disturbance cases; combination-analysis denominator Not reported · Left EEG abnormality · ictalPDF p.3, Results, paragraph preceding Table I; PDF p.4, Results
  • Speech automatism plus speech arrest n=2combined ictal speech disturbancesCount · Reported ictal speech-disturbance cases; combination-analysis denominator Not reported · Speech automatism + speech arrest · ictalPDF p.3, Results, paragraph preceding Table I; PDF p.4, Results
  • Aphasic fit plus speech automatism n=0combined ictal speech disturbancesCount · Reported ictal speech-disturbance cases; combination-analysis denominator Not reported · Aphasic fit + speech automatism · ictalPDF p.3, Results, paragraph preceding Table I; PDF p.4, Results
  • Combined speech-automatism/speech-arrest cases with right EEG abnormality n=1combined ictal speech disturbancesCount · n/N 1/2 · Reported ictal speech-disturbance cases; combination-analysis denominator Not reported · Right EEG abnormality · ictalPDF p.3, Results, paragraph preceding Table I; PDF p.4, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

Normal ictal speechReported: Non-dominant hemisphere3 manuscripts · 3 findings · 4 reported values
Weighted evidence supportevidence weight 2 across 3 manuscripts · 1 manuscript weight pending · 1 structured design not resolved · 2 narrative, educational, or cited context

Prior studies associated normal ictal speech with nondominant temporal onset; the current cohort only showed a nonsignificant right-temporal trend for verbal automatisms. Normal ictal speech was associated with nondominant-hemisphere onset in 83% of cited cases. The occurrence counts alone do not provide a lateralizing direction.

Evidence by contributing manuscript 3

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 2 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.772
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • normal speech / ictal identifiable speechNormal speech, defined as ictal identifiable words or phrases, occurred in 25 seizures in 12 patients (34.2% of patients); it was always ictal and was either repetitive or nonrepetitive.PDF p.1, abstract; PDF p.3, Table 2 and Results; PDF p.5, Discussion
Reported values
  • Seizures with normal ictal speech n=25normal speech / ictal identifiable speechCount · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · ictalPDF p.1, abstract; PDF p.3, Table 2 and Results; PDF p.5, Discussion
  • Patients with normal ictal speech 12/35 (34.2%)normal speech / ictal identifiable speechPercentage · n/N 12/35 · 35 patients and 100 seizures with intractable temporal-lobe epilepsy · ictalPDF p.1, abstract; PDF p.3, Table 2 and Results; PDF p.5, Discussion
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • normal ictal speechGabr et al. observed normal speech in 12.5% of cases, 83% of which arose from the nondominant hemisphere.PDF p.9, section 4.1
Reported values
  • 83%normal ictal speechPercentage · cases evaluated for speech manifestations in temporal lobe seizures · cases with normal ictal speech · ictalPDF p.9, section 4.1
  • 12.5%normal ictal speechPercentage · cases evaluated for speech manifestations in temporal lobe seizures · temporal lobe seizure speech evaluations · ictalPDF p.9, section 4.1
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdfNarrative, educational, or cited context · 1 finding
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study retrospectively evaluated 55 patients with medically intractable unilateral temporal lobe epilepsy selected from 132 consecutive surgical-evaluation patients seen in Rennes (1994–1997) and Marseille (1997–2001). A total of 187 SEEG-recorded seizures were analyzed, with a reported mean of 3.4 seizures per patient. Clinical variables included initial ictal subjective symptoms, early and late ictal signs, loss of contact, seizure duration, and postictal deficits. Clinical data were acquired during video-SEEG testing and retrospectively reviewed by two independent investigators; seizure onset and termination were determined from the earliest and latest ictal SEEG changes. Group comparisons used Pearson’s chi-square or Fisher’s exact test, with two-sided p<0.05 considered significant. The tabulated percentages use patient subgroup sizes M=24, ML=18, and L=13 unless otherwise stated.
Findings
  • nondominant temporal lateralization of normal ictal speechThe discussion states that prior studies showed a nondominant temporal lateralization of “normal ictal speech,” while the current cohort showed a nonsignificant trend toward right temporal lateralization of verbal automatisms.PDF p.8, Vocal verbal and nonverbal automatisms

3 contributing manuscripts; source-reported values remain separate and are not pooled.

Conduction aphasiaReported: Left hemisphereAlso reported: Right hemisphere2 manuscripts · 3 findings · 0 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The review cites left dorsal STG or temporoparietal-junction damage in conduction aphasia; no seizure-side result is reported. The review proposes a left auditory-motor or speech-perception disruption with possible right-hemisphere compensation; no seizure lateralization result is reported. No lateralizing direction is reported for the cited conduction-aphasia case.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 2 findings
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • conduction aphasia and left dorsal STG or temporoparietal-junction lesionsThe review reports that damage to the left dorsal STG or temporoparietal junction is associated with conduction aphasia, characterized by good comprehension but frequent phonemic errors in speech production. It states that errors are more likely for longer, lower-frequency words and verbal repetition of strings with little semantic constraint, and that current evidence favors cortical dysfunction rather than a simple arcuate-fasciculus disconnection account.PDF p.8, “Lesion evidence for a sensorimotor dorsal stream”
  • conduction aphasia as auditory-motor interface disruptionThe authors interpret conduction aphasia as disruption of an auditory-motor interface, particularly at the segment-sequence level. They propose that comprehension is preserved because ventral pathways are spared and/or right-hemisphere speech systems compensate for left-hemisphere disruption, while phonological errors arise because sensory speech representations cannot provide online guidance for speech-sound sequencing.PDF p.8, conduction-aphasia interpretation immediately after lesion evidence
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Ictal conduction aphasiaThe review describes ictal conduction aphasia as inability to repeat with phonemic paraphasias and intact receptive language, naming, auditory, and written language; it was considered related to an arcuate fasciculus lesion but has also been observed during stimulation of the posterior superior temporal gyrus.PDF p.6, section 1.9

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal ear pluggingReported: Contralateral2 manuscripts · 2 findings · 3 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The review table restates unilateral ear plugging as contralateral to the seizure focus in TLE. The cited series reports unilateral ear plugging with seizure onset in the contralateral temporal-lobe auditory cortex.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • unilateral ear pluggingTable 2 lists unilateral ear plugging as a lateralizing sign associated with the superior temporal gyrus and contralateral lateralization in TLE.PDF p.5, Table 2
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Unilateral ear pluggingClarke et al. reported unilateral ear plugging in three cases, with seizure onset lateralized to the contralateral temporal lobe auditory cortex; the epileptogenic zone was confirmed by seizure freedom after surgery in two and presurgical epilepsy evaluation in one.PDF p.3, section 2.4 Auditory auras
Reported values
  • twoUnilateral ear pluggingCount · n/N 2/3 · Three case reports with unilateral ear plugging · unilateral ear-plugging cases · Ictal auraPDF p.3, section 2.4 Auditory auras
  • three casesUnilateral ear pluggingCount · n/N 3/3 · Three case reports with unilateral ear plugging · unilateral ear plugging · Ictal auraPDF p.3, section 2.4 Auditory auras
  • oneUnilateral ear pluggingCount · n/N 1/3 · Three case reports with unilateral ear plugging · unilateral ear-plugging cases · Ictal auraPDF p.3, section 2.4 Auditory auras

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal eye closureReported: Contralateral2 manuscripts · 4 findings · 2 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 case report or observation

The cited stimulation report elicited contralateral eye movement and eye closure in two patients. One depth-recorded case reports eye movements contralateral to the seizure discharge. No lateralizing direction is reported. No source lateralization is reported.

Source-defined result groups 3
Lateralization: ContralateralObserved proportion 100.0%All reported · ipsilateral eye movement · case1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · no contralateral eye response · patients1 manuscript · 1 reported value · not pooled
Localization: OccipitalSource-defined values retained separatelyAll reported · no contralateral eye response · patients1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfCase report or observation · 2 findings
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • cognitive ACC expressionMilder expressions such as discontent, disappointment, disagreement, or doubt, with closed eyes and without hypermotor features, were linked to the dorsal “cognitive” ACC.PDF p.8, Discussion
  • forced eye closureForced eye closure preceded or accompanied the chapeau de gendarme sign in the Figure 2 case.PDF p.7, Figure 2
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfCase report or observation · 2 findings · 2 reported values
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • contralateral eye movement and eye closure after stimulationContralateral eye movement and eye closure were elicited in two patients after stimulation of the lateral occipital cortex.PDF p.15, Cortical stimulation
  • contralateral eye movement in depth-recorded caseIn one patient studied with depth electrodes, eye movements were contralateral to the seizure discharge.PDF p.6, Results, Non-visual manifestations
Reported values
  • 2 patientscontralateral eye movement and eye closure after stimulationCount · two cited patients · stimulation responsePDF p.15, Cortical stimulation
  • 1 casecontralateral eye movement in depth-recorded caseCount · n/N 1/1 · one depth-recorded cohort patient · ictal manifestationPDF p.6, Results, Non-visual manifestations

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal piloerection (goosebumps)Reported: Ipsilateral2 manuscripts · 2 findings · 5 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

No lateralizing relationship is reported for piloerection. Unilateral or initially unilateral ictal piloerection was ipsilateral to the seizure focus in 4 of 5 recent-series cases and 12 of 14 literature-review cases.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • piloerection localizationThe source states that epileptic piloerection occurs predominantly in patients with TL seizures but has also been reported from frontal, fronto-parietal, fronto-temporal, parieto-occipital, and insular cortices.PDF p.8, Autonomic symptoms
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 5 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • Ictal piloerectionLoddenkemper et al. observed ictal piloerection in 14 of 3500 patients undergoing video/EEG monitoring; 5 of 14 had unilateral or initially unilateral piloerection, and 4 of these 5 were ipsilateral to the seizure focus, alongside 12 of 14 ipsilateral cases in the literature review.PDF p.3, section 2.6 Ipsilateral ictal piloerection
Reported values
  • 5 of 14 unilateral or initially unilateralIctal piloerectionPercentage · n/N 5/14 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · unilateral or initially unilateral · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 12 of 14 literature-review cases ipsilateralIctal piloerectionPercentage · n/N 12/14 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · literature review · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 84% as reportedIctal piloerectionPercentage · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · combined summary · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 4 of 5 recent-series cases ipsilateralIctal piloerectionPercentage · n/N 4/5 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · recent series · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection
  • 14 of 3500Ictal piloerectionPercentage · n/N 14/3500 · 3500 patients undergoing video/EEG monitoring; 14 with ictal piloerection; 5 with unilateral or initially unilateral piloerection · ictal piloerection · IctalPDF p.3, section 2.6 Ipsilateral ictal piloerection

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal speech or verbal automatismReported: Dominant hemisphereAlso reported: Non-dominant hemisphere2 manuscripts · 2 findings · 2 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 1 case report or observation · 1 narrative, educational, or cited context

The review restates opposite language-sign directions for aphasia and ictal speech/verbalization, with paraphasia described as not clearly lateralizing. No source-supported lateralizing direction is reported for the cited occipital-plus organization summary.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • aphasia; ictal speech; ictal verbalizationThe article states that aphasic seizures or aphasia are associated with dominant temporal/hemisphere seizures, whereas ictal speech or verbalization is generally interpreted as a non-dominant temporal/hemisphere sign.PDF p.2, Introduction; PDF p.3, Discussion
mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • altered conscious level; automatic motor behavior; verbal automatismsThe review reports that Marchi et al. (2016) found widespread epileptogenic-zone organization typical of occipital-plus epilepsy, with temporal and/or parietal cortex commonly involved; altered conscious level was more common with widespread posterior neocortical onset, while automatic motor behavior and/or verbal automatisms were more often seen with occipitotemporal organization.PDF p.6, Table 2, Occipital lobe row
Reported values
  • 29 subjectsaltered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy and 194 seizures · occipital-lobe epilepsy study · Seizure onset and semiologic expressionPDF p.6, Table 2, Occipital lobe row
  • 194 seizuresaltered conscious level; automatic motor behavior; verbal automatismsCount · 29 subjects with occipital-lobe epilepsy and 194 seizures · occipital-lobe epilepsy study · Seizure onset and semiologic expressionPDF p.6, Table 2, Occipital lobe row

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Ictal tongue biting / tongue deviation (contralateral)Source terms: Ictal tongue biting/deviation; Ictal tongue biting / tongue deviationReported: Ipsilateral2 manuscripts · 2 findings · 3 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

Unilateral tongue biting was ipsilateral to the epileptogenic side in five of seven focal-epilepsy patients. The handbook lists lateral tongue biting as ipsilateral but does not specify the reference side or viewpoint.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Lateral tongue bitingBoth tables list Lateral tongue biting as Ipsilateral.PDF p.2, Lateralizing signs/Localization table row "Lateral tongue biting" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Lateral tongue biting" (printed p.5)
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral tongue bitingIn focal epilepsy, unilateral tongue biting was ipsilateral to the epileptogenic side in five of seven patients.PDF p.11, section 5.7
Reported values
  • 7 focal-epilepsy patients had unilateral bitingunilateral tongue bitingCount · 106 patients; 7 focal-epilepsy patients and 1 generalized-epilepsy patient had unilateral tongue biting · focal epilepsy · peri-ictalPDF p.11, section 5.7
  • 5/7 focal-epilepsy patients (71%) ipsilateralunilateral tongue bitingPercentage · n/N 5/7 · 106 patients; 7 focal-epilepsy patients and 1 generalized-epilepsy patient had unilateral tongue biting · focal epilepsy · peri-ictalPDF p.11, section 5.7
  • 1 generalized-epilepsy patient had unilateral bitingunilateral tongue bitingCount · 106 patients; 7 focal-epilepsy patients and 1 generalized-epilepsy patient had unilateral tongue biting · generalized epilepsy · peri-ictalPDF p.11, section 5.7

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Lower facial weaknessReported: Contralateral2 manuscripts · 2 findings · 5 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The review restates predominantly contralateral lower facial weakness relative to a unilateral temporal-lobe focus, reported in 3/4 of the cited sample. The review restates predominantly contralateral emotional lower facial weakness relative to a unilateral temporal focus: 27/37 (73%) contralateral versus 13% ipsilateral, with facial asymmetry in 33% of controls.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Lower facial weakness or facial asymmetryLower facial weakness was reported contralateral to a unilateral temporal-lobe focus in 3/4 of a sample of 50 patients and was more prominent with mimetic movements.PDF p.5, facial weakness paragraph
Reported values
  • weakness more prominent with mimetic movementsLower facial weakness or facial asymmetryCount · n/N 3/4 · 50-patient sample with unilateral temporal-lobe focus as reported by the review. · Ictal facial manifestationPDF p.5, facial weakness paragraph
  • 3/4 of a sample of 50 patientsLower facial weakness or facial asymmetryCount · n/N 3/4 · 50-patient sample with unilateral temporal-lobe focus as reported by the review. · Ictal facial manifestationPDF p.5, facial weakness paragraph
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • emotional lower facial weaknessRemillard et al. found contralateral lower facial weakness more often than ipsilateral asymmetry in patients with a unilateral temporal focus.PDF p.7, section 3.11
Reported values
  • 27/37 (73%)emotional lower facial weaknessPercentage · n/N 27/37 · 50 prospectively examined patients, including 37 with a unilateral temporal focus, plus 25 controls without epilepsy · unilateral temporal focus · interictal examinationPDF p.7, section 3.11
  • 33%emotional lower facial weaknessPercentage · 50 prospectively examined patients, including 37 with a unilateral temporal focus, plus 25 controls without epilepsy · controls without epilepsy · interictal examinationPDF p.7, section 3.11
  • 13%emotional lower facial weaknessPercentage · 50 prospectively examined patients, including 37 with a unilateral temporal focus, plus 25 controls without epilepsy · unilateral temporal focus · interictal examinationPDF p.7, section 3.11

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Nocturnal hypermotor seizures from insular cortex (mimicking NFLE)Reported: Left hemisphere2 manuscripts · 2 findings · 0 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 1 narrative, educational, or cited context · 1 case report or observation

The sleep-related hypermotor phenotype record provides no lateralizing information. In this single case, seizure onset was in the left hemisphere, and right-sided sensory pain was contralateral to the left insular-opercular onset.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

mcgonigal-frontal-lobe-seizures-overview-update-2022.pdfNarrative, educational, or cited context · 1 finding
mcgonigal-frontal-lobe-seizures-overview-update-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This document is a review/Neurological Update and reports or synthesizes observations from multiple SEEG, intracerebral-recording, and other cited series rather than a single study population. It specifically describes a cited SEEG series of 54 patients with FLE and a cited series of 42 patients with prefrontal seizures for emotional prevalence; other cited cohort sizes, ascertainment details, reference standards, and region-specific denominators are not reported in the document. The review frames its electroclinical correlations as group-level aids for presurgical sublobar hypotheses. It states that both seizure onset and propagation contribute to semiological expression and distinguishes elementary motor signs from complex motor behavior.
Findings
  • sleep-related hypermotor phenotype with frontal and extra-frontal localizationsThe review states that many previously termed nocturnal frontal lobe epilepsy cases had confirmed frontal localizations on intracerebral EEG, including orbitofrontal cortex, anterior cingulate, and supplementary motor area, while similar sleep-related hypermotor seizure phenotypes may also arise from extra-frontal localizations including insula; it presents Sleep-Related Hypermotor Epilepsies as broader terminology reflecting this localization range.PDF p.5, Frontal seizures and genetics
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 2 left posterior/midposterior insular and opercular localizationIn Case 2, unilateral left interictal abnormalities, centro-temporal seizure onset, right-sided sensory pain and auditory auras, and late hypermotor manifestations were interpreted as favoring a left posterior or midposterior insular and temporo-parietal opercular origin with frontal propagation rather than primary frontal onset; invasive recordings showed preictal spikes over parietal-opercular and posterior-insular contacts followed by low-voltage fast activity in the same contacts, and the patient remained seizure-free 1.5 years after left posterior insulectomy and partial parietal opercular resection.PDF p.13, Video-EEG data; PDF p.14, What locations should be sampled based on semiology and EEG findings?; PDF p.15, invasive findings and auditory triggers

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal or peri-ictal amnesiaReported: Bilateral2 manuscripts · 2 findings · 0 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The cited studies are restated as linking absent aura experience with bitemporal dysfunction. The review states that postictal amnesia likely reflects bilateral hippocampal impairment and that retrograde/anterograde amnesia is variable.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • amnesia of aura and bitemporal dysfunctionThe source states that some cited studies found lack of aura experience to correlate strongly with indicators of bitemporal dysfunction.PDF p.9, Post-ictal signs
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Amnesia and bilateral hippocampal impairmentThe review states that patients with CPSs may be unaware of a recent seizure and may have variable retrograde and anterograde amnesia; it attributes postictal amnesia likely to bilateral impairment of hippocampal function.PDF p.2, section 2.4 Amnesia

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal verbal memory impairmentReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere2 manuscripts · 3 findings · 2 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The review assigns postictal verbal-memory impairment and aphasia to dominant-hemisphere suggestion and visual-memory impairment to nondominant-hemisphere suggestion. The review associates immediate postictal verbal-memory decline with left temporal seizures and visual-memory decline with right temporal seizures. The cited study associated impaired 24-hour verbal retention with left, but not right, temporal seizures.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal verbal and visual memory impairment and postictal aphasiaPostictal verbal memory impairment is suggestive of a dominant-hemisphere temporal focus, visual memory impairment of a nondominant-hemisphere focus, and postictal aphasia strongly suggests a dominant-hemisphere focus.PDF p.9, Postictal state
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal verbal and visual memory impairmentLeft temporal seizures are associated with immediate postictal verbal-memory decline, whereas right temporal seizures are associated with visual-memory decline.PDF p.11, section 5.9
  • verbal memory impairment across a 24-hour retention intervalLeft, but not right, temporal seizures were associated with impaired verbal memory over a 24-hour retention interval.PDF p.11, section 5.9
Reported values
  • memory was significantly better on days without seizuresverbal memory impairment across a 24-hour retention intervalCount · 10 patients with unilateral TLE demonstrated by video/EEG · postictal 24-hour retention intervalPDF p.11, section 5.9
  • 10 patientsverbal memory impairment across a 24-hour retention intervalCount · 10 patients with unilateral TLE demonstrated by video/EEG · postictal 24-hour retention intervalPDF p.11, section 5.9

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal visual memory impairmentReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphereAlso reported: Right hemisphere2 manuscripts · 2 findings · 0 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The review assigns postictal verbal-memory impairment and aphasia to dominant-hemisphere suggestion and visual-memory impairment to nondominant-hemisphere suggestion. The review associates immediate postictal verbal-memory decline with left temporal seizures and visual-memory decline with right temporal seizures.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal verbal and visual memory impairment and postictal aphasiaPostictal verbal memory impairment is suggestive of a dominant-hemisphere temporal focus, visual memory impairment of a nondominant-hemisphere focus, and postictal aphasia strongly suggests a dominant-hemisphere focus.PDF p.9, Postictal state
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal verbal and visual memory impairmentLeft temporal seizures are associated with immediate postictal verbal-memory decline, whereas right temporal seizures are associated with visual-memory decline.PDF p.11, section 5.9

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Auditory verbal hallucinations (voices, speech, words)Source terms: Auditory verbal hallucinationsReported: Left hemisphereAlso reported: Right hemisphere2 manuscripts · 2 findings · 3 reported values
Weighted evidence supportevidence weight 1.9 across 2 manuscripts · 2 case report or observation

A left-hemisphere seizure was maximal in the temporal region with right facial, hand, and somatic signs; sound laterality was not identified. The synthesis reports a right-hemisphere stimulation predominance for verbal hallucinations, with no general hemisphere rule for all auditory percept types.

Source-defined result groups 2
Lateralization: Left hemisphere / Right hemisphereSource-defined values retained separatelyAll reported · Seizure/event1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizure/event1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 1 finding · 2 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)In the cortical-stimulation synthesis, SH were mainly induced by posterior insula and Heschl’s gyrus (HG); CH by STG, STS, mesiotemporal structures, and insula; I by STG, HG, STS, and temporal plane with about one-third from extratemporal structures; VH included 60% produced by right-hemisphere stimulation, mostly STG; MH involved STG, HG, temporal plane, and SMG; HD involved temporal structures and insula, especially PLST, posterior STG, and HG; and few PAL reports were identified.PDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
Reported values
  • Verbal hallucinations from right-hemisphere stimulation 60%simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Verbal hallucinations · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • Auditory illusions from extratemporal stimulation about one-thirdsimple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Auditory illusions · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
palinacousis-seven-new-cases.pdfCase report or observation · 1 finding · 1 reported value
palinacousis-seven-new-cases.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • ictal repeating television voicesDuring recurrent continuous-EEG seizures in a woman with mainly left-sided glioblastoma, television voices repeated throughout the seizure for 1 to 2 minutes alongside right facial twitching, worsened aphasia, and a right-hand sensation, without identified auditory laterality.PDF p.1, Results case 3; PDF p.2, Table 1 case 3; PDF p.4, Discussion
Reported values
  • Repeating voices lasted for the seizure duration, reported as 1-2 minutesictal repeating television voicesCount · 58-year-old woman with mainly left-sided glioblastoma multiforme and left parietal lesion with adjacent left insular and temporal abnormalities in Table 1 · IctalPDF p.1, Results case 3; PDF p.2, Table 1 case 3; PDF p.4, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Bilateral tonic seizureReported: Bilateral2 manuscripts · 3 findings · 0 reported values
Weighted evidence supportevidence weight 1.9 across 2 manuscripts · 2 case report or observation

The case reports right orbitofrontal onset with later bilateral tonic propagation. The case reports bilateral asymmetric tonic manifestations without a cerebral side assignment. Case 3 had bilateral asymmetric tonic manifestations.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfCase report or observation · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • hyperkinetic seizure; bilateral tonic seizureIn an illustrative 24-year-old man with sleep-related hyperkinetic seizures, PET and stereo-EEG supported a right orbitofrontal source; seizures progressed to bilateral tonic seizures with loss of awareness, and the patient was seizure-free after right orbitofrontal resection.PDF p.4, Video case 2 and Figure 3 caption
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdfCase report or observation · 2 findings
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study enrolled seven consecutive PCE patients; six had SEEG-identified posterior cingulate ictal onset and one had an MRI-identified postcingulate tumour. Four patients underwent CCEP. SEEG and scalp EEG were retrospectively analyzed with video-documented ictal semiology; the source used the Lüders seizure-classification scheme. The posterior cingulate was operationally defined caudal to the vertical posterior commissure line.
Findings
  • Case 2 bilateral tonic spreadDuring Case 2 bilateral asymmetric tonic manifestations, ictal activity spread to the anterior and posterior cingulate gyri and the supplementary motor area.PDF p.5, Ictal semiology and SEEG findings; PDF p.3, Figure 1
  • Case 3 bilateral tonic spreadDuring Case 3 bilateral asymmetric tonic manifestations, ictal activity spread to the anterior cingulate gyrus, supplementary motor area, precuneus, dorsolateral premotor area, postcentral gyrus, and inferior parietal lobule.PDF p.5, Ictal semiology and SEEG findings; PDF p.3, Figure 1

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal apneaReported: Left hemisphere2 manuscripts · 2 findings · 4 reported values
Weighted evidence supportevidence weight 1.9 across 2 manuscripts · 1 narrative, educational, or cited context · 1 case report or observation

The illustrated apnea occurred during one source-labeled left frontotemporal seizure. No lateralizing direction is reported for ictal versus postictal central apnoea.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfCase report or observation · 1 finding · 4 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • ictal apnea extending into the postictal period in case MO#12In the illustrated MO#12 left frontotemporal seizure, apnea began 20 seconds before scalp EEG seizure onset, persisted for about 15 seconds after EEG termination, and was followed by two brief postictal apnea episodes with progressive oxygen desaturation to below 80%.PDF p.7, Figure 2A caption
Reported values
  • below 80%ictal apnea extending into the postictal period in case MO#12Threshold · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • two brief postictal apnea episodesictal apnea extending into the postictal period in case MO#12Count · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • approximately 15 secondsictal apnea extending into the postictal period in case MO#12Other reported value · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
  • 20 seconds beforeictal apnea extending into the postictal period in case MO#12Other reported value · Individual patient MO#12 with a left frontotemporal lobe seizure · case MO#12 · preictal/ictal-to-postictal and postictalPDF p.7, Figure 2A caption
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdfNarrative, educational, or cited context · 1 finding
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study enrolled 2632 children and adults with epilepsy at nine epilepsy-monitoring centres in the USA and UK between 2011 and 2021; 164 were lost to follow-up and 2468 participants were included in the primary follow-up analyses. There were 38 SUDEP outcomes and two near-SUDEP events. During admission, 1660 participants had seizures captured, 1432 had analysable seizures, and the report describes 1091 analysable generalised convulsive seizures and 2117 non-convulsive seizures. The primary endpoint was time to SUDEP or censoring due to other causes. Cox proportional hazards models assessed clinical and electroclinical predictors; repeated seizure predictors were aggregated to the most severe feature per patient, using the maximum for continuous features or presence for categorical features. Analyses used prolonged video-EEG, ECG, pulse oximetry, and chest/abdominal inductance plethysmography. Statistical significance in primary analyses required two-sided p<0.05 after Bonferroni correction; the report states that secondary-analysis confidence intervals were not intended for hypothesis testing. Main-text results include varying denominators and missing data, which are retained below.
Findings
  • ictal central apnoea; postictal central apnoeaThe Discussion restates that ictal central apnoea is associated with postictal central apnoea, suggesting that individuals with ictal central apnoea are more likely to develop postictal breathing cessation.PDF p.9, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

clinically eloquent insular stimulationReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1.8 across 1 manuscript · 1 narrative, educational, or cited context

The 237 right-insula and 313 left-insula responses report the distribution of sampled eloquent responses, not a lateralizing direction or side-specific response rate.

Source-defined result groups 1
Localization: InsularObserved proportion 82.2%clinically eloquent without postdischarge · non-eloquent stimulation · stimulation1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.80 · 1 × 0.9 × 2
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • clinically eloquent insular stimulationIn the authors' stimulation series, 550 of 669 insular stimulations (82.2%) evoked a clinical response in the absence of a postdischarge; 237 responses followed right-insula stimulation and 313 followed left-insula stimulation (43% and 57%).PDF p.1, abstract; PDF p.3, Results; PDF p.6, Discussion
Reported values
  • 313/550 (57%)clinically eloquent insular stimulationPercentage · n/N 313/550 · 222 patients undergoing presurgical SEEG; 669 insular stimulation sites · left-insula stimulation · stimulation-evoked clinical responsePDF p.1, abstract; PDF p.3, Results; PDF p.6, Discussion
  • 237/550 (43%)clinically eloquent insular stimulationPercentage · n/N 237/550 · 222 patients undergoing presurgical SEEG; 669 insular stimulation sites · right-insula stimulation · stimulation-evoked clinical responsePDF p.1, abstract; PDF p.3, Results; PDF p.6, Discussion
  • 550 of 669 (82.2%)clinically eloquent insular stimulationPercentage · n/N 550/669 · 222 patients undergoing presurgical SEEG; 669 insular stimulation sites · clinically eloquent without postdischarge · stimulation-evoked clinical responsePDF p.1, abstract; PDF p.3, Results; PDF p.6, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

distal hand muscles belonging to the thenar eminence contractReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1.8 across 1 manuscript · 1 independent primary study

MCC stimulation S6 was associated with a source-table label of upper-limb distribution contralateral to stimulation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • distal hand muscles belonging to the thenar eminence contractMCC stimulation S6 in Patient 5 elicited a feeling that distal hand muscles belonging to the thenar eminence contracted, although no movement of the hand or fingers was observed.PDF p.5, Section 3.1 Clinical effects; PDF p.7, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

group-level network reorganization in SYM versus NS conditionsReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1.8 across 1 manuscript · 1 independent primary study

SYM stimulation showed a group-level left-versus-right asymmetry in network connectivity, with region-specific increases and decreases in each hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdfIndependent primary study · 1 finding
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
Patients underwent phase-two invasive presurgical evaluation at the University Emergency Hospital Bucharest or Strasbourg University Hospital between 2000 and 2017. The source reviewed 110 patients whose cingulate cortex was sampled and functionally mapped and included 12 right-handed patients with body-perception changes: 8 from Bucharest and 4 from Strasbourg. All had focal drug-resistant epilepsy; the epileptogenic zone was frontal in 9 patients, temporo-basal in 1, insular-opercular in 1, and insular in 1. Patients were selected when at least one electrode sampled cingulate cortex outside the epileptogenic zone; cognitive or psychiatric comorbidity judged likely to interfere with reliable interaction was excluded. Structures and stimulation sites were selected for clinical presurgical purposes, not for this study. The source reports no visible MRI lesion in the included patients and states that the stimulated locations did not overlap the delineated epileptogenic zone in the two patients who did not undergo surgery. Functional mapping used bipolar high-frequency stimulation at 50 Hz for 5 s through adjacent contacts with biphasic 1 ms pulses; current was gradually increased from 0.1 to 3 mA until a clinical or electrical response. Patients reported psychological or physical changes during or after stimulation. Body-representation changes were analyzed at the lowest intensity that evoked a symptom (SYM target group) and compared with typically half-intensity stimulations without a symptom (NS control group); after-discharges, auras, and seizures were excluded. Repeated trials, including 0 mA sham trials, were used for response consistency and psychogenic-event control. The separate connectivity analysis used h2 values from nonstimulated contacts in 10-s PRESTIM and 5-s POSTSTIM epochs; those network measurements are kept distinct from the semiologic findings below. No independent reference standard was reported for the subjective stimulation responses.
Findings
  • group-level network reorganization in SYM versus NS conditionsThe source's group-level network summary associates SYM stimulation with generally fewer connections in the left hemisphere, except increased connectivity in VMPFC', MOFC', and OpF', and with increased connectivity in right ACC, MCC, SMA, R, S, F, MTG, ITG, aI, pI, and O but decreased connectivity in right MOFC, A, Hc, OpF, and PCC.PDF p.8, Section 3.4 Network characterization; PDF p.10, Discussion; PDF p.11, Figure 7 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

transient nominal dysphasia after operationReported: Dominant hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1.8 across 1 manuscript · 1 independent primary study

Transient nominal dysphasia after dominant temporal surgery is postoperative context, not a seizure lateralizing sign.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdfIndependent primary study · 1 finding · 1 reported value
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
Independent primary study · Class II · Evidence weight 1.80 · 2 × 0.9 × 1
The first 100 consecutive patients with temporal lobe epilepsy operated on by anterior temporal lobectomy were studied; pre-operative documentation recorded the presence or absence and nature of speech disturbance connected with fits, and follow-up was mostly by personal interview for 2-10 years. The operated side was used as an imperfect reference for the presumed primary epileptogenic site: Group A comprised 53 patients who became seizure-free or almost so and were presumed correctly diagnosed, while Group B comprised 47 patients with continuing attacks and lower localization validity, including 30 improved patients and 17 slightly benefited or unchanged patients. Table I reports 56 left-sided and 44 right-sided resections. All patients had pre-operative psychomotor seizures and many also had grand mal attacks. All but three patients were right-handed for ordinary tasks; cerebral speech dominance was presumed from left-sided resection in right-handed persons because intracarotid sodium amytal testing had not yet been used in doubtful cases.
Findings
  • transient nominal dysphasia after operationThe authors report transient nominal dysphasia in the first post-operative month in about half of the pre-operative ictal-dysphasia cases, whereas post-operative dysphasia was minimal in patients with speech automatisms or no recorded speech disorder who underwent dominant temporal lobectomy.PDF p.9, discussion point (2)
Reported values
  • about half of the pre-operative ictal-dysphasia casestransient nominal dysphasia after operationPercentage · Patients with pre-operative ictal dysphasia compared with patients with speech automatisms or no recorded speech disorder undergoing dominant temporal lobectomy · pre-operative ictal dysphasia · First post-operative monthPDF p.9, discussion point (2)

1 contributing manuscript; source-reported values remain separate and are not pooled.

vestibular direction, laterality, and classificationReported: Left hemisphereAlso reported: Right hemisphereNo single reliable side1 manuscript · 1 finding · 15 reported values
Weighted evidence supportevidence weight 1.62 across 1 manuscript · 1 narrative, educational, or cited context

Insular stimulation evoked mixed vestibular directions: fall direction was unrelated to stimulation side, and clockwise responses followed right-sided stimulation in 3/5 and left-sided stimulation in 2/5.

Source-defined result groups 2
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 60.0%clockwise response after right-sided stimulation · left-sided stimulation · evoked vestibular response1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Does not lateralize / Right hemisphereObserved proportion 40.0%clockwise response after left-sided stimulation · right-sided stimulation · evoked vestibular response1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 15 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.62 · 1 × 0.9 × 1.806
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • vestibular direction, laterality, and classificationVestibular responses included translation illusions in 14/41 (34.1%) and rotation illusions in 9/41 (21.9%); translation included levitation/flying (5/14), rising (3/14), or falling (6/14), and fall direction was unrelated to stimulation side. Yaw-plane rotation was most common (7/9), with source-reported clockwise 5/7 and counterclockwise 2/5 responses; clockwise responses followed right-sided stimulation in 3/5 and left-sided stimulation in 2/5, roll-plane illusions numbered 2, and 18/41 (43.9%) responses could not be precisely classified.PDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
Reported values
  • 14/41 (34.1%)vestibular direction, laterality, and classificationPercentage · n/N 14/41 · 41 vestibular responses in the 550-response series · translation illusions · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 3/5vestibular direction, laterality, and classificationCount · n/N 3/5 · 41 vestibular responses in the 550-response series · clockwise response after right-sided stimulation · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 18/41 (43.9%)vestibular direction, laterality, and classificationPercentage · n/N 18/41 · 41 vestibular responses in the 550-response series · not precisely classified · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 5/14vestibular direction, laterality, and classificationCount · n/N 5/14 · 41 vestibular responses in the 550-response series · levitation or flying · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 6/14vestibular direction, laterality, and classificationCount · n/N 6/14 · 41 vestibular responses in the 550-response series · falling · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • n=14vestibular direction, laterality, and classificationCount · n/N 14/18 · 41 vestibular responses in the 550-response series · head spinning · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 2/5vestibular direction, laterality, and classificationCount · n/N 2/5 · 41 vestibular responses in the 550-response series · clockwise response after left-sided stimulation · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • n=1vestibular direction, laterality, and classificationCount · n/N 1/18 · 41 vestibular responses in the 550-response series · loss of visual landmarks · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 7/9vestibular direction, laterality, and classificationCount · n/N 7/9 · 41 vestibular responses in the 550-response series · yaw-plane rotation · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 2/5vestibular direction, laterality, and classificationCount · n/N 2/5 · 41 vestibular responses in the 550-response series · counterclockwise yaw-plane rotation · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 9/41 (21.9%)vestibular direction, laterality, and classificationPercentage · n/N 9/41 · 41 vestibular responses in the 550-response series · rotation illusions · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 3/14vestibular direction, laterality, and classificationCount · n/N 3/14 · 41 vestibular responses in the 550-response series · rising · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • n=3vestibular direction, laterality, and classificationCount · n/N 3/18 · 41 vestibular responses in the 550-response series · instability · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 5/7vestibular direction, laterality, and classificationCount · n/N 5/7 · 41 vestibular responses in the 550-response series · clockwise yaw-plane rotation · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B
  • 2vestibular direction, laterality, and classificationCount · 41 vestibular responses in the 550-response series · roll-plane illusions · stimulation-evoked vestibular responsePDF p.5, Other Types of Evoked Sensations; PDF p.6, continuation and Fig. 5B

1 contributing manuscript; source-reported values remain separate and are not pooled.

to bilateral tonic-clonic seizuresReported: Bilateral1 manuscript · 2 findings · 2 reported values
Weighted evidence supportevidence weight 1.58 across 1 manuscript · 1 narrative, educational, or cited context

The source reports absence of focal-to-bilateral tonic-clonic seizures in this cohort, not a lateralizing sign. The finding reports focal-to-bilateral evolution, not lateralization.

Source-defined result groups 1
Localization: OFC-extended EZNObserved proportion 18.2%OFC-extended EZN group · patients with FBTC1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.58 · 1 × 0.9 × 1.759
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • focal to bilateral tonic-clonic seizures; restricted OFCNo restricted-OFC case was reported to have a focal to bilateral tonic-clonic seizure.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • focal to bilateral tonic-clonic seizures; OFC-extended EZNFocal to bilateral tonic-clonic seizures were reported in six of 33 OFC-extended cases.PDF p.3, Semiological patterns of seizures with EZN extending beyond the OFC
Reported values
  • 0 casesfocal to bilateral tonic-clonic seizures; restricted OFCCount · n/N 0/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictal evolutionPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
  • 6/33 (18.1%)focal to bilateral tonic-clonic seizures; OFC-extended EZNPercentage · n/N 6/33 · OFC-extended EZN group · OFC-extended EZN group · ictal evolutionPDF p.3, Semiological patterns of seizures with EZN extending beyond the OFC

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal forced eye deviationReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1.5 across 1 manuscript · 1 case report or observation

Both reported cases had forced eye deviation ipsilateral to the epileptic focus as the initial clinical sign.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdfCase report or observation · 1 finding
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
Case report or observation · Class III · Evidence weight 1.50 · 1 × 1.5 × 1
This is a two-case report with no control or comparator group. Case-1 was a 24-year-old right-handed man; 32 habitual seizures were recorded during 3 days of scalp video-EEG, with two followed by secondary GTCS, and two right-hemisphere SEEG implantations were performed 4 months apart. Case-2 was a 19-year-old right-handed man; three habitual seizures were captured on video-EEG and right temporal neocortical, temporal-pole, and medial-structure regions were explored with SEEG. The source describes scalp EEG, MRI, FDG-PET, SEEG onset and propagation, anatomical reconstruction, cortical resection, and seizure-free follow-up of 17 months for Case-1 and 25 months for Case-2. Case-1 MRI/FDG-PET was reported unremarkable for an evaluable lesion; Case-2 MRI and PET findings were reported in the right middle-posterior inferior temporal/fusiform and medial temporal regions. No cohort-wide denominator for ipsiversive eye deviation, no control comparison, and no population-level frequency or diagnostic statistic are reported.
Findings
  • Two-case ipsiversive eye deviation with inferioposterior temporal and MT/MST-overlap localizationAcross the two reported cases, the source reports forced ipsilateral eye deviation as the initial clinical sign and ictal SEEG localization of the epileptogenic zones to the inferioposterior temporal region; the authors further report overlap between the epileptogenic zones and the human MT/MST complex, especially human MST on the anterior/dorsal bank of AOS.PDF p.1, Abstract; PDF p.8, Discussion; PDF p.9, Discussion and Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Preserved ictal speechReported: Dominant hemisphereAlso reported: Non-dominant hemisphere2 manuscripts · 3 findings · 3 reported values
Weighted evidence supportevidence weight 1 across 2 manuscripts · 1 manuscript weight pending · 1 structured design not resolved · 1 narrative, educational, or cited context

Normal ictal speech occurred in nine nondominant-hemisphere seizures from two patients and in no dominant-hemisphere seizures. The discussion restates nondominant temporal onset for ictal normal speech and dominant-hemisphere onset for dysphasia. The review states that preserved ictal speech predicts a nondominant-hemisphere seizure origin.

Source-defined result groups 3
Lateralization: Non-dominant hemisphereSource-defined values retained separatelyNondominant-hemisphere seizures (NHS) · Dominant-hemisphere seizures (DHS) · patient1 manuscript · 1 reported value · not pooled
Lateralization: Non-dominant hemisphereObserved proportion 0.0%Dominant-hemisphere seizures (DHS) · Nondominant-hemisphere seizures (NHS) · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Non-dominant hemisphereObserved proportion 7.8%Nondominant-hemisphere seizures (NHS) · Dominant-hemisphere seizures (DHS) · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Ictal speech preservationIctal speech preservation reliably predicts seizures of nondominant-hemisphere origin.PDF p.4, Table 2; PDF p.5, language-disturbances paragraph
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 2 findings · 3 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • ictal normal speechNormal speech during seizures was associated with nondominant-hemisphere onset rather than dominant-hemisphere onset in the source cohort.PDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • ictal normal speech and dysphasia in prior video/EEG reportsThe discussion states that prior video/EEG analyses confirmed the source’s directional language conclusion: ictal normal speech with nondominant temporal onset and dysphasia with dominant-hemisphere onset.PDF p.6, Discussion
Reported values
  • 2 patients with NHS seizures and ictal normal speechictal normal speechCount · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Nondominant-hemisphere seizures (NHS) · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • DHS 0/116 seizures (0%)ictal normal speechPercentage · n/N 0/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Dominant-hemisphere seizures (DHS) · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion
  • NHS 9/116 seizures (8%)ictal normal speechPercentage · n/N 9/116 · 19 patients with unilateral TLE; 65 NHS seizures and 51 DHS seizures · Nondominant-hemisphere seizures (NHS) · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.5, Figure 2; PDF p.6, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

ALA speech-dominance lateralizationReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Strictly unilateral posterior-inferior-frontal speech arrest during naming correctly identified language dominance in the cited four-patient study.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • ALA speech-dominance lateralizationThe review reports that Alonso et al. used bilateral symmetric implantation in four patients and obtained speech arrest only after strictly unilateral posterior inferior frontal gyrus ECS during naming, correctly lateralizing ALA language dominance.PDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

AlexiaReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review associates paraphasic errors and alexia with seizures originating in the dominant hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Paraphasic errors and alexiaParaphasic errors and alexia are reported as clearly associated with CPSs originating in the dominant hemisphere.PDF p.5, language-disturbances paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

anterior temporal lobe (ATL) syntactic and compositional processingReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes bilateral semantic-dementia atrophy with broader temporal, caudate, and right thalamic involvement, without a seizure-related hemispheric direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • anterior temporal lobe (ATL) syntactic and compositional processingThe review states that functional-imaging studies show portions of the ATL are more active for sentences than for unstructured lists of words or sounds, and that ATL damage has been linked to deficits in comprehending complex syntactic structures. It also reports contradictory semantic-dementia evidence, including good sentence-level comprehension, and concludes that neuroimaging supports an ATL role in syntactic or compositional operations while neuropsychological evidence remains equivocal.PDF p.6, anterior temporal and lexical-semantic discussion; PDF p.7, ATL summary

1 contributing manuscript; source-reported values remain separate and are not pooled.

anterotemporal IED lateralization and spike-rate prognostic associationsReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review states that anterotemporal interictal discharges predicted ipsilateral temporal seizure onset and that predominance on the surgical side was prognostically favorable.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • anterotemporal IED lateralization and spike-rate prognostic associationsIEDs predominantly localized to the surgical side often predict good outcome, and anterotemporal IEDs accurately predicted seizure onset in the ipsilateral temporal lobe in the cited TLE description; high spike rates were associated with longer epilepsy duration, while low spike rates were proposed to correlate with less severe epilepsy.PDF p.12, Lateralizing and prognostic value of IEDs on TLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

AnxiolysisReported: Left hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The left stimulation site is procedural context, not a lateralizing semiologic relationship.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • positive affect and anxiolysis; left dorsal anterior cingulum bundle stimulationThe source reports that its group evoked positive affect and anxiolysis by stimulating the left dorsal anterior cingulum bundle in four patients and used the response during intraoperative cognitive mapping without anesthesia sedation.PDF p.13, socio-emotional stimulation paragraph
Reported values
  • total tested-patient denominator not reportedpositive affect and anxiolysis; left dorsal anterior cingulum bundle stimulationCount · Four patients in the cited cingulum-stimulation report · stimulation-induced emotional response during cognitive mappingPDF p.13, socio-emotional stimulation paragraph
  • positive affect and anxiolysis evoked in 4 patientspositive affect and anxiolysis; left dorsal anterior cingulum bundle stimulationCount · Four patients in the cited cingulum-stimulation report · stimulation-induced emotional response during cognitive mappingPDF p.13, socio-emotional stimulation paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

aphasic fit and speech arrest distinctionReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates that right lesions were frequently found in speech-arrest cases, without a seizure-origin lateralization estimate.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

ictal-speech-disturbance-cerebral-dominance.pdfNarrative, educational, or cited context · 1 finding
ictal-speech-disturbance-cerebral-dominance.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors collected about 43 cases with ictal speech disturbances over 8 years. Interictal EEG was examined at least twice per case; laterality was defined by a spike or sharp-wave focus, unilateral dominant spike or sharp wave, or unilateral slow wave corresponding to same-region brain damage or tumor. Laterality was confirmed in 36 cases; 7 cases with independent foci, no laterality, or normal findings were excluded. The statistical report concerns 34 right-handed epileptics because 2 left-handed patients could not be tested statistically. A control pool comprised 243 right-handed patients with unilateral abnormal EEG findings, 136 left and 117 right, and was assessed by t test.
Findings
  • aphasic fit and speech arrest distinctionThe current article reports that Hecaen and colleagues did not discriminate between aphasic fit and speech arrest, and that right lesions were also frequently found in the speech-arrest cases.PDF p.4, Discussion paragraph beginning “The present results are in complete accordance”

1 contributing manuscript; source-reported values remain separate and are not pooled.

auditory detection after pulvinar lesionReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

A cited lesion case detected sounds ipsilateral to a right pulvinar lesion; this is lesion-side sensory performance, not seizure lateralization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfCase report or observation · 1 finding
e236615-full.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • auditory detection after pulvinar lesionThe source reports that Hugdahl and colleagues described a patient performing above average in detecting sounds ipsilateral to a right pulvinar lesion.PDF p.4, Discussion; PDF p.5, reference 32

1 contributing manuscript; source-reported values remain separate and are not pooled.

auditory-motor integration and phonological short-term memoryReported: Dominant hemisphereAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review model describes the proposed auditory dorsal stream as strongly left-dominant.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • auditory-motor integration and phonological short-term memoryThe authors propose that the auditory dorsal stream interfaces with the motor system, serves speech development and continues to function in adults, and provides basic mechanisms for phonological short-term memory. They distinguish segment-level auditory-motor processes for acquisition and maintenance of articulatory phonetic skills from segment-sequence processes for new vocabulary and online guidance of speech sequences.PDF p.7, “The need for auditory-motor integration”; PDF p.7, segment and segment-sequence discussion; PDF p.9, summary

1 contributing manuscript; source-reported values remain separate and are not pooled.

Automatism + contralateral posturing combined (AP sign)Reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited Dupont series is restated as predominantly ipsilateral automatisms in mesial TLE, exclusively contralateral automatisms in neocortical TLE, and contralateral dystonia plus ipsilateral automatisms only in mesial TLE.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • unilateral motor automatisms with dystonic posturingDupont et al. reported predominantly ipsilateral automatisms in mesial TLE, exclusively contralateral automatisms in neocortical TLE, and the combination of contralateral dystonia with ipsilateral automatisms only in mesial TLE.PDF p.6, section 3.9
Reported values
  • 26/60 had unilateral motor automatismsunilateral motor automatisms with dystonic posturingCount · n/N 26/60 · 60 patients with temporal lobe epilepsy, including 26 with unilateral motor automatisms · ictalPDF p.6, section 3.9

1 contributing manuscript; source-reported values remain separate and are not pooled.

basal temporal language area (BTLA)Reported: Dominant hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review places the BTLA in dominant or left ventral temporal structures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • basal temporal language area (BTLA)The review places the BTLA in dominant or left ventral temporal structures including fusiform, inferior temporal, and parahippocampal gyri about 1-9 cm from the temporal pole, and reports extension of its mapped territory to the lateral occipito-temporal sulcus with sEEG.PDF p.5, Figure 1 and caption; PDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG
Reported values
  • 1-9 cm from the temporal polebasal temporal language area (BTLA)Count · published ECoG and sEEG BTLA mapping studies; study-specific populations vary and are not pooled · ECS language mappingPDF p.5, Figure 1 and caption; PDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Bilateral asymmetric tonic seizure (BATS) at secondary generalizationReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review states that tonic face and versive signs point contralaterally, M2e points contralateral to the raised arm, and the sign of four points contralateral to the extended arm.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • motor sequence in secondarily generalized tonic-clonic seizuresThe review describes a sequence beginning with version and tonic pulling of the face to the contralateral side, followed by the M2e fencing position and then asymmetric tonic limb posturing called the “sign of four.” It states that confidence in lateralizing the epileptogenic zone increases when at least two of the four signs are observed; the tonic face and versive signs point contralaterally, M2e points to the hemisphere contralateral to the raised arm, and the sign of four to the hemisphere contralateral to the extended arm. These signs lateralize but do not localize seizure origin.PDF p.4, Tonic seizures
Reported values
  • Confidence stated when 2 or more of 4 signs are observedmotor sequence in secondarily generalized tonic-clonic seizuresCount · n/N 2/4 · Patients with secondarily generalized tonic-clonic seizures; no cohort reported · Ictal motor sequence before secondary generalizationPDF p.4, Tonic seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

Bilateral asymmetric, axial, and generalized modifiersReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

An educational classification framework permits bilateral, asymmetric, axial, and generalized modifiers.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Bilateral asymmetric, axial, and generalized modifiersBilateral asymmetric denotes bilateral symptoms with significant asymmetry and suggests focal epilepsy; generalized denotes widespread manifestations with approximately equal involvement of both sides and distal and proximal segments; axial denotes predominant trunk and proximal-extremity involvement, and the source cautions that focal epilepsies may have axial or generalized seizures and generalized epilepsies may have focal elements.PDF p.6, Table 2; PDF p.6, Somatotopic modifiers

1 contributing manuscript; source-reported values remain separate and are not pooled.

bilateral speech recognition and word deafnessReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited literature describes at least one speech-recognition pathway in each hemisphere, bilateral superior-temporal damage with word deafness, and rare focal unilateral exceptions.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • bilateral speech recognition and word deafnessThe review reports that evidence from unilateral damage to either hemisphere, split-brain patients, and Wada procedures indicates that probably at least one pathway in each hemisphere can process speech sufficiently to access the mental lexicon. It also reports that bilateral superior-temporal damage is associated with severe speech-recognition deficits termed word deafness, whereas focal unilateral lesions can rarely produce word deafness and are described as an exception rather than the rule.PDF p.3, “Parallel computations and bilateral organization”; PDF p.3, unilateral and bilateral lesion discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

bilateral STG and STS activation during speech processingReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review characterizes speech-perception activation as predominantly bilateral in dorsal STG/STS, while acknowledging occasional left-only results.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • bilateral STG and STS activation during speech processingThe review characterizes bilateral STG activation, including dorsal STG and STS, as a consistent finding when speech listening is contrasted with rest, and states that most speech-versus-non-speech studies find bilateral STS activation. It notes that some studies show more extensive activation or activation only in the left hemisphere, but argues that such findings do not refute bilateral speech processing because control subtraction and non-categorical right-hemisphere representations can obscure functional participation.PDF p.1, early functional-imaging discussion; PDF p.3, “Functional imaging evidence” discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

bilateral temporal IEDsReported: Bilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Bilateral temporal IEDs do not establish bilateral seizure onset; unilateral IED predominance may retain prognostic value.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • bilateral temporal IEDsBilateral temporal IEDs occur in 20%–40% of TLE descriptions and become more likely with longer EEG monitoring; although they increase the likelihood of independent bilateral seizure origin, intracranial EEG found unilateral seizure origin in the vast majority of such patients, and unilateral IED predominance was more prognostically informative than bilateral abnormality alone.PDF p.12, Lateralizing and prognostic value of IEDs on TLE
Reported values
  • 20%–40%bilateral temporal IEDsRange · patients with TLE, including patients with independent bitemporal abnormalities · TLE · interictal with relation to ictal onset and postsurgical outcomePDF p.12, Lateralizing and prognostic value of IEDs on TLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

bilateral tonic-clonic seizuresReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited Chassoux series restatement includes bilateral tonic-clonic seizures alongside oro-alimentary, salivation, dystonic, and head-deviation phenomena.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • Chassoux cohort; oro-alimentary automatisms; salivation; dystonic signs; head deviation; bilateral tonic-clonic seizuresThe review restates that Chassoux et al. described 33 patients with oro-alimentary automatisms, salivation, motor signs including dystonia and head deviation, and bilateral tonic-clonic seizures in the medio-lateral context.PDF p.4, Medio-lateral temporal origin

1 contributing manuscript; source-reported values remain separate and are not pooled.

bitemporal ictal activity and delayed contralateral propagationReported: BilateralAlso reported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review synthesis separates early bilateral or independent activity from delayed contralateral propagation and reports the latter as common without implying poor prognosis.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • bitemporal ictal activity and delayed contralateral propagationEarly bilateralization at seizure onset, switch of lateralization, intradischarge asynchrony, or clearly independent bilateral seizures indicate bitemporal epileptic foci and are associated with worse prognosis, whereas delayed contralateral temporal propagation is common and is not associated with poor prognosis; severe unilateral HS can even produce an ictal scalp discharge localized to the opposite temporal lobe despite excellent surgical outcomes, and about 13% of ictal scalp patterns are hemispheric or nonlocalizing.PDF p.13, Bitemporal ictal activity; PDF p.14, Ictal scalp EEG in TLE
Reported values
  • about 13% hemispheric or nonlocalizing ictal scalp patternsbitemporal ictal activity and delayed contralateral propagationPercentage · patients with TLE, MTLE-HS, or temporal surgery evaluations · ictal onset, propagation, and postsurgical prognosisPDF p.13, Bitemporal ictal activity; PDF p.14, Ictal scalp EEG in TLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

brain regions involved in ictal dysprosody; right frontal operculumReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The review places the dysprosody network primarily in the right frontal operculum while leaving adjacent-region contribution unresolved.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • brain regions involved in ictal dysprosody; right frontal operculumFrom the patient’s electroclinical data, the authors conclude that regions involved in his dysprosody primarily include the right frontal operculum, while cautioning that SEEG anatomical sampling cannot exclude adjacent regions.PDF p.5, left column, paragraph beginning “Accordingly, the electroclinical data”; PDF p.4, Figure 3 caption; PDF p.1, abstract

1 contributing manuscript; source-reported values remain separate and are not pooled.

broad sensory-motor networks; basal ganglia; hyperexcitabilityReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Left and bilateral regions are components of a broad sensory-motor network synthesis, not a side-specific lateralizing relationship for one sign.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • broad sensory-motor networks; basal ganglia; hyperexcitabilityThe authors interpret the case's electrophysiological and neuroradiological findings as showing involvement and hyperexcitability of broad sensory-motor networks, including the basal ganglia, in reflex seizures, and conclude that the epileptic networks involved include broad sensory-motor networks and the basal ganglia.PDF p.1, Abstract; PDF p.3, Discussion; PDF p.4, Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

BTLA resection and postoperative namingReported: Dominant hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates a clear left predominance of BTLA sites and, in bilaterally implanted cases, strict lateralization presumed to be in the dominant hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • BTLA resection and postoperative namingThe review presents BTLA postoperative outcomes as discordant: Krauss et al. reported worse early 6-12 month confrontation naming after BTLA resection, Lüders et al. reported no lasting language deficit, and Abdallah et al. found almost 60% early clinically significant visual-naming decline when resection included BTLA-positive sites versus 9% when BTLA was spared; the review states that resected positive sites were within 30 mm of the temporal tip on average 24.5 mm and that early deficits could partially recover by 2 years.PDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG; PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG
Reported values
  • almost 60% early clinically significant visual-naming decline with BTLA-positive-site resectionBTLA resection and postoperative namingPercentage · separate BTLA resection cohorts from Krauss et al., Lüders et al., and Abdallah et al.; Table 1 lists 29 subjects for Abdallah et al.; endpoint denominators not reported · BTLA-positive resection · early postoperative outcome at 6-12 months or within 1 year, with late outcome at 2 yearsPDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG; PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG
  • average distance 24.5 mm from temporal tipBTLA resection and postoperative namingMean · separate BTLA resection cohorts from Krauss et al., Lüders et al., and Abdallah et al.; Table 1 lists 29 subjects for Abdallah et al.; endpoint denominators not reported · BTLA-positive resection · early postoperative outcome at 6-12 months or within 1 year, with late outcome at 2 yearsPDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG; PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG
  • 9% early clinically significant visual-naming decline when BTLA was sparedBTLA resection and postoperative namingPercentage · separate BTLA resection cohorts from Krauss et al., Lüders et al., and Abdallah et al.; Table 1 lists 29 subjects for Abdallah et al.; endpoint denominators not reported · BTLA spared · early postoperative outcome at 6-12 months or within 1 year, with late outcome at 2 yearsPDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG; PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG
  • resected positive sites were within 30 mm of the temporal tipBTLA resection and postoperative namingOther reported value · separate BTLA resection cohorts from Krauss et al., Lüders et al., and Abdallah et al.; Table 1 lists 29 subjects for Abdallah et al.; endpoint denominators not reported · BTLA-positive resection · early postoperative outcome at 6-12 months or within 1 year, with late outcome at 2 yearsPDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG; PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

BTLA visual naming and semantic matchingReported: BilateralAlso reported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Cited stimulation-positive visual-naming sites occurred in either right or left ventral temporal cortex across patients but were strictly unilateral within each individual.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • BTLA visual naming and semantic matchingThe review reports that Bédos Ulvin et al. found anomia or paraphasia during visual naming with preserved performance on a control semantic-matching task, and found positive sites in both right and left VTC across patients but strictly unilateral representation within each individual.PDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language; PDF p.6, Table 1; PDF p.8, Mapping Dispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Case 1 anterior-inferior insular/orbitofrontal localizationReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The multimodal and invasive observations in Case 1 consistently lateralized the investigated network to the right hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 1 anterior-inferior insular/orbitofrontal localizationIn Case 1, fronto-temporal EEG findings and the described semiology led the chapter to favor a right anterior-inferior insular or orbitofrontal focus, with MEG at the junction of the anterior insula and posterior orbitofrontal cortex; invasive recordings showed preictal spiking over orbitofrontal, opercular, and anterior-insular contacts, spread to the middle insula and anterior middle frontal gyrus, and stimulation of the anterior-inferior insula reproduced the typical aura and clinical seizure.PDF p.9, What locations should be sampled based on semiology and EEG findings?; PDF p.10, Figure 17.3; PDF p.11, Invasive studies and outcome

1 contributing manuscript; source-reported values remain separate and are not pooled.

Case 2 left posterior/midposterior insular and opercular localizationReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

In this single case, seizure onset was in the left hemisphere, and right-sided sensory pain was contralateral to the left insular-opercular onset.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfCase report or observation · 1 finding · 1 reported value
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • Case 2 left posterior/midposterior insular and opercular localizationIn Case 2, unilateral left interictal abnormalities, centro-temporal seizure onset, right-sided sensory pain and auditory auras, and late hypermotor manifestations were interpreted as favoring a left posterior or midposterior insular and temporo-parietal opercular origin with frontal propagation rather than primary frontal onset; invasive recordings showed preictal spikes over parietal-opercular and posterior-insular contacts followed by low-voltage fast activity in the same contacts, and the patient remained seizure-free 1.5 years after left posterior insulectomy and partial parietal opercular resection.PDF p.13, Video-EEG data; PDF p.14, What locations should be sampled based on semiology and EEG findings?; PDF p.15, invasive findings and auditory triggers
Reported values
  • Seizure-free at 1.5 years follow-upCase 2 left posterior/midposterior insular and opercular localizationCount · Individual Case 2 · Interictal, ictal, preictal, stimulation-triggered auditory seizure, and postoperative outcomePDF p.13, Video-EEG data; PDF p.14, What locations should be sampled based on semiology and EEG findings?; PDF p.15, invasive findings and auditory triggers

1 contributing manuscript; source-reported values remain separate and are not pooled.

Case Study 2 frontal seizure semiology and invasive localizationReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphereNo single reliable side1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

This single case contains rightward head version, bilateral frontal interictal abnormalities with greater left amplitude, and nonlateralized or artifact-obscured ictal scalp EEG.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfCase report or observation · 1 finding
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • Case Study 2 frontal seizure semiology and invasive localizationIn Case Study 2, a man had sudden facial distortion, rhythmic jerking of both lower extremities, vocalization with impaired consciousness, and later right-arm clonic seizures; recorded seizures included sudden tonic upper-extremity posturing, vocalization, facial distortion, and one rightward head version followed by generalized tonic-clonic activity. Interictal abnormalities were bilateral frontal but higher in amplitude on the left, while ictal scalp EEG was nonlateralized or obscured by movement artifact; invasive recording showed onset over multiple contacts of the frontal convexity anterior to the precentral gyrus with rapid spread to temporal and mesial frontal regions.PDF p.12, Case Study 2, presenting seizure semiology; PDF p.13, Case Study 2, recorded seizures and EEG; PDF p.13, Case Study 2, invasive localization and Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

categorical versus non-categorical acoustic representationsReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review hypothesizes more categorical acoustic representation in the left hemisphere and less categorical representation sufficient for lexical access in the right hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • categorical versus non-categorical acoustic representationsThe authors discuss as a further possibility that the left hemisphere is predisposed to represent acoustic information more categorically than the right hemisphere, while less categorical right-hemisphere representations may still be sufficient for lexical access; they present this as a possible explanation for speech-perception asymmetries and lesion findings.PDF p.4, end of “Multi-time resolution processing”; PDF p.5, opening paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

Cited presumed saccadic-versus-smooth-pursuit directionality mechanismReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The cited-study restatement contrasts contralateral eye deviation attributed to cortical saccadic areas with ipsilateral ocular deviation during stimulation of cortical smooth-pursuit areas.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdfCase report or observation · 1 finding
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a two-case report with no control or comparator group. Case-1 was a 24-year-old right-handed man; 32 habitual seizures were recorded during 3 days of scalp video-EEG, with two followed by secondary GTCS, and two right-hemisphere SEEG implantations were performed 4 months apart. Case-2 was a 19-year-old right-handed man; three habitual seizures were captured on video-EEG and right temporal neocortical, temporal-pole, and medial-structure regions were explored with SEEG. The source describes scalp EEG, MRI, FDG-PET, SEEG onset and propagation, anatomical reconstruction, cortical resection, and seizure-free follow-up of 17 months for Case-1 and 25 months for Case-2. Case-1 MRI/FDG-PET was reported unremarkable for an evaluable lesion; Case-2 MRI and PET findings were reported in the right middle-posterior inferior temporal/fusiform and medial temporal regions. No cohort-wide denominator for ipsiversive eye deviation, no control comparison, and no population-level frequency or diagnostic statistic are reported.
Findings
  • Cited presumed saccadic-versus-smooth-pursuit directionality mechanismThe current report states that prior work presumed contralateral eye deviation to result from involvement of cortical saccadic areas, whereas stimulation of cortical smooth-pursuit areas during epileptic seizures causes ipsilateral ocular deviation.PDF p.6, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

clinical features differentiating exclusive TLE from temporal plus epilepsyReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited temporal-plus comparison reports contralateral head rotation and ipsilateral tonic signs as distinct lateralized components.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • clinical features differentiating exclusive TLE from temporal plus epilepsyCompared with exclusive TLE, temporal plus epilepsy was more associated with gustatory hallucinations, auditory illusions or vertigo, focal impaired awareness seizures with contralateral head rotation or ipsilateral tonic motor signs, and postictal dysphoria; exclusive TLE was more associated with epigastric sensations, gestural automatisms, and postictal amnesia.PDF p.10, Temporal “plus” epilepsy

1 contributing manuscript; source-reported values remain separate and are not pooled.

Complex motor phenomenonReported: Bilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited pediatric review restates bilateral or symmetric tonic, clonic, or myoclonic manifestations in very young TLE, with age-dependent semiology and no fixed hemispheric direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • age-dependent complex motor semiologyIn children younger than 3–4 years with TLE, tonic, clonic, or myoclonic movements may be bilateral and symmetric and resemble generalized epilepsy, and automatisms are less elaborate and restricted to the orobuccal region. After age 6, TLE manifestations are similar to adults; very young posterior-cortex epilepsy more often presents with decreased motor activity or hypomotor seizures.PDF p.4, section 3.3 Complex motor seizures
Reported values
  • After age 6age-dependent complex motor semiologyThreshold · children with TLE and very young patients with posterior-cortex epilepsy · children with TLE · ictalPDF p.4, section 3.3 Complex motor seizures
  • younger than 3–4 yearsage-dependent complex motor semiologyRange · children with TLE and very young patients with posterior-cortex epilepsy · young children with TLE · ictalPDF p.4, section 3.3 Complex motor seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

conversation-related temporal-lobe stimulation experiencesReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The cited case is described as left temporal epilepsy during implanted-electrode stimulation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

palinacousis-seven-new-cases.pdfCase report or observation · 1 finding
palinacousis-seven-new-cases.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • conversation-related temporal-lobe stimulation experiencesAs restated by the source, six detailed interviews in one patient with left temporal epilepsy undergoing implanted-electrode stimulation found that experiences elicited by temporal-lobe stimulation were often related to the ongoing conversation.PDF p.3, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

developmental and acquired pathology effects on language lateralityReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review states that developmental lesions and early-onset seizures are thought not to displace language cortex from prenatally determined sites, whereas acquired lesions before age 5 may relocate language areas to the opposite hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • developmental and acquired pathology effects on language lateralityThe review states that developmental lesions and early-onset seizures are thought not to displace language cortex from prenatally determined sites, whereas acquired lesions before age 5 may relocate language areas to the opposite hemisphere.PDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language
Reported values
  • acquired lesions before age 5developmental and acquired pathology effects on language lateralityOther reported value · developmental versus acquired pathology language-cortex study; cohort details not reported in this review · acquired lesions · language-cortex organization in the setting of epilepsy or lesion onsetPDF p.4, Procedural Considerations for Electrical Stimulation Mapping of Language

1 contributing manuscript; source-reported values remain separate and are not pooled.

distributed language sites after naming ECSReported: BilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates bilateral positive language sites with left predominance during naming ECS.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • distributed language sites after naming ECSThe review reports that Perrone-Bertolotti et al. found bilateral, left-predominant, widespread positive language sites in frontal, temporal, and parietal lobes in 29 patients using a naming task, without postoperative outcome correlation.PDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Dominant hemisphere and maintenance of wakefulness in cited studiesReported: Dominant hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Dominant versus nondominant hemisphere

Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Dominant hemisphere and maintenance of wakefulness in cited studiesThe current paper states that several cited studies suggested a major role for the dominant hemisphere in maintaining wakefulness, while noting that some analyses limited to responsiveness to noxious stimulation found no hemispheric difference.PDF p.5, Discussion, rapid-return paragraph
Reported values
  • Studies finding no hemispheric difference under noxious-stimulation responsiveness n=3Dominant hemisphere and maintenance of wakefulness in cited studiesCount · Cited studies as summarized by the current paper · Analyses limited to noxious-stimulation responsiveness · Postictal recovery/consciousnessPDF p.5, Discussion, rapid-return paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

dominant mesial temporal lobe stimulation during verbal memory taskReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study is summarized as showing a timing-dependent verbal-memory disruption from dominant mesial-temporal stimulation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • dominant mesial temporal lobe stimulation during verbal memory taskThe source reports that stimulation of the dominant mesial temporal lobe had a timing-dependent disruptive effect on verbal memory, with stimulation during the interval between learning and recall most strongly disrupting recall.PDF p.11, memory timing paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

Dominant-hemisphere consciousness effects in cited studiesReported: Dominant hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

One cited intracarotid-amobarbital study reported more frequent and prolonged loss of consciousness after dominant-hemisphere injection, while another did not confirm the result.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfNarrative, educational, or cited context · 1 finding
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Dominant-hemisphere consciousness effects in cited studiesThe current paper reports that Serafetinides et al. (1965) observed more frequent and prolonged loss of consciousness after intracarotid amobarbital injection into the dominant hemisphere, whereas Rosadini and Rossi (1967) did not confirm that result.PDF p.5, Discussion, rapid-return paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

dual-stream model of speech processingReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

In the educational dual-stream speech model, the ventral stream is largely bilateral whereas the dorsal stream is strongly left-hemisphere dominant.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • dual-stream model of speech processingThe authors propose that a ventral stream involving superior and middle temporal structures processes speech signals for comprehension or recognition, whereas a dorsal stream involving posterior frontal, posterior dorsal temporal, and parietal-opercular structures translates acoustic speech into frontal articulatory representations; speech-perception tasks rely more on dorsal circuitry and speech-recognition tasks more on ventral circuitry with shared tissue in the left STG. They further propose bilateral ventral organization with computational differences between hemispheres and strong left dominance of the dorsal stream.PDF p.1, abstract; PDF p.2, “Dual-stream model of speech processing”; PDF p.3, Figure 1 diagram and caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

electrical-stimulation speech effectsReported: Dominant hemisphereNo single reliable side1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited stimulation account links dysphasia to dominant-hemisphere speech areas but describes vocalization from motor speech areas in either hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfNarrative, educational, or cited context · 1 finding
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • electrical-stimulation speech effectsThe source reports that electrical stimulation of speech areas in the dominant hemisphere produced dysphasia, whereas stimulation of motor speech areas in either hemisphere produced vocalization.PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

electroclinical status epilepticus criteria and semiologic axesReported: Bilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational framework lists focal, multifocal, lateralized, bilateral, and generalized discharge patterns without assigning a semiologic hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • electroclinical status epilepticus criteria and semiologic axesThe source organizes status epilepticus by prominent motor symptoms and coma or impaired awareness, including focal motor status, ictal paresis, adversive status, focal aware or impaired-awareness nonconvulsive status, and focal onset evolving to bilateral convulsive status; for nonconvulsive status, discharges above 2.5 Hz or slower/rhythmic patterns with clinical or EEG improvement after intravenous antiseizure medication, subtle clinical ictal signs, or spatiotemporal evolution support the diagnosis.PDF p.196; PDF p.266; PDF p.268; PDF p.269; PDF p.270; PDF p.273
Reported values
  • epileptiform discharges >2.5 Hzelectroclinical status epilepticus criteria and semiologic axesCount · clinical status epilepticus and critical-care EEG teaching groups · ongoing ictal activity and status evolutionPDF p.196; PDF p.266; PDF p.268; PDF p.269; PDF p.270; PDF p.273

1 contributing manuscript; source-reported values remain separate and are not pooled.

emotional prosody; fronto-opercular and temporal activationReported: BilateralAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The review's healthy-subject fMRI synthesis emphasizes non-dominant, particularly right fronto-opercular and temporal, emotional-prosody processing while summarizing cited studies as bilateral but right-predominant.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • emotional prosody; fronto-opercular and temporal activationThe discussion’s healthy-subject fMRI synthesis is that emotional-prosody processing involves the non-dominant hemisphere, particularly right fronto-opercular and temporal cortices, with the cited studies summarized as bilateral but right-predominant temporal/frontal or fronto-opercular activation.PDF p.5, left column, paragraphs beginning “The brain regions involved in recognition of prosody” and “Overall, results from these studies”

1 contributing manuscript; source-reported values remain separate and are not pooled.

Example 2: left temporal lobe epilepsy due to hippocampal atrophyReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational example combines a left temporal epileptic focus with right versive head/eye turning and bilateral temporal sharp waves.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a proposal and narrative synthesis, not a primary empirical study. The authors review prior classification approaches, define the five dimensions, provide tables and conceptual figures, and demonstrate the proposed format with illustrative profiles. The framework is stated to apply to patients with epilepsy, defined here as at least two spontaneous epileptic seizures; for patients with unclear epileptic or nonepileptic events, the source recommends the term paroxysmal event. Clinical history, seizure semiology, EEG, MRI, other diagnostic studies, and etiologic information are translated into a best available working classification that can be refined as information accrues. No formal study cohort, sampling method, reference standard, comparator cohort, or statistical analysis is reported.
Findings
  • Example 2: left temporal lobe epilepsy due to hippocampal atrophyIn an illustrative 33-year-old right-handed man, the initial profile lists left temporal EZ, abdominal aura to automotor seizure to right versive seizure to generalized tonic-clonic seizure, unknown etiology pending MRI, persistent frequency, and febrile convulsions in infancy; after MRI and video-EEG, the profile is refined to left mesial temporal EZ and left hippocampal sclerosis, with the same semiologic sequence, persistent frequency, and predominantly nocturnal seizures.PDF p.5, Example 2 clinical history and initial profile; PDF p.5, MRI/video-EEG refinement and updated profile; PDF p.7, focal temporal-lobe illustrative profile
Reported values
  • three occasionsExample 2: left temporal lobe epilepsy due to hippocampal atrophyCount · One illustrative 33-year-old right-handed man with habitual seizures beginning at age 15; not a study cohort · right-sided head and eye turning · Habitual ictal semiology before and after MRI/video-EEG refinementPDF p.5, Example 2 clinical history and initial profile; PDF p.5, MRI/video-EEG refinement and updated profile; PDF p.7, focal temporal-lobe illustrative profile
  • about monthlyExample 2: left temporal lobe epilepsy due to hippocampal atrophyOther reported value · One illustrative 33-year-old right-handed man with habitual seizures beginning at age 15; not a study cohort · lip smacking and hand-movement episodes · Habitual ictal semiology before and after MRI/video-EEG refinementPDF p.5, Example 2 clinical history and initial profile; PDF p.5, MRI/video-EEG refinement and updated profile; PDF p.7, focal temporal-lobe illustrative profile

1 contributing manuscript; source-reported values remain separate and are not pooled.

Facial motor alteration (unspecified type)Reported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

No general lateralization direction is reported for facial alterations; contralateral direction is stated only conditionally for facial weakness.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Facial alterationsTable 3 associates facial alterations with activation of emotional-network structures or emotional facial movements in cingulum and lists contralateral lateralisation if facial weakness.PDF p.4, Table 3

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ferrier auditory-cortex stimulation observationReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Historical monkey stimulation of the superior temporal gyrus produced contralateral ear holding and contralateral head turning.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

palinacousis-seven-new-cases.pdfCase report or observation · 1 finding
palinacousis-seven-new-cases.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This retrospective case series included seven patients seen at The Mount Sinai Hospital epilepsy clinic or EMU between July 2009 and May 2016 who experienced palinacousis. All patients had epilepsy; EEG and MRI were performed at some point during their clinical course, and the authors reviewed those records after identifying the phenomenon by history. No comparator, uniform event-time reference standard, or inferential statistical analysis was reported.
Findings
  • Ferrier auditory-cortex stimulation observationThe source states that Ferrier identified the superior temporal gyrus as a focus for audition and that stimulation of this area in monkeys caused holding of the contralateral ear and contralateral head turning.PDF p.3, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Fig. 10.4 language mapping; crucial nodes of the language networkReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The educational case explicitly describes left temporo-perisylvian epilepsy and left-sided language-mapping context.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfCase report or observation · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • Fig. 10.4 language mapping; crucial nodes of the language networkIn the source’s 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging, stimulation produced site-specific effects: occipital lateral stimulation caused a visual perceptive naming deficit, anterior BTLA stimulation caused a lexical deficit with semantic access preserved, IFG pars triangularis stimulation prolonged naming latency, sTPJ stimulation disrupted word repetition and phonological-loop maintenance, premotor stimulation slowed automatic speech and repetitive gesture, and auditory-cortex stimulation produced an auditory hallucination or illusion; IFG/precentral stimulation produced no deficit in the displayed table.PDF p.10, Fig. 10.4 panels A-C; PDF p.11, Fig. 10.4 caption and continuation

1 contributing manuscript; source-reported values remain separate and are not pooled.

focal, generalized, focal-to-bilateral, and unknown-onset classificationReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The classification distinguishes focal one-hemisphere onset, bilateral generalized onset, and unknown onset.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • focal, generalized, focal-to-bilateral, and unknown-onset classificationThe source's 2017 classification separates focal-onset seizures beginning in one hemisphere, generalized-onset seizures engaging both hemispheres, focal-to-bilateral tonic-clonic seizures, and unknown-onset seizures; focal seizures are further described by awareness and motor or nonmotor onset.PDF p.45; PDF p.46; PDF p.47; PDF p.48

1 contributing manuscript; source-reported values remain separate and are not pooled.

focal-to-bilateral lateralizing motor signsReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review synthesis preserves ipsilateral and contralateral components of focal-to-bilateral motor signs, including figure-of-four posturing, without treating any one component as universally reliable.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • focal-to-bilateral lateralizing motor signsDuring transition from focal onset to bilateral tonic-clonic activity, versive head turning, contralateral tonic or clonic activity, figure-of-four posturing with contralateral arm extension and ipsilateral arm flexion, asymmetry or asynchrony, and asymmetric termination may support focal lateralization, but each can be altered by propagation and can occur in primary generalized seizures.PDF p.49; PDF p.57

1 contributing manuscript; source-reported values remain separate and are not pooled.

frontal interictal epileptiform activityReported: Bilateral1 manuscript · 1 finding · 8 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review synthesizes mixed interictal-spiking distributions without a semiologic hemisphere result.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 8 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • frontal interictal epileptiform activityIn one large series, interictal spiking was bilaterally synchronous in 37%, lobar in 32%, multilobar in 24%, focal in 12%, and hemispheric-independent in 9% of cases; epileptiform activity occurred exclusively outside the frontal lobes in 20%-50%, was restricted to the frontal lobes in only 25%, and spiking was absent in 20%-70%.PDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
Reported values
  • 20%–50% exclusively outside the frontal lobesfrontal interictal epileptiform activityRange · One large series of patients with frontal lobe epilepsy; exact cohort not reported · outside-frontal only · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 37% bilaterally synchronousfrontal interictal epileptiform activityPercentage · One large series of patients with frontal lobe epilepsy; exact cohort not reported · bilaterally synchronous · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 20%–70% spiking absentfrontal interictal epileptiform activityRange · One large series of patients with frontal lobe epilepsy; exact cohort not reported · spiking absent · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 12% focalfrontal interictal epileptiform activityPercentage · One large series of patients with frontal lobe epilepsy; exact cohort not reported · focal · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 25% restricted to the frontal lobesfrontal interictal epileptiform activityPercentage · One large series of patients with frontal lobe epilepsy; exact cohort not reported · frontal-restricted · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 24% multilobarfrontal interictal epileptiform activityPercentage · One large series of patients with frontal lobe epilepsy; exact cohort not reported · multilobar · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 32% lobarfrontal interictal epileptiform activityPercentage · One large series of patients with frontal lobe epilepsy; exact cohort not reported · lobar · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph
  • 9% hemispheric-independentfrontal interictal epileptiform activityPercentage · One large series of patients with frontal lobe epilepsy; exact cohort not reported · hemispheric-independent · interictalPDF p.6, Frontal lobe epilepsy, interictal EEG paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

frontal, parietal, and occipital ictal EEG patternsReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Occipital scalp discharges may appear bilateral because of volume conduction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • frontal, parietal, and occipital ictal EEG patternsFrontal seizures often spread rapidly and can be difficult to distinguish from generalized activity, but high-frequency focal fast onset can localize the epileptogenic region; parietal scalp EEG can falsely appear temporal or frontal; occipital discharges may be bilateral from volume conduction, and activity above the calcarine fissure tends to spread frontally while activity below it tends to spread temporally.PDF p.220; PDF p.221; PDF p.229; PDF p.230

1 contributing manuscript; source-reported values remain separate and are not pooled.

functional imaging evidence for a sensorimotor dorsal streamReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

In cited auditory-motor functional-imaging studies, posterior STS activity was bilateral, area Spt was left-dominant, and posterior frontal activity was left-sided.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • functional imaging evidence for a sensorimotor dorsal streamThe review reports that cited functional-imaging studies asked individuals to listen to pseudowords and then subvocally reproduce them, identifying a network active during both perceptual and motor-related phases. The network included posterior STS bilaterally, a left-dominant site in the Sylvian fissure at the parietotemporal boundary called area Spt, and left posterior frontal regions; the authors propose that posterior STS supports sensory speech coding and Spt translates sensory codes to the motor system.PDF p.8, “Functional imaging evidence for a sensorimotor dorsal stream”; PDF p.9, Figure 4 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

generalized absence seizuresReported: Bilateral1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Typical generalized absence is described in a generalized bilateral network with bilateral 2.5–4 Hz spike-and-wave activity.

Source-defined result groups 4
Lateralization: BilateralSource-defined values retained separatelytypical generalized absence · atypical and myoclonic absence · EEG discharge1 manuscript · 1 reported value · not pooled
Lateralization: BilateralSource-defined values retained separatelyatypical absence · typical absence · EEG discharge1 manuscript · 1 reported value · not pooled
Lateralization: BilateralSource-defined values retained separatelymyoclonic absence · typical and atypical absence · EEG discharge1 manuscript · 1 reported value · not pooled
Lateralization: BilateralSource-defined values retained separatelytypical generalized absence · atypical and myoclonic absence · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • generalized absence seizuresTypical generalized absence seizures are abrupt, usually lack an aura, commonly last less than 15 seconds, terminate abruptly without a postictal state, and are associated with generalized 2.5-4 Hz spike-and-wave activity; arrest, simple or perseverative automatisms, blinking, subtle myoclonus, eye or neck movements, atonic slumping, and autonomic signs may occur. Atypical absence is slower than 2.5 Hz with slower onset or recovery and more prominent motor manifestations; myoclonic absence has prominent clonic activity at approximately 2.5-3.5 Hz.PDF p.55; PDF p.56; PDF p.299; PDF p.300
Reported values
  • approximately 2.5–3.5 Hzgeneralized absence seizuresRange · typical, atypical, and myoclonic absence seizure teaching groups · myoclonic absence · ictalPDF p.55; PDF p.56; PDF p.299; PDF p.300
  • usually <15 secondsgeneralized absence seizuresDuration · typical, atypical, and myoclonic absence seizure teaching groups · typical generalized absence · ictalPDF p.55; PDF p.56; PDF p.299; PDF p.300
  • 2.5–4 Hzgeneralized absence seizuresRange · typical, atypical, and myoclonic absence seizure teaching groups · typical generalized absence · ictalPDF p.55; PDF p.56; PDF p.299; PDF p.300
  • <2.5 Hzgeneralized absence seizuresFrequency · typical, atypical, and myoclonic absence seizure teaching groups · atypical absence · ictalPDF p.55; PDF p.56; PDF p.299; PDF p.300

1 contributing manuscript; source-reported values remain separate and are not pooled.

generalized EEG patterns with focal-appearing featuresReported: Bilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational source describes a generalized bilateral network despite possible shifting asymmetry or focal-appearing fragments.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • generalized EEG patterns with focal-appearing featuresGeneralized spike-wave activity supports generalized epilepsy when it is appropriately generalized and clinically concordant; typical absence commonly shows abrupt synchronous 2.5-4 Hz activity, juvenile myoclonic epilepsy shows faster irregular generalized or polyspike activity, and shifting asymmetry or focal fragments can occur within generalized epilepsies without proving a focal onset.PDF p.205; PDF p.209; PDF p.212; PDF p.240; PDF p.301
Reported values
  • 2.5–4 Hzgeneralized EEG patterns with focal-appearing featuresRange · generalized epilepsy and absence/JME teaching groups · typical absence · interictal and ictalPDF p.205; PDF p.209; PDF p.212; PDF p.240; PDF p.301
  • 3–6 Hz or fastergeneralized EEG patterns with focal-appearing featuresRange · generalized epilepsy and absence/JME teaching groups · juvenile myoclonic epilepsy · interictal and ictalPDF p.205; PDF p.209; PDF p.212; PDF p.240; PDF p.301

1 contributing manuscript; source-reported values remain separate and are not pooled.

generalized tonic-clonic signs, unknown-onset seizures, and focal evolutionReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Late bilateral motor signs, including changing versive direction, do not by themselves establish focal onset or a lateralizing hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • generalized tonic-clonic signs, unknown-onset seizures, and focal evolutionGeneralized tonic-clonic seizures may evolve from generalized absence or myoclonic seizures; versive head turning may change direction across generalized seizures and alone does not establish focal onset. In an uncaptured tonic-clonic seizure, versive head turning, figure-of-four posture, asymmetrical or asynchronous clonus, and asymmetric termination are more frequent in focal-to-bilateral seizures but can also occur in primary generalized seizures, so none is definitive individually; generalized-onset seizures with focal evolution are described as uncommon.PDF p.56; PDF p.57

1 contributing manuscript; source-reported values remain separate and are not pooled.

Graded precision of semiological descriptionReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The source uses right arm only as an educational symptom-side example in progressively specific seizure labels.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Graded precision of semiological descriptionThe authors state that inadequate information limits precision but the SSC permits progressively more specific labels as evidence permits: epileptic seizure, motor seizure, right arm motor seizure, right arm simple motor seizure, and finally right arm clonic seizure.PDF p.7, Summary of the essential characteristics, item 6

1 contributing manuscript; source-reported values remain separate and are not pooled.

hippocampal language involvementReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

No resolved lateralization information is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • hippocampal language involvementThe review states that hippocampal ECS does not consistently produce overt language impairment, so the hippocampus is not currently considered an eloquent language region, while intracranial HFA and latency studies suggest a role in naming; it reports no consensus on dominant hippocampal resection effects or ECS methods that predict them.PDF p.9, Mapping Dispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal aggressionReported: Bilateral1 manuscript · 2 findings · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited review reports bilateral massive hypersynchronization between frontal and temporal regions during the late seizure period containing aggression. The cited case summary reports bilateral massive hypersynchronization between frontal and temporal regions during late-seizure aggression.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

mcgonigal-on-seizure-semiology-2021-5ba29d.pdfNarrative, educational, or cited context · 2 findings · 2 reported values
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf; mcgonigal-on-seizure-semiology-2021-9127f2.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The article reports a narrative critical overview rather than a systematic search, primary cohort, or pooled quantitative analysis; search and study-selection methods are not reported. Its emphasis is on spontaneous seizures in patients with intractable focal epilepsy undergoing presurgical evaluation, with additional discussion of SEEG stimulation studies, functional imaging, and broader epilepsy classification. The cited-study summaries in Tables 1 and 2 report study-level numbers of subjects and, where available, seizures; exact subgroup denominators and statistical uncertainty are often not provided in this document.
Findings
  • ictal aggressionThe review reports that Bartolomei et al. (2017) observed aggression in the last part of a seizure, during which functional-connectivity analysis showed bilateral massive hypersynchronization between frontal and temporal regions.PDF p.5, Table 1, Ictal aggression row
  • ictal aggressionIn the summarized Bartolomei et al. case, aggression occurred in the last part of the seizure and functional-connectivity analysis showed bilateral massive hypersynchronization between frontal and temporal regions during that period.PDF p.5, Table 1 (continued), Bartolomei et al. 2017 row
Reported values
  • n=1 subjectictal aggressionCount · 1 subject with temporal-lobe epilepsy · Last part of the seizurePDF p.5, Table 1, Ictal aggression row
  • Participant in stimulation study n=1ictal aggressionCount · 1 subject with temporal-lobe epilepsy; number of seizures Not reported · late ictal periodPDF p.5, Table 1 (continued), Bartolomei et al. 2017 row

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal auditory lossReported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The synthesis reports a right-hemisphere stimulation predominance for verbal hallucinations, with no general hemisphere rule for all auditory percept types.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 1 finding · 2 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)In the cortical-stimulation synthesis, SH were mainly induced by posterior insula and Heschl’s gyrus (HG); CH by STG, STS, mesiotemporal structures, and insula; I by STG, HG, STS, and temporal plane with about one-third from extratemporal structures; VH included 60% produced by right-hemisphere stimulation, mostly STG; MH involved STG, HG, temporal plane, and SMG; HD involved temporal structures and insula, especially PLST, posterior STG, and HG; and few PAL reports were identified.PDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
Reported values
  • Verbal hallucinations from right-hemisphere stimulation 60%simple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Verbal hallucinations · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2
  • Auditory illusions from extratemporal stimulation about one-thirdsimple hallucinations (SH), complex hallucinations (CH), illusions (I), verbal hallucinations (VH), musical hallucinations (MH), hypoacusis/deafness (HD), and palinacousis (PAL)Percentage · Cortical-stimulation reports stratified by AP semiology · Auditory illusions · Electrically induced APPDF p.4, section 5; PDF p.5, section 5 and Table 1; PDF p.6, Figure 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal cognitive disturbanceReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review associates memory/language deficits with dominant temporal seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Memory, language, orientation, and expressive speech deficitsThe review states that dominant temporal lobe seizures result in memory and language deficits, whereas frontal seizures result in loss of orientation and expressive speech function.PDF p.3, section 1.3

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal depersonalizationReported: Non-dominant hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review associates ictal derealization/depersonalization with nondominant-hemisphere and other symptom-specific contexts.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal derealization and depersonalizationIctal derealization was reported more frequently in MTLE in one cited study (85% of that study’s MTLE patients), while derealization and depersonalization were associated with nondominant-hemisphere involvement; depersonalization was more frequent in frontal lobe epilepsy, and another study linked it to parietal rather than frontal or temporal hypermetabolism.PDF p.8, Ictal dissociative-like experiences
Reported values
  • 85% MTLE frequency for ictal derealization in the cited studyictal derealization and depersonalizationPercentage · cited patients with MTLE or other focal epilepsy; study denominators not reported in the chapter · ictalPDF p.8, Ictal dissociative-like experiences

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal derealizationReported: Non-dominant hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review associates ictal derealization/depersonalization with nondominant-hemisphere and other symptom-specific contexts.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal derealization and depersonalizationIctal derealization was reported more frequently in MTLE in one cited study (85% of that study’s MTLE patients), while derealization and depersonalization were associated with nondominant-hemisphere involvement; depersonalization was more frequent in frontal lobe epilepsy, and another study linked it to parietal rather than frontal or temporal hypermetabolism.PDF p.8, Ictal dissociative-like experiences
Reported values
  • 85% MTLE frequency for ictal derealization in the cited studyictal derealization and depersonalizationPercentage · cited patients with MTLE or other focal epilepsy; study denominators not reported in the chapter · ictalPDF p.8, Ictal dissociative-like experiences

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal head/eye deviationReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes head/eye deviation as suggesting an ipsilateral focus and other listed unilateral motor signs as usually indicating a contralateral focus.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • unilateral dystonic posturing, head/eye deviation, clonic or tonic movements, and hypokinesiaSecondary motor signs related to propagation outside the temporal lobe may lateralize the seizure-onset zone: unilateral dystonic posturing is usually contralateral to the focus, head or eye deviation suggests an ipsilateral focus, and other unilateral clonic or tonic movements or limb immobility usually indicate a contralateral focus.PDF p.8, Focal impaired awareness seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal hypokinesiaReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes head/eye deviation as suggesting an ipsilateral focus and other listed unilateral motor signs as usually indicating a contralateral focus.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • unilateral dystonic posturing, head/eye deviation, clonic or tonic movements, and hypokinesiaSecondary motor signs related to propagation outside the temporal lobe may lateralize the seizure-onset zone: unilateral dystonic posturing is usually contralateral to the focus, head or eye deviation suggests an ipsilateral focus, and other unilateral clonic or tonic movements or limb immobility usually indicate a contralateral focus.PDF p.8, Focal impaired awareness seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal inner speechReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Ictal inner speech has been associated with seizures arising from the left supplementary motor area.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • ictal inner speechThe article reports that ictal inner speech has been associated with seizures arising from the left supplementary motor area.PDF p.2, Introduction

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal lacrimationReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review reports a possible right-hemispheric lateralization for ictal lacrimation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal lacrimationIctal lacrimation has been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal leaving or wandering behaviorReported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

A cited report describes ictal leaving behavior as a possible sign of nondominant mesial temporal lobe epilepsy.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal leaving behaviorIctal leaving behavior, consisting of walking or running away, has been mentioned as a possible sign of nondominant MTLE.PDF p.8, Focal impaired awareness seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal mydriasisReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The table reports contralateral lateralization for mesial frontal cortex and ipsilateral lateralization for mesial temporal/insular cortex, respectively.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • MydriasisTable 2 associates mydriasis with mesial frontal and mesial temporal/insular cortex and lists contralateral and ipsilateral lateralisation, respectively.PDF p.3, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal pallorReported: IpsilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review assigns ipsilateral direction to marching piloerection, left-temporal onset context to pallor in one pediatric series, and no lateralizing value to flushing.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • ictal piloerection, pallor, and flushingIctal piloerection presents as marching goose bumps involving a limb ipsilateral to seizure onset and is most common in TLE. Ictal pallor, usually occurring with other cutaneous signs, was associated with left temporal onset in one pediatric series, whereas ictal flushing involving mainly the face has no localizing value.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal panic attackReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review lists ictal panic attacks among features possibly lateralizing to the right hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal panic attacksIctal panic attacks have been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal scalp EEG during aura and focal unaware or hypermotor seizuresReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

When ictal EEG is lateralized, it is described as ipsilateral to the seizure focus; aura and hypermotor contexts limit observability.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdfNarrative, educational, or cited context · 1 finding
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
No formal search strategy, eligibility criteria, pooled analysis, common comparator, or uniform reference standard is reported. The chapter includes two individual case observations: Case 1 is a 27-year-old right-handed woman with seizure onset at age 9, and Case 2 is a 46-year-old right-handed man with seizures since age 16. Other populations are cited literature populations as reported in individual findings, including a review of 153 patients and a 22-patient nonlesional operculo-insular series; these are not an original chapter cohort.
Findings
  • ictal scalp EEG during aura and focal unaware or hypermotor seizuresIctal EEG changes are described as rare during auras; during focal unaware seizures they are generally lateralizing, except that some hypermotor seizures may show more widespread or artifact-masked changes, and a lateralized change occurs ipsilateral to the seizure focus.PDF p.6, Scalp EEG; PDF p.14, What locations should be sampled based on semiology and EEG findings?

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal scalp EEG patterns in TLEReported: Ipsilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review summarizes temporal ictal scalp EEG patterns, including ipsilateral or diffuse attenuation, mesial-associated regular 5–9 Hz inferior-temporal rhythm, lateral-associated irregular 2–5 Hz rhythm, basal/polar vertex activity, and wider temporal-plus distributions.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • ictal scalp EEG patterns in TLEIctal scalp EEG in TLE may show temporal rhythmic delta or theta-alpha activity, ipsilateral or diffuse background attenuation, focal temporal spikes or sharp waves, or less commonly rapid focal discharges; patterns from seizures initially restricted to mesial structures may be minimal, and scalp patterns are not sufficient by themselves to identify the EZ anatomically. Regular 5–9 Hz inferior-temporal rhythm is associated with temporo-mesial onset, irregular polymorphic 2–5 Hz rhythm with lateral onset, basal or polar onset with vertex activity, and temporal plus with wider frontal, temporoparietal, or central distribution.PDF p.13, Ictal scalp EEG in TLE
Reported values
  • Mesial-associated regular inferior-temporal rhythm 5–9 Hzictal scalp EEG patterns in TLERange · patients with TLE undergoing ictal scalp EEG · Temporo-mesial onset pattern · ictal onset and propagationPDF p.13, Ictal scalp EEG in TLE
  • Lateral-associated irregular polymorphic rhythm 2–5 Hzictal scalp EEG patterns in TLERange · patients with TLE undergoing ictal scalp EEG · Lateral onset pattern · ictal onset and propagationPDF p.13, Ictal scalp EEG in TLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal visual field deficitReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review gives right occipital seizure with left homonymous hemianopia as an example and reports 100% predictive value for contralateral onset.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Visual field defect and homonymous hemianopiaThe review states that clear identification of a visual-field defect establishes involvement of symptomatogenic cortex; a right occipital seizure could produce left homonymous hemianopia, and the deficit had a reported 100% predictive value for contralateral onset in reported series.PDF p.6, section 1.12
Reported values
  • Reported 100% predictive value for contralateral onsetVisual field defect and homonymous hemianopiaPercentage · Reported occipital-lobe seizure series; exact population not reported · ictal or postictalPDF p.6, section 1.12

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal visuospatial disorientation / spatial neglectSource terms: Ictal spatial neglectReported: Non-dominant hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited review restates a right-sided lesion tendency for unilateral spatial neglect and nondominant parietal stimulation associations.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • unilateral spatial neglect; nondominant parietal spatial judgment and face processingThe source states that unilateral spatial neglect tends to occur more often after right-sided lesions and, in its cited stimulation-mapping summary, localizes spatial-neglect responses to the posterior right STG and MTG, IPL, inferior postcentral gyrus and IFG, SLF II, and SOFF; it also associates spatial judgment and basic face processing with nondominant parietal stimulation, particularly the parietal-occipital junction.PDF p.12-13, Visual-spatial processing, construction, navigation; PDF p.19, Table 10.1, Visuo-Perceptual/Visual-Spatial

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal yawningReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review reports a possible right-hemispheric association for ictal yawning, retained as non-independent and uncertain.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • ictal yawningIctal yawning has been associated with possible right-hemispheric lateralization.PDF p.12, Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

IEH EEG patternsReported: BilateralAlso reported: Right hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

IEH-related EEG descriptions include right temporo-occipital, bilateral, and generalized patterns.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • IEH EEG patternsReported EEG descriptions associated with IEH include 11-12-Hz activity and spikes over the right temporo-occipital region, theta activity with sharp waves over occipital regions, continuous bilateral spike-and-slow-wave discharges, and generalized discharges.PDF p.3, Localization
Reported values
  • Right temporo-occipital EEG activity 11–12 HzIEH EEG patternsRange · Reported IEH cases summarized by the review · Right temporo-occipital pattern · Ictal or seizure-associated EEG period; exact timing varies by reportPDF p.3, Localization

1 contributing manuscript; source-reported values remain separate and are not pooled.

illustrative profiles for juvenile absence epilepsy, benign focal epilepsy of childhood, and temporal lobe epilepsyReported: ContralateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational examples mention left perirolandic and left mesial temporal EZs paired with right clonic/versive phenomena, while explicitly stating that no causal or contralateral rule is asserted.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdfNarrative, educational, or cited context · 1 finding
loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a proposal and narrative synthesis, not a primary empirical study. The authors review prior classification approaches, define the five dimensions, provide tables and conceptual figures, and demonstrate the proposed format with illustrative profiles. The framework is stated to apply to patients with epilepsy, defined here as at least two spontaneous epileptic seizures; for patients with unclear epileptic or nonepileptic events, the source recommends the term paroxysmal event. Clinical history, seizure semiology, EEG, MRI, other diagnostic studies, and etiologic information are translated into a best available working classification that can be refined as information accrues. No formal study cohort, sampling method, reference standard, comparator cohort, or statistical analysis is reported.
Findings
  • illustrative profiles for juvenile absence epilepsy, benign focal epilepsy of childhood, and temporal lobe epilepsyThe source contrasts a generalized juvenile-absence profile associated with typical absence seizures and 3-Hz spike-and-wave complexes, a benign-focal-epilepsy-of-childhood profile with left perirolandic EZ and right clonic seizures, and a temporal-lobe profile with left mesial temporal EZ, abdominal aura to automotor seizure to right versive seizure to generalized tonic-clonic seizure, left hippocampal sclerosis, and febrile convulsions during infancy.PDF p.7, illustrative juvenile-absence, benign-focal-epilepsy-of-childhood, and temporal-lobe profiles

1 contributing manuscript; source-reported values remain separate and are not pooled.

indispensable ALA and PLA surgical sparingReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited indispensable language regions were described in the left hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • indispensable ALA and PLA surgical sparingThe review reports Ius et al.'s low-grade-glioma awake-surgery observation that ALA could be largely and safely resected if a small portion anterior to the left ventral premotor cortex and contiguous with subcortical language tracts was spared, with the same observation for the angular gyrus and posterior superior temporal gyrus of PLA.PDF p.5, Mapping Indispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

inducing factors of reflex seizures; disconnection of this circuitReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The left-sided network is single-case mechanistic context rather than lateralizing evidence for a semiologic sign.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • inducing factors of reflex seizures; disconnection of this circuitThe authors state that increased proprioceptive feedback via startle responses and hyperexcitability of motor-related areas are thought to induce reflex seizures, and that medial frontal resection might disconnect this circuit and stop the patient's reflex seizures.PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

inferior frontal versus anterior temporal F7 fieldReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

In this single case, the EEG field and lesion were left-sided, right versive head-eye deviation was contralateral to that left onset interpretation, and bilateral tonic-clonic activity represented later spread.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • inferior frontal versus anterior temporal F7 fieldIn the illustrated case with speech arrest, automatisms, postictal aphasia, and right versive head and eye deviation during rare bilateral tonic-clonic progression, recurrent sharp waves and ictal activity maximal at F7 were interpreted as left inferior frontal rather than anterior temporal because the field involved Fp1 and F3 more than Sp1 and T7; MRI showed a left inferior frontal lesion.PDF p.405; PDF p.406; PDF p.407

1 contributing manuscript; source-reported values remain separate and are not pooled.

insular versus SI and SII somato-sensory responsesReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 5 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

In the cited stimulation comparison, SI responses were strictly contralateral except poorly lateralized perioral sensations, whereas insular responses could be bilateral or ipsilateral and strictly ipsilateral responses were exclusive to insular stimulation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 5 reported values
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • insular versus SI and SII somato-sensory responsesRestating its cited comparison study, the source says insular somato-sensory responses involve larger skin territories than SI/SII responses, can be bilateral or ipsilateral rather than the SI pattern of strict contralaterality except for poorly lateralized perioral sensations, and that pain occurs after both SII and insular stimulation at about 10% with similar 4-9/10 intensity and stimulus threshold; SII responses were bilateral in 36% versus 30% for insular responses, and strictly ipsilateral responses were exclusive to insular stimulation.PDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
Reported values
  • SII responses bilateral in 36%insular versus SI and SII somato-sensory responsesPercentage · Cited comparison of somato-sensory responses after SI, SII, and insular stimulation · SII stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Pain about 10% after SII stimulationinsular versus SI and SII somato-sensory responsesPercentage · Cited comparison of somato-sensory responses after SI, SII, and insular stimulation · SII stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Pain intensity 4–9/10insular versus SI and SII somato-sensory responsesRange · n/N 9/10 · Cited comparison of somato-sensory responses after SI, SII, and insular stimulation · SII and insular stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Insular responses bilateral in 30%insular versus SI and SII somato-sensory responsesPercentage · Cited comparison of somato-sensory responses after SI, SII, and insular stimulation · Insular stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses
  • Pain about 10% after insular stimulationinsular versus SI and SII somato-sensory responsesPercentage · Cited comparison of somato-sensory responses after SI, SII, and insular stimulation · Insular stimulation · stimulation-evoked somato-sensory responsePDF p.4, Somato-sensory Responses; PDF p.7, Somato-sensory Responses

1 contributing manuscript; source-reported values remain separate and are not pooled.

interictal SEEG activity in TLEReported: Ipsilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates preferential propagation from hippocampal activity to the ipsilateral entorhinal cortex and amygdala and to posterior cingulate, with distant synchrony indicating network involvement.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • interictal SEEG activity in TLESEEG detected 25% more discharges than scalp EEG and showed broader IED distribution; synchronous activity between distant interconnected structures, multifocal independent spikes, and preferential hippocampal spread to ipsilateral entorhinal cortex, amygdala, and posterior cingulate can reveal network connectivity and propagation.PDF p.15, Interictal SEEG activity in TLE
Reported values
  • 25% more discharges detected by SEEG than scalp EEGinterictal SEEG activity in TLEPercentage · patients with TLE undergoing SEEG · interictalPDF p.15, Interictal SEEG activity in TLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

Interictal versus postictal language testingReported: Dominant hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study found interictal and postictal language testing equally accurate for lateralising language-dominant temporal-lobe seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Interictal versus postictal language testingOne LTM study of 212 seizures in 60 patients found interictal and postictal language testing equally accurate for lateralising language-dominant temporal-lobe seizures after use of the Boston Naming Test.PDF p.6, section 1.9
Reported values
  • 212 seizuresInterictal versus postictal language testingCount · 212 seizures in 60 patients with language-dominant temporal-lobe seizures · LTM language-testing study · interictal and postictalPDF p.6, section 1.9

1 contributing manuscript; source-reported values remain separate and are not pooled.

Jaw jerkingReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Reading-triggered right-predominant jaw/facial jerks were associated with brief EEG discharges often showing left predominance or left lateralization, although generalized fields can occur.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • reading epilepsy with jaw jerksIn the illustrated reflex epilepsy case, right-predominant facial twitching was triggered by reading and a single brief spike-and-wave or sharp-theta discharge was temporally associated with the subtle jaw jerks; the source notes that such discharges may be generalized, bifrontocentrotemporal with left predominance, or lateralized to the left hemisphere.PDF p.405; PDF p.406

1 contributing manuscript; source-reported values remain separate and are not pooled.

juvenile myoclonic epilepsy and generalized EEG fragmentsReported: Bilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review preserves unilateral and bilateral myoclonus, generalized activity, and focal-appearing fragments as context-dependent features of juvenile myoclonic epilepsy.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • juvenile myoclonic epilepsy and generalized EEG fragmentsIn juvenile myoclonic epilepsy, myoclonic seizures may be unilateral or bilateral and generalized tonic-clonic or absence seizures may coexist; EEG usually shows a normal background with generalized 3-6 Hz spike-wave or irregular polyspike activity with frontal predominance, although a minority of patients have focal or markedly lateralized fragments of generalized discharges.PDF p.301; PDF p.302
Reported values
  • generalized 3–6 Hz spike-wave or irregular polyspike activityjuvenile myoclonic epilepsy and generalized EEG fragmentsRange · juvenile myoclonic epilepsy teaching groups · Juvenile myoclonic epilepsy · interictal and ictalPDF p.301; PDF p.302

1 contributing manuscript; source-reported values remain separate and are not pooled.

lateralized or localized ictal patterns in frontal epilepsyReported: BilateralAlso reported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Frontal epilepsy may show lateralized patterns, bilateral synchrony, or paradoxical apparent contralateral scalp lateralization from an interhemispheric generator.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • lateralized or localized ictal patterns in frontal epilepsyLateralized or localized ictal patterns were reported in 33%-50% of frontal epilepsy cases; the chapter also describes secondary bilateral synchrony and a paradoxical ictal lateralization pattern when a generator near the interhemispheric fissure projects an obliquely oriented dipole to the opposite hemisphere.PDF p.7, Frontal lobe epilepsy, paragraph before "Electroencephalography in Parietal Lobe Epilepsy"
Reported values
  • 33%-50% lateralized or localized ictal patternslateralized or localized ictal patterns in frontal epilepsyPercentage · Patients with frontal lobe epilepsy; exact cohorts not reported · ictalPDF p.7, Frontal lobe epilepsy, paragraph before "Electroencephalography in Parietal Lobe Epilepsy"

1 contributing manuscript; source-reported values remain separate and are not pooled.

lateralized rhythmic temporal activity at seizure onsetReported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates lateralized rhythmic temporal activity as usually predicting ipsilateral temporal onset, with reported false lateralization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • lateralized rhythmic temporal activity at seizure onsetLateralized rhythmic alpha or theta activity in the ipsilateral temporal region within the first 30 seconds of clinical or electrographic onset was observed in approximately 80% of patients with mesial temporal origin and correctly predicted ipsilateral temporal onset in over 80% of invasively confirmed TLE; false lateralization with scalp electrodes occurred in 3%-13% of MTLE patients.PDF p.4, Temporal lobe seizures, paragraph on lateralized rhythmic activity
Reported values
  • Correct ipsilateral temporal-onset prediction over 80%lateralized rhythmic temporal activity at seizure onsetPercentage · Patients with mesial temporal origin or invasively confirmed temporal lobe epilepsy · Invasively confirmed TLE · ictal onsetPDF p.4, Temporal lobe seizures, paragraph on lateralized rhythmic activity
  • False scalp-EEG lateralization 3%–13%lateralized rhythmic temporal activity at seizure onsetRange · Patients with mesial temporal origin or invasively confirmed temporal lobe epilepsy · MTLE · ictal onsetPDF p.4, Temporal lobe seizures, paragraph on lateralized rhythmic activity
  • Lateralized rhythmic temporal activity observed in approximately 80%lateralized rhythmic temporal activity at seizure onsetPercentage · Patients with mesial temporal origin or invasively confirmed temporal lobe epilepsy · Mesial temporal origin · ictal onsetPDF p.4, Temporal lobe seizures, paragraph on lateralized rhythmic activity

1 contributing manuscript; source-reported values remain separate and are not pooled.

left and right hippocampal stimulation; word-recognition and face-recognition memory deficitsReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited stimulation comparison reports left hippocampal stimulation with word-recognition deficits and right hippocampal stimulation with face-recognition deficits.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • left and right hippocampal stimulation; word-recognition and face-recognition memory deficitsThe source reports hemisphere-specific memory deficits in which left hippocampal stimulation produced word-recognition memory deficits, whereas right hippocampal stimulation produced face-recognition memory deficits.PDF p.11, hemisphere-specific memory paragraph; PDF p.19, Table 10.1, Memory Functions

1 contributing manuscript; source-reported values remain separate and are not pooled.

left-hemisphere distribution of language sitesReported: BilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study restatement reports language sites in both hemispheres, at least three patients with bilateral fMRI representation, and a left-hemisphere distribution across temporal, frontal, and parietal lobes.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • left-hemisphere distribution of language sitesThe review reports that Cuisenier et al. found language sites in both hemispheres, with at least three patients showing bilateral fMRI language representation; among left-hemisphere language sites, more than half were temporal, one fifth frontal, and 5% parietal.PDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
Reported values
  • 5% parietalleft-hemisphere distribution of language sitesPercentage · Cuisenier et al. sEEG study; Table 1 lists 42 subjects, while the bilateral-fMRI statement gives at least three patients; endpoint denominators not reported · parietal · sEEG language mapping and comparison with fMRI representationPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • one fifth frontalleft-hemisphere distribution of language sitesPercentage · Cuisenier et al. sEEG study; Table 1 lists 42 subjects, while the bilateral-fMRI statement gives at least three patients; endpoint denominators not reported · frontal · sEEG language mapping and comparison with fMRI representationPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • at least three patients showing bilateral fMRI language representationleft-hemisphere distribution of language sitesCount · Cuisenier et al. sEEG study; Table 1 lists 42 subjects, while the bilateral-fMRI statement gives at least three patients; endpoint denominators not reported · bilateral fMRI representation · sEEG language mapping and comparison with fMRI representationPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • more than half were temporalleft-hemisphere distribution of language sitesPercentage · Cuisenier et al. sEEG study; Table 1 lists 42 subjects, while the bilateral-fMRI statement gives at least three patients; endpoint denominators not reported · temporal · sEEG language mapping and comparison with fMRI representationPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

Left/right and named somatotopic area modifiersReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational classification states that left and right refer to the somatotopic body side of the symptom, not to a brain region, with left-hand, throat, and left-foot examples.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Left/right and named somatotopic area modifiersWhen symptom somatotopy is well defined, the classification specifies the involved body region; “left” and “right” refer strictly to somatotopic localization of symptoms rather than to a brain region, with examples such as left hand clonic seizure, throat somatosensory aura, and left foot tonic seizure.PDF p.6, Table 2; PDF p.6, Somatotopic modifiers

1 contributing manuscript; source-reported values remain separate and are not pooled.

Left/right hemispheric modifierReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational statement pairs postictal aphasia with a left-language-dominant left-hemisphere example and left-hand/arm dystonia with right-hemispheric classification, while also naming preserved consciousness and ictal speech as possible lateralizing signs.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Left/right hemispheric modifierThe authors state that dystonic posturing during a complex motor seizure, preserved consciousness or ictal speech during an automotor seizure, and postictal aphasia may identify the hemisphere of seizure origin, and that the presence of such signs strongly suggests that hemisphere; if the patient is left-hemisphere dominant for language, postictal aphasia is used in the source’s left-hemispheric example, while preserved consciousness with left-hand/arm dystonia is classified as a right-hemispheric automotor seizure.PDF p.6, Table 2; PDF p.6, Left and right hemispheric; PDF p.6, examples

1 contributing manuscript; source-reported values remain separate and are not pooled.

LTLE, temporopolar, and temporal-plus interictal EEG distributionsReported: Contralateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review reports about one-third of LTLE patients with anterior-temporal IEDs, lateral-temporal predominance, contralateral IEDs in 10%–20% of LTLE versus MTLE, temporopolar suggestion from anterior temporo-basal amplitude, and precentral IEDs in temporal plus epilepsy.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • LTLE, temporopolar, and temporal-plus interictal EEG distributionsAbout one-third of LTLE patients show IEDs over anterior temporal electrodes, while most have lateral-temporal predominance; contralateral IEDs are less frequent in LTLE than MTLE (10%–20%), maximal anterior temporal or anterior temporo-basal amplitude can suggest temporopolar epilepsy, and temporal plus epilepsy more often has precentral IEDs.PDF p.11, Localization value of interictal epileptiform discharges
Reported values
  • about one-thirdLTLE, temporopolar, and temporal-plus interictal EEG distributionsOther reported value · patients with LTLE, temporopolar epilepsy, or temporal plus epilepsy · LTLE · interictalPDF p.11, Localization value of interictal epileptiform discharges
  • 10%–20%LTLE, temporopolar, and temporal-plus interictal EEG distributionsRange · patients with LTLE, temporopolar epilepsy, or temporal plus epilepsy · LTLE · interictalPDF p.11, Localization value of interictal epileptiform discharges

1 contributing manuscript; source-reported values remain separate and are not pooled.

mesial temporal seizure spreadReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited literature is restated as ipsilateral temporal/frontal neocortical spread followed by spread to the contralateral hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfNarrative, educational, or cited context · 1 finding
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • mesial temporal seizure spreadThe discussion states that, in mesial TLE, the most common spreading ictal EEG pattern involves ipsilateral temporal and frontal neocortex before spreading to the contralateral hemisphere.PDF p.5, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

minimum seizure count for independent bilateral temporal patternsReported: Bilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

No sign-specific lateralizing information is present.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • minimum seizure count for independent bilateral temporal patternsA minimum of four seizures was required to identify 100% of 18 patients whose ictal patterns arose independently from both temporal regions.PDF p.11, Surgical Evaluation, paragraph on the number of seizures needed
Reported values
  • Minimum seizure count for identification n=4minimum seizure count for independent bilateral temporal patternsCount · 18 patients with ictal patterns arising independently from both temporal regions · ictalPDF p.11, Surgical Evaluation, paragraph on the number of seizures needed
  • Patients identified 18/18 (100%)minimum seizure count for independent bilateral temporal patternsPercentage · n/N 18/18 · 18 patients with ictal patterns arising independently from both temporal regions · ictalPDF p.11, Surgical Evaluation, paragraph on the number of seizures needed

1 contributing manuscript; source-reported values remain separate and are not pooled.

motor sequence in secondarily generalized tonic-clonic seizuresReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review states that tonic face and versive signs point contralaterally, M2e points contralateral to the raised arm, and the sign of four points contralateral to the extended arm.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • motor sequence in secondarily generalized tonic-clonic seizuresThe review describes a sequence beginning with version and tonic pulling of the face to the contralateral side, followed by the M2e fencing position and then asymmetric tonic limb posturing called the “sign of four.” It states that confidence in lateralizing the epileptogenic zone increases when at least two of the four signs are observed; the tonic face and versive signs point contralaterally, M2e points to the hemisphere contralateral to the raised arm, and the sign of four to the hemisphere contralateral to the extended arm. These signs lateralize but do not localize seizure origin.PDF p.4, Tonic seizures
Reported values
  • Confidence stated when 2 or more of 4 signs are observedmotor sequence in secondarily generalized tonic-clonic seizuresCount · n/N 2/4 · Patients with secondarily generalized tonic-clonic seizures; no cohort reported · Ictal motor sequence before secondary generalizationPDF p.4, Tonic seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

multi-time resolution processingReported: Bilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes right selectivity for longer-timescale integration, less-selective left processing, and more bilateral shorter-timescale processing.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • multi-time resolution processingThe authors describe segmental information as requiring temporal windows of approximately 20–50 ms and suprasegmental or syllabic information as occurring over roughly 150–300 ms. They propose concurrent processing on these timescales, with functional MRI evidence of hemispheric asymmetry: the right hemisphere shows selectivity for longer-term integration, the left hemisphere is less selective, longer-timescale integration is predominantly right-hemisphere, and shorter-timescale integration is more bilateral.PDF p.4, “Multi-time resolution processing”
Reported values
  • roughly 150–300 msmulti-time resolution processingRange · Behavioral and functional-imaging speech-processing evidence; exact cohorts Not reported · suprasegmental or syllabic information · Speech processing across segmental and syllabic timescalesPDF p.4, “Multi-time resolution processing”
  • approximately 20–50 msmulti-time resolution processingRange · Behavioral and functional-imaging speech-processing evidence; exact cohorts Not reported · segmental information · Speech processing across segmental and syllabic timescalesPDF p.4, “Multi-time resolution processing”

1 contributing manuscript; source-reported values remain separate and are not pooled.

occipital interictal and ictal EEGReported: Bilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review reports bilateral or diffuse epileptiform activity, occipital-restricted activity, and spread from occipital regions to mesial temporal, SMA, or dorsolateral frontal regions.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • occipital interictal and ictal EEGOccipital interictal EEG commonly involves posterior temporal regions; bilateral independent, bilateral synchronous, or diffuse epileptiform activity was reported in 30%-50% of cases, occipital-restricted epileptiform activity in 8%-18%, and ictal onset restricted to the occipital lobe in less than 20%. Invasive recordings showed spread from occipital regions to mesial temporal structures, the supplementary motor area, or dorsolateral frontal convexity before generalization.PDF p.9, Occipital lobe epilepsy, interictal EEG paragraph; PDF p.10, continuation before "Surgical Evaluation"
Reported values
  • less than 20% occipital-restricted ictal onsetoccipital interictal and ictal EEGPercentage · Patients with occipital lobe epilepsy · occipital-restricted · interictal and ictalPDF p.9, Occipital lobe epilepsy, interictal EEG paragraph; PDF p.10, continuation before "Surgical Evaluation"
  • 30%–50% bilateral independent, bilateral synchronous, or diffuse epileptiform activityoccipital interictal and ictal EEGRange · Patients with occipital lobe epilepsy · bilateral or diffuse · interictal and ictalPDF p.9, Occipital lobe epilepsy, interictal EEG paragraph; PDF p.10, continuation before "Surgical Evaluation"
  • 8%–18% occipital-restricted epileptiform activityoccipital interictal and ictal EEGRange · Patients with occipital lobe epilepsy · occipital-restricted · interictal and ictalPDF p.9, Occipital lobe epilepsy, interictal EEG paragraph; PDF p.10, continuation before "Surgical Evaluation"

1 contributing manuscript; source-reported values remain separate and are not pooled.

occipital lobe seizure visual semiologyReported: Contralateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review states that suprasylvian spread from occipital seizures to mesial frontal regions can produce contralateral tonic posturing.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • occipital lobe seizure visual semiologyOccipital lobe epilepsy comprises 8% of focal epilepsy cases. SPS may involve elementary visual phenomena, ocular movement sensations, nystagmus, eye flutter or forced blinking, ictal amaurosis, and versive head or eye movements; elementary visual hallucinations were the most common manifestation in 50%-60% of cases. Infrasylvian spread to temporal regions was associated with altered awareness and automatisms, suprasylvian spread to mesial frontal regions with contralateral tonic posturing, and lateral spread with focal motor or sensory seizures; multiple seizure types occurred in one-third to one-half of patients.PDF p.9, Electroencephalography in Occipital Lobe Epilepsy, clinical manifestations paragraphs
Reported values
  • 8%occipital lobe seizure visual semiologyPercentage · Patients with occipital lobe epilepsy · occipital lobe epilepsy · ictalPDF p.9, Electroencephalography in Occipital Lobe Epilepsy, clinical manifestations paragraphs
  • 50%–60%occipital lobe seizure visual semiologyRange · Patients with occipital lobe epilepsy · occipital lobe epilepsy · ictalPDF p.9, Electroencephalography in Occipital Lobe Epilepsy, clinical manifestations paragraphs
  • one-third to one-halfoccipital lobe seizure visual semiologyRange · Patients with occipital lobe epilepsy · occipital lobe epilepsy · ictalPDF p.9, Electroencephalography in Occipital Lobe Epilepsy, clinical manifestations paragraphs

1 contributing manuscript; source-reported values remain separate and are not pooled.

occipital manifestationsReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational source lists contralateral eye deviation when specified among source-reported occipital manifestations; other listed ocular signs have no supplied direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdfNarrative, educational, or cited context · 1 finding
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source reports 42 medically refractory patients with clinically and electrographically supported occipital lobe epilepsy who underwent surgery during 1930-1991. Clinical history, serial scalp EEG, imaging when available, pre- and post-excision electrocorticography, depth recordings in selected patients, and intra-operative cortical stimulation were used. The EEG and electrocorticography denominators vary by available study and are preserved per result. The source’s operational occipital localization and its historical terminology are retained without adding a Brodmann-area mapping or a Lüders/ILAE classification not stated by the source.
Findings
  • other occipital manifestationsThe source lists contralateral tonic eye deviation, clonic eye deviation, nystagmoid eye movements, blinking, and a sensation of ocular movement at seizure onset as reported occipital manifestations.PDF p.2-3, Introduction

1 contributing manuscript; source-reported values remain separate and are not pooled.

opercular language responsesReported: BilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited naming-task ECS study found bilateral frontal-opercular language sites with larger left volume and left-only posterior temporal-opercular responses.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdfNarrative, educational, or cited context · 1 finding · 4 reported values
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is not an original cohort or pooled analysis. The review discusses published sEEG/ECS, subdural ECS, intraoperative ECS, intracranial recording, fMRI, and surgical-outcome studies; Table 1 lists 16 reviewed depth-electrode studies with study-level subject counts ranging from 1 to 172, including pediatric and adult populations. The source does not define one aggregate analysis population, does not report a pooled estimate, and states that no proper comparison has been made between resections with and without extra-operative or intra-operative language mapping. Stimulation protocols and language-task choices are described as methodological context; findings below retain study-specific populations and units where the review reports them.
Findings
  • opercular language responsesThe review reports that Mălîia et al. found bilateral positive language sites producing speech arrest in the frontal operculum with a larger left-hemisphere volume distribution of about 1.1 cm3; 90% of naming-task responses were expressive aphasia and the remainder mixed, while posterior temporal operculum responses occurred only on the left in 11% of stimulated contacts and produced expressive aphasia in two thirds of cases; one parietal site produced expressive language deficit.PDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
Reported values
  • about 1.1 cm3 larger left-hemisphere frontal-opercular volume distributionopercular language responsesOther reported value · 31-subject Mălîia et al. study listed in Table 1; endpoint denominators not reported · Left frontal operculum · ECS during a naming taskPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • one parietal site produced expressive language deficitopercular language responsesCount · 31-subject Mălîia et al. study listed in Table 1; endpoint denominators not reported · Parietal site · ECS during a naming taskPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • 11% of stimulated contacts in posterior temporal operculum produced responsesopercular language responsesPercentage · 31-subject Mălîia et al. study listed in Table 1; endpoint denominators not reported · Left posterior temporal operculum · ECS during a naming taskPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG
  • 90% of naming-task responses were expressive aphasiaopercular language responsesPercentage · 31-subject Mălîia et al. study listed in Table 1; endpoint denominators not reported · Frontal operculum · ECS during a naming taskPDF p.6, Table 1; PDF p.7, Mapping Indispensable Eloquent Language Cortex Using sEEG

1 contributing manuscript; source-reported values remain separate and are not pooled.

operculo-insular and SI functional pain processingReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

No source-supported hemispheric direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 1 finding
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • operculo-insular and SI functional pain processingFunctional neuroimaging studies are summarized as showing increased bilateral operculo-insular activity during discrimination of stimuli above a painful threshold and with progressive pain intensity; SI is described as having sparse nociceptive responses and being more involved in tactile qualitative and localizing functions than in pain perception.PDF p.5, Somatosensory Pain as a Symptom of Seizures, Localization

1 contributing manuscript; source-reported values remain separate and are not pooled.

Oral phenomenaReported: ContralateralAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational opercular-seizure description associates oral symptoms and speech difficulty with focal clonic movements of the contralateral face.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfNarrative, educational, or cited context · 1 finding
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • oral symptoms; sialorrhea; speech difficulties; focal clonic movements of the contralateral faceThe source's introductory clinical description associates opercular seizures with oral symptoms such as sialorrhea and speech difficulties, together with focal clonic movements of the contralateral face.PDF p.2, Introduction

1 contributing manuscript; source-reported values remain separate and are not pooled.

parietal and occipital seizure manifestationsReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

This review describes contralateral version and clonic activity after posterior-cortex seizure spread; it does not provide an independent lateralization estimate.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • parietal and occipital seizure manifestationsParietal epileptogenic lesions may produce vertigo, body-image disturbance, and visual illusions or hallucinations; tonic posturing is associated with superior-parietal involvement and automatisms with inferior-parietal involvement. Occipital seizures may include contralateral eye deviation, blinking, eye-movement sensations, nystagmus, and contralateral head version, while spread to dorsolateral frontal cortex, SSMA, or limbic structures produces contralateral version and clonic activity, hypermotor or asymmetric tonic seizures, or oral and gestural automatisms, respectively.PDF p.6, section 8.2 Parieto-occipital lobe epilepsy

1 contributing manuscript; source-reported values remain separate and are not pooled.

parietal and occipital semiologyReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review links a parietal sensory march and selected visual-field findings with contralateral postcentral or visual cortex.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • parietal and occipital semiologyA parietal sensory march suggests postcentral primary sensory cortex involvement contralateral to the ictal discharge, while a sensory aura without march may arise from the second sensory area or parietal operculum; focal weakness may represent a parietal inhibitory motor seizure. Occipital seizures are suggested by elementary visual aura or a contralateral visual-field deficit, complex scenes by occipitotemporal involvement, and variable spread to temporal or frontal regions by oroalimentary or asymmetric tonic manifestations.PDF p.54; PDF p.55

1 contributing manuscript; source-reported values remain separate and are not pooled.

parietal lobe seizure somatosensory and motor semiologyReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review synthesis describes parietal seizures as commonly producing contralateral extremity or facial somatosensory symptoms and contralateral version, with some bilateral somatosensory manifestations.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • parietal lobe seizure somatosensory and motor semiologyParietal lobe seizures comprise 5%-6% of focal epilepsy cases in medical and surgical series. SPS commonly involve contralateral extremity or facial somatosensory symptoms, sometimes bilaterally, including paresthesias, numbness, pain, or cold/burning sensations; parietal CPS may show asymmetric tonic limb posturing, unilateral clonic activity, and contralateral version, with frontal activation or temporal spread producing the stated motor or awareness/automatisms patterns.PDF p.7, Electroencephalography in Parietal Lobe Epilepsy, clinical semiology paragraphs
Reported values
  • 5%-6% of focal epilepsy casesparietal lobe seizure somatosensory and motor semiologyPercentage · Medical and surgical series of parietal lobe epilepsy · ictalPDF p.7, Electroencephalography in Parietal Lobe Epilepsy, clinical semiology paragraphs

1 contributing manuscript; source-reported values remain separate and are not pooled.

pathological hippocampus in the EZ; left hippocampus outside the EZReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited comparison contrasts a pathological hippocampus included in the EZ with a left hippocampus outside the EZ in a patient with right temporal-lobe seizure onset.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • pathological hippocampus in the EZ; left hippocampus outside the EZIn a cited comparison, stimulation of a pathological hippocampus included in the EZ failed to induce a verbal memory deficit, whereas electrical stimulation of the left hippocampus outside the EZ in a patient with right temporal-lobe seizure onset interfered with verbal learning performance.PDF p.12, memory stimulation and EZ paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

pediatric epileptic spasms and Lennox-Gastaut syndromeReported: Bilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The pediatric syndrome description is multifocal or generalized rather than consistently lateralizing.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • pediatric epileptic spasms and Lennox-Gastaut syndromeEpileptic spasms may have normal waking EEG but multifocal epileptiform activity and electrodecrement emerging in sleep, while Lennox-Gastaut syndrome is associated with multiple seizure types including tonic, atonic, tonic-clonic, and absence-type seizures, slow spike-wave complexes below 2.5 Hz, and tonic seizures with overall voltage attenuation or electrodecrement-like activity.PDF p.294; PDF p.296
Reported values
  • slow spike-wave frequency <2.5 Hz in Lennox-Gastaut syndromepediatric epileptic spasms and Lennox-Gastaut syndromeCount · children with epileptic spasms or Lennox-Gastaut syndrome · interictal, sleep, and ictalPDF p.294; PDF p.296

1 contributing manuscript; source-reported values remain separate and are not pooled.

pediatric left frontal cortical dysplasia with delayed clinical onsetReported: Left hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

A left frontal seizure-generation region was associated with right eye deviation and head turning, with electrographic onset preceding clinical onset.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • pediatric left frontal cortical dysplasia with delayed clinical onsetIn the pediatric case, seizures began clinically with right eye deviation and head turning, while interictal activity was frequent in the left frontal region and ictal EEG became organized and rhythmic over left frontal-central electrodes; electrographic onset preceded clinical onset by about 10 seconds, MRI showed left frontal cortical dysplasia, and stereo-EEG defined a left frontal seizure-generation region with intermittent spread.PDF p.408; PDF p.409; PDF p.410
Reported values
  • EEG onset preceded clinical onset by approximately 10 secondspediatric left frontal cortical dysplasia with delayed clinical onsetCount · 38-month-old girl with early-onset seizures and left frontal cortical dysplasia · interictal and ictal onset/propagationPDF p.408; PDF p.409; PDF p.410

1 contributing manuscript; source-reported values remain separate and are not pooled.

pediatric right perituberal frontal onset with rapid spreadReported: Right hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The case observation records right central/right perituberal frontal onset, right temporal spread, and a left-sided motor manifestation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • pediatric right perituberal frontal onset with rapid spreadIn the pediatric tuberous-sclerosis case, a right central rhythmic EEG discharge preceded a head drop by about 12 seconds; the clinical pattern included an abrupt facial grimace, left-arm grabbing by the right hand, and head drops, and stereo-EEG confirmed right perituberal/right frontal onset with rapid secondary spread to the right temporal lobe.PDF p.410; PDF p.411
Reported values
  • electrographic onset preceded head drop by approximately 12 secondspediatric right perituberal frontal onset with rapid spreadCount · 4-year-old boy with tuberous sclerosis complex and focal seizures · ictal onset and propagationPDF p.410; PDF p.411

1 contributing manuscript; source-reported values remain separate and are not pooled.

perceived side of AP during cortical stimulationReported: ContralateralAlso reported: IpsilateralNo single reliable side1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Among 13 stimulation cases with individual side information, perceived auditory phenomena were predominantly contralateral (9), with one ipsilateral and three bilateral/inside-head cases.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 1 finding · 3 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • perceived side of AP during cortical stimulationIndividual perceived-side information was rarely reported; among 13 stimulation cases with individual information, AP were contralateral to the stimulated area in 9 cases and ipsilateral in 1, while the remaining cases were described as bilateral or inside the head rather than lateralized to one ear.PDF p.5, section 5, cortical-stimulation lateralization paragraph
Reported values
  • nine casesperceived side of AP during cortical stimulationCount · Individual cortical-stimulation cases with perceived-side information · contralateral AP · Electrically induced APPDF p.5, section 5, cortical-stimulation lateralization paragraph
  • 13 casesperceived side of AP during cortical stimulationCount · Individual cortical-stimulation cases with perceived-side information · bilateral or inside the head · Electrically induced APPDF p.5, section 5, cortical-stimulation lateralization paragraph
  • one caseperceived side of AP during cortical stimulationCount · Individual cortical-stimulation cases with perceived-side information · ipsilateral AP · Electrically induced APPDF p.5, section 5, cortical-stimulation lateralization paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

perceived side of AP in the Jaroszynski seriesReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The cited Jaroszynski series reports bilateral, contralateral, and ipsilateral perceived auditory phenomena relative to stimulation.

Source-defined result groups 3
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelycontralateral · Bilateral versus contralateral versus ipsilateral AP · Auditory response1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelybilateral · Bilateral versus contralateral versus ipsilateral AP · Auditory response1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralSource-defined values retained separatelyipsilateral · Bilateral versus contralateral versus ipsilateral AP · Auditory response1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 1 finding · 3 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • perceived side of AP in the Jaroszynski seriesThe review states that Jaroszynski et al. reported 70 bilateral AP, 57 contralateral AP, and 4 AP ipsilateral to stimulation.PDF p.5, section 5, cortical-stimulation lateralization paragraph
Reported values
  • bilateral 70perceived side of AP in the Jaroszynski seriesCount · Cited Jaroszynski cortical-stimulation series · bilateral · Electrically induced APPDF p.5, section 5, cortical-stimulation lateralization paragraph
  • contralateral 57perceived side of AP in the Jaroszynski seriesCount · Cited Jaroszynski cortical-stimulation series · contralateral · Electrically induced APPDF p.5, section 5, cortical-stimulation lateralization paragraph
  • ipsilateral 4perceived side of AP in the Jaroszynski seriesCount · Cited Jaroszynski cortical-stimulation series · ipsilateral · Electrically induced APPDF p.5, section 5, cortical-stimulation lateralization paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

perceived side of AP in the Mazzola insular-stimulation seriesReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The cited Mazzola stimulation series is restated as 58% contralateral, 36% bilateral, and 6% ipsilateral perceived auditory phenomena.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 1 finding · 3 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • perceived side of AP in the Mazzola insular-stimulation seriesThe review states that the Mazzola series reported AP predominantly contralateral to stimulation (58%), followed by bilateral (36%) and rarely ipsilateral (6%) responses.PDF p.5, section 5, cortical-stimulation lateralization paragraph
Reported values
  • Ipsilateral perceived AP 6%perceived side of AP in the Mazzola insular-stimulation seriesPercentage · Cited Mazzola et al. presurgical insular-stimulation series · Ipsilateral · Electrical stimulation responsePDF p.5, section 5, cortical-stimulation lateralization paragraph
  • Bilateral perceived AP 36%perceived side of AP in the Mazzola insular-stimulation seriesPercentage · Cited Mazzola et al. presurgical insular-stimulation series · Bilateral · Electrical stimulation responsePDF p.5, section 5, cortical-stimulation lateralization paragraph
  • Contralateral perceived AP 58%perceived side of AP in the Mazzola insular-stimulation seriesPercentage · Cited Mazzola et al. presurgical insular-stimulation series · Contralateral · Electrical stimulation responsePDF p.5, section 5, cortical-stimulation lateralization paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

phonological processing and the superior temporal sulcus (STS)Reported: BilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes bilateral phonological STS organization with a possible mild leftward bias.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • phonological processing and the superior temporal sulcus (STS)The review states that portions of the STS are important for phonological representation or processing, are activated during speech perception, speech production, and active maintenance of phonemic information, and can respond preferentially to phonemic acoustic signals relative to complex non-speech signals. It reports that STS activity is modulated by phonological-neighborhood density, with middle-to-posterior STS activation in both hemispheres greater for high- than low-density words, and proposes a crucial phonological STS region extending from the most anterolateral Heschl’s gyrus to the posterior-most Sylvian fissure, with bilateral organization and a mild leftward bias.PDF p.6, “Phonological processing and the STS”; PDF p.7, Figure 3 caption and surrounding discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

planum temporale (PT) heterogeneity and competing functionsReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review limits strong left dominance to a proposed dorsal circuit and cautions that PT and area Spt are not one speech-specific module.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • planum temporale (PT) heterogeneity and competing functionsThe review cautions that the PT should not be treated as one speech-specific module: it reports PT activation for tone sequences, music, spatial signals, visual speech, sign language, and visual motion, and notes four cytoarchitectonic fields in the region. It contrasts the authors’ sensorimotor-integration account with an alternative computational-hub account involving segregation and spectrotemporal pattern matching, allows that sensorimotor and spatial-hearing functions could coexist, and limits the proposed strongly left-dominant dorsal circuit to only part of the PT rather than general cortical auditory or PT function.PDF p.8, “Area Spt is located within the planum temporale”; PDF p.9, limitation of the proposed dorsal circuit

1 contributing manuscript; source-reported values remain separate and are not pooled.

Positive affectReported: Left hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The left stimulation site is procedural context, not a lateralizing semiologic relationship.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • positive affect and anxiolysis; left dorsal anterior cingulum bundle stimulationThe source reports that its group evoked positive affect and anxiolysis by stimulating the left dorsal anterior cingulum bundle in four patients and used the response during intraoperative cognitive mapping without anesthesia sedation.PDF p.13, socio-emotional stimulation paragraph
Reported values
  • total tested-patient denominator not reportedpositive affect and anxiolysis; left dorsal anterior cingulum bundle stimulationCount · Four patients in the cited cingulum-stimulation report · stimulation-induced emotional response during cognitive mappingPDF p.13, socio-emotional stimulation paragraph
  • positive affect and anxiolysis evoked in 4 patientspositive affect and anxiolysis; left dorsal anterior cingulum bundle stimulationCount · Four patients in the cited cingulum-stimulation report · stimulation-induced emotional response during cognitive mappingPDF p.13, socio-emotional stimulation paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

posterior lateral temporal lexical and semantic accessReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes the posterior middle temporal lexical-semantic network as predominantly left-dominant while retaining some bilateral capability and right-hemisphere word comprehension.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • posterior lateral temporal lexical and semantic accessThe review reports strong evidence that posterior middle temporal regions participate in lexical and semantic access from auditory input. It states that damage particularly along the middle temporal gyrus has long been associated with auditory-comprehension deficits, an effect confirmed in a cited large-scale study involving 101 patients; direct cortical stimulation implicates the middle temporal gyrus but also a broader network including most of the superior temporal lobe, anterior portions, and inferior frontal lobe. The review says most evidence indicates left-dominant organization, while the right hemisphere can comprehend words reasonably well, implying bilateral capability with computational differences.PDF p.6, “Lexical, semantic and grammatical linkages”; PDF p.7, summary of posterior lateral temporal access

1 contributing manuscript; source-reported values remain separate and are not pooled.

posterior-cortex semiologyReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Contralateral somatosensory aura suggests parietal origin; simple visual aura suggests occipital origin

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • posterior-cortex semiologyRapid propagation from parieto-occipital seizures to frontal and temporal lobes can produce misleading electroclinical features. The most reliable posterior-cortex semiology includes contralateral somatosensory auras and simple visual auras, which are highly suggestive of parietal and occipital seizure origin, respectively.PDF p.6, section 8.2 Parieto-occipital lobe epilepsy

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal bilateral weaknessReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The sign is explicitly bilateral and therefore non-lateralizing.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Bilateral weaknessThe review identifies bilateral weakness as a rare variant of postictal weakness from SMA seizures.PDF p.4, section 1.6

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal gaze deviation toward EZ (ipsilateral)Reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates contralateral lateralization above 90% under specified timing/quality conditions and 100% under other cited conditions.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdfNarrative, educational, or cited context · 1 finding
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors screened 1,970 patients admitted to adult and pediatric epilepsy monitoring units at University Hospitals of Case Medical Center, Cleveland, Ohio, from 2009 through 2014; 236 had a documented secondarily generalized motor seizure. Inclusion required focal epilepsy, a video-captured seizure manifesting at least two defined motor signs, and evolution to a generalized motor seizure. Exclusions were more than one or an ill-defined EZ, focal motor signs in generalized epilepsy, or no secondary generalization during EMU monitoring. The final cohort was 47 patients: 26 with temporal lobe epilepsy, 13 with frontal lobe epilepsy, and 8 with other epilepsy types (1 parietal, 2 parieto-occipital, 3 hemispheric, 1 fronto-temporal, and 1 central). One representative seizure per patient was selected from the available video and history to reflect the patient's habitual seizure components; the face, trunk, and all limbs were visible in the selected recordings. Three investigators independently reviewed the videos while blinded to all clinical and electrographic data; a motor component was accepted when at least two readers agreed, and Fleiss Kappa quantified inter-observer agreement. The study's sign and sequence analyses therefore use one representative seizure per patient, although the manuscript alternates “patients” and “seizures” for some subset descriptions. EZ localization and lateralization were based on extensive presurgical evaluation including surface and/or invasive EEG, available MRI, PET, and SPECT, followed by presentation at a weekly patient-management conference where an expert panel agreed on each EZ using concordance across modalities; the authors call this their gold standard. The analysis was restricted to simple motor seizures and excluded complex motor seizures such as automatisms. Sequence analysis retained signs meeting the source's “reliable” PPV criterion and required at least two reliable signs; the source uses both PPV ≥80% and PPV >80% wording, documented below without resolving the discrepancy.
Findings
  • version; versive head and eye movementsThe current paper reports that defined versive head and eye deviation lateralized the EZ to the contralateral hemisphere, describes a value above 90% when version occurred within 10 seconds or less before motor generalization, and reports 100% contralateral lateralization under the cited conditions of neck extension and late ipsiversion after the end of a generalized tonic-clonic seizure.PDF p.7, Version definition and cited value; PDF p.13, discussion of version; PDF p.14, discussion of cited version conditions

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal hemispatial neglectReported: Non-dominant hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study associates postictal spatial neglect with right parietal foci and describes it as usually non-dominant, while acknowledging dominant-parietal exceptions.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Postictal hemispatial neglectIn a study of 33 patients, spatial neglect was found on postictal but not interictal examination in patients with right parietal foci and was maximal for left-positioned lines; the review states that neglect is usually non-dominant but can occur with dominant parietal involvement.PDF p.6, section 1.12

1 contributing manuscript; source-reported values remain separate and are not pooled.

postictal language reading testReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study is restated as showing reading within 1 minute after right temporal seizures and disruption beyond 1 minute after dominant-left temporal seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • postictal language reading testThe source restates a cited postictal language study in which all patients with right temporal seizures read a test sentence correctly within 1 minute of seizure termination, whereas patients with dominant left temporal foci had reading disruption for more than 1 minute; atypical language representation limits the generality of the lateralizing interpretation.PDF p.51; PDF p.105; PDF p.442
Reported values
  • within 1 minute versus more than 1 minute postictal reading impairmentpostictal language reading testCount · patients with right or dominant left temporal seizures in the cited postictal language study · postictalPDF p.51; PDF p.105; PDF p.442

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal spatial disorientationReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study is summarized as finding place disorientation more often after right- than left-hemispheric seizures, 11/32 versus 2/33.

Source-defined result groups 2
Lateralization: Left hemisphere / Right hemisphereObserved proportion 6.1%Left hemisphere · Right hemisphere · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 34.4%Right hemisphere · Left hemisphere · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • postictal disorientation for placePlace disorientation occurred more often after right than left hemispheric seizures.PDF p.11, section 5.5
Reported values
  • Place disorientation after right-hemispheric seizures 11/32postictal disorientation for placePercentage · n/N 11/32 · 19 patients contributing 32 right and 33 left hemispheric seizures · Right hemisphere · postictalPDF p.11, section 5.5
  • Place disorientation after left-hemispheric seizures 2/33postictal disorientation for placePercentage · n/N 2/33 · 19 patients contributing 32 right and 33 left hemispheric seizures · Left hemisphere · postictalPDF p.11, section 5.5

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal speech productionReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Educational table assigns immediate postictal speech to the dominant hemisphere.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Immediate postictal speechThe p.3 table lists Immediate postictal speech as Dominant hemisphere.PDF p.3, Lateralizing signs/Localization table row "Immediate postictal speech" (printed p.5)

1 contributing manuscript; source-reported values remain separate and are not pooled.

precentral and bilateral interictal scalp-EEG abnormalitiesReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited restatement contrasts precentral and fronto-temporal interictal abnormalities and notes bilateral abnormalities in the cited temporal-lobe context.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfNarrative, educational, or cited context · 1 finding
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • precentral and bilateral interictal scalp-EEG abnormalitiesThe source contrasts T+ precentral interictal abnormalities with fronto-temporal blunt sharp waves described in mesial-temporal epilepsy and states that bilateral interictal abnormalities had previously been associated with worse surgical outcome in temporal lobe epilepsy.PDF p.9, Scalp-EEG findings

1 contributing manuscript; source-reported values remain separate and are not pooled.

prefrontal seizure case comparison in Fig. 4Reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Rightward head deviation in one illustrated case cannot be converted to a lateralizing direction without the ictal-side relationship.

Source-defined result groups 2
Localization: FrontalSource-defined values retained separatelyFigure 4 panel B · panels A and C · seizure1 manuscript · 1 reported value · not pooled
Localization: FrontalSource-defined values retained separatelyFigure 4 case comparison · Three cases with overlapping regions but different discharge propagation and clinical expression · illustrated patient/seizure panel1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdfCase report or observation · 1 finding · 2 reported values
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with no single study cohort, unified eligibility population, or common comparator. The evidence discussed spans heterogeneous SEEG recordings, cortical stimulation observations, clinical/video studies, ictal SPECT, and cited cases or series. Finding-specific populations and analysis units are retained below; where the review does not report a denominator, it is marked Not reported rather than inferred.
Findings
  • prefrontal seizure case comparison in Fig. 4Fig. 4 shows three SEEG-recorded frontal seizure cases involving common areas but different clinical patterns: in A, fast lateral-premotor activity spreading to medial premotor and anterior or middle cingulate accompanied asymmetric trunk and four-limb posturing, rightward head deviation, and later four-limb clonus; in B, a medial orbital-frontal discharge was initially silent and after 10 seconds spread to anterior cingulate and lateral prefrontal cortex with distal stereotypies and utilization behavior; in C, medial orbital-frontal spiking accompanied subjective fear, followed by simultaneous anterior cingulate and premotor fast activity with standing and frightened screaming.PDF p.7, Fig. 4 and caption; PDF p.8, section 9
Reported values
  • three SEEG-recorded frontal seizure casesprefrontal seizure case comparison in Fig. 4Count · Three illustrated patients with frontal seizures recorded by SEEG; additional cohort details are not reported · Figure 4 case comparison · Ictal onset and propagation; panel B includes a 10-second delay before the second discharge phasePDF p.7, Fig. 4 and caption; PDF p.8, section 9
  • after 10 secondsprefrontal seizure case comparison in Fig. 4Duration · Three illustrated patients with frontal seizures recorded by SEEG; additional cohort details are not reported · Figure 4 panel B · Ictal onset and propagation; panel B includes a 10-second delay before the second discharge phasePDF p.7, Fig. 4 and caption; PDF p.8, section 9

1 contributing manuscript; source-reported values remain separate and are not pooled.

Preserved ictal languageReported: Dominant hemisphereAlso reported: Left hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Preserved language during language-dominant left temporal epilepsy is restated as rare, approximately 5%, with possible limited temporal propagation or false surface-EEG lateralization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 1 finding · 1 reported value
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • preserved language during language-dominant left temporal lobe seizuresThe review states that preserved language during language-dominant left temporal lobe epilepsies is rare, reported at approximately 5%, and may reflect limited seizure propagation within the temporal lobe or false seizure lateralization on surface EEG.PDF p.5, §6
Reported values
  • Rare, approximately 5%preserved language during language-dominant left temporal lobe seizuresPercentage · Patients with language-dominant left temporal lobe epilepsies · ictalPDF p.5, §6

1 contributing manuscript; source-reported values remain separate and are not pooled.

Preserved ictal responsivenessReported: Left hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study reports greater impairment with bitemporal or left-temporal seizures and more preserved consciousness with nondominant-temporal seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Impaired or spared consciousnessA further cited study found consciousness was most commonly impaired in bitemporal or left temporal seizures and more frequently spared in non-dominant temporal lobe seizures.PDF p.3, section 1.3

1 contributing manuscript; source-reported values remain separate and are not pooled.

ProsopagnosiaReported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited stimulation cases reporting selective face-recognition impairment involved right-sided sites.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • transient selective impairment in face recognition; prosopagnosiaThe source reports transient selective face-recognition impairment or prosopagnosia after stimulation of the right inferior occipital gyrus and, in a second patient, the right middle fusiform gyrus; it relates the inferior-occipital site to the right occipital face area and also associates stimulation of the right ventral visual stream with familiar-face recognition deficits.PDF p.12, Face Recognition; PDF p.15, visual perceptive impairments; PDF p.19, Table 10.1, Visuo-Perceptual/Visual-Spatial
Reported values
  • broader tested-patient denominator not reportedtransient selective impairment in face recognition; prosopagnosiaCount · Two patients with stimulation-induced prosopagnosia in the cited visual study, plus patients in additional tumor or epilepsy reports; broader denominator not reported · stimulation-induced face-recognition task responsePDF p.12, Face Recognition; PDF p.15, visual perceptive impairments; PDF p.19, Table 10.1, Visuo-Perceptual/Visual-Spatial
  • prosopagnosia observed in 2 patientstransient selective impairment in face recognition; prosopagnosiaCount · Two patients with stimulation-induced prosopagnosia in the cited visual study, plus patients in additional tumor or epilepsy reports; broader denominator not reported · stimulation-induced face-recognition task responsePDF p.12, Face Recognition; PDF p.15, visual perceptive impairments; PDF p.19, Table 10.1, Visuo-Perceptual/Visual-Spatial

1 contributing manuscript; source-reported values remain separate and are not pooled.

PSS pain matrixReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

No lateralizing direction is reported for the PSS pain network.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hwang-painful-seizures-review-ictal-pain-2019.pdfNarrative, educational, or cited context · 1 finding
hwang-painful-seizures-review-ictal-pain-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative literature review; no original study population or independent patient-level analysis is reported. The review summarizes retrospective cohorts, EMU series, case series, individual cases, electrical-stimulation and functional-neuroimaging studies, and prior reviews. Populations therefore vary by finding and include patients with epilepsy, focal or temporal/occipital epilepsy, EMU admissions, painful somatosensory seizures, abdominal epilepsy, and cited literature case collections. Exact ascertainment, subgroup denominators, and reference standards are retained only where the source reports them.
Findings
  • PSS pain matrixThe review describes a PSS pain network involving primary sensory cortex (SI), parieto-opercular secondary somatosensory cortex (SII), insula, cingulate gyrus, and lateral thalamus, with possible contributions from amygdala, mesial fronto-parietal secondary somatosensory area, motor cortex, and posterior parietal cortex.PDF p.2, Table 1; PDF p.4, Somatosensory Pain as a Symptom of Seizures, Localization

1 contributing manuscript; source-reported values remain separate and are not pooled.

Pupillary dilationReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The handbook lists unilateral pupillary dilatation as contralateral to the frontal lobe but does not specify the reference side/viewpoint.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

epilepsy-fellowship-handbook-semiologyreferences.pdfNarrative, educational, or cited context · 1 finding
epilepsy-fellowship-handbook-semiologyreferences.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Not reported. The excerpt is an educational handbook table and reports no study design, setting, cohort, analysis population, ascertainment method, comparator, reference standard, sample size, or statistical analysis.
Findings
  • Unilateral pupillary dilatationBoth tables list Unilateral pupillary dilatation as Contralateral frontal lobe; p.2 marks the term with an asterisk and p.3 does not.PDF p.2, Lateralizing signs/Localization table row "Unilateral pupillary dilatation*" (printed p.7); PDF p.3, Lateralizing signs/Localization table row "Unilateral pupillary dilatation" (printed p.5)

1 contributing manuscript; source-reported values remain separate and are not pooled.

pure insular epilepsy sequenceReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

In the cited pure-insular sequence, unilateral sensory and focal motor signs are usually contralateral to the EZ.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • pure insular epilepsy sequencePure insular epilepsy has a typical sequence beginning with laryngeal discomfort and thoraco-abdominal constriction or dyspnea, followed by unpleasant perioral or large-area paresthesias or warmth, dysarthria or dysphonia, and focal motor manifestations. Consciousness is not impaired in seizures restricted to the insula, and unilateral sensory symptoms and focal motor activity are usually contralateral to the epileptogenic zone.PDF p.6, section 8.3 Insular lobe epilepsy

1 contributing manuscript; source-reported values remain separate and are not pooled.

recognition memory; bilateral versus unilateral hippocampal stimulationReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited study is restated as suggesting recognition can be processed by either hippocampus, with deficits after bilateral but not unilateral stimulation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • recognition memory; bilateral versus unilateral hippocampal stimulationA separate cited study summarized by the source suggested that recognition can be processed independently by the hippocampus of either hemisphere and described memory deficits with bilateral hippocampal stimulation but not unilateral stimulation.PDF p.11-12, memory hemisphere and stimulation-parameter paragraphs

1 contributing manuscript; source-reported values remain separate and are not pooled.

relationship between SOZ side and perceived side of ASReported: BilateralAlso reported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 17 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

In the review aggregate, unilateral auditory phenomena were more often perceived contralateral than ipsilateral to the SOZ; bilateral/inside-head phenomena and auditory subtypes showed different side patterns, including more left than right SOZ in the bilateral/inside-head category.

Source-defined result groups 9
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 11.4%Right SOZ to bilateral · Other relation categories · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 19.3%Left SOZ to bilateral · Other relation categories · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 7.9%Left SOZ to inside-head · Other relation categories · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 1.8%Right SOZ to inside-head · Other relation categories · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 43.9%Contralateral · Other relation categories · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereSource-defined values retained separatelyUnilateral; ipsilateral · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 15.8%Ipsilateral · Other relation categories · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereSource-defined values retained separatelyUnilateral; contralateral · auditory seizure1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / Ipsilateral / Left hemisphere / Right hemisphereObserved proportion 92.3%PAL; unilateral · Ipsilateral versus contralateral; bilateral versus inside-head; AS semiology subgroups · auditory seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 1 finding · 17 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • relationship between SOZ side and perceived side of ASAcross 114 paired AS, 44% were perceived contralateral and 16% ipsilateral to the SOZ; among the 68 AS heard in one ear, 74% were contralateral and 26% ipsilateral, while bilateral/inside-head AS more often had a left than right SOZ and subtype patterns varied.PDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
Reported values
  • Unilateral auditory seizures ipsilateral to SOZ 26% of 68relationship between SOZ side and perceived side of ASPercentage · AS with both perceived side and SOZ side reported · Unilateral; ipsilateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Right SOZ to inside-head 2/114 (2%)relationship between SOZ side and perceived side of ASPercentage · n/N 2/114 · AS with both perceived side and SOZ side reported · Right SOZ to inside-head · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • PAL auditory seizures n=17relationship between SOZ side and perceived side of ASCount · n/N 17/114 · AS with both perceived side and SOZ side reported · PAL · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Contralateral 50/114 (44%)relationship between SOZ side and perceived side of ASPercentage · n/N 50/114 · AS with both perceived side and SOZ side reported · Contralateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • VH auditory seizures n=22relationship between SOZ side and perceived side of ASCount · n/N 22/114 · AS with both perceived side and SOZ side reported · VH · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • MH auditory seizures n=15relationship between SOZ side and perceived side of ASCount · n/N 15/114 · AS with both perceived side and SOZ side reported · MH · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • I auditory seizures n=6relationship between SOZ side and perceived side of ASCount · n/N 6/114 · AS with both perceived side and SOZ side reported · I · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Unilateral auditory seizures contralateral to SOZ 74% of 68relationship between SOZ side and perceived side of ASPercentage · AS with both perceived side and SOZ side reported · Unilateral; contralateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • CH auditory seizures n=8relationship between SOZ side and perceived side of ASCount · n/N 8/114 · AS with both perceived side and SOZ side reported · CH · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • HD auditory seizures n=10relationship between SOZ side and perceived side of ASCount · n/N 10/114 · AS with both perceived side and SOZ side reported · HD · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Unilateral PAL cases contralateral 12/13relationship between SOZ side and perceived side of ASPercentage · n/N 12/13 · AS with both perceived side and SOZ side reported · PAL; unilateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Left SOZ to inside-head 9/114 (8%)relationship between SOZ side and perceived side of ASPercentage · n/N 9/114 · AS with both perceived side and SOZ side reported · Left SOZ to inside-head · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Left SOZ to bilateral 22/114 (19%)relationship between SOZ side and perceived side of ASPercentage · n/N 22/114 · AS with both perceived side and SOZ side reported · Left SOZ to bilateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Right SOZ to bilateral 13/114 (11%)relationship between SOZ side and perceived side of ASPercentage · n/N 13/114 · AS with both perceived side and SOZ side reported · Right SOZ to bilateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • Ipsilateral 18/114 (16%)relationship between SOZ side and perceived side of ASPercentage · n/N 18/114 · AS with both perceived side and SOZ side reported · Ipsilateral · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • SH auditory seizures n=33relationship between SOZ side and perceived side of ASCount · n/N 33/114 · AS with both perceived side and SOZ side reported · SH · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion
  • NS auditory seizures n=3relationship between SOZ side and perceived side of ASCount · n/N 3/114 · AS with both perceived side and SOZ side reported · NS · Ictal ASPDF p.1, Abstract; PDF p.6, section 6.1; PDF p.7, Table 2 and section 6.1; PDF p.9, Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

right-hemisphere pathways in singing-based therapyReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited aphasia-therapy literature is outside seizure semiology lateralization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdfNarrative, educational, or cited context · 1 finding
pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Forty-five adults with chronic aphasia more than 6 months after a clinically confirmed left-hemisphere stroke were recruited in Helsinki and Turku in 2017-2019; all were Finnish native speakers, over 18 years, and had no hearing deficit, severe cognitive impairment, substance abuse, or neurological/psychiatric comorbidity. Connected spoken-language production was mean correct information units per minute across three discourse tasks; connected singing was correct words per minute while singing the familiar song Jaakko-kulta; two connected-singing recordings were lost, leaving n=43 for that analysis. Repetition used 16 identical 1-5-word phrases in spoken and melodically intoned formats, with the first attempt scored and correct words per minute calculated. Six participant-level local-connectome regression models used age and lesion volume as covariates; tract tracking used a T-score threshold of 3, 2,000 permutations, and FDR <0.0083 after Bonferroni correction.
Findings
  • right-hemisphere pathways in singing-based therapyThe source states that prior small case-series literature on nonfluent aphasia and singing-based or intonation-based therapy focused on treatment-associated tract changes in the right hemisphere.PDF p.8, Discussion, prior right-hemisphere therapy literature; PDF p.9, Discussion, small case-series limitation

1 contributing manuscript; source-reported values remain separate and are not pooled.

right-hemisphere prosodic specialization; lesion-study conflictReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The discussion reports conflicting lesion literature on hemispheric specialization for prosody.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • right-hemisphere prosodic specialization; lesion-study conflictThe discussion presents conflicting lesion-study evidence: some cited authors reported right-hemisphere specialization or a right-sided functional-anatomic organization for prosody, whereas several series found no significant prosody difference between right- and left-brain-damaged patients; it also describes competing right-emotional versus left-linguistic-cue hypotheses.PDF p.4, right column, paragraph beginning “In fact, the neuroanatomic substrates”

1 contributing manuscript; source-reported values remain separate and are not pooled.

SEEG indicationsReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited indications include bihemispheric exploration for bilateral or network hypotheses.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

laoprasert-stereoelectroencephalography-seeg-mset-2018.pdfNarrative, educational, or cited context · 1 finding
laoprasert-stereoelectroencephalography-seeg-mset-2018.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Document type: educational slide deck. No source-wide cohort, prospective protocol, sampling frame, or unified analysis population is reported. The deck combines heterogeneous cited studies, article screenshots, modality tables, conceptual diagrams, and individual cases. Study-specific populations, analysis units, denominators, comparators, and follow-up intervals are retained only where stated on the relevant slide; no source-wide denominator is inferred.
Findings
  • SEEG indicationsThe cited SEEG indications include MRI-negative epilepsy, deep or difficult-to-cover regions such as bottom-of-sulcus FCD, mesial temporal, operculo-insular, cingulate, interhemispheric, and posterior orbitofrontal regions, prior failed subdural exploration, bihemispheric exploration, and suspected anatomo-functional network involvement with normal MRI.PDF p.18

1 contributing manuscript; source-reported values remain separate and are not pooled.

Seizure-associated aphasiaReported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 2 findings · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The review says seizure-associated aphasia most often relates to the dominant hemisphere and has limited fine-localizing value. Cited-study restatement describes left hemispheric origin or right-to-left propagation for seizure-associated aphasia.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 2 findings
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • seizure-associated aphasia (SAA)The review concludes that seizure-associated aphasia has good or high lateralizing significance, while its closer localizing value is limited; language disturbances most frequently lateralize to the dominant hemisphere.PDF p.1, abstract; PDF p.5, §6; PDF p.6, §7
  • seizure-associated aphasia in different focal epilepsiesThe review reports that SAA in the study attributed to Lösch et al. occurred either with left hemispheric seizure origin or with seizures spreading from the right to the left hemisphere; SAA was most common in parieto-occipital epilepsy, followed by temporal, focal-not-further-localized, and frontal epilepsy, and the authors concluded that SAA has high lateralizing but limited localizing value.PDF p.5, §6

1 contributing manuscript; source-reported values remain separate and are not pooled.

Seizure-associated speech disturbanceReported: Dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Cited-study restatement associates speech abnormalities with dominant-hemisphere seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfNarrative, educational, or cited context · 1 finding
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • speech abnormalities in dominant-hemisphere seizuresThe source attributes to John Hughlings Jackson the observation that seizures in the dominant hemisphere could result in speech abnormalities.PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Seizure-associated speech/language disturbanceReported: Dominant hemisphereAlso reported: Non-dominant hemisphereNo single reliable side1 manuscript · 1 finding · 5 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited series reports ictal speech predominantly in the nondominant temporal lobe and postictal aphasia in the dominant temporal lobe, with other listed disturbances nonlateralizing.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding · 5 reported values
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • speech and language manifestations of complex motor seizuresIn a series of patients with TLE, vocalizations occurred in 49% and abnormal speech in 51% of cases; ictal speech, defined as clearly intelligible speech during altered consciousness, occurred in 34% and localized to the nondominant temporal lobe in 83% of cases; postictal aphasia occurred in 12% and was virtually always localized to the dominant temporal lobe. Vocalizations, dysarthria, dysphasia, speech arrest, and nonidentifiable speech had no lateralizing value.PDF p.5, section 6 Speech and language manifestations of complex motor seizures; PDF p.5, Table 2
Reported values
  • 49%speech and language manifestations of complex motor seizuresPercentage · patients with TLE · TLE · ictal altered consciousness for ictal speech; postictal for aphasiaPDF p.5, section 6 Speech and language manifestations of complex motor seizures; PDF p.5, Table 2
  • 51%speech and language manifestations of complex motor seizuresPercentage · patients with TLE · TLE · ictal altered consciousness for ictal speech; postictal for aphasiaPDF p.5, section 6 Speech and language manifestations of complex motor seizures; PDF p.5, Table 2
  • 12%speech and language manifestations of complex motor seizuresPercentage · patients with TLE · TLE · ictal altered consciousness for ictal speech; postictal for aphasiaPDF p.5, section 6 Speech and language manifestations of complex motor seizures; PDF p.5, Table 2
  • 34%speech and language manifestations of complex motor seizuresPercentage · patients with TLE · ictal speech · ictal altered consciousness for ictal speech; postictal for aphasiaPDF p.5, section 6 Speech and language manifestations of complex motor seizures; PDF p.5, Table 2
  • 83%speech and language manifestations of complex motor seizuresPercentage · patients with TLE · ictal speech · ictal altered consciousness for ictal speech; postictal for aphasiaPDF p.5, section 6 Speech and language manifestations of complex motor seizures; PDF p.5, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

Semiological seizure classification versus epileptic syndrome classificationReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The educational syndrome-classification statement includes left mesial-temporal and right-frontal examples but no general side rule.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Semiological seizure classification versus epileptic syndrome classificationThe authors distinguish classification of seizure semiology from classification of the epileptic syndrome: the syndrome requires semiological type plus interictal and ictal EEG, functional and anatomic neuroimaging, seizure evolution, neurological examination, and other clinical information; because many syndromes may share the same semiological seizure types, a dialeptic seizure alone does not distinguish generalized absence epilepsy from a focal syndrome with different treatment implications.PDF p.1, Introduction; PDF p.6, Epilepsy classification; PDF p.7, illustrative examples; PDF p.8, Advantages

1 contributing manuscript; source-reported values remain separate and are not pooled.

sleep-related seizuresReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Left hemisphere is single-case diagnostic context for sleep-related seizures.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

jobst-insula-and-its-epilepsies-2019.pdfCase report or observation · 1 finding
jobst-insula-and-its-epilepsies-2019.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a multi-author narrative review with educational sections and cited-study restatements rather than a single primary cohort. Denominators therefore belong to the cited series named in each finding. The review includes insular stimulation series, noninvasive-test series, SEEG observations, and case reports. The source's own distinctions between insular, operculo-insular, insulo-opercular, extrainsular, temporal-like, and frontal-like are preserved.
Findings
  • sleep-related seizures in left insular SUDEP caseThe SEEG-proven left-insular case had sleep-related seizures.PDF p.8, Is SUDEP Risk Increased in Insular Epilepsy?

1 contributing manuscript; source-reported values remain separate and are not pooled.

Somatosensory body-schema illusionReported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review links somatosensory body-schema illusions, specifically, to nondominant inferior parietal or TPO activation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • well-localized somatosensory auras and somatosensory illusionsWell-localized somatosensory auras that evolve to motor features are usually associated with a perirolandic epileptogenic zone close to the symptomatogenic zone, whereas illusions of swelling, shrinking, or movement of body parts are often elicited by activation of the nondominant inferior parietal lobe or TPO junction.PDF p.2, section 3.1 Auras

1 contributing manuscript; source-reported values remain separate and are not pooled.

spatial extent of temporal FDG-PET hypometabolism and outcomeReported: BilateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review associates restricted ipsilateral anterior mesial temporal hypometabolism with better outcomes and wider, bilateral, extratemporal, or propagation-related hypometabolism with less favorable or less specific localization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • spatial extent of temporal FDG-PET hypometabolism and outcomeIn MTLE-HS, more restricted or strong focal anterior mesial temporal hypometabolism was associated with better surgical outcomes, while hypometabolism sparing the hippocampus, extending laterally or extratemporally, involving both hemispheres, or reflecting propagated activity was associated with less favorable or less specific localization; unilateral temporal hypometabolism with normal MRI could still have excellent outcomes after anterior temporal lobectomy.PDF p.19, Interictal PET in TLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

speech and singing production; lesion-symptom mappingReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

No separate lateralizing axis is reported for the cited speech and singing lesion-symptom mapping.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdfNarrative, educational, or cited context · 1 finding
pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Forty-five adults with chronic aphasia more than 6 months after a clinically confirmed left-hemisphere stroke were recruited in Helsinki and Turku in 2017-2019; all were Finnish native speakers, over 18 years, and had no hearing deficit, severe cognitive impairment, substance abuse, or neurological/psychiatric comorbidity. Connected spoken-language production was mean correct information units per minute across three discourse tasks; connected singing was correct words per minute while singing the familiar song Jaakko-kulta; two connected-singing recordings were lost, leaving n=43 for that analysis. Repetition used 16 identical 1-5-word phrases in spoken and melodically intoned formats, with the first attempt scored and correct words per minute calculated. Six participant-level local-connectome regression models used age and lesion volume as covariates; tract tracking used a T-score threshold of 3, 2,000 permutations, and FDR <0.0083 after Bonferroni correction.
Findings
  • speech and singing production; lesion-symptom mappingThe source restates that a prior VBM/VLSM study associated impaired connected spoken-language production and repetition, and sung repetition, with damage to left frontal, temporal, and parietal structures, whereas impaired singing of familiar-song words was associated with left middle and superior temporal gyri and temporal poles.PDF p.2, Introduction, prior VBM/VLSM study; PDF p.8, Discussion, prior left temporal lesion finding

1 contributing manuscript; source-reported values remain separate and are not pooled.

startle-sensory-motor circuit; proprioceptive feedback; hyperexcitabilityReported: BilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The review proposes left caudate-putamen, left SMA, and left paracentral involvement with bilateral postcentral/posterior-parietal sensory components.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • startle-sensory-motor circuit; proprioceptive feedback; hyperexcitabilityThe authors propose that ictal-SPECT hyperperfusion of the left caudate-putamen and sensory tracts may reflect startle responses and increased proprioceptive input, respectively, while hyperperfusion plus invasive irritability and ictal involvement of the left SMA and paracentral lobule indicates hyperexcitability of those motor areas.PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Status epilepticus in the SSCReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The SSC uses “right foot clonic status” as a classification example, not as a lateralizing rule.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 1 finding
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors describe a classification based exclusively on ictal seizure semiology as reported by patients or observers or analyzed during video monitoring. EEG and other test results do not influence the semiological classification, although EEG may be used to distinguish epileptic from nonepileptic paroxysmal events. The authors state that the classification had been tested for more than 10 years in selected epilepsy centers and that the present version or variants had been used in daily practice for more than 10 years, without reporting a defined cohort, eligibility criteria, sample size, or evaluation design.
Findings
  • Status epilepticus in the SSCEssentially any seizure form described in the SSC can manifest as status epilepticus, which is classified in the same way as the corresponding seizure by replacing “seizure” with “status,” such as dialeptic status or right foot clonic status.PDF p.6, Status epilepticus

1 contributing manuscript; source-reported values remain separate and are not pooled.

supplementary motor area seizuresReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Supplementary motor area seizures are described with bilateral, asymmetrical tonic posturing and no fixed side.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • supplementary motor area seizuresSupplementary motor area seizures are characterized by sudden bilateral, asymmetrical tonic posturing associated with vocalization and preservation of consciousness.PDF p.5, Frontal lobe epilepsy, paragraph beginning "Supplementary motor area"

1 contributing manuscript; source-reported values remain separate and are not pooled.

syllable discrimination and identificationReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates that left frontal or inferior parietal lesions were associated with syllable-task deficits; no body-side direction is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

hickok-poeppel-cortical-organization-speech-processing-2007.pdfNarrative, educational, or cited context · 1 finding
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
Narrative opinion/review; no single study cohort, eligibility rule, comparator set, or reference standard is reported for the document as a whole. The review discusses aphasia and lesion evidence, functional MRI, direct cortical stimulation, Wada and split-brain evidence, and normal speech perception, recognition, production, and auditory-motor tasks. Cited-study sample sizes, finding denominators, and effect sizes are generally not reported in this document.
Findings
  • syllable discrimination and identificationThe review reports that damage to left frontal or inferior parietal areas caused deficits on speech-syllable discrimination or identification tasks, while syllable discrimination or identification and auditory word comprehension doubly dissociated: some patients had impaired syllable performance with good word comprehension and others had the reverse pattern.PDF p.1, frontal and inferior-parietal lesion discussion; PDF p.2, task-dependence and definitions discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal aura subtype and motor profileReported: IpsilateralAlso reported: Left hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The teaching review assigns different directions to different aura subtypes: multiple sequential auras suggest nondominant localization, chills or goosebumps favor left temporal foci and are usually ipsilateral when unilateral, and viscerosensory or experiential auras show only a right-temporal trend.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfNarrative, educational, or cited context · 1 finding
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • temporal aura subtype and motor profileMultiple sequential auras suggest a nondominant, often temporal, localization; chills or goosebumps are more common with left temporal foci and are usually ipsilateral; olfactory and gustatory auras are uncommon in mesial temporal epilepsy and are associated in the source with mesial temporal tumors; auditory aura suggests lateral temporal involvement, while cephalic, somatosensory, and visual auras more often suggest extratemporal onset.PDF p.49; PDF p.50

1 contributing manuscript; source-reported values remain separate and are not pooled.

Temporal seizure semiological sequence (orderly progression: aura->arrest->oral->manual->dystonia)Reported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Cited-study restatement reports a strong right-temporal association for epigastric sensation and ictal vomiting within a broader symptom-cluster description.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Temporal-lobe symptom clusters and sequenceIn an analysis of 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset, 18 common symptoms formed four subclusters: epigastric aura with ictal emesis, alimentary and hand automatisms; behavioural arrest with complete loss of consciousness, staring and bilateral facial contraction; unilateral dystonic arm posturing with mimetic automatisms, complex gestures, ictal speech and partial loss of consciousness; and looking around with agitation, vocalizations and whole-body movements. Epigastric sensation and ictal vomiting were strongly associated with right temporal foci, and the commonest sequence was behavioural arrest, alimentary and hand automatisms, random gazing, then whole-body movements.PDF p.6, section 7
Reported values
  • 31 Engel class 1 patientsTemporal-lobe symptom clusters and sequenceCount · 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset. · Symptom clusters and seizure progressionPDF p.6, section 7
  • 18 common symptomsTemporal-lobe symptom clusters and sequenceCount · 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset. · Symptom clusters and seizure progressionPDF p.6, section 7
  • four subclustersTemporal-lobe symptom clusters and sequenceCount · 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset. · Symptom clusters and seizure progressionPDF p.6, section 7

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal start-stop-start ictal onsetReported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

This case observed right-sided inferomesial temporal onset followed by wider right frontotemporal propagation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdfCase report or observation · 1 finding · 3 reported values
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The complete native PDF page set 1-473 was reviewed as one source. Per-page text was read in coherent sections with targeted consolidation of repeated headers, references, medication material, and non-in-scope management content. Renderings were additionally inspected for the vision-required pages and for selected semiology diagrams, EEG traces, montages, tables, captions, and case figures where visual field, waveform evolution, or extraction uncertainty carried scientific meaning. Populations are heterogeneous and the source's own: educational descriptions, selected cited-study restatements, and distinct illustrated patient cases are kept separate below. Quantitative values are reported only when the source states them.
Findings
  • temporal start-stop-start ictal onsetIn the illustrated temporal epilepsy case, an initial 8-second focal 6 Hz rhythm at right inferomesial temporal electrodes was followed by attenuation and then a wider right frontotemporal rhythmic discharge; the source interprets the first focal start as the ictal onset zone, the attenuation as transient propagation away from the surface, and the second start as a less clearly localizing wider field, with four of ten right inferomesial temporal seizures showing the start-stop-start phenomenon.PDF p.401; PDF p.403; PDF p.404; PDF p.405
Reported values
  • initial 6 Hz rhythmtemporal start-stop-start ictal onsetFrequency · 48-year-old woman with ten recorded right inferomesial temporal seizures · illustrated event · ictal onset, transient attenuation, and propagationPDF p.401; PDF p.403; PDF p.404; PDF p.405
  • initial rhythm lasted 8 secondstemporal start-stop-start ictal onsetDuration · 48-year-old woman with ten recorded right inferomesial temporal seizures · illustrated event · ictal onset, transient attenuation, and propagationPDF p.401; PDF p.403; PDF p.404; PDF p.405
  • 4/10 recorded ictal discharges showed start-stop-starttemporal start-stop-start ictal onsetPercentage · n/N 4/10 · 48-year-old woman with ten recorded right inferomesial temporal seizures · ictal onset, transient attenuation, and propagationPDF p.401; PDF p.403; PDF p.404; PDF p.405

1 contributing manuscript; source-reported values remain separate and are not pooled.

Temporal-lobe symptom clusters and sequenceReported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Cited-study restatement reports a strong right-temporal association for epigastric sensation and ictal vomiting within a broader symptom-cluster description.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Temporal-lobe symptom clusters and sequenceIn an analysis of 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset, 18 common symptoms formed four subclusters: epigastric aura with ictal emesis, alimentary and hand automatisms; behavioural arrest with complete loss of consciousness, staring and bilateral facial contraction; unilateral dystonic arm posturing with mimetic automatisms, complex gestures, ictal speech and partial loss of consciousness; and looking around with agitation, vocalizations and whole-body movements. Epigastric sensation and ictal vomiting were strongly associated with right temporal foci, and the commonest sequence was behavioural arrest, alimentary and hand automatisms, random gazing, then whole-body movements.PDF p.6, section 7
Reported values
  • 31 Engel class 1 patientsTemporal-lobe symptom clusters and sequenceCount · 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset. · Symptom clusters and seizure progressionPDF p.6, section 7
  • 18 common symptomsTemporal-lobe symptom clusters and sequenceCount · 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset. · Symptom clusters and seizure progressionPDF p.6, section 7
  • four subclustersTemporal-lobe symptom clusters and sequenceCount · 31 Engel class 1 patients with complex partial seizures of temporal-lobe onset. · Symptom clusters and seizure progressionPDF p.6, section 7

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal-plus epilepsyReported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review reports that temporal-plus epilepsy is often associated with ipsilateral tonic signs, but this is a non-independent restatement of Barba et al. 2007.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • temporal-plus epilepsyTemporal-plus epilepsy involves the temporal lobe and a connected network including orbitofrontal region, insula, frontal or parietal operculum, and TPO junction. Hippocampal sclerosis on MRI cannot reliably differentiate pure TLE from temporal-plus epilepsy, whereas semiology distinguishes them: pure TLE more often has abdominal auras evolving to automatisms and postictal amnesia, while temporal-plus epilepsy is associated with gustatory, auditory, or vertiginous auras, version, piloerection, ipsilateral tonic signs, and postictal dysphoria.PDF p.6, section 8.4 Temporal-plus epilepsies

1 contributing manuscript; source-reported values remain separate and are not pooled.

types of ictal language disturbances in relation to epilepsy typeReported: BilateralAlso reported: Dominant hemisphereAlso reported: Left hemisphereAlso reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

Table 5 places language-disturbance categories in dominant temporal, bilateral and/or non-dominant temporal, and left centro-parietal source contexts; it does not establish a single lateralizing direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

unterberger-epileptic-aphasia-critical-appraisal-2021.pdfCase report or observation · 1 finding
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report an extensive literature search on the term “epileptic aphasia,” analysis of semiology and terminology indicating language-associated seizure symptoms, and an overview of EEG, etiology, brain imaging, and ictal language disorders. The document is not a single-cohort study; its evidence base includes cited case reports, case series, and studies involving ictal aphasia, aphasic status epilepticus (ASE), temporal/frontal/other focal epilepsies, and postictal language dysfunction. The review does not report one pooled analysis population or common denominator.
Findings
  • types of ictal language disturbances in relation to epilepsy typeTable 5 presents a qualitative cross-category comparison of speech arrest, receptive aphasia, global/undifferentiated aphasia, expressive aphasia, mixed aphasia, jargon aphasia, dysphasia, and non-speech vocalization across dominant temporal lobe epilepsy, bilateral and/or non-dominant temporal lobe epilepsy, frontal lobe epilepsy, and other conditions including occipital, centro-parietal, parieto-occipital, left centro-parietal, subcortical demyelinating, focal NCSE, metabolic encephalopathy, absence seizures, and generalized spikes and waves.PDF p.5, Table 5

1 contributing manuscript; source-reported values remain separate and are not pooled.

Typical mesial temporal seizure progressionReported: BilateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited review restates ipsilateral facial or oral contraction/head deviation followed by bilateral facial or axial motor phenomena in a mesial-temporal sequence.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Typical mesial temporal seizure progressionThe review says mesial temporal seizures may begin with rising epigastric, déjà vu, affective, or experiential auras, followed by frequently ipsilateral face or mouth contraction or head deviation and bilateral face or axial motor phenomena; behavioural arrest and oral automatisms are common, and bitemporal spread heralds altered consciousness, amnesia, autonomic changes, and prominent tonic or dystonic motor automatisms.PDF p.3, section 3 Mesial Temporal Lobe Seizures and Neocortical Temporal Lobe Seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

typical, atypical, and atypical right language representation; specialized language hemisphereReported: BilateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review distinguishes typical left, distributed left-right, and atypical right language representations for functional mapping.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • typical, atypical, and atypical right language representation; specialized language hemisphereThe source distinguishes a typical language representation with principal left-hemisphere involvement, atypical configurations spanning left-right involvement, and atypical right-hemisphere representation; it states that chronic epilepsy or a brain lesion may increase atypical representation and that hemispheric specialization should be assessed region by region.PDF p.5-6, Language and Stimulation and hemispheric organization

1 contributing manuscript; source-reported values remain separate and are not pooled.

Unilateral epileptic spasmsReported: Contralateral1 manuscript · 2 findings · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Predominantly unilateral spasms are helpful in lateralizing the epileptogenic zone to the contralateral hemisphere. Predominantly unilateral spasms were contralateral to the epileptogenic zone in the four cited infants with confirmatory seizure-free surgical outcome.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdfNarrative, educational, or cited context · 2 findings · 1 reported value
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review with a subjective selection of semiological features. The summarized populations vary across epilepsy monitoring units, focal epilepsy and temporal/frontal/occipital lobe epilepsy cohorts, infants, surgical series, case reports, and stimulation or lesion studies. Reference standards include video/EEG, EEG, MRI, CT, PET, SPECT, Wada testing, presurgical evaluation, seizure freedom or seizure reduction after surgery, and combinations of these; the source frequently states when the standard was incomplete or unavailable.
Findings
  • predominantly unilateral spasmsPredominantly unilateral spasms are helpful in lateralizing the epileptogenic zone to the contralateral hemisphere.PDF p.6, section 3.7
  • predominantly unilateral spasms in surgical infantsThe contralateral lateralizing result for predominantly unilateral spasms was confirmed in 4 of 19 infants who became seizure free after surgery.PDF p.6, section 3.7
Reported values
  • 4/19 infants confirmed the result and became seizure free after surgerypredominantly unilateral spasms in surgical infantsCount · n/N 4/19 · 19 infants evaluated for lateralizing signs, including 4 with the confirming sign and postoperative seizure freedom · ictalPDF p.6, section 3.7

1 contributing manuscript; source-reported values remain separate and are not pooled.

Urogenital phenomenon (unspecified type)Reported: Non-dominant hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates a possible association of ictal urinary urge and orgasmic phenomena with nondominant temporal origin.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • urogenital manifestationsIncontinence, ictal urinary urge, orgasmic sensations, and genital sensations are rare and not extensively studied; the review states that ictal urinary urge and orgasmic phenomena may suggest seizure origin in the nondominant temporal lobe.PDF p.4, section 3.5 Autonomic seizures; PDF p.2, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

Visual hallucinations or illusionsReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited stimulation series describes left superior temporal stimulation effects that vary by task and subregion, including auditory phenomena, phonological errors, and naming or reading deficits.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdfNarrative, educational, or cited context · 1 finding
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The source describes clinical SEEG functional mapping using stimulation of sampled contacts during patient-specific tasks and summarizes cited studies involving patients with epilepsy, plus selected non-SEEG and awake-mapping studies in Table 10.1. Cited-study populations, sampling frames, analysis units, and denominators are frequently not reported in this chapter. One source-described clinical example is a 17-year-old patient with left temporo-perisylvian epilepsy and MRI-negative imaging (Fig. 10.4). The source distinguishes stimulation-induced clinical/electrophysiological responses from spontaneous seizures and treats afterdischarges as interpretation context.
Findings
  • hallucinations or illusions; auditory symptoms; articulatory or phonological errors; naming or reading deficitsIn the posterior left superior temporal region, the source reports task- and subregion-specific effects: word-repetition stimulation of Heschl’s gyrus induced hallucinations or illusions without language deficit; planum temporale stimulation induced auditory symptoms with comprehension deficit; left planum temporale or Spt stimulation during word or pseudoword repetition elicited articulatory or phonological errors and difficulty maintaining the phonological loop; and posterior left STS stimulation during naming or reading produced naming or reading deficits without positive auditory symptoms, including the source’s reported “graphene” decoding, comprehension, and “graphene to phoneme” deficits.PDF p.7, posterior left superior temporal gyrus paragraph; PDF p.8, Fig. 10.3 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

Young-child temporal-lobe seizure semiologyReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited synthesis says young-child ictal features provide few lateralizing clues and that motor features may be bilateral and symmetrical.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Young-child temporal-lobe seizure semiologyIn young children, ictal features are said to provide few localizing or lateralizing clues; preschool children may initially show arousal with eye opening, sitting up, or axial jerking, and motor features are often bilateral, symmetrical, and more typical of secondarily generalized seizures.PDF p.5, section 6 Semiology of Childhood Onset Temporal Lobe Epilepsy

1 contributing manuscript; source-reported values remain separate and are not pooled.

Peri-ictal central apneaReported: Left hemisphere2 manuscripts · 2 findings · 5 reported values
Weighted evidence supportevidence weight 0.9 across 2 manuscripts · 1 manuscript weight pending · 1 structured design not resolved · 1 case report or observation

Left temporal onset is single-case context for the sleep/wake apnea-duration comparison. The authors interpret premortem peri-ictal breathing dysfunction, specifically prolonged ictal and postictal central apnoea, as a potential SUDEP risk marker and propose >14 seconds for postictal central apnoea and >17 seconds for ictal central apnoea as study-derived thresholds that could inform development of a validatable risk index; the Discussion separately describes >=15 seconds as prolonged postictal central apnoea and calls for further prospective validation.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdfCase report or observation · 1 finding · 2 reported values
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Consecutive patients older than 13 years admitted to the Epilepsy Monitoring Unit at Baggiovara Civil Hospital, Modena Academic Hospital, Italy, from April 2020 through December 2023 were studied with long-term video-EEG and cardiorespiratory polygraphy; 71 met inclusion, 2 were discarded for technical artifact, 5 focal seizures with bilateral tonic-clonic evolution were excluded, and the final analysis comprised 69 patients and 406 focal-onset seizures. MRI analyses included 22 patients with ICA/PICA, 31 patients without seizure-related breathing disorders, and 30 healthy controls; analyses adjusted for age, sex, and intracranial volume and used false-discovery-rate correction.
Findings
  • seizure-related apnea during wake and sleep in case MO#01In the illustrated young patient with focal left temporal seizures due to herpes virus encephalitis, wake seizures were shorter with brief postictal apnea periods, whereas sleep seizures showed prolonged and persistent apnea events; the patient was not actively tested in any of the four recordings.PDF p.9, Figure 4 caption
Reported values
  • Illustrated recordings n=4seizure-related apnea during wake and sleep in case MO#01Count · Individual young patient MO#01 with focal left temporal seizures due to herpes virus encephalitis · ictal and postictalPDF p.9, Figure 4 caption
  • Recordings with active testing 0/4seizure-related apnea during wake and sleep in case MO#01Percentage · n/N 0/4 · Individual young patient MO#01 with focal left temporal seizures due to herpes virus encephalitis · ictal and postictalPDF p.9, Figure 4 caption
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdfStructured design not resolved · 1 finding · 3 reported values
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The study enrolled 2632 children and adults with epilepsy at nine epilepsy-monitoring centres in the USA and UK between 2011 and 2021; 164 were lost to follow-up and 2468 participants were included in the primary follow-up analyses. There were 38 SUDEP outcomes and two near-SUDEP events. During admission, 1660 participants had seizures captured, 1432 had analysable seizures, and the report describes 1091 analysable generalised convulsive seizures and 2117 non-convulsive seizures. The primary endpoint was time to SUDEP or censoring due to other causes. Cox proportional hazards models assessed clinical and electroclinical predictors; repeated seizure predictors were aggregated to the most severe feature per patient, using the maximum for continuous features or presence for categorical features. Analyses used prolonged video-EEG, ECG, pulse oximetry, and chest/abdominal inductance plethysmography. Statistical significance in primary analyses required two-sided p<0.05 after Bonferroni correction; the report states that secondary-analysis confidence intervals were not intended for hypothesis testing. Main-text results include varying denominators and missing data, which are retained below.
Findings
  • prolonged peri-ictal central apnoeaThe authors interpret premortem peri-ictal breathing dysfunction, specifically prolonged ictal and postictal central apnoea, as a potential SUDEP risk marker and propose >14 seconds for postictal central apnoea and >17 seconds for ictal central apnoea as study-derived thresholds that could inform development of a validatable risk index; the Discussion separately describes >=15 seconds as prolonged postictal central apnoea and calls for further prospective validation.PDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion
Reported values
  • >17 seconds ictalprolonged peri-ictal central apnoeaDuration · Source-authored interpretation based on the primary cohort’s peri-ictal apnoea analyses · Proposed study-derived threshold · ictal and postictalPDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion
  • >14 seconds postictalprolonged peri-ictal central apnoeaDuration · Source-authored interpretation based on the primary cohort’s peri-ictal apnoea analyses · Proposed study-derived threshold · ictal and postictalPDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion
  • ≥15 seconds postictalprolonged peri-ictal central apnoeaOther reported value · Source-authored interpretation based on the primary cohort’s peri-ictal apnoea analyses · Discussion definition of prolonged postictal central apnoea · ictal and postictalPDF p.1, Interpretation; PDF p.6, Figure 2 description and Results; PDF p.9, Discussion; PDF p.10, Conclusion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

auditory acuityReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

No lateralization axis information is reported for the normal auditory-acuity observation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfCase report or observation · 1 finding
e236615-full.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • auditory acuityAuditory acuity testing in the index patient was within normal limits.PDF p.1, Summary; PDF p.2, Investigations

1 contributing manuscript; source-reported values remain separate and are not pooled.

Case-1 inferioposterior temporal ictal SEEG onset and early propagationReported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Both Case-1 recordings involved right inferioposterior temporal onset/early network activity.

Source-defined result groups 2
Localization: Frontal / Occipital / Parietal / TemporalSource-defined values retained separatelysecond SEEG recording · first SEEG recording · SEEG recording/seizure1 manuscript · 1 reported value · not pooled
Localization: Frontal / Occipital / Parietal / TemporalSource-defined values retained separatelyfirst SEEG recording · second SEEG recording · SEEG recording/seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdfCase report or observation · 1 finding · 2 reported values
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a two-case report with no control or comparator group. Case-1 was a 24-year-old right-handed man; 32 habitual seizures were recorded during 3 days of scalp video-EEG, with two followed by secondary GTCS, and two right-hemisphere SEEG implantations were performed 4 months apart. Case-2 was a 19-year-old right-handed man; three habitual seizures were captured on video-EEG and right temporal neocortical, temporal-pole, and medial-structure regions were explored with SEEG. The source describes scalp EEG, MRI, FDG-PET, SEEG onset and propagation, anatomical reconstruction, cortical resection, and seizure-free follow-up of 17 months for Case-1 and 25 months for Case-2. Case-1 MRI/FDG-PET was reported unremarkable for an evaluable lesion; Case-2 MRI and PET findings were reported in the right middle-posterior inferior temporal/fusiform and medial temporal regions. No cohort-wide denominator for ipsiversive eye deviation, no control comparison, and no population-level frequency or diagnostic statistic are reported.
Findings
  • Case-1 inferioposterior temporal ictal SEEG onset and early propagationAcross the Case-1 SEEG recordings, the source reports initial ictal discharges or polyspikes followed by high-frequency oscillations in the inferioposterior temporal region; the second recording’s initial discharge originated in posterior inferior temporal gyrus, with propagation to the posterior inferior temporal sulcus, anterior and posterior banks of AOS, lateral occipital sulcus, and the frontal eye-field region within 400 ms, while the first recording showed wider propagation including temporo-occipital, supramarginal, angular, and intraparietal regions within 600 ms.PDF p.3, Case-1 SEEG results; PDF p.4, Results and Fig. 5 caption; PDF p.5, Results and Fig. 6 caption; PDF p.9, Discussion
Reported values
  • within 400 msCase-1 inferioposterior temporal ictal SEEG onset and early propagationOther reported value · Case-1; two SEEG implantations/recordings · second SEEG recording · ictal onset and early propagationPDF p.3, Case-1 SEEG results; PDF p.4, Results and Fig. 5 caption; PDF p.5, Results and Fig. 6 caption; PDF p.9, Discussion
  • within 600 msCase-1 inferioposterior temporal ictal SEEG onset and early propagationOther reported value · Case-1; two SEEG implantations/recordings · first SEEG recording · ictal onset and early propagationPDF p.3, Case-1 SEEG results; PDF p.4, Results and Fig. 5 caption; PDF p.5, Results and Fig. 6 caption; PDF p.9, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

concordant noninvasive localization of left rostral frontal epilepsyReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

A nonlesional case showed concordant left rostral frontal localization across ictal-SPECT hyperperfusion, FDG-PET hypometabolism, and MEG discharges.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

laoprasert-stereoelectroencephalography-seeg-mset-2018.pdfCase report or observation · 1 finding
laoprasert-stereoelectroencephalography-seeg-mset-2018.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Document type: educational slide deck. No source-wide cohort, prospective protocol, sampling frame, or unified analysis population is reported. The deck combines heterogeneous cited studies, article screenshots, modality tables, conceptual diagrams, and individual cases. Study-specific populations, analysis units, denominators, comparators, and follow-up intervals are retained only where stated on the relevant slide; no source-wide denominator is inferred.
Findings
  • concordant noninvasive localization of left rostral frontal epilepsyAn illustrated nonlesional case shows concordant left rostral frontal localization across focal ictal SPECT hyperperfusion, focal FDG-PET hypometabolism, and focal MEG discharges, despite absent MRI lesion.PDF p.68

1 contributing manuscript; source-reported values remain separate and are not pooled.

Correlation matrix between cortical areas and clinical featuresReported: Contralateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 non-independent primary or overlapping context

The sign-area matrix links contralateral versive and tonic signs and somesthetic aura to caudal regions, while staring and speech arrest map toward rostral/frontopolar regions.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfNon-independent primary or overlapping context · 1 finding · 1 reported value
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf
Non-independent primary or overlapping context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Consecutive presurgical SEEG series from Timone Hospital, Marseille, February 2000-November 2010: 54 patients in whom SEEG-defined EZ was within the frontal lobe, selected from 180 SEEG explorations; patients with inconclusive intracranial recording (n=1) or a nonpredominantly frontal EZ were excluded. All patients had noninvasive presurgical assessment and video-SEEG after complete or partial antiepileptic-drug withdrawal; 374 seizures were recorded and analyzed. The cohort included 22 male and 32 female patients, mean age 24.9 +/- 9.5 years, mean epilepsy duration 16.9 +/- 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed VEEG and electrical data; 31 ictal signs and 24 brain-area variables were scored 0-1-2 per patient, with rank-based PCA, hierarchical clustering, correlation matrices, and Kendall tests at p < 0.05. The source describes sampling 20 cortical regions in one methods passage and distinguishes the SEEG-defined EZ from the source-defined early spread network.
Findings
  • Correlation matrix between cortical areas and clinical featuresThe ordered sign-area matrix showed a diagonal posterior-to-anterior correlation pattern. Early clonic signs, contralateral versive signs, contralateral tonic posture, and somesthetic localized aura were associated with caudal regions including primary motor cortex and rolandic operculum, whereas staring, speech arrest, manipulation behavior, and fixed facial expression were associated with rostral or frontopolar regions. The diagonal pattern persisted for significant correlations at p < 0.05; early clonic signs and manipulation behavior were described as more specific to posterior and anterior regions respectively, while hyperkinetic movements and impaired consciousness were weaker, more distributed indicators.PDF p.4, Figure 1 and caption; PDF p.7, Cluster analysis and anatomic-electroclinical correlations
Reported values
  • p < 0.05Correlation matrix between cortical areas and clinical featuresP value · 54 patients; 31 clinical-sign variables and the source’s brain-area score matrix · Alternate source version; non-independent · Ictal clinical signs during the early-spread analysis windowPDF p.4, Figure 1 and caption; PDF p.7, Cluster analysis and anatomic-electroclinical correlations

1 contributing manuscript; source-reported values remain separate and are not pooled.

cortical dysplasia (ILAE type Ic)Reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The pathology finding provides no sign-based lateralization relationship.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • cortical dysplasia (ILAE type Ic)Histopathology from the second resection demonstrated cortical dysplasia classified as ILAE type Ic.PDF p.2, Case Report; PDF p.3, Fig. 2(e-f) caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

cortical stimulationReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

No seizure lateralization is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfCase report or observation · 1 finding
e236615-full.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • cortical stimulationDuring awake surgery nine days after admission, stimulation of the superior temporal gyrus did not reproduce palinacousis; phenytoin had been administered before surgery to prevent seizures.PDF p.2, Treatment; PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

daily focal seizures with right frontocentral scalp EEG concordanceReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The case has a right frontal BOSD and concordant right frontocentral interictal and ictal scalp EEG.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdfCase report or observation · 1 finding
jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study included consecutive children with focal epilepsy and MRI-defined BOSD evaluated at The Hospital for Sick Children in Toronto between January 2007 and July 2019; patients with less than 1 year of postsurgical follow-up were excluded. Forty-one children were included. Medical-record data included seizure semiology, seizure frequency, age at seizure onset, antiseizure medications, and comorbidities. Mean age at surgery was 9.7 years (SD 4.5), 29 patients were male (70.7%), and mean age at seizure onset was 4.7 years (SD 3.5). Table 1 reported daily seizures in 30 of 41 patients (73.2%), weekly seizures in 9 (22.0%), monthly seizures in 1 (2.4%), yearly seizures in 1 (2.4%), and a history of focal status epilepticus requiring hospitalization in 8 (19.5%); these are cohort descriptors, not separate findings here. Presurgical evaluation included scalp video EEG, MEG, FDG-PET, and invasive video EEG when indicated. Thirty-seven patients underwent IVEEG, and 34 had available ictal data. Forty patients underwent MEG. MRI context included left-sided lesions in 23 of 41 patients (56.1%) and right-sided lesions in 18 (43.9%); lesion distributions were frontal 21 (51.2%), parietal 6 (14.6%), temporal 2 (4.9%), insular 4 (9.8%), and pre- or postcentral 8 (19.5%). These lesion-distribution and treatment details are contextual only and are not findings in this report.
Findings
  • daily focal seizures with right frontocentral scalp EEG concordanceFigure 3 describes a 3-year-old developmentally normal male with daily focal seizures and a right frontal BOSD; interictal and ictal scalp EEG were concordant with the right frontocentral region, where characteristic EKG-like spike waves were also shown.PDF p.6, Figure 3 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

EEGReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Post-event EEG showed focal slowing in the left temporal region without epileptiform abnormalities; this is EEG context only.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfCase report or observation · 1 finding
e236615-full.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • EEGEEG obtained a few days after palinacousis had ceased showed focal slowing in the left temporal region without epileptiform abnormalities.PDF p.1, Summary; PDF p.2, Investigations; PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

equivalent current dipoles (ECDs) of interictal spikesReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The first MEG analysis found interictal-spike ECDs in the left paracentral lobule and left precuneus.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • equivalent current dipoles (ECDs) of interictal spikesThe first MEG analysis localized ECDs of interictal spikes to the left paracentral lobule and left precuneus.PDF p.1, Case Report; PDF p.2, Fig. 1(d) caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

first resection; left paracentral lobule sparingReported: Left hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The case report supplies no lateralizing semiologic relationship for the first resection.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding · 1 reported value
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • first resection; left paracentral lobule sparingThe first operation resected the left middle cingulate gyrus, parts of the precuneus, and the superior parietal lobule while sparing the left paracentral lobule to prevent a right-foot motor deficit; seizures ceased temporarily and recurred three months after surgery.PDF p.1, Case Report; PDF p.2, Fig. 1(g) caption
Reported values
  • Resection extent and temporary seizure cessation with recurrence at 3 monthsfirst resection; left paracentral lobule sparingCount · Single reported patient · First postoperative coursePDF p.1, Case Report; PDF p.2, Fig. 1(g) caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

functional mapping; SMA symptomsReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Functional mapping of left medial frontal areas produced right upper-limb motor function considered likely to represent SMA symptoms.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • functional mapping; SMA symptomsFunctional mapping showed that the left medial frontal areas identified during the second evaluation controlled motor function of the right upper limb, which the authors considered likely to represent SMA symptoms.PDF p.2, Case Report

1 contributing manuscript; source-reported values remain separate and are not pooled.

Group 2 illustrative anatomic-electroclinical caseReported: Bilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The case included asymmetric bilateral facial contraction and left- and right-sided limb manifestations, but no sign-side relationship to the seizure-onset hemisphere is supplied.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfCase report or observation · 1 finding
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This single-center presurgical series included 54 patients whose SEEG-defined epileptogenic zone (EZ) predominantly involved the frontal lobe, selected from 180 SEEG explorations performed from February 2000 through November 2010; one inconclusive exploration and nonpredominantly frontal cases were excluded. The cohort included 22 male and 32 female patients, mean age 24.9 ± 9.5 years, mean epilepsy duration 16.9 ± 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed all seizures and scored presence/absence of 31 ictal signs; each patient's sign was assigned 0, 1, or 2 according to reproducibility. The “early spread network” was the cortical tissue involved from electrical onset through completion of clinical semiology and was explicitly distinguished from the EZ. SEEG sampling is described as 20 frontal cortical regions, while the later matrices are described as containing 24 brain-area variables. Analyses used correlation matrices, Kendall tests with p < 0.05, PCA on rank-transformed sign scores, hierarchical clustering, and value-test ≥ 2 to identify characteristic variables.
Findings
  • Group 2 illustrative anatomic-electroclinical caseFigure 3 illustrates one Group 2 patient with nonintegrated gestural behavior and proximal stereotypies of the pelvis, trunk, and left upper limb, asymmetric bilateral facial contraction, tonic/dystonic posture of the right upper limb, and vocalization. SEEG showed low-voltage rapid discharge at electrical onset in ventrolateral prefrontal BA 45, BA 9/46V, and BA 44, followed at clinical onset by fast activity in BA 8V, BA 9, SMA, and lateral BA 6 and slower activity in the temporopolar region.PDF p.9, Figure 3 and caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

Groups 1-4; Table 1 semiologic features; early spread networksReported: ContralateralAlso reported: IpsilateralAlso reported: Right hemisphere1 manuscript · 1 finding · 62 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 non-independent primary or overlapping context

Group 1 was characterized by contralateral tonic and contralateral versive signs; Group 3 showed negative v-tests for contralateral tonic and ipsilateral versive signs. The source reports relative-sided signs, not a left/right hemispheric preference.

Source-defined result groups 4
Lateralization: ContralateralSource-defined values retained separatelyG3 · For variables not used to build clustering, occurrence in one group versus the whole population; for active variables, similarity between ictal signs and groups · Patient group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyG3 · For variables not used to build clustering, occurrence in one group versus the whole population; for active variables, similarity between ictal signs and groups · Patient group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyG1 · For variables not used to build clustering, occurrence in one group versus the whole population; for active variables, similarity between ictal signs and groups · Patient group1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyG1 · For variables not used to build clustering, occurrence in one group versus the whole population; for active variables, similarity between ictal signs and groups · Patient group1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfNon-independent primary or overlapping context · 1 finding · 62 reported values
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf
Non-independent primary or overlapping context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Consecutive presurgical SEEG series from Timone Hospital, Marseille, February 2000-November 2010: 54 patients in whom SEEG-defined EZ was within the frontal lobe, selected from 180 SEEG explorations; patients with inconclusive intracranial recording (n=1) or a nonpredominantly frontal EZ were excluded. All patients had noninvasive presurgical assessment and video-SEEG after complete or partial antiepileptic-drug withdrawal; 374 seizures were recorded and analyzed. The cohort included 22 male and 32 female patients, mean age 24.9 +/- 9.5 years, mean epilepsy duration 16.9 +/- 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed VEEG and electrical data; 31 ictal signs and 24 brain-area variables were scored 0-1-2 per patient, with rank-based PCA, hierarchical clustering, correlation matrices, and Kendall tests at p < 0.05. The source describes sampling 20 cortical regions in one methods passage and distinguishes the SEEG-defined EZ from the source-defined early spread network.
Findings
  • Groups 1-4; Table 1 semiologic features; early spread networksHierarchical clustering identified Group 1 (16 patients) with elementary motor signs including early clonic, contralateral tonic or versive, somesthetic localized aura, asymmetric tonic, and asymmetric facial signs, with gestural motor behavior and emotional features absent; rolandic BA4, low-BA4 rolandic operculum, parietal cortex, and other caudal or premotor regions were involved. Group 2 (23 patients) combined symmetric proximal or axial tonic posture or chapeau de gendarme with nonintegrated gestural motor behavior, often nonlocalized aura or vocalization, while integrated behavior, distal stereotypies, early clonic signs, and fixed facial expression were absent; premotor and lateral prefrontal regions were frequently co-involved, commonly with lateral-to-medial propagation. Group 3 (10 patients) showed integrated gestural behavior with distal stereotypies, fixed facial or positive emotional expression, proximal stereotypies, and speech production, with elementary motor signs absent; the early spread network involved rostral ventrolateral prefrontal BA47/12, BA10, BA11, BA46 and rostral cingulate BA32 or rostral BA24. Group 4 (5 patients) showed integrated fearful behavior, sometimes hyperkinetic, with fight or escape attempts, frightened expression, occasional screaming or swearing, and autonomic signs, with elementary motor signs absent; orbital or medial prefrontal BA14, BA32/24r, BA10 propagated to amygdala and anterior temporal regions but not lateral frontal cortex.PDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
Reported values
  • G4 +2.47 hyperkinetic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 +3.75 chapeau*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +3.76 elementary motor*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 +2.24 elementary motorGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • Group 4: 5 patientsGroups 1-4; Table 1 semiologic features; early spread networksCount · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · Group 4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +2.01 rictus/asymmetric facialGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +4.59 early clonic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +5.33 fixed facial*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.59 fear/anxiety/rage*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +2.90 proximal stereotypies*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +2.09 impaired consciousnessGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +4.97 integrated*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 +2.43 nonlocalized aura*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 -4.73 elementary motor*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.09 chapeauGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 -2.09 contralateral tonicGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +3.00 positive affect*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +5.77 negative affect*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 -2.40 symmetric axial tonicGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -3.78 impaired consciousness*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +2.66 impaired consciousness*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +3.04 autonomic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +4.86 manipulation*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +3.61 contralateral tonic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 -3.34 integrated*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 -2.00 manipulationGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 -2.15 late clonicGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +2.07 speechGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 +3.76 nonintegrated*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -3.83 nonlocalized auraGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +3.16 tonic vocalization*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • Group 3: 10 patientsGroups 1-4; Table 1 semiologic features; early spread networksCount · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · Group 3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • negative v-test threshold < -2Groups 1-4; Table 1 semiologic features; early spread networksThreshold · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · method · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +4.58 fear/anxiety/rage*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +3.33 asymmetric tonic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +3.45 contralateral versive*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.36 proximal stereotypies*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 -2.07 ipsilateral versiveGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.21 distal stereotypiesGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 -2.94 distal stereotypies*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 -3.39 elementary motor*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • positive v-test threshold >2Groups 1-4; Table 1 semiologic features; early spread networksThreshold · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · method · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -3.12 integrated*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +2.49 nonlocalized aura*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +3.56 somesthetic aura*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.10 nonintegratedGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.19 hyperkineticGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 +2.12 vocalizationGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +4.21 speech*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • Group 2: 23 patientsGroups 1-4; Table 1 semiologic features; early spread networksCount · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · Group 2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 +2.04 GTCSGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 -2.57 early clonic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.11 autonomicGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 -2.51 tonic vocalization*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.08 speechGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • Group 1: 16 patientsGroups 1-4; Table 1 semiologic features; early spread networksCount · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · Group 1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G3 +7.16 distal stereotypies*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G3 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 -2.19 fixed facialGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 -2.17 speechGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G2 +4.38 symmetric axial tonic*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G2 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G1 -2.09 negative affectGroups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G1 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4
  • G4 +3.94 integrated*Groups 1-4; Table 1 semiologic features; early spread networksOther reported value · 54 patients partitioned into Group 1 n=16, Group 2 n=23, Group 3 n=10, and Group 4 n=5 · G4 · Ictal semiology and the early spread network from electrical onset through emergence of clinical signsPDF p.1, Summary; PDF p.5, Figure 2; PDF p.8, Table 1; PDF p.9, Results, Group 1; PDF p.10, Results, Groups 2-4

1 contributing manuscript; source-reported values remain separate and are not pooled.

highly epileptogenic middle and posterior insular short gyri in Patient 2Reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The left-sided finding is patient-specific onset and resection anatomy, not semiologic lateralization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfCase report or observation · 1 finding
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • highly epileptogenic middle and posterior insular short gyri in Patient 2In Patient 2, the EI map showed the middle and posterior insular short gyri as highly epileptogenic, and the postoperative MRI showed resection including anterior and posterior long gyri and posterior and middle short gyri in the left insular lobe.PDF p.11, Figure 5 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal forced head versionReported: IpsilateralAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

In Case 1, forced right eye deviation and right head turning were ipsilateral to the right temporo-occipital focus, while later left-leg tonic posturing and left version were contralateral during seizure progression.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdfCase report or observation · 1 finding
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
This is a two-case report with no control or comparator group. Case-1 was a 24-year-old right-handed man; 32 habitual seizures were recorded during 3 days of scalp video-EEG, with two followed by secondary GTCS, and two right-hemisphere SEEG implantations were performed 4 months apart. Case-2 was a 19-year-old right-handed man; three habitual seizures were captured on video-EEG and right temporal neocortical, temporal-pole, and medial-structure regions were explored with SEEG. The source describes scalp EEG, MRI, FDG-PET, SEEG onset and propagation, anatomical reconstruction, cortical resection, and seizure-free follow-up of 17 months for Case-1 and 25 months for Case-2. Case-1 MRI/FDG-PET was reported unremarkable for an evaluable lesion; Case-2 MRI and PET findings were reported in the right middle-posterior inferior temporal/fusiform and medial temporal regions. No cohort-wide denominator for ipsiversive eye deviation, no control comparison, and no population-level frequency or diagnostic statistic are reported.
Findings
  • Case-1 forced eye deviation and head turningIn the Case-1 habitual seizure chronology, forced eye deviation to the right was followed by right-sided head turning, left-leg tonic posturing, left version, and GTCS in the described sequence.PDF p.2, Case-1 case presentation; PDF p.2, Fig. 1 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal onset in adjacent superior parietal cortex with spread to the lesionReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Intracranial EEG onset and the radiological lesion were in the right parietal region.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdfCase report or observation · 1 finding
jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study included consecutive children with focal epilepsy and MRI-defined BOSD evaluated at The Hospital for Sick Children in Toronto between January 2007 and July 2019; patients with less than 1 year of postsurgical follow-up were excluded. Forty-one children were included. Medical-record data included seizure semiology, seizure frequency, age at seizure onset, antiseizure medications, and comorbidities. Mean age at surgery was 9.7 years (SD 4.5), 29 patients were male (70.7%), and mean age at seizure onset was 4.7 years (SD 3.5). Table 1 reported daily seizures in 30 of 41 patients (73.2%), weekly seizures in 9 (22.0%), monthly seizures in 1 (2.4%), yearly seizures in 1 (2.4%), and a history of focal status epilepticus requiring hospitalization in 8 (19.5%); these are cohort descriptors, not separate findings here. Presurgical evaluation included scalp video EEG, MEG, FDG-PET, and invasive video EEG when indicated. Thirty-seven patients underwent IVEEG, and 34 had available ictal data. Forty patients underwent MEG. MRI context included left-sided lesions in 23 of 41 patients (56.1%) and right-sided lesions in 18 (43.9%); lesion distributions were frontal 21 (51.2%), parietal 6 (14.6%), temporal 2 (4.9%), insular 4 (9.8%), and pre- or postcentral 8 (19.5%). These lesion-distribution and treatment details are contextual only and are not findings in this report.
Findings
  • ictal onset in adjacent superior parietal cortex with spread to the lesionIn the Figure 4 case, intracranial EEG showed ictal onset in the adjacent superior parietal cortex with subsequent spread to the radiological lesion; intraictal fast ripples were prominent in both the adjacent cortex and the radiological lesion.PDF p.7, Figure 4 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal onset zone; seizure onset and spread areasReported: Left hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The case observation records a left-sided ictal onset and subsequent spread, with source-reported spread categories of <10 seconds and <20 seconds.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding · 2 reported values
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • ictal onset zone; seizure onset and spread areasDuring the first invasive evaluation, the ictal onset zone was localized to the left middle cingulate gyrus, with spread to the left paracentral lobule, pre- and postcentral gyri, and superior parietal lobule; Fig. 1f labels source-reported spread categories of <10 s and <20 s.PDF p.1, Case Report; PDF p.2, Fig. 1(f) caption
Reported values
  • Seizure spread category <20 secondsictal onset zone; seizure onset and spread areasDuration · Single reported patient · Later spread category · First invasive evaluation; ictal onset and spreadPDF p.1, Case Report; PDF p.2, Fig. 1(f) caption
  • Seizure spread category <10 secondsictal onset zone; seizure onset and spread areasDuration · Single reported patient · Earlier spread category · First invasive evaluation; ictal onset and spreadPDF p.1, Case Report; PDF p.2, Fig. 1(f) caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal SPECT hyperperfusion; broad sensory-motor networksReported: BilateralAlso reported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Ictal SPECT showed left-sided and bilateral hyperperfusion across the source-described sensory-motor network.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • ictal SPECT hyperperfusion; broad sensory-motor networksDuring a seizure provoked by sudden right-foot sensory stimulation, ictal SPECT showed hyperperfusion in broad sensory-motor networks including the dorsal column-medial lemniscus pathways, left thalamus, bilateral postcentral gyri and posterior parietal cortices, left supplementary motor area, left paracentral lobule, and left caudate-putamen.PDF p.1, Abstract; PDF p.2, Case Report; PDF p.3, Fig. 2(a) caption and Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

illustrative SVT prediction exampleReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

In one illustrative case, the semiology sets correctly predicted a right-hemisphere focus.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfCase report or observation · 1 finding
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • illustrative SVT prediction exampleIn the source’s illustrative case, both initial and combined set-of-semiology correctly lateralized the seizure focus to the right hemisphere and localized it to the frontal lobe, but neither localized it to the inferior frontal gyrus.PDF p.4, Fig. 2 caption and panels A-F

1 contributing manuscript; source-reported values remain separate and are not pooled.

interictal epileptiform discharges; ictal onset zones; low voltage fast activityReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Interictal discharges and ictal onset zones in the second invasive evaluation were left-sided.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • interictal epileptiform discharges; ictal onset zones; low voltage fast activityDuring the second invasive evaluation, interictal epileptiform discharges and ictal onset zones were localized to the left medial frontal lobes, specifically the SMA, middle cingulate gyrus, and part of the paracentral lobule; Fig. 2d depicts low-voltage fast activity beginning at the red arrow.PDF p.2, Case Report; PDF p.3, Fig. 2(c-d) caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

interictal scalp epileptiform discharges; ictal activitiesReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Interictal discharges were reported in the left posterior quadrant, while ictal activities were nonlocalizable on long-term video EEG.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • interictal scalp epileptiform discharges; ictal activitiesInitial scalp monitoring localized interictal epileptiform discharges to the left posterior quadrant, whereas ictal activities were nonlocalizable on long-term video EEG monitoring.PDF p.1, Case Report

1 contributing manuscript; source-reported values remain separate and are not pooled.

interictal SEEG abnormalitiesReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Interictal abnormalities were most prominent in the right amygdala and right temporal pole, with occasional extension through right temporolimbic structures; left-amygdala slow waves were also present.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • interictal SEEG abnormalitiesThe prominent interictal abnormalities were spikes and slow waves in the right amygdala, sometimes extending through right temporolimbic structures; intermittent pseudo-rhythmic sharp waves occurred in the right temporal pole and slow waves in the left amygdala.PDF p.2, right column, paragraph beginning “The most prominent interictal abnormalities”

1 contributing manuscript; source-reported values remain separate and are not pooled.

language lateralisation; memory impairmentReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

Intracarotid amobarbital testing showed strictly left-sided language lateralisation and right-sided memory impairment in one patient.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • language lateralisation; memory impairmentIntracarotid amobarbital testing demonstrated strictly left-sided language lateralisation and right-sided memory impairment in the patient.PDF p.2, left column, paragraph beginning “Seizures remained drug-resistant”

1 contributing manuscript; source-reported values remain separate and are not pooled.

left temporal anatomo-electro-clinical correlationReported: ContralateralAlso reported: Left hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The case reports left anterior/mid-temporal ictal activity with propagation to contralateral temporal and midline regions.

Source-defined result groups 2
Lateralization: Contralateral / Left hemisphereSource-defined values retained separatelyAll reported · Seizure1 manuscript · 3 reported values · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · Seizure1 manuscript · 3 reported values · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdfCase report or observation · 1 finding · 3 reported values
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case assessed by clinical history, examination, brain MRI, video-EEG, and pathology; 12 typical seizures were recorded; no comparator or formal independent reference standard was reported, and the authors used an anatomo-electro-clinical correlation.
Findings
  • left temporal anatomo-electro-clinical correlationMRI showed a left anterior temporal lesion, interictal spikes were seen in the left anterior and mid-temporal region, and ictal EEG during 12 typical seizures with loss of awareness and paraphasia showed rhythmic evolving delta over the left anterior/mid-temporal region with propagation to the contralateral temporal region; Figure 2 also shows propagation toward midline regions.PDF p.2, Materials and Methods; PDF p.3, Figure 1 caption; PDF p.4, Figure 2 caption
Reported values
  • paraphasias during eventsleft temporal anatomo-electro-clinical correlationCount · One 73-year-old right-handed woman; 12 typical recorded seizures · Interictal and ictalPDF p.2, Materials and Methods; PDF p.3, Figure 1 caption; PDF p.4, Figure 2 caption
  • 12 typical seizures recordedleft temporal anatomo-electro-clinical correlationCount · One 73-year-old right-handed woman; 12 typical recorded seizures · Interictal and ictalPDF p.2, Materials and Methods; PDF p.3, Figure 1 caption; PDF p.4, Figure 2 caption
  • left temporal ictal activity with propagationleft temporal anatomo-electro-clinical correlationCount · One 73-year-old right-handed woman; 12 typical recorded seizures · Interictal and ictalPDF p.2, Materials and Methods; PDF p.3, Figure 1 caption; PDF p.4, Figure 2 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

postoperative courseReported: Left hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The postoperative-course record does not establish a lateralizing sign.

Source-defined result groups 3
Localization: TemporalSource-defined values retained separatelyindex patient · preoperative aphasia · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyindex patient · preoperative symptomatic state · patient1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyindex patient · preoperative symptomatic state · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

e236615-full.pdfCase report or observation · 1 finding · 3 reported values
e236615-full.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The index report concerns one 24-year-old Caucasian right-handed woman with a ruptured left temporal cavernous malformation. The review searched PubMed for the word “palinacousis,” found 26 reports including 3 reviews, cross-referenced all publications, excluded reports without perseveration of previously heard sounds or words and all review articles, and retained 22 articles with 35 cases; the authors added their own case. No year or primary-language exclusions were applied. The source does not state a diagnostic reference standard or provide complete denominators for several review percentages; the index EEG was performed after symptoms had ceased.
Findings
  • postoperative courseAfter the haematoma was suctioned and the cavernoma resected while preserving the associated venous developmental anomaly, there was no recurrence of palinacousis at two months and the patient was symptom-free at six months; the report also states complete resolution of aphasia.PDF p.1, Summary; PDF p.2, Outcome and follow-up
Reported values
  • symptom-free at six monthspostoperative courseOther reported value · Same index patient · index patient · Postoperative follow-up at two and six monthsPDF p.1, Summary; PDF p.2, Outcome and follow-up
  • complete resolution of aphasiapostoperative courseOther reported value · Same index patient · index patient · Postoperative follow-up at two and six monthsPDF p.1, Summary; PDF p.2, Outcome and follow-up
  • no recurrence ... at two monthspostoperative courseOther reported value · n/N 0/1 patient · Same index patient · index patient · Postoperative follow-up at two and six monthsPDF p.1, Summary; PDF p.2, Outcome and follow-up

1 contributing manuscript; source-reported values remain separate and are not pooled.

remission of reflex seizures and hypermotor seizuresReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

At one-year follow-up after the second resection, reflex and hypermotor seizures were in remission with improved daily activities.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding · 2 reported values
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • remission of reflex seizures and hypermotor seizuresAt one-year follow-up after the second resection, reflex seizures and hypermotor seizures were in remission, with remarkable improvement in daily activities including gait, wearing stockings, and foot care.PDF p.2, Case Report; PDF p.3, Discussion; PDF p.4, Discussion
Reported values
  • Hypermotor seizures in remission at 1 yearremission of reflex seizures and hypermotor seizuresOther reported value · Single reported patient · Hypermotor seizures · One-year postoperative follow-upPDF p.2, Case Report; PDF p.3, Discussion; PDF p.4, Discussion
  • Reflex seizures in remission at 1 yearremission of reflex seizures and hypermotor seizuresOther reported value · Single reported patient · Reflex seizures · One-year postoperative follow-upPDF p.2, Case Report; PDF p.3, Discussion; PDF p.4, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

right amygdala ictal discharge; seizure propagationReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

All five seizures began in the right amygdala, with later spread involving both right-sided structures and the left amygdala.

Source-defined result groups 3
Localization: Frontal / Insular / TemporalObserved proportion 100.0%All reported · seizures1 manuscript · 1 reported value · not pooled
Localization: Frontal / Insular / TemporalSource-defined values retained separatelyAll reported · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 100.0%All reported · seizures1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding · 3 reported values
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • right amygdala ictal discharge; seizure propagationIn all five spontaneous electroclinical seizures, a 2–3-Hz spike-and-wave rhythmic discharge began in the right amygdala about 20 seconds before the first ictal symptom, propagated to the right anterior hippocampus and parahippocampal gyrus during nausea, and then involved the left amygdala, right insula, right lower SMA, and right anterior cingulate in association with staring, loss of awareness, oro-alimentary automatisms, and rightward oculocephalic version.PDF p.2, right column, paragraph beginning “In all five seizures”; PDF p.3, left column, paragraph beginning “the right anterior cingulate gyrus”
Reported values
  • in all five seizuresright amygdala ictal discharge; seizure propagationCount · n/N 5/5 · one patient; five stereotyped spontaneous electroclinical seizures · ictal onset and propagationPDF p.2, right column, paragraph beginning “In all five seizures”; PDF p.3, left column, paragraph beginning “the right anterior cingulate gyrus”
  • about 20 seconds before the first ictal symptomright amygdala ictal discharge; seizure propagationDuration · one patient; five stereotyped spontaneous electroclinical seizures · ictal onset and propagationPDF p.2, right column, paragraph beginning “In all five seizures”; PDF p.3, left column, paragraph beginning “the right anterior cingulate gyrus”
  • 2–3 Hzright amygdala ictal discharge; seizure propagationRange · one patient; five stereotyped spontaneous electroclinical seizures · ictal onset and propagationPDF p.2, right column, paragraph beginning “In all five seizures”; PDF p.3, left column, paragraph beginning “the right anterior cingulate gyrus”

1 contributing manuscript; source-reported values remain separate and are not pooled.

right temporal seizure onset; right mesial temporal findingsReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The right side is patient-specific onset and imaging anatomy, not a lateralizing direction of a the source's own sign.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdfCase report or observation · 1 finding
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The report concerns one 35-year-old right-handed man with drug-resistant partial epilepsy. Long-term video-EEG captured 6 electroclinical seizures; SEEG recorded 5 stereotyped spontaneous electroclinical seizures using 11 right-hemisphere electrodes and 1 left-amygdala electrode. The report also describes high-frequency stimulation of the right amygdala and right precentral operculum. No control group or independent reference standard is reported.
Findings
  • right temporal seizure onset; right mesial temporal findingsPresurgical video-EEG and ictal semiology suggested right temporal seizure onset; FDG-PET showed right-amygdala hypometabolism extending to the right temporal pole and anterior hippocampus, while ictal SPECT showed increased blood flow centered on the right amygdala.PDF p.2, left column, paragraph beginning “Seizures remained drug-resistant”; PDF p.2, Figure 1 caption; PDF p.3, right column, paragraph beginning “Right mesial TLE was diagnosed”

1 contributing manuscript; source-reported values remain separate and are not pooled.

right- versus left-sided insular stimulationReported: Left hemisphereAlso reported: Right hemisphereNo single reliable side1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 narrative, educational, or cited context

The source found no significant difference in evoked-sensation type between right- and left-insula stimulation.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • right- versus left-sided insular stimulationThe source found no significant difference in the type of evoked sensation between right- and left-sided insular stimulations.PDF p.3, Results
Reported values
  • P=0.10right- versus left-sided insular stimulationP value · 550 clinically eloquent responses: 237 after right-insula and 313 after left-insula stimulation · stimulation-evoked clinical responsePDF p.3, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

second MEG analysis; ECD clustersReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The second presurgical MEG analysis found left-sided ECD clusters.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdfCase report or observation · 1 finding
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Single case report: an 18-year-old right-handed girl with medically refractory reflex and spontaneous seizures since age 12. The evaluation included MRI, FDG-PET, scalp and long-term video EEG, two MEG analyses, two chronic subdural-electrode evaluations with functional mapping, ictal SPECT during provocation, resections, histopathology, and postoperative follow-up. No comparator or reference standard was reported.
Findings
  • second MEG analysis; ECD clustersThe second MEG analysis of interictal spikes revealed ECD clusters in the left supplementary motor area and left paracentral lobules.PDF p.2, Case Report; PDF p.3, Fig. 2(b) caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

temporal-to-insular/opercular spreadReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The illustrated SEEG exploration was left-sided.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

laoprasert-stereoelectroencephalography-seeg-mset-2018.pdfCase report or observation · 1 finding
laoprasert-stereoelectroencephalography-seeg-mset-2018.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
Document type: educational slide deck. No source-wide cohort, prospective protocol, sampling frame, or unified analysis population is reported. The deck combines heterogeneous cited studies, article screenshots, modality tables, conceptual diagrams, and individual cases. Study-specific populations, analysis units, denominators, comparators, and follow-up intervals are retained only where stated on the relevant slide; no source-wide denominator is inferred.
Findings
  • temporal-to-insular/opercular spreadAn illustrated left temporal, perisylvian, and insular exploration used SEEG to evaluate possible spread of temporal discharge to insular and opercular regions suggested by the patient’s clinical seizure features.PDF p.46

1 contributing manuscript; source-reported values remain separate and are not pooled.

wide right frontal ictal onset zoneReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 0.9 across 1 manuscript · 1 case report or observation

The case reports a right frontal ictal onset zone on intracranial EEG.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdfCase report or observation · 1 finding
jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdf
Case report or observation · Class III · Evidence weight 0.90 · 1 × 0.9 × 1
The study included consecutive children with focal epilepsy and MRI-defined BOSD evaluated at The Hospital for Sick Children in Toronto between January 2007 and July 2019; patients with less than 1 year of postsurgical follow-up were excluded. Forty-one children were included. Medical-record data included seizure semiology, seizure frequency, age at seizure onset, antiseizure medications, and comorbidities. Mean age at surgery was 9.7 years (SD 4.5), 29 patients were male (70.7%), and mean age at seizure onset was 4.7 years (SD 3.5). Table 1 reported daily seizures in 30 of 41 patients (73.2%), weekly seizures in 9 (22.0%), monthly seizures in 1 (2.4%), yearly seizures in 1 (2.4%), and a history of focal status epilepticus requiring hospitalization in 8 (19.5%); these are cohort descriptors, not separate findings here. Presurgical evaluation included scalp video EEG, MEG, FDG-PET, and invasive video EEG when indicated. Thirty-seven patients underwent IVEEG, and 34 had available ictal data. Forty patients underwent MEG. MRI context included left-sided lesions in 23 of 41 patients (56.1%) and right-sided lesions in 18 (43.9%); lesion distributions were frontal 21 (51.2%), parietal 6 (14.6%), temporal 2 (4.9%), insular 4 (9.8%), and pre- or postcentral 8 (19.5%). These lesion-distribution and treatment details are contextual only and are not findings in this report.
Findings
  • wide right frontal ictal onset zoneFigure 5, describing the Figure 3 patient, reports a wide right frontal ictal onset zone on intracranial EEG; the MEG cluster was discordant with the lesion.PDF p.8, Figure 5 caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

Rapid postictal recoveryReported: Right hemisphere2 manuscripts · 2 findings · 4 reported values
Weighted evidence supportevidence weight pending · 2 structured design not resolved

Rapid postictal return to baseline occurred in 20/54 right temporal seizures (37%) and in 0/73 left temporal seizures. No hemisphere or body-side direction is reported.

Source-defined result groups 4
Localization: typical anterior cingulate lesion groupObserved proportion 100.0%All reported · patients1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 37.0%RTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 100.0%RTL rapid-return seizures · RTL versus LTL · seizure with rapid return1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 0.0%LTL · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 2

Alphabetical by manuscript.

alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdfStructured design not resolved · 1 finding · 1 reported value
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.389
The authors retrospectively identified consecutive cases from Cleveland Clinic and University of Texas Southwestern databases, using MRI-defined lesions confined to the cingulate gyrus and source-defined follow-up/outcome criteria. Visual MRI analysis divided the cingulate into anterior and posterior portions using Talairach and Tournoux coordinates; invasive data were used when lesion overlap made localization uncertain. Fourteen cases were included, with 10 anterior and 4 posterior cingulate lesions; the report’s direct EEG/PET denominators are retained only where stated.
Findings
  • typical anterior quick recoveryQuick recovery was seen in all six typical anterior patients.PDF p.5, Clinical Presentation
Reported values
  • 6/6 quick recoverytypical anterior quick recoveryProportion · n/N 6/6 · 6 typical anterior cingulate cases · postictal phasePDF p.5, Clinical Presentation
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 3 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Rapid return to baseline postictallyRapid return to baseline occurred only in RTL seizures.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
Reported values
  • all ... 20 ... CPSRapid return to baseline postictallyPercentage · n/N 20/20 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL rapid-return seizures · Postictal; rapid means within 1 minute after the ictal discharge endedPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • 0/73Rapid return to baseline postictallyPercentage · n/N 0/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · Postictal; rapid means within 1 minute after the ictal discharge endedPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • 20/54 (37%)Rapid return to baseline postictallyPercentage · n/N 20/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · Postictal; rapid means within 1 minute after the ictal discharge endedPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Aura presentReported: ContralateralAlso reported: IpsilateralAlso reported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Auras preceding complex partial seizures and psychomotor epilepsy seizures were more common in the RTL group than the LTL group.

Source-defined result groups 2
Lateralization: presence of auraObserved proportion 46.3%RTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Lateralization: presence of auraObserved proportion 26.0%LTL · RTL versus LTL · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 3 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Presence of auraAuras preceding CPS and PE seizures were more common in RTL than in LTL seizures.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
Reported values
  • p=0.03Presence of auraP value · RTL seizure group, n=54, versus LTL seizure group, n=73 · Preictal aura preceding CPS or PE seizurePDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • RTL 25/54 seizures (46%)Presence of auraPercentage · n/N 25/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL · Preictal aura preceding CPS or PE seizurePDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5
  • LTL 19/73 seizures (26%)Presence of auraPercentage · n/N 19/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL · Preictal aura preceding CPS or PE seizurePDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5

1 contributing manuscript; source-reported values remain separate and are not pooled.

Axial motor movementReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Ventral posterior-insula stimulation evoked trunk rotation toward contralateral space with gaze shift in the same direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

simone-anatomo-functional-organization-insular-networks-2025.pdfStructured design not resolved · 1 finding
simone-anatomo-functional-organization-insular-networks-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The paper summarizes prior macaque ICMS mapping performed with 200-microsecond biphasic pulses at 50 Hz, 4 mA, for 3 seconds; a behavior entered the dataset when two observers recognized it and it was evoked in more than 50% of trials. The present analyses used ICMS maps and insular tracer injections in two male rhesus macaques (Mk1 and Mk2), indirect tracer data from 22 additional animals, and resting-state fMRI from 12 male macaques aged 4-8 years. The authors warped the ICMS maps and injection sites onto the INIA19 macaque template and delineated six insular fields. No seizure cohort, ictal or postictal observations, or clinical localization reference standard was studied.
Findings
  • proximal movements; axial movements; tremorsIn macaques, ICMS of the caudalmost insular region produced simple limb-muscle reactions, axial movements, and bodily tremors: proximal movements clustered in the dorsal posterior sector, axial movements occupied the ventral posterior sector, and tremors occurred across both sectors. The source also describes posterior-insula responses including tremors coupled with limb or axial movements, postural adjustments, and ventral-sector trunk rotation toward contralateral space with a gaze shift in the same direction.PDF p.5, Fig. 1D, E and caption; PDF p.12, §4.5.1; PDF p.15, Fig. 9A and caption; PDF p.16, §§4.5.2-4.5.3; PDF p.19, §5.4

1 contributing manuscript; source-reported values remain separate and are not pooled.

Complex partial seizures (CPS) and partial evolving to generalized (PE) seizuresReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The primary result reports LTL seizures as 54/73 CPS (74%) and 19/73 PE (26%), versus RTL 50/54 CPS (93%) and 4/54 PE (7%).

Source-defined result groups 4
Lateralization: Left hemisphere / Right hemisphereObserved proportion 26.0%LTL; PE · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 74.0%LTL; CPS · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 7.4%RTL; PE · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Left hemisphere / Right hemisphereObserved proportion 92.6%RTL; CPS · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 4 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Complex partial seizures (CPS) and partial evolving to generalized (PE) seizuresAmong the recorded seizures, the LTL group had 54 CPS and 19 PE seizures, whereas the RTL group had 50 CPS and 4 PE seizures.PDF p.1, Summary; PDF p.3, Results, seizure-type paragraph
Reported values
  • LTL CPS 54/73 (74%)Complex partial seizures (CPS) and partial evolving to generalized (PE) seizuresPercentage · n/N 54/73 · 9 LTL/LTLE patients versus 10 RTL/RTLE patients · LTL; CPS · ictalPDF p.1, Summary; PDF p.3, Results, seizure-type paragraph
  • LTL PE 19/73 (26%)Complex partial seizures (CPS) and partial evolving to generalized (PE) seizuresPercentage · n/N 19/73 · 9 LTL/LTLE patients versus 10 RTL/RTLE patients · LTL; PE · ictalPDF p.1, Summary; PDF p.3, Results, seizure-type paragraph
  • RTL CPS 50/54 (93%)Complex partial seizures (CPS) and partial evolving to generalized (PE) seizuresPercentage · n/N 50/54 · 9 LTL/LTLE patients versus 10 RTL/RTLE patients · RTL; CPS · ictalPDF p.1, Summary; PDF p.3, Results, seizure-type paragraph
  • RTL PE 4/54 (7%)Complex partial seizures (CPS) and partial evolving to generalized (PE) seizuresPercentage · n/N 4/54 · 9 LTL/LTLE patients versus 10 RTL/RTLE patients · RTL; PE · ictalPDF p.1, Summary; PDF p.3, Results, seizure-type paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

connected singing efficacyReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Post-stroke singing efficacy involved left ventral language pathways and a right middle cerebellar peduncle finding, without seizure-axis evidence.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdfStructured design not resolved · 1 finding · 1 reported value
pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Forty-five adults with chronic aphasia more than 6 months after a clinically confirmed left-hemisphere stroke were recruited in Helsinki and Turku in 2017-2019; all were Finnish native speakers, over 18 years, and had no hearing deficit, severe cognitive impairment, substance abuse, or neurological/psychiatric comorbidity. Connected spoken-language production was mean correct information units per minute across three discourse tasks; connected singing was correct words per minute while singing the familiar song Jaakko-kulta; two connected-singing recordings were lost, leaving n=43 for that analysis. Repetition used 16 identical 1-5-word phrases in spoken and melodically intoned formats, with the first attempt scored and correct words per minute calculated. Six participant-level local-connectome regression models used age and lesion volume as covariates; tract tracking used a T-score threshold of 3, 2,000 permutations, and FDR <0.0083 after Bonferroni correction.
Findings
  • connected singing efficacyIn the current study, better connected singing efficacy was associated primarily with the left ventral stream and left projection pathways, with a right middle cerebellar peduncle association also reported.PDF p.3, Results, networks supporting connected spoken language production and connected singing efficacy; PDF p.4, Fig. 1b caption and tract panel; PDF p.7, Discussion; PDF p.9, Conclusion
Reported values
  • FDR <0.0083connected singing efficacyP value · Participants with chronic post-stroke aphasia and an available connected-singing recording; connectometry n=43PDF p.3, Results, networks supporting connected spoken language production and connected singing efficacy; PDF p.4, Fig. 1b caption and tract panel; PDF p.7, Discussion; PDF p.9, Conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

connected singing efficacy by spoken language deficit severityReported: Bilateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Less-severe and more-severe post-stroke aphasia groups show shared left networks plus subgroup-specific bilateral/right and left pathway patterns.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdfStructured design not resolved · 1 finding · 2 reported values
pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Forty-five adults with chronic aphasia more than 6 months after a clinically confirmed left-hemisphere stroke were recruited in Helsinki and Turku in 2017-2019; all were Finnish native speakers, over 18 years, and had no hearing deficit, severe cognitive impairment, substance abuse, or neurological/psychiatric comorbidity. Connected spoken-language production was mean correct information units per minute across three discourse tasks; connected singing was correct words per minute while singing the familiar song Jaakko-kulta; two connected-singing recordings were lost, leaving n=43 for that analysis. Repetition used 16 identical 1-5-word phrases in spoken and melodically intoned formats, with the first attempt scored and correct words per minute calculated. Six participant-level local-connectome regression models used age and lesion volume as covariates; tract tracking used a T-score threshold of 3, 2,000 permutations, and FDR <0.0083 after Bonferroni correction.
Findings
  • connected singing efficacy by spoken language deficit severityAfter a median split by connected spoken-language production efficacy, better connected singing efficacy was associated with distinct tract patterns in less-severe and more-severe spoken-language deficit groups.PDF p.3, Results, networks supporting connected singing in relation to severity; PDF p.5, Fig. 2 caption and panels; PDF p.8, Discussion
Reported values
  • FDR <0.0083connected singing efficacy by spoken language deficit severityP value · Chronic post-stroke aphasia; less-severe/higher spoken-language efficacy group n=22, mean=52.0 SD=16.4, and more-severe/lower efficacy group n=21, mean=9.4 SD=12.0 · Less-severe/higher spoken-language efficacy group (n=22, mean=52.0 SD=16.4)PDF p.3, Results, networks supporting connected singing in relation to severity; PDF p.5, Fig. 2 caption and panels; PDF p.8, Discussion
  • FDR <0.0083connected singing efficacy by spoken language deficit severityP value · Chronic post-stroke aphasia; less-severe/higher spoken-language efficacy group n=22, mean=52.0 SD=16.4, and more-severe/lower efficacy group n=21, mean=9.4 SD=12.0 · More-severe/lower spoken-language efficacy group (n=21, mean=9.4 SD=12.0)PDF p.3, Results, networks supporting connected singing in relation to severity; PDF p.5, Fig. 2 caption and panels; PDF p.8, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Correlation matrix between ictal signs and cortical areasReported: Contralateral1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The sign-area correlation matrix links contralateral motor signs and somesthetic aura with caudal regions and staring/speech/manipulation signs with rostral-frontopolar regions.

Source-defined result groups 2
Localization: FrontalSource-defined values retained separatelyAll reported · Ordered signs and ordered cortical areas across the series · Patient-level semiologic score and cortical-area involvement matrix1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyAll reported · Ordered signs and ordered cortical areas across the series · Patient-level semiologic score and cortical-area involvement matrix1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfStructured design not resolved · 1 finding · 2 reported values
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
This single-center presurgical series included 54 patients whose SEEG-defined epileptogenic zone (EZ) predominantly involved the frontal lobe, selected from 180 SEEG explorations performed from February 2000 through November 2010; one inconclusive exploration and nonpredominantly frontal cases were excluded. The cohort included 22 male and 32 female patients, mean age 24.9 ± 9.5 years, mean epilepsy duration 16.9 ± 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed all seizures and scored presence/absence of 31 ictal signs; each patient's sign was assigned 0, 1, or 2 according to reproducibility. The “early spread network” was the cortical tissue involved from electrical onset through completion of clinical semiology and was explicitly distinguished from the EZ. SEEG sampling is described as 20 frontal cortical regions, while the later matrices are described as containing 24 brain-area variables. Analyses used correlation matrices, Kendall tests with p < 0.05, PCA on rank-transformed sign scores, hierarchical clustering, and value-test ≥ 2 to identify characteristic variables.
Findings
  • Correlation matrix between ictal signs and cortical areasThe sign-area correlation matrix showed a diagonal posterior-to-anterior pattern. Early clonic signs, contralateral versive signs, contralateral tonic posture, and somesthetic localized aura correlated with more caudal areas such as primary motor cortex and rolandic operculum, whereas staring, speech arrest, manipulation behavior, and fixed facial expression correlated with more rostral/frontopolar areas. Early clonic signs and manipulation behavior were relatively region-specific, while hyperkinetic movements and impairment of consciousness were weaker, more distributed associations involving caudal and rostral prefrontal regions; the diagonal pattern remained for significant correlations.PDF p.4, Figure 1; PDF p.7, Cluster analysis and anatomic-electroclinical correlations
Reported values
  • p < 0.05Correlation matrix between ictal signs and cortical areasP value · 54-patient series; 31 ictal signs and the sampled cortical areas · Ictal; early spread networkPDF p.4, Figure 1; PDF p.7, Cluster analysis and anatomic-electroclinical correlations
  • significant matrix correlations marked at p < 0.05Correlation matrix between ictal signs and cortical areasCount · 54-patient series; 31 ictal signs and the sampled cortical areas · Ictal; early spread networkPDF p.4, Figure 1; PDF p.7, Cluster analysis and anatomic-electroclinical correlations

1 contributing manuscript; source-reported values remain separate and are not pooled.

cortical mechanism of ictal contraversionReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The initial versive movement is contralateral to the seizure-onset hemisphere, while the implicated frontal contraversive centers are in the same hemisphere as seizure onset.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

wyllie1986.pdfStructured design not resolved · 1 finding
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • cortical mechanism of ictal contraversionThe authors interpret contraversion as primarily resulting from transcortical propagation of seizure discharge to frontal contraversive centers in the hemisphere of seizure onset, with the first versive movement clinically similar to movements elicited by electrical stimulation of Brodmann area 6 or 8; they note that contraversion occurred with frontal, temporal, parietal, and occipital onset seizures.PDF p.4, discussion of frontal contraversive fields and transcortical propagation; PDF p.4, paragraph on occipital onset; PDF p.5, conclusion

1 contributing manuscript; source-reported values remain separate and are not pooled.

dysphasia subtypesReported: Non-dominant hemisphere1 manuscript · 1 finding · 16 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Expressive and receptive dysphasia and isolated anomia occurred only with dominant-temporal origin in Table 5, whereas isolated paraphasia occurred only with nondominant-temporal origin.

Source-defined result groups 16
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyReceptive dysphasia; Nondominant-origin · Dominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated anomia; Nondominant-origin · Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyExpressive dysphasia; Nondominant-origin · Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated anomia; Nondominant-origin · Dominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyExpressive dysphasia; Nondominant-origin · Dominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated paraphasia; Nondominant-origin · Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated paraphasia; Dominant-origin · Nondominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyReceptive dysphasia; Dominant-origin · Nondominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyReceptive dysphasia; Nondominant-origin · Dominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated anomia; Dominant-origin · Nondominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated anomia; Dominant-origin · Nondominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated paraphasia; Nondominant-origin · Dominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyExpressive dysphasia; Dominant-origin · Nondominant-origin · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyIsolated paraphasia; Dominant-origin · Nondominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyExpressive dysphasia; Dominant-origin · Nondominant-origin · patient1 manuscript · 1 reported value · not pooled
Lateralization: Dominant hemisphere / Non-dominant hemisphereSource-defined values retained separatelyReceptive dysphasia; Dominant-origin · Nondominant-origin · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 16 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • dysphasia subtypesTable 5 reports expressive dysphasia in 8 patients/15 seizures from the dominant group and none from the nondominant group, receptive dysphasia in 4/11 dominant and none nondominant, isolated paraphasia in 2/3 nondominant and none dominant, and isolated anomia in 1/1 dominant and none nondominant.PDF p.4, Table 5 and footnotes
Reported values
  • Isolated anomia, Nondominant-origin: 0 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated anomia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Expressive dysphasia, Dominant-origin: 8 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Expressive dysphasia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Expressive dysphasia, Dominant-origin: 15 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Expressive dysphasia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated paraphasia, Nondominant-origin: 3 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated paraphasia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Expressive dysphasia, Nondominant-origin: 0 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Expressive dysphasia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated paraphasia, Nondominant-origin: 2 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated paraphasia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Receptive dysphasia, Nondominant-origin: 0 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Receptive dysphasia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Receptive dysphasia, Dominant-origin: 11 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Receptive dysphasia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated anomia, Nondominant-origin: 0 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated anomia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated paraphasia, Dominant-origin: 0 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated paraphasia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Expressive dysphasia, Nondominant-origin: 0 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Expressive dysphasia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated paraphasia, Dominant-origin: 0 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated paraphasia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Receptive dysphasia, Nondominant-origin: 0 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Receptive dysphasia; Nondominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Receptive dysphasia, Dominant-origin: 4 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Receptive dysphasia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated anomia, Dominant-origin: 1 patientsdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated anomia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes
  • Isolated anomia, Dominant-origin: 1 seizuresdysphasia subtypesCount · Dysphasia subtypes among the 14 patients and 30 seizures with dysphasia · Isolated anomia; Dominant-origin · mixed; the table is not phase-stratifiedPDF p.4, Table 5 and footnotes

1 contributing manuscript; source-reported values remain separate and are not pooled.

EEG lateralization at onset of contraversive movementReported: ContralateralAlso reported: Right hemisphere1 manuscript · 1 finding · 10 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Source reports that EEG remained clearly lateralized into contraversive movement in most seizures, with EMG-obscured, nonlateralized, and bitemporal-spread exceptions.

Source-defined result groups 6
Lateralization: ContralateralSource-defined values retained separatelyfull versive-seizure cohort · EEG pattern retained versus obscured or nonlateralized at contraversion · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyEEG remained clearly lateralized · obscured or nonlateralized at contraversion · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelynonlateralized EEG onset · other EEG patterns · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelytemporal onset with equal bitemporal spread · other EEG patterns · seizure1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyEEG remained clearly lateralized · remaining patients · patient1 manuscript · 1 reported value · not pooled
Lateralization: ContralateralSource-defined values retained separatelyremaining EEG patterns · retained lateralization or EMG-obscured · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

wyllie1986.pdfStructured design not resolved · 1 finding · 10 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • EEG lateralization at onset of contraversive movementThe ictal EEG pattern remained clearly lateralized into onset of the contraversive movement in 54 seizures from 24 patients; 3 previously lateralized seizures were obscured by EMG artifact, and 4 remaining seizures included 3 with nonlateralized EEG onset and 1 with temporal onset spreading equally to both temporal lobes before contraversion.PDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
Reported values
  • 1 seizureEEG lateralization at onset of contraversive movementCount · n/N 1/61 versive seizures · 61 versive seizures from 27 patients · temporal onset with equal bitemporal spread · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 24 patientsEEG lateralization at onset of contraversive movementCount · n/N 24/27 patients · 61 versive seizures from 27 patients · EEG remained clearly lateralized · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 79 secondsEEG lateralization at onset of contraversive movementDuration · 61 versive seizures from 27 patients · illustrative bitemporal-spread seizure · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 4 seizuresEEG lateralization at onset of contraversive movementCount · n/N 4/61 versive seizures · 61 versive seizures from 27 patients · remaining EEG patterns · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 61 versive seizuresEEG lateralization at onset of contraversive movementCount · 61 versive seizures from 27 patients · full versive-seizure cohort · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 54 seizuresEEG lateralization at onset of contraversive movementCount · n/N 54/61 versive seizures · 61 versive seizures from 27 patients · EEG remained clearly lateralized · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 3 patientsEEG lateralization at onset of contraversive movementCount · n/N 3/27 patients · 61 versive seizures from 27 patients · EMG-obscured seizures · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 3 seizuresEEG lateralization at onset of contraversive movementCount · n/N 3/61 versive seizures · 61 versive seizures from 27 patients · EMG-obscured seizures · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 3 seizuresEEG lateralization at onset of contraversive movementCount · n/N 3/61 versive seizures · 61 versive seizures from 27 patients · nonlateralized EEG onset · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure
  • 75 secondsEEG lateralization at onset of contraversive movementDuration · 61 versive seizures from 27 patients · illustrative bitemporal-spread seizure · Ictal EEG onset through contraversion; one seizure after spread to both temporal lobesPDF p.2, paragraphs describing EEG lateralization and the bitemporal-spread seizure

1 contributing manuscript; source-reported values remain separate and are not pooled.

epileptogenicity profile and seizure thresholdReported: Left hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

No in-scope sign-specific lateralization evidence is present.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdfStructured design not resolved · 1 finding
loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
This is a proposal and narrative synthesis, not a primary empirical study. The authors review prior classification approaches, define the five dimensions, provide tables and conceptual figures, and demonstrate the proposed format with illustrative profiles. The framework is stated to apply to patients with epilepsy, defined here as at least two spontaneous epileptic seizures; for patients with unclear epileptic or nonepileptic events, the source recommends the term paroxysmal event. Clinical history, seizure semiology, EEG, MRI, other diagnostic studies, and etiologic information are translated into a best available working classification that can be refined as information accrues. No formal study cohort, sampling method, reference standard, comparator cohort, or statistical analysis is reported.
Findings
  • epileptogenicity profile and seizure thresholdFigure 2 presents a conceptual profile for a sample patient with left temporal lobe epilepsy in which rising epileptogenicity in a circumscribed brain region reaches a seizure threshold and produces a seizure from that area; the source states that individual patients can instead have focal, multilobar, multifocal, hemispheric, or generalized epileptogenicity profiles.PDF p.6, Figure 2 and caption

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal posturingReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Relative to the seizure-onset hemisphere, focal posturing was predominantly contralateral in the late ictal phase (12/54 RTL and 22/73 LTL), with late ipsilateral posturing in 0/54 RTL and 3/73 LTL; early contralateral posturing was rare, and no RTL-LTL comparison was significant.

Source-defined result groups 6
Lateralization: Contralateral / IpsilateralObserved proportion 0.0%RTL; ipsilateral late · LTL at same phase/direction · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 1.9%RTL; contralateral early · LTL at same phase/direction · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 22.2%RTL; contralateral late · LTL at same phase/direction · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 0.0%LTL; contralateral early · RTL at same phase/direction · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 30.1%LTL; contralateral late · RTL at same phase/direction · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Contralateral / IpsilateralObserved proportion 4.1%LTL; ipsilateral late · RTL at same phase/direction · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 6 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Focal posturingFocal posturing showed no significant RTL-LTL difference in the reported early contralateral, late contralateral, or late ipsilateral comparisons.PDF p.4, Table 5
Reported values
  • 1/54 (2%)Focal posturingPercentage · n/N 1/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL; contralateral early · Early and late ictal phasesPDF p.4, Table 5
  • 0/54Focal posturingPercentage · n/N 0/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL; ipsilateral late · Early and late ictal phasesPDF p.4, Table 5
  • 3/73 (4%)Focal posturingPercentage · n/N 3/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL; ipsilateral late · Early and late ictal phasesPDF p.4, Table 5
  • 22/73 (30%)Focal posturingPercentage · n/N 22/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL; contralateral late · Early and late ictal phasesPDF p.4, Table 5
  • 0/73Focal posturingPercentage · n/N 0/73 · RTL seizure group, n=54, versus LTL seizure group, n=73 · LTL; contralateral early · Early and late ictal phasesPDF p.4, Table 5
  • 12/54 (22%)Focal posturingPercentage · n/N 12/54 · RTL seizure group, n=54, versus LTL seizure group, n=73 · RTL; contralateral late · Early and late ictal phasesPDF p.4, Table 5

1 contributing manuscript; source-reported values remain separate and are not pooled.

hand field; hand-related movementsReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Macaque insular stimulation evoked simple contralateral hand movements.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

simone-anatomo-functional-organization-insular-networks-2025.pdfStructured design not resolved · 1 finding
simone-anatomo-functional-organization-insular-networks-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The paper summarizes prior macaque ICMS mapping performed with 200-microsecond biphasic pulses at 50 Hz, 4 mA, for 3 seconds; a behavior entered the dataset when two observers recognized it and it was evoked in more than 50% of trials. The present analyses used ICMS maps and insular tracer injections in two male rhesus macaques (Mk1 and Mk2), indirect tracer data from 22 additional animals, and resting-state fMRI from 12 male macaques aged 4-8 years. The authors warped the ICMS maps and injection sites onto the INIA19 macaque template and delineated six insular fields. No seizure cohort, ictal or postictal observations, or clinical localization reference standard was studied.
Findings
  • hand field; hand-related movementsIn macaques, the ICMS-defined hand field localized to the dorsal middle insula: stimulation elicited simple contralateral hand twitches, wrist rotation or flexion, finger extension or closure, and complex goal-related movements ranging from hand-to-mouth actions to actions directed to specific body parts; the most posterior dorsal sites were intermingled with proximal-movement sites and were treated as a separate field.PDF p.5, Fig. 1B, E and caption; PDF p.9, §4.3.1; PDF p.10, Fig. 5A and caption; PDF p.12, §§4.3.2-4.3.3; PDF p.18, §5.2

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal motor signs as lateralizing patternsReported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The authors synthesize motor signs as contralateral and unilateral eye blinking or automatism as ipsilateral to the seizure focus.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 1 finding
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • ictal motor signs as lateralizing patternsThe authors’ synthesis is that unilateral dystonia, tonic posture, clonic jerking, and head version strongly suggest contralateral hemisphere seizure origin, while unilateral eye blinking and unilateral automatism indicate ipsilateral seizure focus.PDF p.1, Abstract; PDF p.4, Figure 1 discussion; PDF p.5, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

interictal EEG foci in versive and nonversive seizuresReported: BilateralAlso reported: ContralateralAlso reported: Ipsilateral1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Versive patients usually had only a focus contralateral to movement (22/27), with 5 bilateral and none only ipsilateral; nonversive patients were mostly bilateral (7/10), with 2 only contralateral and 1 only ipsilateral.

Source-defined result groups 6
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 18.5%Versive; Bilateral foci · Nonversive · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 0.0%Versive; Only ipsilateral focus · Nonversive · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 10.0%Nonversive; Only ipsilateral focus · Versive · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 81.5%Versive; Only contralateral focus · Nonversive · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 70.0%Nonversive; Bilateral foci · Versive · patient1 manuscript · 1 reported value · not pooled
Lateralization: Bilateral / Contralateral / IpsilateralObserved proportion 20.0%Nonversive; Only contralateral focus · Versive · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

wyllie1986.pdfStructured design not resolved · 1 finding · 6 reported values
wyllie1986.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.716
Thirty-nine patients aged 1-48 years (mean 22) were selected for lateral head and eye movement during seizures; 2 were excluded because electromyographic artifact obscured electroencephalographic seizure onset. The analyzed sample was 37 patients with 74 spontaneous seizures: 20 patients were studied for complex partial seizures with or without secondary generalization and 17 for partial motor seizures with or without altered consciousness or secondary generalization. All seizures occurred spontaneously in the EEG laboratory, were recorded from onset, and had high-quality synchronized audio-video and EEG recordings; scalp, nasopharyngeal or sphenoidal electrodes were used, and 8 patients also had chronic subdural electrode arrays. Video and EEG were analyzed independently, and movement classification was performed without knowledge of EEG or clinical data. Ictal EEG seizure-onset location was used for all seizures except 3 with generalized ictal EEG onset, which were assigned to the location of the interictal focus because of other lateralizing EEG data. Table 1 onset totals were frontal 39 (12 patients), temporal 31 (22), parietal 2 (2), and occipital 2 (1); table values are seizures with patient counts in parentheses.
Findings
  • interictal EEG foci in versive and nonversive seizuresInterictal EEG findings supported the movement-direction distinction: among patients with versive seizures, 22 had only a focus contralateral to the direction of head and eye movement, 5 had bilateral foci, and none had only an ipsilateral focus; among patients with nonversive seizures, 7 had bilateral foci, 2 only contralateral, and 1 only ipsilateral.PDF p.2, paragraph beginning “The interictal EEG data supported these findings”
Reported values
  • Nonversive Only ipsilateral focus 1/10interictal EEG foci in versive and nonversive seizuresPercentage · n/N 1/10 · 27 patients with versive seizures and 10 patients with nonversive seizures · Nonversive; Only ipsilateral focus · interictal EEG assessed in relation to ictal head and eye movement direction and the seizure-onset hemispherePDF p.2, paragraph beginning “The interictal EEG data supported these findings”
  • Nonversive Only contralateral focus 2/10interictal EEG foci in versive and nonversive seizuresPercentage · n/N 2/10 · 27 patients with versive seizures and 10 patients with nonversive seizures · Nonversive; Only contralateral focus · interictal EEG assessed in relation to ictal head and eye movement direction and the seizure-onset hemispherePDF p.2, paragraph beginning “The interictal EEG data supported these findings”
  • Versive Bilateral foci 5/27interictal EEG foci in versive and nonversive seizuresPercentage · n/N 5/27 · 27 patients with versive seizures and 10 patients with nonversive seizures · Versive; Bilateral foci · interictal EEG assessed in relation to ictal head and eye movement direction and the seizure-onset hemispherePDF p.2, paragraph beginning “The interictal EEG data supported these findings”
  • Nonversive Bilateral foci 7/10interictal EEG foci in versive and nonversive seizuresPercentage · n/N 7/10 · 27 patients with versive seizures and 10 patients with nonversive seizures · Nonversive; Bilateral foci · interictal EEG assessed in relation to ictal head and eye movement direction and the seizure-onset hemispherePDF p.2, paragraph beginning “The interictal EEG data supported these findings”
  • Versive Only ipsilateral focus 0/27 (0%)interictal EEG foci in versive and nonversive seizuresPercentage · n/N 0/27 · 27 patients with versive seizures and 10 patients with nonversive seizures · Versive; Only ipsilateral focus · interictal EEG assessed in relation to ictal head and eye movement direction and the seizure-onset hemispherePDF p.2, paragraph beginning “The interictal EEG data supported these findings”
  • Versive Only contralateral focus 22/27 (81%)interictal EEG foci in versive and nonversive seizuresPercentage · n/N 22/27 · 27 patients with versive seizures and 10 patients with nonversive seizures · Versive; Only contralateral focus · interictal EEG assessed in relation to ictal head and eye movement direction and the seizure-onset hemispherePDF p.2, paragraph beginning “The interictal EEG data supported these findings”

1 contributing manuscript; source-reported values remain separate and are not pooled.

Medial versus lateral distinction for localizationReported: Right hemisphere1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

No source lateralization is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdfStructured design not resolved · 1 finding
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
This single-center presurgical series included 54 patients whose SEEG-defined epileptogenic zone (EZ) predominantly involved the frontal lobe, selected from 180 SEEG explorations performed from February 2000 through November 2010; one inconclusive exploration and nonpredominantly frontal cases were excluded. The cohort included 22 male and 32 female patients, mean age 24.9 ± 9.5 years, mean epilepsy duration 16.9 ± 8 years, and 27/54 with normal MRI. Three epileptologists independently reviewed all seizures and scored presence/absence of 31 ictal signs; each patient's sign was assigned 0, 1, or 2 according to reproducibility. The “early spread network” was the cortical tissue involved from electrical onset through completion of clinical semiology and was explicitly distinguished from the EZ. SEEG sampling is described as 20 frontal cortical regions, while the later matrices are described as containing 24 brain-area variables. Analyses used correlation matrices, Kendall tests with p < 0.05, PCA on rank-transformed sign scores, hierarchical clustering, and value-test ≥ 2 to identify characteristic variables.
Findings
  • Medial versus lateral distinction for localizationThe authors conclude that a semiologic trait during the early-spread interval could not be attributed only to a lateral or medial discharge origin because propagation also mattered. They observed lateral prefrontal discharge tending to propagate to anterior cingulate and pre-SMA, and SMA/pre-SMA discharge tending to propagate to lateral areas 6 and 8; medial premotor and cingulate regions were proposed as a possible “final common pathway” for anterior frontal seizure organization.PDF p.12, Is medial versus lateral distinction a reliable indicator for localization?

1 contributing manuscript; source-reported values remain separate and are not pooled.

Mesiotemporal sclerosis (MTS) on MRIReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

MRI MTS showed a nonsignificant right-versus-left temporal cohort difference.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.5
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Mesiotemporal sclerosis (MTS) on MRIAn MRI diagnosis of MTS was more common in the RTL group than in the LTL group, but the difference was not significant.PDF p.3, Results, Imaging and surgical outcome; PDF p.3, Tables 3-4
Reported values
  • 5 of 10Mesiotemporal sclerosis (MTS) on MRIPercentage · n/N 5/10 · 10 RTL/RTLE patients and 9 LTL/LTLE patients · RTL/RTLEPDF p.3, Results, Imaging and surgical outcome; PDF p.3, Tables 3-4
  • 2 of 9Mesiotemporal sclerosis (MTS) on MRIPercentage · n/N 2/9 · 10 RTL/RTLE patients and 9 LTL/LTLE patients · LTL/LTLEPDF p.3, Results, Imaging and surgical outcome; PDF p.3, Tables 3-4

1 contributing manuscript; source-reported values remain separate and are not pooled.

No ictal speech manifestationReported: Non-dominant hemisphere1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The only patient with no speech manifestations in all four seizures belonged to the nondominant-origin group.

Source-defined result groups 1
Lateralization: Non-dominant hemisphereObserved proportion 2.9%nondominant-origin group; all 4 seizures lacked speech manifestations · other cohort patients · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 3 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • no speech manifestationsNo speech manifestations occurred in 21 of 100 seizures in 12 patients; only 1 patient had no speech manifestations in all 4 of that patient’s seizures, and this patient belonged to the nondominant group.PDF p.2, speech-manifestation definition and Results; PDF p.2, Table 1
Reported values
  • in 12 patientsno speech manifestationsCount · n/N 21/100 · 100 seizures from 35 patients with intractable temporal-lobe epilepsy · patients contributing seizures without speech manifestations · absence of spontaneous ictal speech with normal postictal speech function when tested, according to the source definitionPDF p.2, speech-manifestation definition and Results; PDF p.2, Table 1
  • 21 of 100 seizures (21%)no speech manifestationsPercentage · n/N 21/100 · 100 seizures from 35 patients with intractable temporal-lobe epilepsy · seizures without speech manifestations · absence of spontaneous ictal speech with normal postictal speech function when tested, according to the source definitionPDF p.2, speech-manifestation definition and Results; PDF p.2, Table 1
  • only 1 patient ... in all 4 ... seizuresno speech manifestationsCount · n/N 1/35 · 100 seizures from 35 patients with intractable temporal-lobe epilepsy · nondominant-origin group; all 4 seizures lacked speech manifestations · absence of spontaneous ictal speech with normal postictal speech function when tested, according to the source definitionPDF p.2, speech-manifestation definition and Results; PDF p.2, Table 1

1 contributing manuscript; source-reported values remain separate and are not pooled.

number of speech phenomena per seizureReported: Non-dominant hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Among 79 speech-manifestation seizures, one speech phenomenon occurred in 55 (70%) and more than one in 24 (30%); multiple-phenomenon status did not correlate with seizure-onset lateralization.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 2 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.949
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • number of speech phenomena per seizureOf the 79 seizures with speech manifestations, 55 (70%) had one speech phenomenon and 24 (30%) had more than one; the presence or absence of multiple phenomena did not correlate with seizure-onset lateralization.PDF p.2, Results
Reported values
  • 55/79 seizures (70%) with one speech phenomenonnumber of speech phenomena per seizurePercentage · n/N 55/79 · 79 seizures with speech manifestations from the 35-patient temporal-lobe epilepsy cohort · one phenomenon · mixed ictal/postictal phenomena; one phase was not assigned to this multiplicity analysisPDF p.2, Results
  • 24/79 (30%) with more than onenumber of speech phenomena per seizurePercentage · n/N 24/79 · 79 seizures with speech manifestations from the 35-patient temporal-lobe epilepsy cohort · more than one phenomenon · mixed ictal/postictal phenomena; one phase was not assigned to this multiplicity analysisPDF p.2, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postoperative seizures in one patient with habitual RTL onsetReported: Left hemisphereAlso reported: Right hemisphere1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The patient had right temporal habitual seizures and right MTS preoperatively, then left frontal spikes with different postoperative events.

Source-defined result groups 1
Localization: Frontal / TemporalObserved proportion 5.3%All reported · Habitual preoperative RTL seizures versus postoperative events · patient and seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 2 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.639
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Postoperative seizures in one patient with habitual RTL onsetOnly one patient had more than rare postoperative seizures; all of that patient's recorded seizures before surgery had RTL onset and classic right MTS, whereas postoperative events included generalized tonic-clonic seizures and staring spells without motor manifestations, with left frontal spikes recorded postoperatively.PDF p.3, Results, Imaging and surgical outcome
Reported values
  • no additional rate reported.Postoperative seizures in one patient with habitual RTL onsetCount · n/N 1/19 · One patient within the 19-patient surgical-evaluation cohort · Preoperative habitual seizures and postoperative eventsPDF p.3, Results, Imaging and surgical outcome
  • One patient with more than rare postoperative seizuresPostoperative seizures in one patient with habitual RTL onsetCount · n/N 1/19 · One patient within the 19-patient surgical-evaluation cohort · Preoperative habitual seizures and postoperative eventsPDF p.3, Results, Imaging and surgical outcome

1 contributing manuscript; source-reported values remain separate and are not pooled.

Proximal limb movementReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Ventral posterior-insula stimulation evoked trunk rotation toward contralateral space with gaze shift in the same direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

simone-anatomo-functional-organization-insular-networks-2025.pdfStructured design not resolved · 1 finding
simone-anatomo-functional-organization-insular-networks-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The paper summarizes prior macaque ICMS mapping performed with 200-microsecond biphasic pulses at 50 Hz, 4 mA, for 3 seconds; a behavior entered the dataset when two observers recognized it and it was evoked in more than 50% of trials. The present analyses used ICMS maps and insular tracer injections in two male rhesus macaques (Mk1 and Mk2), indirect tracer data from 22 additional animals, and resting-state fMRI from 12 male macaques aged 4-8 years. The authors warped the ICMS maps and injection sites onto the INIA19 macaque template and delineated six insular fields. No seizure cohort, ictal or postictal observations, or clinical localization reference standard was studied.
Findings
  • proximal movements; axial movements; tremorsIn macaques, ICMS of the caudalmost insular region produced simple limb-muscle reactions, axial movements, and bodily tremors: proximal movements clustered in the dorsal posterior sector, axial movements occupied the ventral posterior sector, and tremors occurred across both sectors. The source also describes posterior-insula responses including tremors coupled with limb or axial movements, postural adjustments, and ventral-sector trunk rotation toward contralateral space with a gaze shift in the same direction.PDF p.5, Fig. 1D, E and caption; PDF p.12, §4.5.1; PDF p.15, Fig. 9A and caption; PDF p.16, §§4.5.2-4.5.3; PDF p.19, §5.4

1 contributing manuscript; source-reported values remain separate and are not pooled.

Sniffing automatismsReported: Left hemisphere1 manuscript · 1 finding · 20 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Deglutition, sexual automatism, sniffing, fumbling, and spitting showed no statistically significant right-versus-left temporal-lobe-epilepsy difference.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdfStructured design not resolved · 1 finding · 20 reported values
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The study included 19 patients with unilateral TLE who underwent anterior temporal lobectomy with amygdalohippocampectomy. Long-term video/EEG monitoring used scalp and sphenoidal electrodes; hippocampal depth electrodes were used in five patients. The epileptogenic zone was determined from ictal EEG, MRI findings including mesial temporal sclerosis, ictal SPECT, regional temporal PET, and surgical outcome; Wada-test results were used for dominant versus nondominant hemisphere classification. Two to ten seizures per patient were reviewed (mean 6.1); the cohort included 10 females and 9 males, mean age 28.7 years (range 12-43). Sixty-five seizures were classified as nondominant-hemisphere onset and 51 as dominant-hemisphere onset; 85 seizures arose from the right temporal lobe and 31 from the left. Chi-square testing was used for statistical analysis.
Findings
  • other categories of automatismsThe source reports no statistically significant right-versus-left TLE difference for the listed other automatisms.PDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
Reported values
  • LTE 1 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 0 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 2 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 0 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 0 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 3 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 3 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 0 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • LTE 6 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · LTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 4 seizuresother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 0 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion
  • RTE 1 patientsother categories of automatismsCount · 19 patients with unilateral TLE; right-versus-left TLE seizure comparison · RTE · ictalPDF p.1, Abstract; PDF p.4, Results and Table 2; PDF p.7, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

spoken repetition versus sung repetition efficacyReported: Bilateral1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight pending · 1 structured design not resolved

The visual comparison showed strong overlap between spoken and sung repetition in the left ventral stream and bilateral projection pathways, while the left dorsal stream had a stronger link to spoken than sung repetition.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdfStructured design not resolved · 1 finding · 1 reported value
pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
Forty-five adults with chronic aphasia more than 6 months after a clinically confirmed left-hemisphere stroke were recruited in Helsinki and Turku in 2017-2019; all were Finnish native speakers, over 18 years, and had no hearing deficit, severe cognitive impairment, substance abuse, or neurological/psychiatric comorbidity. Connected spoken-language production was mean correct information units per minute across three discourse tasks; connected singing was correct words per minute while singing the familiar song Jaakko-kulta; two connected-singing recordings were lost, leaving n=43 for that analysis. Repetition used 16 identical 1-5-word phrases in spoken and melodically intoned formats, with the first attempt scored and correct words per minute calculated. Six participant-level local-connectome regression models used age and lesion volume as covariates; tract tracking used a T-score threshold of 3, 2,000 permutations, and FDR <0.0083 after Bonferroni correction.
Findings
  • spoken repetition versus sung repetition efficacyThe visual comparison showed strong overlap between spoken and sung repetition in the left ventral stream and bilateral projection pathways, while the left dorsal stream had a stronger link to spoken than sung repetition.PDF p.6, Fig. 3c caption and visual comparison; PDF p.7, Results, visual comparison of spoken and sung repetition
Reported values
  • FDR <0.0083spoken repetition versus sung repetition efficacyP value · Participants with chronic post-stroke aphasia; comparison of spoken and sung repetition connectomes, n=45 for each analysisPDF p.6, Fig. 3c caption and visual comparison; PDF p.7, Results, visual comparison of spoken and sung repetition

1 contributing manuscript; source-reported values remain separate and are not pooled.

TremorReported: Contralateral1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Ventral posterior-insula stimulation evoked trunk rotation toward contralateral space with gaze shift in the same direction.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

simone-anatomo-functional-organization-insular-networks-2025.pdfStructured design not resolved · 1 finding
simone-anatomo-functional-organization-insular-networks-2025.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1
The paper summarizes prior macaque ICMS mapping performed with 200-microsecond biphasic pulses at 50 Hz, 4 mA, for 3 seconds; a behavior entered the dataset when two observers recognized it and it was evoked in more than 50% of trials. The present analyses used ICMS maps and insular tracer injections in two male rhesus macaques (Mk1 and Mk2), indirect tracer data from 22 additional animals, and resting-state fMRI from 12 male macaques aged 4-8 years. The authors warped the ICMS maps and injection sites onto the INIA19 macaque template and delineated six insular fields. No seizure cohort, ictal or postictal observations, or clinical localization reference standard was studied.
Findings
  • proximal movements; axial movements; tremorsIn macaques, ICMS of the caudalmost insular region produced simple limb-muscle reactions, axial movements, and bodily tremors: proximal movements clustered in the dorsal posterior sector, axial movements occupied the ventral posterior sector, and tremors occurred across both sectors. The source also describes posterior-insula responses including tremors coupled with limb or axial movements, postural adjustments, and ventral-sector trunk rotation toward contralateral space with a gaze shift in the same direction.PDF p.5, Fig. 1D, E and caption; PDF p.12, §4.5.1; PDF p.15, Fig. 9A and caption; PDF p.16, §§4.5.2-4.5.3; PDF p.19, §5.4

1 contributing manuscript; source-reported values remain separate and are not pooled.

Unintelligible ictal speechReported: Non-dominant hemisphere1 manuscript · 1 finding · 6 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Nonidentifiable speech occurred with both dominant- and nondominant-origin temporal seizures and had no lateralizing significance.

Source-defined result groups 2
Lateralization: Does not lateralizeSource-defined values retained separatelynondominant-origin · dominant-origin versus nondominant-origin nonidentifiable-speech observations · patient and seizure1 manuscript · 1 reported value · not pooled
Lateralization: Does not lateralizeSource-defined values retained separatelydominant-origin · dominant-origin versus nondominant-origin nonidentifiable-speech observations · patient and seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdfStructured design not resolved · 1 finding · 6 reported values
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 2
Thirty-five patients aged 12-39 years (mean 24.6) were selected from an epilepsy-surgery population; all had intractable temporal-lobe epilepsy and subsequently underwent temporal lobectomy. The investigators reviewed up to four good-quality videotaped seizures per patient until 100 seizures were reached; 94 were spontaneous, 3 hyperventilation-induced, and 3 Metrazol-activated. The cohort comprised 80 complex partial seizures and 20 complex partial seizures with secondary generalization; 48 seizures arose from the dominant temporal lobe in 16 patients and 52 from the nondominant temporal lobe in 19 patients. Simultaneous scalp and chronically implanted subdural EEG-video monitoring was used, speech dominance was determined by intracarotid amobarbital testing, and patients with bihemispheric speech representation were excluded. One author reviewed the videotapes without knowledge of EEG localization or eventual surgical management.
Findings
  • nonidentifiable speechNonidentifiable speech occurred in 10 seizures in 6 patients, was ictal in 8 seizures and postictal in 2, and neither the phenomenon overall nor its repetitive/nonrepetitive subdivisions had lateralizing significance.PDF p.3, Table 3 and Results; PDF p.4, Results
Reported values
  • 4 nondominant-origin seizuresnonidentifiable speechCount · 6 patients and 10 nonidentifiable-speech seizures in the 35-patient temporal-lobe epilepsy cohort · nondominant-origin · 8 ictal seizures and 2 postictal seizuresPDF p.3, Table 3 and Results; PDF p.4, Results
  • 2 postictal seizuresnonidentifiable speechCount · 6 patients and 10 nonidentifiable-speech seizures in the 35-patient temporal-lobe epilepsy cohort · postictal · 8 ictal seizures and 2 postictal seizuresPDF p.3, Table 3 and Results; PDF p.4, Results
  • 6 patients with nonidentifiable speechnonidentifiable speechCount · 6 patients and 10 nonidentifiable-speech seizures in the 35-patient temporal-lobe epilepsy cohort · 8 ictal seizures and 2 postictal seizuresPDF p.3, Table 3 and Results; PDF p.4, Results
  • 6 dominant-origin seizuresnonidentifiable speechCount · 6 patients and 10 nonidentifiable-speech seizures in the 35-patient temporal-lobe epilepsy cohort · dominant-origin · 8 ictal seizures and 2 postictal seizuresPDF p.3, Table 3 and Results; PDF p.4, Results
  • 10 seizures with nonidentifiable speechnonidentifiable speechCount · 6 patients and 10 nonidentifiable-speech seizures in the 35-patient temporal-lobe epilepsy cohort · 8 ictal seizures and 2 postictal seizuresPDF p.3, Table 3 and Results; PDF p.4, Results
  • 8 ictal seizuresnonidentifiable speechCount · 6 patients and 10 nonidentifiable-speech seizures in the 35-patient temporal-lobe epilepsy cohort · ictal · 8 ictal seizures and 2 postictal seizuresPDF p.3, Table 3 and Results; PDF p.4, Results

1 contributing manuscript; source-reported values remain separate and are not pooled.

Well-formed ictal speechReported: Right hemisphere1 manuscript · 1 finding · 4 reported values
Weighted evidence supportevidence weight pending · 1 structured design not resolved

Well-formed ictal speech occurred in 17 of 54 right-temporal seizures and in 0 of 73 left-temporal seizures.

Source-defined result groups 2
Lateralization: Right hemisphereObserved proportion 31.5%RTL; Table 5 · seizure1 manuscript · 1 reported value · not pooled
Lateralization: Right hemisphereObserved proportion 0.0%LTL; Table 5 · RTL Table 5 · seizure1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

fakhoury-right-left-temporal-lobe-clinical-features-1994.pdfStructured design not resolved · 1 finding · 4 reported values
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
Structured design not resolved · Class pending · Evidence weight pending · 0 × 0.9 × 1.932
Patients were admitted to an epilepsy unit over 30 months and underwent 5-14 days of scalp and sphenoidal EEG-CCTV monitoring with antiepileptic-drug discontinuation; all had head MRI, 16 had PET, 18 had neuropsychological testing, 16 had Wada testing, and 6 had repeat monitoring with implanted subdural grids. The 19 patients were divided by unilateral temporal onset using interictal discharges, ictal EEG onset, MRI lesions including mesiotemporal sclerosis, PET hypometabolism, neuropsychological testing, Wada testing, preoperative evaluation, and surgical outcome; 10 patients had RTL onset and 9 had LTL onset, yielding 54 and 73 recorded seizures, respectively. Only complex partial seizures (CPS) and secondarily generalized or partial-evolving-to-generalized (PE) seizures were analyzed. Clinical features were compared with chi-square or Fisher's exact tests.
Findings
  • Well-formed ictal speechWell-formed ictal speech occurred only in RTL-origin seizures; Table 5 reports 17 RTL seizures (33%) versus 0 LTL seizures, while the discussion restates the result as 33% of RTLE patients versus no LTLE patients.PDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
Reported values
  • 33% of patients with RTLEWell-formed ictal speechPercentage · RTL seizure group, n=54, versus LTL seizure group, n=73; discussion also uses the 10- versus 9-patient group wording · RTLE; discussion restatement · IctalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • no patients with LTLEWell-formed ictal speechOther reported value · RTL seizure group, n=54, versus LTL seizure group, n=73; discussion also uses the 10- versus 9-patient group wording · LTLE; discussion restatement · IctalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • 0/73 seizuresWell-formed ictal speechPercentage · n/N 0/73 · RTL seizure group, n=54, versus LTL seizure group, n=73; discussion also uses the 10- versus 9-patient group wording · LTL; Table 5 · IctalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion
  • 17/54 seizures (33%)Well-formed ictal speechPercentage · n/N 17/54 · RTL seizure group, n=54, versus LTL seizure group, n=73; discussion also uses the 10- versus 9-patient group wording · RTL; Table 5 · IctalPDF p.1, Summary; PDF p.4, numbered clinical-feature results; PDF p.4, Table 5; PDF p.5, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Autonomic auraDoes not lateralizeNo directional estimate16 manuscripts · 122 findings · 89 reported values
Weighted evidence supportevidence weight 38.66 across 16 manuscripts · 7 systematic review or meta-analysis · 2 independent primary study · 7 narrative, educational, or cited context

The cited table restates autonomic aura as non-lateralising. The review restates autonomic auras as nonlateralizing while discussing insular, anterior-cingulate, SSMA, amygdala, and hypothalamic relay anatomy. The primary table result gives no hemisphere or lateralizing direction for autonomic aura (palpitation). No hemisphere or body-side direction is reported. No lateralizing direction is reported. The row reports the number of autonomic-aura studies, not lateralization evidence. The row reports a sample size, not lateralization evidence. No lateralization axis information is reported for the autonomic-aura odds confidence interval. No lateralization axis information is reported for the autonomic-aura heterogeneity test. No lateralization axis information is reported for the autonomic-aura study comparison. No lateralization axis information is reported for the 40 lateral-TLE patients assessed for autonomic aura. No lateralization axis information is reported for the 71 mesial-TLE patients assessed for autonomic aura. The review classification of ictal feature categories reports no lateralizing direction. No hemisphere or body-side direction is reported for the clustered manifestations. No lateralization information is reported. No lateralization axis information is reported for autonomic features. The primary result reports autonomic features in a source-defined fronto-temporal subgroup and does not assign a hemisphere or lateralizing direction. The primary result reports autonomic features in a source-defined temporo-frontal subgroup and does not assign a hemisphere or lateralizing direction. The autonomic-hyperkinetic association coefficient provides no lateralizing information. Autonomic signs preceding hyperkinetic behavior provide no lateralizing information. No lateralization axis information is reported for autonomic aura with temporal-lobe onset. No lateralization axis information is reported for autonomic aura with mesial-temporal onset. No lateralization axis information is reported for autonomic aura with frontal-lobe sources. No lateralization axis information is reported for the review's autonomic-phenomena frequency. The review table reports autonomic phenomena in 22 basal-temporal cases (27%) with no hemisphere or lateralizing direction. The review reports autonomic phenomena in 18/60 high- or very-high-confidence basal-temporal EZ cases (30%) with no hemisphere or lateralizing direction. The review distinguishes subjective autonomic auras from objectively documented autonomic seizures and reports no hemisphere or lateralizing direction. The cited emotional-expression statement reports no hemisphere or lateralization direction. The source distinguishes autonomic aura from autonomic seizure by evidentiary criteria but reports no hemisphere or anatomical localization. No lateralization axis information is reported for the motor-gestural versus affective/autonomic comparison. No lateralization axis information is reported for loss of consciousness versus affective/autonomic aura. No lateralization axis information is reported for post-ictal confusion/behavior change disinhibition versus affective/autonomic aura. No lateralization axis information is reported for chapeau de gendarme versus affective/autonomic aura. No lateralization axis information is reported for dystonic posturing versus affective/autonomic aura. No lateralization axis information is reported for head-eye deviation versus affective/autonomic aura. No lateralization axis information is reported for laughter versus affective/autonomic aura. No lateralization axis information is reported for oro-alimentary automatisms versus affective/autonomic aura. No lateralization axis information is reported for tonic-clonic activity versus affective/autonomic aura. No lateralization axis information is reported for focal-to-bilateral tonic-clonic activity versus affective/autonomic aura. No lateralization axis information is reported for vocalization/verbalization versus autonomic signs. No lateralization axis information is reported for affective/autonomic aura versus autonomic signs. No lateralization axis information is reported for facial expression change versus autonomic signs. The source reports OR 0.8 for motor gestural automatisms relative to autonomic signs; no hemisphere direction is reported. No lateralization evidence is reported. This finding provides no lateralization information. No lateralization axis information is reported for head-eye deviation versus autonomic signs. The claim states OR 0.2 for laughter relative to autonomic signs, while the supplied statistic record states OR 0.1; no hemisphere direction is reported. No lateralizing semiology is reported for the tonic-clonic versus autonomic-sign odds comparison. No lateralization axis information is reported for focal-to-bilateral tonic-clonic activity versus autonomic signs. No lateralization axis information is reported for affective/autonomic aura versus facial expression change. No lateralization axis information is reported for autonomic signs versus facial expression change. No lateralization axis information is reported for affective/autonomic aura versus motor-gestural automatisms. No seizure lateralization is reported. Figure 6 reports OR 2.3 for Affective/autonomic aura relative to Loss of consciousness, with no hemisphere or lateralization direction. Figure 6 reports OR 2.9 for Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibition, with no hemisphere or lateralization direction. Figure 6 reports OR 4.9 for Affective/autonomic aura relative to Chapeau de gendarme, with no hemisphere or lateralization direction. Figure 6 reports OR 5.2 for Affective/autonomic aura relative to Dystonic posturing, with no hemisphere or lateralization direction. Figure 6 reports OR 7.7 for Affective/autonomic aura relative to Head-eye deviation, with no hemisphere or lateralization direction. Figure 6 reports OR 5.7 for Autonomic signs relative to Head-eye deviation, with no hemisphere or lateralization direction. Figure 6 reports OR 11.7 for Affective/autonomic aura relative to Laughter, with no hemisphere or lateralization direction. Figure 6 reports OR 13.3 for Affective/autonomic aura relative to Oro-alimentary automatisms, with no hemisphere or lateralization direction. Figure 6 reports OR 21.9 for Affective/autonomic aura relative to Tonic-clonic, with no hemisphere or lateralization direction. No lateralizing semiology is reported for the reciprocal autonomic-signs versus tonic-clonic odds comparison. Figure 6 reports OR 21.9 for Affective/autonomic aura relative to F to BTC, with no hemisphere or lateralization direction. Figure 6 reports OR 16.2 for Autonomic signs relative to F to BTC, with no hemisphere or lateralization direction.

Source-defined result groups 12
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Autonomic aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Autonomic aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: Frontal / TemporalSource-defined values retained separatelyAll reported · other symptom-cluster pairs in the same analysis · pairwise symptom-cluster association1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyMotor (gestural) automatisms · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: autonomic aura / hypothalamic sourceSource-defined values retained separatelyhypothalamic localization given autonomic aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyAutonomic signs · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 9.5%All reported · prefrontal operculum versus precentral Rolandic operculum · all included patients1 manuscript · 1 reported value · not pooled
Localization: ACC/cingulate localization / reviewed anterior cingulate cortex seizure casesSource-defined values retained separatelyLaughter · pairwise symptom-occurrence comparison1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelymesial temporal localization given autonomic aura · localizing data point1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: autonomic features / hypothalamusSource-defined values retained separatelyhypothalamic localization relative to all other semiologies · localizing data point1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 16

Alphabetical by manuscript.

alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdfSystematic review or meta-analysis · 15 findings · 7 reported values
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a primary systematic-review/database analysis, not a new prospective cohort. The authors report 11,230 localizing and 2,391 lateralizing data points from 4,643 patients across 309 articles. The analysis uses source-described semiologies, 103 hierarchical regions, mixed ground truths, patient-level normalization, 10,000 bootstrap samples for 95% CIs, and ORs from two-by-two contingency tables. Figure 3 and Figure 4 show plotted values, but exact point estimates for every plotted region/semiology cell are not tabulated in the source; only exact values stated in the prose or printed labels are entered as atomic findings below.
Findings
  • autonomicTable 1 defines or exemplifies the the source's own semiology category “autonomic” as Autonomic symptoms or signs relating to respiratory, cardiovascular, genitourinary, or gastrointestinal systems.PDF p.7, Table 1 Semiology descriptions and frequencies
  • autonomicAutonomic semiology comprised 4.7% of non-topological data.PDF p.7, Table 1 Semiology descriptions and frequencies
  • autonomic; Figure 3 all-data subsetFigure 3 reports N = 731 for the all-data autonomic panel.PDF p.9, Figure 3 and caption
  • autonomic; Figure 3 non-topological subsetFigure 3 reports N = 164 for the non-topological autonomic panel.PDF p.9, Figure 3 and caption
  • autonomic aura; temporal lobeAutonomic aura indicated temporal-lobe onset in 58%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; temporal lobeThe 95% CI for autonomic aura; temporal lobe was 47%, 67%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; mesial temporal structuresAutonomic aura indicated mesial temporal onset in 36%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; mesial temporal structuresThe 95% CI for autonomic aura; mesial temporal structures was 27%, 44%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; frontal lobeAutonomic aura was associated with a frontal source in 13%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; frontal lobeThe 95% CI for autonomic aura; frontal lobe was 7%, 18%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; hypothalamusAutonomic aura was associated with a hypothalamic source in 15%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; hypothalamusThe 95% CI for autonomic aura; hypothalamus was 10%, 21%.PDF p.8, Seizure semiology localizing values
  • autonomic aura; insulaautonomic aura indicated insular localization in 18%.PDF p.8, Seizure semiology localizing values
  • autonomic features; hypothalamusAutonomic features had an intrinsic localizing OR of 2.8 for the hypothalamus.PDF p.8, Relative localizing values of semiologies
  • autonomic features; hypothalamusThe 95% CI for autonomic features; hypothalamus was 1.8–4.4.PDF p.8, Relative localizing values of semiologies
Reported values
  • autonomic 4.7%autonomicPercentage · non-topological Semio2Brain dataPDF p.7, Table 1 Semiology descriptions and frequencies
  • autonomic aura; temporal lobe 58%autonomic aura; temporal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • autonomic aura; mesial temporal structures 36%autonomic aura; mesial temporal structuresPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • autonomic aura; frontal lobe 13%autonomic aura; frontal lobePercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • autonomic aura; hypothalamus 15%autonomic aura; hypothalamusPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • autonomic aura; insula 18%autonomic aura; insulaPercentage · non-topological localizing data points unless otherwise statedPDF p.8, Seizure semiology localizing values
  • OR 2.8autonomic features; hypothalamusOdds ratio · non-topological Semio2Brain data unless otherwise statedPDF p.8, Relative localizing values of semiologies
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdfSystematic review or meta-analysis · 3 findings · 3 reported values
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The authors state that the review followed PRISMA. Eligible peer-reviewed English, French, German, Spanish, or Italian papers had relevant video-EEG, semiology, stimulation, surgical, electrical-source-imaging, or anatomical data focused on basal temporal epilepsy; papers limited to stimulation were excluded. Two reviewers screened and extracted data, with a third resolving disagreements. Descriptive statistics summarized demographics, imaging, semiology, and outcomes. QUADAS-2-guided assessment addressed enrollment and symptom assessment. Epileptogenic-zone (EZ) confidence was graded very high, high, moderate, or low using MRI, intracerebral EEG, and postoperative outcome; selective/tailored surgery was considered for high evidence grading.
Findings
  • autonomic phenomenaAutonomic phenomena were observed in 27% of reviewed cases.PDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • Autonomic phenomena (Table 3)Table 3 reports autonomic phenomena in 22 cases (27%), more at seizure onset.PDF p.6, Table 3
  • Autonomic phenomena (Table 4)In the 60 cases with high or very-high EZ confidence, Table 4 reports autonomic phenomena in 18 cases (30%).PDF p.7, Table 4
Reported values
  • 27% autonomic phenomenaautonomic phenomenaPercentage · reviewed basal temporal seizure cases · ictal; timing not otherwise specified in narrativePDF p.4, Semiology and clinical features; PDF p.6, Table 3
  • 22 cases (27%)Autonomic phenomena (Table 3)Percentage · Table 3 basal temporal seizure cases · onsetPDF p.6, Table 3
  • 18/60 (30%)Autonomic phenomena (Table 4)Percentage · n/N 18/60 · 60 basal temporal seizure cases with high or very-high EZ confidence · ictal; timing not separately stated in Table 4PDF p.7, Table 4
blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Autonomic and emotional auras across childhood maturationAuras with autonomic and emotional features are described as unaffected by the maturational process in childhood TLE.PDF p.5, section 6
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdfSystematic review or meta-analysis · 68 findings · 61 reported values
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review includes 23 studies and 93 patients, with ACC involvement defined through anatomical, invasive-electrophysiological, imaging, and clinical correlations. Study selection, demographic, imaging, surgery, pathology, confidence, and risk-of-bias details are retained as compact population/context here; they are not individual findings unless directly tied to an ictal sign, phase, or localization association. The review extracted aura type, vocalization/verbalization, laughter, autonomic and facial signs, automatisms, hypermotor behavior, dystonic/tonic-clonic signs, deviations, loss of consciousness, postictal confusion, timing, duration, sleep, and interictal behavior, then performed one-sided typicality tests and pairwise odds-ratio comparisons.
Findings
  • emotional and autonomic manifestations; vocalization; facial expression; hypermotor behaviorThe review identifies emotional/autonomic manifestations, vocalization, facial expression changes, complex automatisms, and hypermotor behavior with preserved awareness as the main ACC clinical features.PDF p.11, Anatomical and clinical correlations; PDF p.15, Conclusion
  • affective manifestations; autonomic manifestations; ACC onsetAffective and autonomic manifestations, along with vocalization and facial-expression changes, were postulated to be associated with early ACC involvement.PDF p.10, Anatomical and clinical correlations; PDF p.11
  • autonomic auraThe source reports a frequency of 25% for autonomic aura.PDF p.13, Table 3
  • autonomic aura; reported frequency rangeThe source reports a frequency range of 0–82% for autonomic aura.PDF p.13, Table 3
  • autonomic signsThe source reports a frequency of 48% for autonomic signs.PDF p.13, Table 3
  • autonomic signs; reported frequency rangeThe source reports a frequency range of 0–91% for autonomic signs.PDF p.13, Table 3
  • autonomic signs; ACC association gradeTable 3 assigns the source's High overall association grade to autonomic signs.PDF p.13, Table 3
  • autonomic signs; Figure 4 rateFigure 4 displays a 48.4% rate for autonomic signs.PDF p.10, Figure 4
  • autonomic aura; Figure 4 rateFigure 4 displays a 24.7% rate for autonomic aura.PDF p.10, Figure 4
  • affective and autonomic subjective manifestationsAffective and autonomic subjective manifestations represented 80% of reported auras.PDF p.7, Subjective manifestations
  • affective/autonomic aura typicalityAffective/autonomic aura met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • autonomic signs typicalityAutonomic signs met the source's typicality criterion of significantly exceeding one-third of patients.PDF p.10, Statistical analysis of ictal semiology; PDF p.11, Figure 5
  • affective/autonomic aura; pairwise odds-ratio significanceaffective/autonomic aura showed eight significant pairwise odds-ratio comparisons after Holm correction.PDF p.10, Statistical analysis of ictal semiology
  • autonomic signs; pairwise odds-ratio significanceautonomic signs showed eight significant pairwise odds-ratio comparisons after Holm correction.PDF p.10, Statistical analysis of ictal semiology
  • pairwise OR: Affective/autonomic aura relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.8 for Affective/autonomic aura relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Vocalization/verbalizationFigure 6 reports an odds ratio of 0.6 for Autonomic signs relative to Vocalization/verbalization.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.8 for Affective/autonomic aura relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Hypermotor-complex motor behaviorFigure 6 reports an odds ratio of 0.6 for Autonomic signs relative to Hypermotor-complex motor behavior.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Affective/autonomic auraFigure 6 reports an odds ratio of 1.2 for Vocalization/verbalization relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Affective/autonomic auraFigure 6 reports an odds ratio of 1.2 for Hypermotor-complex motor behavior relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.7 for Autonomic signs relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.7 for Facial expression change relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.6 for Motor (gestural) automatisms relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.4 for Loss of consciousness relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.3 for Post-ictal confusion/behavior change disinhibition relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.2 for Chapeau de gendarme relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.2 for Dystonic posturing relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.1 for Head-eye deviation relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Affective/autonomic auraFigure 6 reports an odds ratio of 0.1 for Laughter relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Affective/autonomic auraFigure 6 reports an odds ratio of <0.1 for Oro-alimentary automatisms relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Affective/autonomic auraFigure 6 reports an odds ratio of <0.1 for Tonic-clonic relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Affective/autonomic auraFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Affective/autonomic aura.PDF p.12, Figure 6
  • pairwise OR: Vocalization/verbalization relative to Autonomic signsFigure 6 reports an odds ratio of 1.7 for Vocalization/verbalization relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Hypermotor-complex motor behavior relative to Autonomic signsFigure 6 reports an odds ratio of 1.6 for Hypermotor-complex motor behavior relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Autonomic signsFigure 6 reports an odds ratio of 1.4 for Affective/autonomic aura relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Facial expression change relative to Autonomic signsFigure 6 reports an odds ratio of 0.9 for Facial expression change relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Motor (gestural) automatisms relative to Autonomic signsFigure 6 reports an odds ratio of 0.8 for Motor (gestural) automatisms relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Loss of consciousness relative to Autonomic signsFigure 6 reports an odds ratio of 0.6 for Loss of consciousness relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Autonomic signsFigure 6 reports an odds ratio of 0.5 for Post-ictal confusion/behavior change disinhibition relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Chapeau de gendarme relative to Autonomic signsFigure 6 reports an odds ratio of 0.3 for Chapeau de gendarme relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Dystonic posturing relative to Autonomic signsFigure 6 reports an odds ratio of 0.3 for Dystonic posturing relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Head-eye deviation relative to Autonomic signsFigure 6 reports an odds ratio of 0.2 for Head-eye deviation relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Laughter relative to Autonomic signsFigure 6 reports an odds ratio of 0.2 for Laughter relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Oro-alimentary automatisms relative to Autonomic signsFigure 6 reports an odds ratio of 0.1 for Oro-alimentary automatisms relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Tonic-clonic relative to Autonomic signsFigure 6 reports an odds ratio of 0.1 for Tonic-clonic relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: F to BTC relative to Autonomic signsFigure 6 reports an odds ratio of <0.1 for F to BTC relative to Autonomic signs.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Facial expression changeFigure 6 reports an odds ratio of 1.5 for Affective/autonomic aura relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Facial expression changeFigure 6 reports an odds ratio of 1.1 for Autonomic signs relative to Facial expression change.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 1.7 for Affective/autonomic aura relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Motor (gestural) automatismsFigure 6 reports an odds ratio of 1.2 for Autonomic signs relative to Motor (gestural) automatisms.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Loss of consciousnessFigure 6 reports an odds ratio of 2.3 for Affective/autonomic aura relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Loss of consciousnessFigure 6 reports an odds ratio of 1.7 for Autonomic signs relative to Loss of consciousness.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 2.9 for Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Post-ictal confusion/behavior change disinhibitionFigure 6 reports an odds ratio of 2.1 for Autonomic signs relative to Post-ictal confusion/behavior change disinhibition.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 4.9 for Affective/autonomic aura relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Chapeau de gendarmeFigure 6 reports an odds ratio of 3.6 for Autonomic signs relative to Chapeau de gendarme.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Dystonic posturingFigure 6 reports an odds ratio of 5.2 for Affective/autonomic aura relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Dystonic posturingFigure 6 reports an odds ratio of 3.9 for Autonomic signs relative to Dystonic posturing.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Head-eye deviationFigure 6 reports an odds ratio of 7.7 for Affective/autonomic aura relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Head-eye deviationFigure 6 reports an odds ratio of 5.7 for Autonomic signs relative to Head-eye deviation.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to LaughterFigure 6 reports an odds ratio of 11.7 for Affective/autonomic aura relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to LaughterFigure 6 reports an odds ratio of 8.6 for Autonomic signs relative to Laughter.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 13.3 for Affective/autonomic aura relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Oro-alimentary automatismsFigure 6 reports an odds ratio of 9.8 for Autonomic signs relative to Oro-alimentary automatisms.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to Tonic-clonicFigure 6 reports an odds ratio of 21.9 for Affective/autonomic aura relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to Tonic-clonicFigure 6 reports an odds ratio of 16.2 for Autonomic signs relative to Tonic-clonic.PDF p.12, Figure 6
  • pairwise OR: Affective/autonomic aura relative to F to BTCFigure 6 reports an odds ratio of 21.9 for Affective/autonomic aura relative to F to BTC.PDF p.12, Figure 6
  • pairwise OR: Autonomic signs relative to F to BTCFigure 6 reports an odds ratio of 16.2 for Autonomic signs relative to F to BTC.PDF p.12, Figure 6
Reported values
  • 25% (frequency range 0–82%)autonomic auraPercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.13, Table 3
  • 48% (frequency range 0–91%)autonomic signsPercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.13, Table 3
  • 48.4%autonomic signs; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.10, Figure 4
  • 24.7%autonomic aura; Figure 4 ratePercentage · Reviewed ACC seizure cases with reported semiology · ictal onsetPDF p.10, Figure 4
  • 80% of reported aurasaffective and autonomic subjective manifestationsPercentage · Reviewed ACC seizure cases with reported semiology · reported auras · Reported ACC aurasPDF p.7, Subjective manifestations
  • 8 significant pairwise comparisonsaffective/autonomic aura; pairwise odds-ratio significanceCount · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.10, Statistical analysis of ictal semiology
  • 8 significant pairwise comparisonsautonomic signs; pairwise odds-ratio significanceCount · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.10, Statistical analysis of ictal semiology
  • OR 0.8pairwise OR: Affective/autonomic aura relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Autonomic signs relative to Vocalization/verbalizationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Affective/autonomic aura relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Autonomic signs relative to Hypermotor-complex motor behaviorOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Vocalization/verbalization relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Hypermotor-complex motor behavior relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Autonomic signs relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.7pairwise OR: Facial expression change relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Motor (gestural) automatisms relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.4pairwise OR: Loss of consciousness relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Chapeau de gendarme relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Dystonic posturing relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Head-eye deviation relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Laughter relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Oro-alimentary automatisms relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Affective/autonomic auraOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Vocalization/verbalization relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.6pairwise OR: Hypermotor-complex motor behavior relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.4pairwise OR: Affective/autonomic aura relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.9pairwise OR: Facial expression change relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.8pairwise OR: Motor (gestural) automatisms relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.6pairwise OR: Loss of consciousness relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.5pairwise OR: Post-ictal confusion/behavior change disinhibition relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Chapeau de gendarme relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.3pairwise OR: Dystonic posturing relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.2pairwise OR: Head-eye deviation relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Laughter relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 0.1pairwise OR: Oro-alimentary automatisms relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: Tonic-clonic relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR <0.1pairwise OR: F to BTC relative to Autonomic signsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.5pairwise OR: Affective/autonomic aura relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.1pairwise OR: Autonomic signs relative to Facial expression changeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Affective/autonomic aura relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.2pairwise OR: Autonomic signs relative to Motor (gestural) automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.3pairwise OR: Affective/autonomic aura relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 1.7pairwise OR: Autonomic signs relative to Loss of consciousnessOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.9pairwise OR: Affective/autonomic aura relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 2.1pairwise OR: Autonomic signs relative to Post-ictal confusion/behavior change disinhibitionOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 4.9pairwise OR: Affective/autonomic aura relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.6pairwise OR: Autonomic signs relative to Chapeau de gendarmeOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.2pairwise OR: Affective/autonomic aura relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 3.9pairwise OR: Autonomic signs relative to Dystonic posturingOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 7.7pairwise OR: Affective/autonomic aura relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 5.7pairwise OR: Autonomic signs relative to Head-eye deviationOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 11.7pairwise OR: Affective/autonomic aura relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 8.6pairwise OR: Autonomic signs relative to LaughterOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 13.3pairwise OR: Affective/autonomic aura relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 9.8pairwise OR: Autonomic signs relative to Oro-alimentary automatismsOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 21.9pairwise OR: Affective/autonomic aura relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 16.2pairwise OR: Autonomic signs relative to Tonic-clonicOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 21.9pairwise OR: Affective/autonomic aura relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
  • OR 16.2pairwise OR: Autonomic signs relative to F to BTCOdds ratio · Reviewed ACC seizure cases with reported semiology · ACC symptom-comparison analysisPDF p.12, Figure 6
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdfSystematic review or meta-analysis · 1 finding
chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The article is labelled a Review and states that it summarizes current literature, focuses on common semiologies, and provides cases from the authors’ centre with online supplemental videos. No systematic search strategy, eligibility criteria, pooled analysis, or formal reference standard is reported. Cited-study populations remain those of the cited reports; the article also describes seven illustrative cases with patient ages, seizure histories, imaging, EEG, and outcomes. Patient consent for publication was obtained. The source integrates history, examination, neuroimaging, neurophysiology, and neuropsychology for presurgical interpretation and repeatedly cautions that semiology may reflect propagation rather than onset.
Findings
  • gustatory; olfactory; vestibular; autonomic auraTable 3 maps gustatory aura to insula or mesiotemporal regions, olfactory aura to insula, mesiotemporal, or orbitofrontal regions, vestibular aura to posterior temporal or parietal regions, and autonomic aura to insula, amygdala, or cingulate regions.PDF p.10, Table 3; PDF p.3, Figure 1
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.54 · 1 × 0.9 × 1.707
This is a narrative/systematic literature review with 21 included studies selected from 171 considered studies. The source reports 87 confidently included cases involving OFC onset, of which 26 were analyzed as OFC-restricted and 33 as OFC-extended based on resection evidence; extended cases were grouped by frontal, insular, or temporal accessory resection. The review applies the proposed ILAE seizure-description framework and a published EZN confidence grading score. Search counts, study-list cells, standalone resection/imaging/surgery/outcome counts, and generic method/risk-of-bias statements remain context here rather than individual findings.
Findings
  • autonomic phenomenaAutonomic phenomena were reported in three of 26 restricted-OFC cases.PDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
Reported values
  • 3/26 (11.6%)autonomic phenomenaPercentage · n/N 3/26 · OFC-restricted EZN cases · OFC-restricted EZN cases · ictalPDF p.2, Semiology patterns of seizures with EZN restricted to the OFC
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Autonomic auraTable 3 reports 3 studies assessing Autonomic aura.PDF p.6, Table 3
  • Autonomic auraTable 3 reports 40 patients assessed for Autonomic aura.PDF p.6, Table 3
  • Autonomic auraTable 3 reports 20–37.5% as the percentage range or value for Autonomic aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Autonomic auraTable 4 reports overall odds of 0.34 for occurrence of Autonomic aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Autonomic auraTable 4 reports a 95% confidence interval of 0.17–0.70 for the overall odds of Autonomic aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Autonomic auraThe heterogeneity test for the Table 4 odds estimate for Autonomic aura has p=0.6498.PDF p.7, Table 4
  • Autonomic aura; lateral versus mesial comparisonTable 5 reports 3 studies comparing Autonomic aura in lateral and mesial TLE.PDF p.9, Table 5
  • Autonomic aura; lateral TLE patient denominatorTable 5 reports 40 lateral-TLE patients assessed for Autonomic aura.PDF p.9, Table 5
  • Autonomic aura; mesial TLE patient denominatorTable 5 reports 71 mesial-TLE patients assessed for Autonomic aura.PDF p.9, Table 5
  • Autonomic aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 20–37.5% for Autonomic aura.PDF p.9, Table 5
  • Autonomic aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 5–48.4% for Autonomic aura.PDF p.9, Table 5
Reported values
  • 20–37.5%Autonomic auraPercentage Range · Lateral temporal epilepsy patients assessed for Autonomic aura · ictalPDF p.6, Table 3
  • odds 0.34odds of occurrence; Autonomic auraOdds · Lateral temporal epilepsy patients assessed for Autonomic aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 20–37.5%Autonomic aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Autonomic aura · Lateral TLE patients assessed for Autonomic aura · ictalPDF p.9, Table 5
  • 5–48.4%Autonomic aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Autonomic aura · Mesial TLE patients assessed for Autonomic aura · ictalPDF p.9, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • autonomic aurasAutonomic auras include cardiorespiratory, gastrointestinal, genitourinary, and cutaneous sensations and are attributed to activation of the insular cortex, anterior cingulum, SSMA, or amygdala; the source notes that these areas share a subcortical relay station with the hypothalamus.PDF p.2, section 3.1 Auras; PDF p.3, section 3.1 Auras; PDF p.2, Table 1
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdfSystematic review or meta-analysis · 4 findings · 3 reported values
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
This is a systematic review of non-idiopathic focal fronto-opercular epilepsy. The included population is 21 patients from 16 studies, including case series and case reports; the source reports 13 adults and 8 children in its population context. The review used anatomical and electroclinical evidence to define the EZ and divided the cohort into 12 prefrontal-operculum and 9 precentral Rolandic-operculum patients. Study-selection counts, Table 1 demographic/exploration cells, publication details, and risk-of-bias statements are retained here as context rather than individual findings. The source states that quantitative meta-analysis was not possible because of heterogeneity and low patient numbers; Fisher's exact tests compared semiological variables between the two EZ groups.
Findings
  • Autonomic aura (palpitation)Table 2 reports 2/21 (10%) for Autonomic aura (palpitation); timing is onset, and the source's overall agreement that the sign is suggestive of fronto-opercular epilepsy is graded Low.PDF p.7, Table 2
  • Autonomic aura (palpitation)Table 2 reports 1/12 patients with Autonomic aura (palpitation) in the prefrontal operculum group.PDF p.7, Table 2
  • Autonomic aura (palpitation)Table 2 reports 1/9 patients with Autonomic aura (palpitation) in the precentral Rolandic operculum group.PDF p.7, Table 2
  • Autonomic aura (palpitation)Fisher's exact comparison of Autonomic aura (palpitation) between the prefrontal and precentral Rolandic operculum groups has p=1.PDF p.7, Table 2
Reported values
  • 2/21 (10%)Autonomic aura (palpitation)Percentage · n/N 2/21 · 21 included fronto-opercular epilepsy patients · OnsetPDF p.7, Table 2
  • 1/12 patientsAutonomic aura (palpitation)Proportion · n/N 1/12 · 12 patients with EZ in the prefrontal operculum · 12 patients with EZ in the prefrontal operculum · OnsetPDF p.7, Table 2
  • 1/9 patientsAutonomic aura (palpitation)Proportion · n/N 1/9 · 9 patients with EZ in the precentral Rolandic operculum · 9 patients with EZ in the precentral Rolandic operculum · OnsetPDF p.7, Table 2
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdfIndependent primary study · 1 finding · 2 reported values
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
Independent primary study · Class II · Evidence weight 5.11 · 2 × 1.35 × 1.893
Electronic records were reviewed for all individuals who underwent frontal lobe epilepsy surgery at the National Hospital for Neurology & Neurosurgery, London, UK, between 1 January 2011 and 31 December 2020; 61 individuals were included after excluding operations performed primarily for reasons other than epilepsy. All had presurgical multidisciplinary review after scalp video-EEG telemetry, neuropsychology and neuropsychiatry assessment, MRI, and, in selected cases, FDG-PET, ictal SPECT, or intracranial EEG. Ictal semiology and its evolution came from video-EEG telemetry reports and multidisciplinary-team summaries, were documented in a predetermined format, and were independently categorized by two investigators with discrepancies resolved by discussion. Surgical records and postoperative MRI identified resection site and extent; the final resection site was the presumed EZ surrogate, and only the first resection was retained for the one individual with more than one procedure. At 12 months, outcomes came from a prospective epilepsy-surgery database and were classified with the ILAE surgery outcome scale. The cohort had median age at surgery 33.9 years (IQR 28.1-43.1) and median epilepsy duration 21.9 years (IQR 21.3-25.1); 43/61 (70%) had abnormal MRI, including 35 (57%) focal and 8 (13%) diffuse abnormalities, while 18 had normal MRI; 41/61 (67%) underwent intracranial EEG. Operations included 52/61 (85%) cortical resections and 9/61 (15%) lesionectomies; resections were left-sided in 32/61 (53%) and right-sided in 29/61 (47%), with orbitofrontal, frontomedial, dorsolateral, frontocentral, and combined extensive resections reported in Table 1. Twenty-three individuals (38%) had anterior cingulate extension and one had insular extension.
Findings
  • AutonomicAutonomic semiology occurred in 2/61 individuals (3%) as initial semiology and 9/61 (15%) in the combined set-of-semiology.PDF p.5, Table 2
Reported values
  • Initial 2/61 (3%)AutonomicPercentage · n/N 2/61 · 61 individuals undergoing frontal lobe epilepsy surgery · initial semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
  • Combined 9/61 (15%)AutonomicPercentage · n/N 9/61 · 61 individuals undergoing frontal lobe epilepsy surgery · combined set-of-semiology · Ictal video-EEG; initial manifestation versus all observed ictal manifestationsPDF p.5, Table 2
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Autonomic auraTable 2 associates autonomic aura with insula, amygdala, anterior cingulum, and SSMA and describes it as non-lateralising.PDF p.3, Table 2
luders-semiological-seizure-classification-1998.pdfNarrative, educational, or cited context · 3 findings
luders-semiological-seizure-classification-1998.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a classification/methods article rather than a cohort study. The proposed classification is based on semiology reported by the patient or observers or observed during video monitoring; the article gives definitions, examples, and clinical-application rationale. No study cohort, eligibility criteria, analysis population, reference standard, diagnostic accuracy analysis, or comparative denominator is reported. The authors state that the system had been tested in selected epilepsy centers for more than 10 years, without presenting a validation cohort or performance estimates in this report.
Findings
  • autonomic aura; autonomic seizureThe source distinguishes an autonomic aura, based on patient-reported symptoms probably produced by autonomic alteration without objective proof, from an autonomic seizure, which requires objective documentation by appropriate polygraphic recording or direct observation; documented autonomic dysfunction may be clinically silent.PDF p.2, Overview; PDF p.3, Auras; PDF p.4, Autonomic seizures
  • Autonomic auraAutonomic alterations that the patient can detect but observers have difficulty identifying are classified as autonomic auras when they most probably represent epileptic autonomic change even without objective proof; objective polygraphic or directly observed autonomic change is classified as an autonomic seizure.PDF p.3, Auras, subsection Autonomic auras; PDF p.2, Overview
  • Autonomic seizureAutonomic seizures are episodic alterations of autonomic function elicited by activation of autonomic cortical centers by an epileptiform discharge; diagnosis requires documentation by appropriate polygraphic recording or direct observation, and documented episodes may be clinically silent.PDF p.2, Overview; PDF p.3, Autonomic seizures; PDF p.4, Autonomic seizures
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdfNarrative, educational, or cited context · 1 finding
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors registered the review in PROSPERO (CRD42024519156) and report PRISMA methods. PubMed, EMBASE, and Scopus were searched through December 1, 2024. Original peer-reviewed studies with individual-level spontaneous ictal descriptions and invasive EEG, surgery/outcome, or imaging data were eligible; case reports were included. EZ confidence was graded as very high, high, moderate, or low using MRI, invasive EEG, and postsurgical outcome, and GRADE was used for overall evidence. Descriptive statistics and Pearson chi-squared tests with Holm-corrected pairwise proportion tests were reported.
Findings
  • affective ACC expressionStronger emotional expressions such as fear or menace, with open eyes, hypermotor, and autonomic features, were linked to the rostroventral “affective” ACC.PDF p.8, Discussion
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdfSystematic review or meta-analysis · 9 findings · 6 reported values
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review included English-language case series and selected case reports of drug-resistant temporal or frontal epilepsy with electroclinical or imaging evidence of temporo-frontal/fronto-temporal network involvement. The reviewed population is 40 articles and 109 patients; the source divides them into a temporo-frontal subgroup (temporal seizure-onset zone with frontal extension) and a fronto-temporal subgroup (frontal onset with temporal involvement). Search counts, duplicate resolution, reviewer roles, eligibility/risk-of-bias details, Table 1 per-study MRI/SEEG/surgery/outcome cells, and standalone surgery/outcome counts are retained only as compact context here. The source uses cluster analysis, Fisher exact comparisons for sign/resection associations, and random-effects prevalence meta-analysis.
Findings
  • automatisms; elementary motor; hyperkinetic; autonomic; emotional; grimace; cognitive; other subjectiveThe source classifies ictal features into automatisms, elementary motor, hyperkinetic, autonomic, emotional, grimace, cognitive, and other subjective categories for the cluster and prevalence analyses.PDF p.4, Statistical analysis
  • emotional; autonomic; cognitive; grimacing; hyperkinetic behaviorThe source identifies a main cluster containing emotional, grimacing, autonomic, cognitive, and hyperkinetic manifestations across the whole group and both subgroups.PDF p.1, Abstract; PDF p.10, Figure 3
  • emotional; autonomic; automatisms; hyperkinetic behavior; grimaceAcross groups, the source places autonomic and emotional features at seizure onset, while automatisms, hyperkinetic behavior, and grimace are associated with propagation.PDF p.2, Key points; PDF p.9, Seizure semiology
  • autonomic features; whole groupAutonomic features were reported in 38% of the whole review group.PDF p.5, All group; PDF p.9, Figure 2
  • autonomic features; fronto-temporal subgroupAutonomic features was reported in 30% of the fronto-temporal subgroup (33 patients).PDF p.5, Fronto-temporal subgroup
  • autonomic features; temporo-frontal subgroupAutonomic features was reported in 41% of the temporo-frontal subgroup (76 patients).PDF p.5, Temporo-frontal subgroup
  • association coefficient; autonomic and hyperkineticThe source reports an association coefficient of 0.606 for autonomic and hyperkinetic in the whole group.PDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient; emotional and autonomicThe source reports an association coefficient of 0.788 for emotional and autonomic in the fronto-temporal subgroup.PDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
  • hyperkinetic behavior preceded by autonomic signsThe source states that hyperkinetic behavior could be preceded by autonomic signs in 38% of cases.PDF p.12, Discussion
Reported values
  • 38%autonomic features; whole groupPercentage · 109 review patients, whole group · ictal onsetPDF p.5, All group; PDF p.9, Figure 2
  • 30%autonomic features; fronto-temporal subgroupPercentage · 33 patients, fronto-temporal subgroup · ictal onsetPDF p.5, Fronto-temporal subgroup
  • 41%autonomic features; temporo-frontal subgroupPercentage · 76 patients, temporo-frontal subgroup · ictal onsetPDF p.5, Temporo-frontal subgroup
  • association coefficient 0.606association coefficient; autonomic and hyperkineticAssociation Coefficient · 109 review patients · ictal symptom co-occurrencePDF p.5, All group; PDF p.10, Figure 3A
  • association coefficient 0.788association coefficient; emotional and autonomicAssociation Coefficient · 33 fronto-temporal subgroup patients · ictal symptom co-occurrencePDF p.5, Fronto-temporal subgroup; PDF p.10, Figure 3B
  • 38%hyperkinetic behavior preceded by autonomic signsPercentage · Source-described hyperkinetic-behavior cases · ictal onset before hyperkinetic propagationPDF p.12, Discussion
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • autonomic auras and autonomic seizuresThe review distinguishes subjective autonomic auras from “autonomic seizures,” which it says should be diagnosed when an autonomic alteration is objectively documented, such as tachycardia on ECG; the symptomatogenic zone of most autonomic auras is stated to be most likely the insular cortex.PDF p.2, Autonomic auras; PDF p.3, Autonomic seizures
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdfIndependent primary study · 1 finding · 2 reported values
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
Independent primary study · Class II · Evidence weight 5.01 · 2 × 1.5 × 1.671
The study retrospectively identified 22 consecutive medication-resistant patients evaluated between January 2015 and March 2018; 12 were adults and 10 were pediatric patients. Insulo-opercular seizure origin was defined by SEEG, and patients without complete presurgical evaluation or clear seizure-semiology video were excluded. At least two habitual seizures were reviewed per patient for scalp video-EEG (53 seizures total), and EI was computed for two habitual seizures per patient. PET visual/MRI-coregistration analyses involved the patient group; the voxel-based PET comparison used 17 patients after excluding three with previous epilepsy surgery and two younger than 7 years, compared with 18 healthy subjects.
Findings
  • autonomic; somatosensory/viscerosensory symptomsIn the 22-patient SEEG-defined insulo-opercular epilepsy series, autonomic symptoms and somatosensory/viscerosensory symptoms, separately or in combination, were the most prevalent auras and/or early seizure semiologies.PDF p.3, Results—Seizure semiology
Reported values
  • Autonomic symptoms 7/22 (32%)autonomic; somatosensory/viscerosensory symptomsPercentage · n/N 7/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology
  • Somatosensory/viscerosensory symptoms 13/22 (59%)autonomic; somatosensory/viscerosensory symptomsPercentage · n/N 13/22 · 22 medication-resistant patients with SEEG-defined insulo-opercular epilepsy · aura and/or early seizure semiologyPDF p.3, Results—Seizure semiology

16 contributing manuscripts; source-reported values remain separate and are not pooled.

Cephalic auraDoes not lateralizeNo directional estimate7 manuscripts · 18 findings · 11 reported values
Weighted evidence supportevidence weight 20.7 across 7 manuscripts · 3 independent primary study · 2 systematic review or meta-analysis · 2 narrative, educational, or cited context

The cited table describes cephalic/whole-body aura as non-lateralising. No lateralizing direction is reported for cephalic auras. No lateralization relationship is reported. The primary table's dizziness/cephalic-aura result reports no hemisphere or lateralization direction. The primary odds result for Dizziness/cephalic aura reports no hemisphere or lateralization direction. The primary lateral-TLE percentage range for Dizziness/cephalic aura reports no hemisphere or lateralization direction. The primary mesial-TLE percentage range for Dizziness/cephalic aura reports no hemisphere or lateralization direction. No lateralization is reported. No linked lateralization assertion is reported for cephalic and whole-body auras. No lateralizing direction is reported for cephalic aura in the temporo-polar synthesis. No lateralizing direction is reported for the 0–14% cephalic-aura range.

Source-defined result groups 7
Localization: TemporalSource-defined values retained separatelyAll reported · Table 3 point estimate 4% · Table 3 between-report frequency range1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · other Table 3 temporo-polar sign estimates · Table 3 sign-frequency estimate1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · reported sign prevalence across included studies1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyMesial TLE patients assessed for Dizziness/cephalic aura · lateral TLE percentage shown separately · reported mesial-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyAll reported · absence of the same sign in lateral TLE · random-effects summary odds of sign occurrence1 manuscript · 1 reported value · not pooled
Localization: TemporalSource-defined values retained separatelyLateral TLE patients assessed for Dizziness/cephalic aura · mesial TLE percentage shown separately · reported lateral-TLE sign prevalence1 manuscript · 1 reported value · not pooled
Localization: FrontalObserved proportion 75.0%All reported · frontal versus nonfrontal SHE and SP1/SP2 versus other SPs · patient1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 7

Alphabetical by manuscript.

barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdfIndependent primary study · 1 finding · 3 reported values
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
Independent primary study · Class II · Evidence weight 5.65 · 2 × 1.5 × 1.882
The study was retrospective and included 80 of 212 consecutive patients with medically intractable seizures operated on after SEEG at Grenoble Hospital from 1990 to 1998. Eligibility required no detectable MRI lesion except hippocampal sclerosis, SEEG involvement of at least mesial and/or lateral temporal structures, SEEG-guided surgery, and at least 5 years of postoperative follow-up. The cohort comprised 42 females and 38 males; the reported mean age at SEEG was 29.3 ± 8.7 years, mean age at epilepsy onset 10.1 ± 7.9 years, mean epilepsy duration 19 ± 8 years, and mean seizure frequency 13.5 ± 17.5 per month. Sixty-six patients had unilateral hippocampal sclerosis; 14 had no clear MRI abnormality before surgery, with hamartoma or non-Taylor cortical dysplasia found in two of those at neuropathology. Long-term scalp video-EEG recorded 432 seizures in 79 patients; SEEG used 888 chronically implanted electrodes and recorded 607 seizures in 79 patients, with one patient not captured because the SEEG study was interrupted. The epileptogenic zone was defined by the first clear preclinical ictal SEEG change consisting of low-voltage fast activity or recruiting fast spikes and by the cortex considered for removal; 58 patients were classified TL and 22 T+, with T+ subgroups temporo-frontal (TF, n=9), temporo-sylvian (TS, n=7), and temporo-parieto-occipital (TPO, n=6). Clinical semiology was assessed on one typical seizure per patient, giving 80 analyzed seizures, because the number of recorded seizures per patient ranged from 1 to 44. The comparison used relative frequencies and contingency tables; Phi and Cramer V significance was set at P≤0.05. Scalp-EEG findings were classified by type, lateralization, and 10–20 localization; ictal onset included low-voltage fast activity, localized flattening, disappearance of localized interictal abnormalities, or rhythmic theta when the other patterns were absent. Tailored resections included at least the temporal pole and mesio-temporal structures; 18 of 22 T+ cases had extension outside the temporal lobe, and postoperative Engel classes were reported as context rather than as semiologic findings. The introduction also cites surgical outcome examples involving temporo-perisylvian, temporo-insular, temporo-parietal, and posterior basal temporal onsets; these cited reports are represented separately only where the outcome is inseparable from the localizing claim.
Findings
  • cephalic auraCephalic auras did not differ significantly between TL and T+ groups.PDF p.6, Table 2
Reported values
  • T+ 4.3%cephalic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · T+ · ictal onsetPDF p.6, Table 2
  • TL 6.8%cephalic auraPercentage · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · TL · ictal onsetPDF p.6, Table 2
  • P=0.8cephalic auraP value · TL group (n=58) versus T+ group (n=22); one analyzed seizure per patient · ictal onsetPDF p.6, Table 2
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdfSystematic review or meta-analysis · 11 findings · 4 reported values
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The review used a PRISMA-based systematic search of PubMed and EMBASE and included six studies with 94 patients; the source states that only an estimated 56–69 patients had unambiguous lateral temporal epilepsy because other neocortical temporal structures were included. The review used random-effects meta-analysis for sign odds and diagnostic accuracy, with sensitivity analysis for studies in which more than half of patients unequivocally had lateral seizure onset. Search/duplicate/exclusion counts, reviewer details, eligibility thresholds, Table 1/2 imaging and surgery cells, and standalone population/outcome facts are retained as compact context here rather than individual findings.
Findings
  • Dizziness/cephalic auraTable 3 reports 3 studies assessing Dizziness/cephalic aura.PDF p.6, Table 3
  • Dizziness/cephalic auraTable 3 reports 47 patients assessed for Dizziness/cephalic aura.PDF p.6, Table 3
  • Dizziness/cephalic auraTable 3 reports 11.8–50% as the percentage range or value for Dizziness/cephalic aura; the overall association grade is Low.PDF p.6, Table 3
  • odds of occurrence; Dizziness/cephalic auraTable 4 reports overall odds of 0.31 for occurrence of Dizziness/cephalic aura in lateral TLE.PDF p.7, Table 4; PDF p.8, Figure 2
  • odds confidence interval; Dizziness/cephalic auraTable 4 reports a 95% confidence interval of 0.10–0.93 for the overall odds of Dizziness/cephalic aura.PDF p.7, Table 4; PDF p.8, Figure 2
  • heterogeneity test; Dizziness/cephalic auraThe heterogeneity test for the Table 4 odds estimate for Dizziness/cephalic aura has p=0.1134.PDF p.7, Table 4
  • Dizziness/cephalic aura; lateral versus mesial comparisonTable 5 reports 2 studies comparing Dizziness/cephalic aura in lateral and mesial TLE.PDF p.9, Table 5
  • Dizziness/cephalic aura; lateral TLE patient denominatorTable 5 reports 25 lateral-TLE patients assessed for Dizziness/cephalic aura.PDF p.9, Table 5
  • Dizziness/cephalic aura; mesial TLE patient denominatorTable 5 reports 40 mesial-TLE patients assessed for Dizziness/cephalic aura.PDF p.9, Table 5
  • Dizziness/cephalic aura; lateral TLE prevalenceTable 5 reports a lateral-TLE percentage of 11.8–50% for Dizziness/cephalic aura.PDF p.9, Table 5
  • Dizziness/cephalic aura; mesial TLE prevalenceTable 5 reports a mesial-TLE percentage of 0–40% for Dizziness/cephalic aura.PDF p.9, Table 5
Reported values
  • 11.8–50%Dizziness/cephalic auraPercentage Range · Lateral temporal epilepsy patients assessed for Dizziness/cephalic aura · ictalPDF p.6, Table 3
  • odds 0.31odds of occurrence; Dizziness/cephalic auraOdds · Lateral temporal epilepsy patients assessed for Dizziness/cephalic aura · ictalPDF p.7, Table 4; PDF p.8, Figure 2
  • 11.8–50%Dizziness/cephalic aura; lateral TLE prevalencePercentage Range · Lateral TLE patients assessed for Dizziness/cephalic aura · Lateral TLE patients assessed for Dizziness/cephalic aura · ictalPDF p.9, Table 5
  • 0–40%Dizziness/cephalic aura; mesial TLE prevalencePercentage Range · Mesial TLE patients assessed for Dizziness/cephalic aura · Mesial TLE patients assessed for Dizziness/cephalic aura · ictalPDF p.9, Table 5
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • cephalic and whole-body aurasCephalic auras are nonvertiginous head sensations that can arise from the amygdala, entorhinal cortex, or lateral temporal neocortex but often have little localizing value, whereas whole-body auras are generalized body sensations that may be elicited by SII and SSMA stimulation.PDF p.3, section 3.1 Nonspecific auras; PDF p.2, Table 1
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdfIndependent primary study · 1 finding · 1 reported value
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
Independent primary study · Class II · Evidence weight 4.36 · 2 × 1.5 × 1.452
The study retrospectively identified 155 patients with drug-resistant sleep-related epilepsy from 1433 consecutive epilepsy-surgery patients treated from October 1997 through July 2015; sleep-related epilepsy required more than 90% of seizures during sleep. After exclusion of 20 patients with nocturnal temporal lobe epilepsy who did not meet confirmed SHE criteria, 135 patients comprised the SHE series. SOZ location was assigned from presurgical anatomo-electroclinical data, including stereo-EEG when performed, postoperative MRI, and postoperative Engel outcome. Six patients with overlapping frontal and extrafrontal SOZs were assigned to the principal SOZ location; seven patients with incomplete resection but confidently localized SOZs were retained using stereo-EEG; 20 patients with unclear or widespread SOZs were excluded from the semiology analysis. The semiology analysis therefore included 115 patients: 74 frontal and 41 extrafrontal, comprising 14 temporal, 18 operculoinsular, and 9 posterior cases. Clinical descriptions came from patients and family members, and the earliest nonmotor manifestation was selected when more than one was reported. All patients had at least one typical sleep-related event captured during video-EEG and stereo-EEG monitoring when performed. Five epileptologists reviewed captured events; two independently categorized the four video-documented semiology patterns, and four reviewed discordant assignments. One semiology pattern was assigned per patient because seizures were considered stereotyped, with early motor semiology weighted more heavily than late semiology. Seventeen patients (15%) required consensus review for discordant categorization. Postictal confusion was assessed from the clinical assessment during ictal recordings. Welch-corrected unpaired t tests, two-tailed Fisher exact tests, and kappa statistics were used; significance was retained at P < 0.05. Context reported by the source: mean seizure-onset age was 5.8 +/- 4.4 years, mean disease duration was 17.9 +/- 10.3 years, 64% had at least one seizure per night, and 90% had at least one seizure per week. An MRI-identifiable lesion was present in 88/135 patients (65%); probable focal cortical dysplasia was the most common MRI diagnosis (52%). The most common postoperative histopathologic diagnosis was FCD type II (67%). At least 2 years of postoperative outcome data were available for 127/135 patients (94%); Engel I outcome occurred in 104/127 (82%) and Engel class Ia in 86/127 (68%). Mortality outcomes were Not reported.
Findings
  • cephalic sensationCephalic symptoms were restricted to the frontal SHE subgroup; 6/8 patients with a cephalic sensation exhibited SP1 or SP2, which the authors state suggests frequent localization to the posterior frontal lobe.PDF p.6, section 3.3; PDF p.7, section 3.3
Reported values
  • Restriction to frontal subgroup and SP1/SP2 association, 6/8cephalic sensationCount · n/N 6/8 · Frontal SHE patients with an early cephalic manifestation · early nonmotor symptom followed by ictal semiology patternPDF p.6, section 3.3; PDF p.7, section 3.3
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Cephalic/whole-body auraTable 2 associates cephalic/whole-body aura with amygdala, entorhinal cortex, temporal neocortex, SSII, and SSMA and describes it as non-lateralising.PDF p.3, Table 2
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdfIndependent primary study · 1 finding · 1 reported value
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
Independent primary study · Class II · Evidence weight 2.70 · 2 × 1.35 × 1
The source studied 82 medically refractory patients whose seizure foci largely involved the parietal association area. Patients with large resections extending into anterior occipital, posterior temporal, or precentral regions and patients with parietal tumours were excluded. Surface EEG was available in 66 patients, seizures were recorded in 36, pre-resection ECoG was performed in 63, and intra-operative cortical stimulation was performed in 80. Denominators remain specific to each modality and subgroup. The source’s “parietal association area,” epileptogenic-zone definition, functional anatomy, and the source's own terms are preserved without a forced Brodmann, Lüders, or ILAE mapping.
Findings
  • cephalic sensation aura entriesTable 1 lists three cephalic-sensation aura entries.PDF p.4, Table 1
Reported values
  • 3 source-reported aura entriescephalic sensation aura entriesCount · 82-patient parietal epilepsy series · aura or seizure onsetPDF p.4, Table 1
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdfSystematic review or meta-analysis · 2 findings · 2 reported values
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
Systematic review or meta-analysis · Class I · Evidence weight 3.00 · 3 × 1 × 1
The source is a systematic review of temporal-polar and medio-lateral temporal seizure semiology. It reports 129 patients overall; the abstract prints 78/129 temporal-pole cases and 51/120 mesio-lateral cases. The temporal-polar section describes 11 publications with a maximum of 23 patients, and the medio-lateral section describes two publications. The printed 51/120 denominator is preserved as source context and is flagged as an internal denominator question below. Search-flow counts, reviewer counts, generic eligibility or risk-of-bias details, and standalone Table 1/2 demographic, imaging, surgery, and outcome cells are not findings.
Findings
  • cephalic auraTable 3 reports cephalic aura in 4% of the temporo-polar synthesis (evidence grade Low).PDF p.5, Table 3
  • cephalic auraTable 3 reports a 0–14% range for cephalic aura across the temporo-polar reports (evidence grade Low).PDF p.5, Table 3
Reported values
  • 4%cephalic auraPercentage · Temporo-polar semiology synthesis represented in Table 3 · clinical onsetPDF p.5, Table 3
  • range 0–14%cephalic auraPercentage Range · Temporo-polar semiology synthesis represented in Table 3 · clinical onsetPDF p.5, Table 3

7 contributing manuscripts; source-reported values remain separate and are not pooled.

Postictal coughDoes not lateralizeNo directional estimate2 manuscripts · 2 findings · 0 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The review states that postictal coughing is not lateralizing. Postictal coughing or sighing is restated as non-lateralizing, with a source-described association with MTLE rather than LTLE.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Postictal coughPostictal coughing is listed as localizing to the temporal lobe but not as lateralizing.PDF p.4, Table 2; PDF p.5, autonomic-phenomena paragraph
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal coughing and sighingPostictal coughing or sighing has no stated lateralizing value but is described as rare and quite specific for MTLE; these signs are usually absent in LTLE.PDF p.9, Postictal state; PDF p.9, Other signs to discriminate between LTLE and MTLE

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Whole-body auraDoes not lateralizeNo directional estimate2 manuscripts · 2 findings · 0 reported values
Weighted evidence supportevidence weight 2 across 2 manuscripts · 2 narrative, educational, or cited context

The cited table describes cephalic/whole-body aura as non-lateralising. No linked lateralization assertion is reported for cephalic and whole-body auras.

Evidence by contributing manuscript 2

Alphabetical by manuscript.

foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdfNarrative, educational, or cited context · 1 finding
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is a narrative review rather than a single original cohort or systematic quantitative synthesis. The discussed populations include patients with focal epilepsy, temporal lobe epilepsy, mesial and neocortical temporal lobe epilepsy, extratemporal and posterior-cortex epilepsy, children and infants, and presurgical epilepsy-surgery candidates. The review draws on clinical history, video/EEG and electrical-stimulation observations and on cited case series and cohorts; a single review-wide analysis population, eligibility rule, reference standard, and common denominator are not reported.
Findings
  • cephalic and whole-body aurasCephalic auras are nonvertiginous head sensations that can arise from the amygdala, entorhinal cortex, or lateral temporal neocortex but often have little localizing value, whereas whole-body auras are generalized body sensations that may be elicited by SII and SSMA stimulation.PDF p.3, section 3.1 Nonspecific auras; PDF p.2, Table 1
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Cephalic/whole-body auraTable 2 associates cephalic/whole-body aura with amygdala, entorhinal cortex, temporal neocortex, SSII, and SSMA and describes it as non-lateralising.PDF p.3, Table 2

2 contributing manuscripts; source-reported values remain separate and are not pooled.

Auditory phenomenon (unspecified type)Does not lateralizeNo directional estimate1 manuscript · 3 findings · 11 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 case report or observation

The review says the small cited auditory-phenomena series did not establish clear SOZ lateralization. No hemisphere or body-side direction is reported. No lateralization information is reported.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdfCase report or observation · 3 findings · 11 reported values
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
Case report or observation · Class III · Evidence weight 1.00 · 1 × 1 × 1
PubMed, Scopus, and Google Scholar were searched without language or date restrictions through 11 December 2022. The review narratively summarized auditory-network anatomy and compiled encountered cortical-stimulation studies reporting auditory phenomena (AP) plus case reports/series with AS-like phenomena and enough information to determine seizure-onset-zone (SOZ) lateralization and/or localization; acute symptomatic seizures and cases without evident auditory semiology were excluded. Level A evidence comprised seizure freedom after surgery with more than 1 year follow-up, seizures demonstrated from a SOZ on intracranial EEG, a concordant structural MRI lesion, or a concordant MEG cluster of at least 6 spike sources within 1 cm; Level B used MEG scatters, scalp EEG, PET/SPECT, and/or other clinical features. Localization and lateralization were analyzed for Level A, but only lateralization for Level B; data were tabulated as count (frequency), missing data were pairwise-deleted, and no comparative statistical tests were performed.
Findings
  • auditory responses in the Penfield and Perot cortical-stimulation seriesThe review states that Penfield and Perot reviewed more than 1,000 focal-epilepsy surgical patients, identified AP in 27 patients, and found auditory responses predominantly with stimulation of the superior and lateral STG; their small AP case number did not establish clear SOZ lateralization.PDF p.4, section 5, Penfield and Perot paragraph; PDF p.6, section 6.1, lateralization discussion
  • auditory phenomena (AP) induced by cortical stimulationAcross 27 articles, 351 AP induced by cortical stimulation were most often associated with temporal structures, but AP were also induced from insular, parietal, frontal, and occipital structures.PDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • auditory responses induced by insular stimulationThe review states that Mazzola et al. reported 44 auditory responses in a review of presurgical insular stimulation, almost all provoked by stimulation of the posteroinferior insula.PDF p.4, section 5; PDF p.5, section 5, cortical-stimulation lateralization paragraph
Reported values
  • more than 1,000auditory responses in the Penfield and Perot cortical-stimulation seriesCount · Cited Penfield and Perot surgical series; 27 patients with AP within a larger series of more than 1,000 patients · cited Penfield and Perot surgical series · Cortical stimulation responses; SOZ lateralization discussionPDF p.4, section 5, Penfield and Perot paragraph; PDF p.6, section 6.1, lateralization discussion
  • 27 patientsauditory responses in the Penfield and Perot cortical-stimulation seriesCount · n/N 27/more than 1,000 · Cited Penfield and Perot surgical series; 27 patients with AP within a larger series of more than 1,000 patients · auditory phenomena · Cortical stimulation responses; SOZ lateralization discussionPDF p.4, section 5, Penfield and Perot paragraph; PDF p.6, section 6.1, lateralization discussion
  • insula 95 APauditory phenomena (AP) induced by cortical stimulationCount · Cortical-stimulation reports in the epilepsy literature · insula · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • 27 articlesauditory phenomena (AP) induced by cortical stimulationCount · Cortical-stimulation reports in the epilepsy literature · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • parietal 22 APauditory phenomena (AP) induced by cortical stimulationCount · Cortical-stimulation reports in the epilepsy literature · parietal · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • temporal 222/351 (63%)auditory phenomena (AP) induced by cortical stimulationPercentage · n/N 222/351 · Cortical-stimulation reports in the epilepsy literature · temporal · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • occipital 1 APauditory phenomena (AP) induced by cortical stimulationCount · Cortical-stimulation reports in the epilepsy literature · occipital · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • frontal 11 APauditory phenomena (AP) induced by cortical stimulationCount · Cortical-stimulation reports in the epilepsy literature · frontal · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • 351 induced APauditory phenomena (AP) induced by cortical stimulationCount · Cortical-stimulation reports in the epilepsy literature · Electrically induced AP; not an ictal phase reported by the reviewPDF p.4, section 5; PDF p.5, Table 1; PDF p.6, Figure 2
  • “almost all” posteroinferior, without a reported numeratorauditory responses induced by insular stimulationCount · Cited Mazzola et al. review of presurgical insular stimulation · Electrical stimulation responsePDF p.4, section 5; PDF p.5, section 5, cortical-stimulation lateralization paragraph
  • 44 auditory responsesauditory responses induced by insular stimulationCount · Cited Mazzola et al. review of presurgical insular stimulation · Electrical stimulation responsePDF p.4, section 5; PDF p.5, section 5, cortical-stimulation lateralization paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal onset and nonlateralized temporal activityDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review describes focal one-electrode ictal onset in approximately a quarter of subjects and diffuse or nonlateralized temporal activity in a broader one-third-to-three-quarters range, especially with bitemporal independent discharges.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • focal ictal onset and nonlateralized temporal activityFocal ictal onset, defined by rhythmic activity or repetitive spiking at one electrode with rhythmic spread, was observed in approximately 25% of subjects; diffuse suppression or nonlateralized rhythmic activity characterized one-third to three-quarters of temporal lobe seizures and was more common with bitemporal independent discharges.PDF p.4, Temporal lobe seizures, paragraph on focal and nonlateralized ictal patterns
Reported values
  • one-third to three-quarters diffuse suppression or nonlateralized rhythmic activityfocal ictal onset and nonlateralized temporal activityRange · Patients with temporal lobe seizures; exact cohorts not reported · temporal-lobe seizures · ictal onset and ictalPDF p.4, Temporal lobe seizures, paragraph on focal and nonlateralized ictal patterns
  • approximately 25% focal ictal onsetfocal ictal onset and nonlateralized temporal activityPercentage · Patients with temporal lobe seizures; exact cohorts not reported · subjects · ictal onset and ictalPDF p.4, Temporal lobe seizures, paragraph on focal and nonlateralized ictal patterns

1 contributing manuscript; source-reported values remain separate and are not pooled.

Gustatory aura (parietal opercular component)Does not lateralizeNo directional estimate1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Gustatory aura is restated as non-lateralising.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

kinney-structured-testing-ictal-postictal-video-eeg-2019.pdfNarrative, educational, or cited context · 1 finding
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors report a PubMed literature review using the search terms “seizure”, “ictal”, “postictal”, “testing”, “examination”, and “interview”, followed by selection of relevant literature and references for a narrative review. The intended setting is an epilepsy long-term monitoring unit with video-EEG and ictal/postictal bedside testing. The source contains no single original cohort, unified analysis population, or uniform reference standard; cited populations and analysis units vary and are retained at the finding level when reported. Cited evidence includes video-EEG seizure series, temporal-lobe cohorts, stereo-EEG language observations, electrical cortical stimulation studies, and PNES diagnostic studies. Cohort demographics, lesion prevalence, etiology, surgery outcomes, and mortality outcomes are not reported as a unified study dataset. The review reports contextual testing metrics, including 27% of seizures assessed within 30 seconds and 50% unassessed in one UK study, and describes PNES comorbidity and induction literature; these are not treated as atlas findings.
Findings
  • Gustatory auraTable 2 associates gustatory aura with Rolandic and parietal operculum, basal/mesial temporal regions, and insula and describes it as non-lateralising.PDF p.3, Table 2

1 contributing manuscript; source-reported values remain separate and are not pooled.

ictal EEG localization in focal epilepsyDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 1 reported value
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited ictal-EEG series reports 40% correct localization and a mostly nonlateralized or uninterpretable remainder.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 1 reported value
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • ictal EEG localization in focal epilepsyIn another series of focal epilepsy, ictal EEG correctly localized 40% of seizures, while most of the remainder was nonlateralized or uninterpretable.PDF p.2, General Concepts, final paragraph before "Electroencephalography in Simple Partial Seizures"
Reported values
  • 40% correctly localizedictal EEG localization in focal epilepsyPercentage · Another focal epilepsy series; exact cohort not reported · ictalPDF p.2, General Concepts, final paragraph before "Electroencephalography in Simple Partial Seizures"

1 contributing manuscript; source-reported values remain separate and are not pooled.

Ictal retchingDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review states that ictal vomiting and retching have no definite lateralizing value.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdfNarrative, educational, or cited context · 1 finding
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document is a narrative literature review organized by a semiological classification of paroxysmal events, auras, autonomic, dialeptic, motor, special, and additional lateralizing signs. It does not report a systematic search method, eligibility criteria, aggregate review population, cohort size, comparator, or common reference standard. Individual findings retain the population, phase, comparator, and cited-study attribution stated in the review.
Findings
  • ictal vomiting and ictal retchingThe review states that ictal vomiting and retching are observed mainly in adult temporal lobe seizures, have no definite lateralizing value, and have some evidence supporting a role for the insula as visceral sensory cortex.PDF p.3, Autonomic seizures

1 contributing manuscript; source-reported values remain separate and are not pooled.

nonlateralized frontal ictal EEGDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 2 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review restates that frontal ictal EEG may be absent or nonlateralized in roughly one-third groups.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 2 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • nonlateralized frontal ictal EEGApproximately one-third of frontal lobe seizures were not accompanied by EEG changes, another one-third showed nonlateralized slowing, rhythmic activity, or repetitive spiking, and focal ictal onsets were less common in frontal than temporal seizures.PDF p.6, Frontal lobe epilepsy, paragraph beginning "Frontal lobe complex partial seizures"
Reported values
  • Another approximately one-third with nonlateralized ictal EEG patternsnonlateralized frontal ictal EEGPercentage · Patients with frontal lobe complex partial seizures; exact cohorts not reported · Nonlateralized slowing, rhythmic activity, or repetitive spiking · ictalPDF p.6, Frontal lobe epilepsy, paragraph beginning "Frontal lobe complex partial seizures"
  • Approximately one-third without ictal EEG changesnonlateralized frontal ictal EEGPercentage · Patients with frontal lobe complex partial seizures; exact cohorts not reported · No EEG change · ictalPDF p.6, Frontal lobe epilepsy, paragraph beginning "Frontal lobe complex partial seizures"

1 contributing manuscript; source-reported values remain separate and are not pooled.

parietal interictal and ictal EEGDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 3 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The review synthesis describes mixed parietal EEG patterns: lateralized, generalized, nonlateralized, and secondary bilateral synchrony.

Source-defined result groups 3
Lateralization: generalized slowing / lateralized EEG pattern / nonlateralized EEG pattern / secondary bilateral synchronySource-defined values retained separatelyAll reported · interictal versus ictal EEG; parietal-localized versus multiregional or absent correlates · patient1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyAll reported · interictal versus ictal EEG; parietal-localized versus multiregional or absent correlates · patient1 manuscript · 1 reported value · not pooled
Localization: ParietalSource-defined values retained separatelyLarge surgical series · interictal versus ictal EEG; parietal-localized versus multiregional or absent correlates · case1 manuscript · 1 reported value · not pooled
Evidence by contributing manuscript 1

Alphabetical by manuscript.

foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdfNarrative, educational, or cited context · 1 finding · 3 reported values
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This is an educational chapter rather than a single primary cohort. The general text synthesizes source-cited series involving focal epilepsy, temporal/mesial temporal epilepsy, and frontal, parietal, or occipital epilepsy, and separately presents three illustrative case observations. The source uses patients, cases, seizures, and source-defined observations as analysis units; no common cohort, eligibility rule, comparator, reference standard, or chapter-wide denominator is reported. The report retains the source's unit and missingness for each finding and does not infer denominators from percentages.
Findings
  • parietal interictal and ictal EEGParietal interictal EEG may be normal or show lateralized/generalized slowing, while epileptiform activity is often multiregional and may suggest areas distant from the epileptogenic zone; centroparietal activity as the sole interictal abnormality was reported in 5%-20%, secondary bilateral synchrony in one-third, SPS often had no EEG correlate, and localized ictal onsets occurred in 6% of a large surgical series.PDF p.7, Parietal lobe epilepsy, interictal paragraph; PDF p.9, continuation before "Electroencephalography in Occipital Lobe Epilepsy"
Reported values
  • Centroparietal activity as sole interictal abnormality 5%–20%parietal interictal and ictal EEGRange · Patients with parietal lobe epilepsy and a large surgical series; exact cohorts not reported · interictal and ictalPDF p.7, Parietal lobe epilepsy, interictal paragraph; PDF p.9, continuation before "Electroencephalography in Occipital Lobe Epilepsy"
  • Secondary bilateral synchrony in one-thirdparietal interictal and ictal EEGPercentage · Patients with parietal lobe epilepsy and a large surgical series; exact cohorts not reported · interictal and ictalPDF p.7, Parietal lobe epilepsy, interictal paragraph; PDF p.9, continuation before "Electroencephalography in Occipital Lobe Epilepsy"
  • Localized ictal onsets 6%parietal interictal and ictal EEGPercentage · Patients with parietal lobe epilepsy and a large surgical series; exact cohorts not reported · Large surgical series · interictal and ictalPDF p.7, Parietal lobe epilepsy, interictal paragraph; PDF p.9, continuation before "Electroencephalography in Occipital Lobe Epilepsy"

1 contributing manuscript; source-reported values remain separate and are not pooled.

polymodal insular representation and spatial overlapDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The authors' synthesis reports no clear hemispheric specialization in the stimulation-response distribution.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdfNarrative, educational, or cited context · 1 finding
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The authors reviewed stimulation data from 222 patients (107 women, 114 men; mean age 35.5 years, range 20-59) explored for atypical temporal or perisylvian epilepsy between March 1997 and April 2015; 669 insular sites were stimulated through transopercular electrodes orthogonal to the midsagittal plane using bipolar 50-Hz stimulation, 0.5-ms pulses, 5-second trains, and 0.2-3.5-mA intensity. Subjective reports and clinical observations were collected immediately after stimulation, with EEG and video reviewed retrospectively; stimulations in or around lesions or inducing an after-discharge were excluded, and multivariate logistic regression compared coordinates of contacts evoking each sensation with all other stimulated contacts, including non-eloquent contacts.
Findings
  • polymodal insular representation and spatial overlapThe authors synthesize that most evoked responses were body-related and usually neutral or unpleasant, with no clear hemispheric specialization; despite functional segregation, representations of different response types clearly overlapped spatially, which may support multimodal functional integration.PDF p.1, abstract; PDF p.7, Discussion

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal sighingDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

Postictal coughing or sighing is restated as non-lateralizing, with a source-described association with MTLE rather than LTLE.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdfNarrative, educational, or cited context · 1 finding
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
This source is a narrative review chapter and does not state a unified search strategy, eligibility set, enrollment cohort, or pooled analysis population. It draws on heterogeneous cited patient cohorts, seizure/event observations, imaging and EEG studies, and case reports, with emphasis on drug-resistant and presurgical temporal lobe epilepsy. Denominators, reference standards, and analysis units therefore remain study-specific; no chapter-level aggregate estimate is established.
Findings
  • postictal coughing and sighingPostictal coughing or sighing has no stated lateralizing value but is described as rare and quite specific for MTLE; these signs are usually absent in LTLE.PDF p.9, Postictal state; PDF p.9, Other signs to discriminate between LTLE and MTLE

1 contributing manuscript; source-reported values remain separate and are not pooled.

Postictal vomitingDoes not lateralizeNo directional estimate1 manuscript · 1 finding · 0 reported values
Weighted evidence supportevidence weight 1 across 1 manuscript · 1 narrative, educational, or cited context

The cited source states that postictal vomiting has no lateralizing value.

Evidence by contributing manuscript 1

Alphabetical by manuscript.

blair-temporal-lobe-epilepsy-semiology-2012.pdfNarrative, educational, or cited context · 1 finding
blair-temporal-lobe-epilepsy-semiology-2012.pdf
Narrative, educational, or cited context · Class III · Evidence weight 1.00 · 1 × 1 × 1
The document reports a narrative review and does not report a systematic-search method, single enrollment cohort, eligibility criteria, pooled analysis, or source-wide reference standard. Population descriptors are claim-specific and heterogeneous, including temporal-lobe, mesial-temporal, neocortical-temporal, frontal-versus-temporal, childhood, older-adult, benign mesial-temporal, and cited study cohorts. The review discusses 31 Engel class 1 patients in one cited symptom-cluster analysis and a 50-patient sample in one cited facial-asymmetry result; those cohort descriptors are retained only with the corresponding findings. It also reports lesion/etiologic context, including mesial temporal sclerosis or hippocampal sclerosis as a common cause of TLE and HS evidence in benign mTLE, but those context statements are not treated as stand-alone semiologic findings. No source-wide analysis unit, surgery-outcome analysis, or mortality-outcome analysis is reported. Cited-study restatements remain unverified against the cited articles under this review boundary.
Findings
  • Postictal vomitingPostictal vomiting is reported to have no lateralizing or localizing value.PDF p.5, autonomic-phenomena paragraph

1 contributing manuscript; source-reported values remain separate and are not pooled.

No lateralization reported in linked evidence 615

No lateralization relationship reported in the currently linked reviewed findings. These signs remain visible.

12-month postsurgical ILAE outcome18F-FET uptake pattern in status epilepticusabdominal epilepsy symptom profileabrupt cessation of interictal epileptiform activityabsence seizureAffective auraAffective/emotional phenomenon (unspecified type)afterdischarge (AD); evoked spike AD; local, remote, or regional ADageAge applicability of the SSCAge at onset, mesial versus neocortical focus, and aurasage-dependent frontal lobe epilepsy semiologyage-specific reliability of pediatric lateralizing signsAging and temporal-lobe seizure elaborationAkinetic seizureAlien limb phenomenon (ictal)Anarthriaanatomical and volumetric estimation of the EZ; anatomical-electroclinical correlationsanatomical correlation and rapid propagation in frontal lobe epilepsyanatomical electroclinical correlation; epileptogenic zoneanterior and posterior cingulate seizuresanterior and posterior insula manifestationsanterior and posterior insular seizure-onset-zone featuresanterior insula manifestations; posterior insula featuresanterior language area (ALA)anterior or inferomesial temporal scalp EEG with extra-temporal seizure originanterior prefrontal integrated behavior and posterior frontal elementary motor signsanterior-to-posterior interictal scalp EEG gradientAnxiety phenomenonAphasia (phase unspecified)area Spt and vocal-tract sensorimotor couplingArrest (unspecified type)Astatic seizureAsymmetric facial movementsatonic motor phenomenonAtonic seizureaudiogenic-evoked reflex seizureAuditory hallucination (unspecified content)Automatism (unspecified type)Benign mesial temporal lobe epilepsy semiologyBilateral leg elevation with cycling/pedaling movementsBilateral symmetric tonic posturingbinding; synchrony; decorrelation; rhythmic pattern generatorBipedal automatismsbipolar organization of major insular functionsBlurred visionBody-part absence illusion (asomatognosia)body-segment distribution of ictal stereotypiesBTLA as a connected language-network hubcardiac rhythm during stimulationcardiac/cardiorespiratory compromisechildhood epilepsies; infantile spasms; electrical status epilepticus during sleepcingulate cortex stimulation effects related to body perceptioncingulate emotional, interoceptive, autonomic, motor, vestibular, and visual responsescingulate epilepsy electroclinical subtypesclear hypothesis must precede the implantationclinical behavior during long-term video EEGclinical expression of seizures; seizure semiologyclinical features differentiating LTLE from MTLEclinical semiology as a lateralizing aidclinical suspicion of insulo-opercular epilepsy and need for SEEGClinical use and testing of the SSCclinically silent local discharge before network recruitmentClinically silent seizure onsetcluster 13cluster 28cluster 3clustered and scattered MEG dipolesCognitive auraCognitive phenomenon (unspecified subtype)combinations of asymmetric motor signscomparative distribution of objective emotional behaviorsComplex automatismsComplex ictal behaviorComplex ictal motor behaviorComplex ictal posturingComplex motor phenomenon (unspecified subtype)complex motor seizurecomplex partial seizuresComplex stereotyped nocturnal motor sequences (quasi-purposeful)concordance of presurgical modalitiesConfusional auraconnected spoken language production efficacyconnected spoken language production versus connected singing efficacyconsistency across repeated stimulation trials and 0 mA sham trialsconventional PET visualizationcortical dysplasia in MRI-negative surgical casescortical gustatory representationcriteria for signs used for localizationDacrystic seizures (ictal crying - associated with hypothalamic hamartoma)dipoles defined by ictal activity; grey matter (EZ); white matter (propagation pathways); over-implantation of presumed ictal onset zonedischarge frequency and positive or negative semiologyDisgust responsedorso-caudal, dorso-mid, and dorso-rostral insular focusDrop attack (mechanism unspecified)dynamic seizure semiology; spatiotemporal frameworkDysembryoplastic neuroepithelial tumours; focal epilepsydystonic seizuresearly involvement of motor or speech areas; Wernicke’s areaearly nonmotor seizure onset and nonmotor manifestation typesearly spread network / early spread zoneearly temporo-polar involvement and temporo-polar seizure onset zoneearly-onset ICA high gamma activityeating-evoked reflex seizureECS versus meta-analytic fMRI language sitesECS-defined language-site surgical marginEcstatic auraEEG findings in reviewed casesEEG localization of ictal speech disturbancesEEG patterns associated with ictal language disturbancesEEG seizure duration in PICA versus ICA-only seizuresEI-based insulo-opercular, opercular, and “pure” insular epilepsy classificationelectrical brain stimulationElectrical onset; clinical onset; completion of clinical semiology; propagationElectrical-to-clinical timing and propagation directionElectroclinical spectrum following a rostrocaudal gradientElectroclinical spectrum; integrated behavior; rostrocaudal axisemotional behaviors across cortical and subcortical seizure localizationsEpigastric rising auraepilepsy associated with BOSDepileptogenic network; anatomical electroclinical correlationepileptogenic network; symptomatogenic zoneepileptogenic zoneepileptogenic zone (EZ); focal, multilobar, hemispheric, multifocal, generalizedepileptogenic zone network and propagation zone networkepileptogenic-zone fingerprintepileptogenicity index values in opercular, insular, and SMA/MCC cortexestimated localizing and lateralizing value of semiologyetiologies underlying ictal language disturbancesetiology in aphasic status epilepticusexaggerated startle response; proprioceptive feedback; hyperexcitable motor cortexextensive resection by intracranial EEG statusextrafrontal SHE semiology pattern distributionextraoperative intracranial EEG indicationsextratemporal AS patterns by semiologyEZ markers for SEEG-guided RF-TC; low-amplitude fast pattern; seizure triggering after direct electric stimulationF to BTCF7/F8 electrode ambiguity and field localizationFalling sensationfalse-negative stimulation; false-positive errorsFamilial mesial temporal lobe seizure semiologyFCDFCD; epileptogenic zoneFCD; focal motor status; epilepsia partialis continuaFDG-PETFDG-PET focal hypermetabolismFDG-PET in MRI-negative epilepsyFeatures favouring PNESFeatures with insufficient evidence to favour PNESfirst ictal scalp-EEG change outside temporal regionsfirst recorded seizure as a representative seizurefirst SEEG ictal modifications; low-voltage fast activity; seizure onset zone; early spreadfive-dimensional, patient-oriented epilepsy classificationfocal-appearing lateralizing signs in generalized epilepsyFOIA and mesial temporal epileptogenic zoneFOIA non-motor onset (dialepsis)Four main groups of patients / electroclinical categorizationFreezing aurafrontal lobe complex partial seizure semiologyfrontal lobe epilepsy manifestations and network connectivityfrontal lobe epilepsy surgery cohort and resection profilefrontal lobe epilepsy; anterior versus posterior; mesial versus dorso-lateralfrontal SHE semiology pattern distributionFrontal-versus-mesial-temporal symptom distinctionsfrontopolar and dorsolateral frontal seizure semiologyfunctional and anatomic connections; startle responsesfunctional coupling and the “tuning” effectfunctional neuroimaging studies; startle responsesfunctional uncoupling and the “release effect”Gelastic seizureGelastic seizures - frontal/ACC origin (non-hamartoma)Gelastic seizures - temporal neocortical origin (non-hamartoma)generalised convulsive seizures; non-generalised convulsive seizuresgeneralized convulsive seizuresGeneralized myoclonic jerkingGeometric formed visual hallucinations (grids, kaleidoscope, checkerboards - without semantic content)gradual onsetGustatory aura (primary insular gustatory cortex)handednessHFO specificity and sensitivity for SOZ identificationhigh-frequency oscillations (HFOs), ripples, and fast rippleshighly epileptogenic posterior insular and opercular structures in Patient 4hippocampal discharge spread into the insulahippocampal-onset inferotemporal rhythmhistology and outcome in MRI-negative epilepsyHypermotor agitated behavior (ACC-dominant type with emotional coloring)Hypermotor vs. hypomotor distinction (primary semiological axis for lobe of origin)hypersynchronous low-frequency periodic high-amplitude spikes (HYP) and low-voltage fast discharge (LVFD)hypothalamic hamartoma-associated epilepsy; EZ independent of the hamartomaIctal anarthriaictal and interictal semiology; functional imagingIctal anomiaIctal autonomic cardiac arrhythmia (right insular predominance)Source terms: Ictal autonomic cardiac arrhythmiaictal baseline-shift dipole in the amygdala-hippocampus complexIctal behavioral changeIctal body rockingIctal consciousness in PNES and epilepsyIctal deafness / hypoacusisIctal defensive/aggressive behaviorIctal discomfort / aversive sensationictal EEG and focal ictal patterns in MRI-negative epilepsyictal EEG evolutionIctal eyelid flutterIctal facial grimacing/distortionIctal fear behaviorIctal fear or anxiety behaviorIctal forced mouth closureIctal head pursuitictal HMPAO-SPECT local hyperperfusionIctal hypotensionIctal mouth contractionIctal nauseaictal onset within MRI-visible BOSD and overlying cortexictal onset zone extending beyond the MRI-visible BOSDIctal open eyesIctal palilaliaIctal palpitationIctal perioral constrictionIctal pleasant sensationIctal prosocial behaviorictal scalp EEG electrical changeictal scalp EEG localized to lesionictal scalp-EEG patternsictal SEEG flattening, slow polarizing shift, and fast activityIctal singing or whistlingictal SPECT in MRI-negative epilepsyictal SPECT localization in frontal lobe epilepsyictal SPECT perfusion patterns in TLEIctal speech disorganizationIctal stereotyped behaviorIctal stereotyped motor behaviorIctal stridorIctal sweatingIctal tonic head versionIctal unresponsivenessIctal verbal help-seekingIctal visual obscurationIctal visual phenomenonIEH epilepsy type and demographic distributionimpaired awareness seizureimpaired consciousness seizuresinconsistent sEEG-positive language siteIndescribable auraindications and limits of SEEG; confirm a main hypothesis and eliminate alternative hypothesesindividualized anatomo-electro-clinical SEEG methodologyinduced high-frequency activity versus ECSinformational redundancyIngestive behaviorinitial fast discharge as seizure-onset areainitial versus combined set-of-semiology localization and lateralizationinsular epilepsy and seizure onsetinsular language responsesinsular seizuresinsular seizuresinsular seizures mimicking other regional seizuresinsulo-opercular seizures; semiologic subgroupsinsulo-opercular semiologic subgroupsintegrated versus non-integrated motor behavior in a 54-patient SEEG seriesIntegration of semiology with other clinical informationinterictal and ictal scalp epileptiform dischargesinterictal epileptiform focus versus ictal onsetinterictal FDG-PET localizing and lateralizing valueinterictal languageinterictal patterns, periodic/rhythmic patterns, and attenuationinterictal scalp EEG abnormalityinterictal scalp-EEG distribution and lateralizationinterictal spikes and sharp wavesinterictal spikes; continuous spikes; 1 spike every 5–10 s; 1 spike every 30–60 sinterictal spikes; irritative zone; subclinical rhythmic dischargesinterpretation of conflicting signsinterval-to-reading language testintracranial EEG status and seizure freedominvasive EEG in TLE and SEEG implantation strategyinvasive recordings in simple partial seizuresIshibashi electrical-stimulation auditory changesKim et al. cited conditional-inference-tree localization resultLaryngeal / throat constriction (tightening, strangling, pressure sensation)Source terms: Laryngeal/throat constrictionlate-onset ICA high gamma activitylatency from EEG ictal onset to hypermotor manifestationlateralized postictal slowing and background attenuationlateralized postictal slowing or background attenuationlearning pointsleft superior temporal gyrus (STG) lesion evidencelesion aetiologylesion aetiology subtypeslesion removal and symptom resolutionlesion-associated interictal EEG signatureslesional and non-lesional presurgical use of semiologylesional epilepsy; intralesional and perilesional electrodeslesional extra-temporal epilepsy; discrepancy between lesion topography and electroclinical semiologyLobar localization in frontal lobe epilepsyLobar localization in occipital lobe epilepsyLobar localization in parietal lobe epilepsyLobar localization in temporal lobe epilepsylobe localisationlocalising and lateralising value of seizure semiologyLocalization comparison with interictal EEG, ictal EEG, and MRILocalization reliability in partial and multifocal epilepsylocalized electrical depression or slowing during the post-ictal period; ictal and post-ictal clinical expressionlocalizing associations of sensory illusions and hallucinationslocalizing value of isolated signs and complete ictal sequenceslow-voltage fast discharge restricted to a malformationM, ML, and L electroclinical patternsmain hypothesis; alternative hypotheses; sampling error; number of electrodesmajor and minor stimulation symptomsmean Talairach stereotactic coordinatesmedial (M), medial-lateral (ML), and lateral (L) subtypesmedial-lateral seizures and epileptogenic-zone extentMEG spike propagation from insular subregionsMemory recall during PNES eventsmesial frontal semiology and electrocortical stimulationmesial temporal sclerosis (MTS) and mesial temporal seizure onsetMesial versus neocortical temporal aura and initial-automation distinctionmesial versus neocortical temporal seizure semiologymesial, lateral, and mesial-lateral temporal seizure typesmesio-lateral temporal seizuresMesiolateral propagation and medial premotor/cingulate pathwayMetamorphopsia (visual shape/form distortion)Source terms: MetamorphopsiaMicrodysgenesis; focal epilepsy; temporal-lobe epilepsy with hippocampal sclerosisMicrodysgenesis; idiopathic generalised epilepsiesmigraine aura-triggered seizure (migralepsy)montage, polarity reversal, and reference effectsmorphometry in self-limiting ICA versus persistent PICAmotor phenomenonmotor responses in other insular stimulation studiesMRI-negative epilepsyMRI-negative epilepsy; visible lesion after localization and MRI restudyMRI; FDG-PETMRI; hippocampal sclerosisMTLE scalp IED pattern and source modelingMTLE-like seizures in TPEMTS and mesial temporal epileptogenic zonemultimodal evaluation required for EZ predictionmultiple lesions; unique or largely predominant EZmultiple seizure typesMultisensory auramyoclonic jerkingNaming difficultyNauseaNegative cognitive-affective expressionNegative emotional expressionNegative motor phenomenaNegative myoclonusNeocortical temporal lobe seizure semiologyneocortical temporal seizure courseneocortical versus mesial temporal aura patternnetwork or focus model; symptomatogenic zonenetwork-based localization of the epileptogenic phenomenonNocturnal brief stereotyped seizures (rapid onset/offset, minimal postictal)Source terms: Nocturnal brief stereotyped seizuresNominal dysphasianon-evoked visual, motor, and deja vu sensationsNon-painful ocular sensationNon-specific auraNon-specific focal aware auranon-specificity of altered awareness and hyperkinetic motor behaviornoneloquent stimulation sitesnumber of antiseizure medications (ASMs)number of generalised convulsive seizures in the previous yearobjectives of SEEG planning; integration of presurgical assessmentobserver bias; description of semiology; recording conditionsOcular auraOculomotor phenomenaOlder-child temporal-lobe seizure semiology and age-dependent lateralizing signsOlfactory hallucination (orbitofrontal secondary olfactory cortex)One-to-one relationship between clinical-ictal semiology and EEG findingsonset, early spread, and secondary involvementopercular and perirolandic seizure semiologyoperculo-insular localization of PSS by SEEG and ESMoperculo-insular seizures; “great mimicker”operculo-insular thermal and laser stimulationOral-lingual-pharyngeal symptomsorbitofrontal-amygdala desynchronization during emotionally charged FLS onsetorolingual motor signOverall lobar localization by seizure semiologyoverall prevalence of ictal emotional symptoms or signs in prefrontal seizuresOverall seizure-semiology lateralizationoxygen desaturation duration and nadiroxygen desaturation severityO’Brien et al. cited history-plus-video distinctionPain from tonic muscle contractionPalilaliaPalinopsiaPallesthesia / vibratory aura (rare)Panayiotopoulos syndrome headache-associated seizure semiologyparietal and posterior cingulate involvement in SP1, SP2, and SP3parietal lobe epilepsyparietal SI localization of PSSParoxysmal eventParoxysmal language disturbancepathology-specific ictal SEEG patternsPCA and hierarchical clustering of semiologic scorespediatric focal syndromes and Rasmussen encephalitispediatric insular seizure semiologyPelvic thrusting / ictal sexual automatismsSource terms: Pelvic thrustingPenfield-Perot auditory responses by temporal cortical regionperi-ictal apnea durationPeri-ictal cardiac arrhythmiaPeri-ictal heart-rate changeperi-ictal hypoxaemia; hypoxaemia severityPerioral symptomsperirolandic areaperisylvian epilepsies; insula and opercula; oblique or orthogonal insular explorationperisylvian-temporal lobe epilepsyPeriventricular heterotopia with hippocampal sclerosis; pseudotemporal clinical presentationPeriventricular heterotopic nodulesperiventricular nodular heterotopia (PNH) networkPET lateralization and localizationPleasant emotional auraPNES movement and duration featuresPNES semiological specificityPolymicrogyria; surrounding cortexpoor performance of initial semiologypoorer connected singing efficacy in the more-severe deficit grouppositive and negative stimulation responses by taskpossible body-perception-related effects at other implanted structuresposterior basal temporal ictal onsetposterior cingulate seizure propagationposterior language area (PLA)posterior or extra-temporal ictal EEG onset and temporal lobectomy failurePostictal asystolePostictal bradycardiaPostictal brainstem posturingPostictal cardiac arrestpostictal EEG suppression in PICApostictal generalised EEG suppressionPostictal language testing in a cited studyPostictal psychiatric symptomsPostictal recovery of consciousnessPostictal respiratory recoveryPostictal stertorous breathingPostictal tachycardiapostoperative right hemiparesisprecentral-premotor co-involvement and lateral-to-medial projectionprecentral/premotor and lateral prefrontal/frontal-pole semiologyprefrontal seizure semiologic subgroupsprefrontal seizure subgroups; DLPFC; VLPFC; DMPFC; VMPFC; OFCPreictal autonomic dynamics in PNESpreictal-to-ictal cellular mechanismpreserved connected singing ability in severe aphasiapreserved singing ability in aphasiaPRESTIM versus POSTSTIM h2 Z-scoresprevalence of specific ILAE epilepsy syndromesprimary and associative cortexprimary motor cortex M1 and EMG couplingPrincipal Component Analysis and hierarchical clusteringProgressive speech difficultypropagation before subjective symptomsproposed mechanism and focal-origin hypothesis for ATLPpsychogenic non-epileptic paroxysmal eventspsychogenic nonepileptic events and scalp EEG caveatpsychomotor seizurepsychomotor seizuresPulling sensationputative mechanisms of semiologic productionRathke et al. cited reliability comparison in patients with two seizure focireduced interictal spiking and seizure-onset recruitment after RFTCReduced tone/hypotonia (phase unspecified)reflex seizurereflex seizuresRepetitive ictal leg movementretinotopic, tonotopic, and somatotopic organizationRetrosternal constrictionrhythmic discharges and cortical dysplasiarhythmic ictal onset in beta, theta, alpha, or delta rangesright frontal bottom-of-sulcus dysplasia (BOSD)rostro-caudal (antero-posterior) hierarchy of frontal ictal motor semiologyrostrocaudal organization of frontal semiologyRotatory body sensation (egocentric body rotation)Source terms: Rotatory body sensationscalp EEG absence, clinical onset, and deep generatorsscalp interictal epileptiform discharges from deep mesial temporal structuresscalp-recorded seizures in extratemporal focal epilepsyscalp-recorded simple partial seizuresSEEG biomarkers of the epileptogenic zoneSEEG ictal low-voltage fast activity and electrical stimulationSEEG in MRI-negative epilepsySEEG procedural safetySEEG stereotactic accuracySEEG-guided radiofrequency thermocoagulation in malformations of cortical developmentSEEG-recorded seizure sample and durationSEEG; implantation strategy; missing electrodeseizure burden during LTVEMseizure classification; site of origin; extent of spread; clinical symptomatologySeizure durationseizure duration in temporal lobe seizures with and without ICAseizure freedom after SEEG-guided surgery in MRI-negative epilepsyseizure frequencySeizure frequency in temporal-versus-frontal differentialseizure mechanismSeizure onset in temporal-versus-frontal differentialSeizure progression in temporal-versus-frontal differentialseizure propagation; symptomatogenic zoneseizure semiology and the epileptogenic zoneseizure semiology as a dynamic data sourceseizure semiology by localizationSeizure semiology in frontal lobe epilepsySeizure semiology in non-lesional patientsSeizure semiology in occipital lobe epilepsySeizure semiology in parietal lobe epilepsySeizure semiology in temporal lobe epilepsyseizure semiology; neural networksSeizure sequence and component notationseizure spread in time and spaceseizure-related MRI abnormalitiesseizure-scene analysis and data aggregationseizures triggered by stimulation; usual clinical pattern; connected regions distant from the EZseizures with impaired awarenesssemiologic hierarchy; elementary signs; complex semiologic patternssemiological seizure classificationSemiological seizure classification (SSC)semiological seizure classification applied in Cleveland and elsewheresemiology and seizure classification systemssemiology as an uncertain prognostic featuresemiology in juvenile myoclonic epilepsysemiology of focal seizures; anatomical-electroclinical correlationsSensorial, consciousness, autonomic, and motor spheresSensory epilepsia partialis continuasequences prior to secondary generalizationSerles et al. cited comparison of surface EEG and seizure semiologysexSimple and complex motor seizuresimple motor seizuresimple motor seizuressimultaneous Video-EEG recordingsinusoidal activity and repetitive epileptiform dischargesSleep activation in temporal-versus-frontal differentialSleep-wake reliability of temporal-lobe semiologySomatosensory Jacksonian march (sensory spread through somatotopic map)Source terms: Somatosensory Jacksonian marchsomatosensory-evoked reflex seizureSP1 broad cortical localization synthesisSP2 and SP3 nonspecific localization and asymmetric featuresSP4 localization synthesisSP4-like semiology with a parietal SOZspatial hierarchy of semiology with respect to cortical localizationspecificity of insular seizure semiologySpeech arrest / ictal mutism (dominant SMA, inhibitory)speech assessment timing and protocolspeech entrainmentSpeech slowingspike–jerk temporal correspondencespoken repetition efficacyspontaneous seizure reproducing the known semiology; seizure homogeneitystartle-induced seizures; parieto-frontal networkstatus epilepticusstereotactic radiofrequency lesioning of solitary PNHStereotypy of PNESstimulation thresholdstimulation trials with afterdischarge; potentially nonfocal effectstimulation-induced seizures; naturally occurring events; epileptogenic and functional networksstrong hypothesis and clear objectivestructural abnormalities on preoperative MRIstructural lesions in testing of seizures with postictal language functionsubclinical seizures and habitual seizures after low-frequency stimulation; hippocampal reproduced habitual seizureSubjective auraSubjective ictal symptomssulcal cortical zones; insulo-opercular system; limbic system; periventricular heterotopia; hypothalamic hamartomasung repetition efficacysuperior temporal gyrus seizure and postictal dysfunction hypothesissuperior temporal gyrus stimulation in prior cases and thought-word noveltysurface electrodes and lesion depthsurgery and seizure outcome in MRI-negative versus MRI-positive epilepsysurvey of 15 French centers regularly performing SEEGSVT accuracy by resection type and siteSVT prediction accuracy and seizure outcomeSVT prediction for elementary motor and hyperkinetic manifestationsSVT prediction scores by MRI abnormality categorySYM versus NS h2 pairwise structure correlationsSymptom progression and frontal-temporal differentiationsymptomatogenic zonesymptomatogenic zone and dynamic interactionsymptomatogenic zone and epileptogenic zonesymptomatogenic zone and seizure propagationsymptoms from functionally silent cortexsynchronized video; detailed and global seizure semiology; EMG polygraphytailored insulo-opercular, insular, and opercular resection; postoperative seizure freedomtask-specific positive sites in ALA and PLAtemporal and suprasylvian opercular seizure onsettemporal ictal EEG localizationtemporal intermittent rhythmic delta activity (TIRDA)temporal lobe epilepsy (TLE) among PICA patientstemporal lobe epilepsy associated with hippocampal sclerosistemporal lobe lesiontemporal lobe seizure onsettemporal lobe seizure subtypes; mesial type; lateral type; mesial-lateral typetemporal lobe seizurestemporal plus epilepsytemporal SEEG seizure with delayed clinical onsettemporal seizure-onset-zone localization in auditory seizurestemporal SOZ patterns by AS semiologytemporal-lobe predominance of lesions outside stimulationtemporo-insular seizure onsettemporo-lateral SEEG onset without medial propagationtemporo-parietal ictal symptoms with inferomesial temporal EEGThoracic heavinessThreat/fear behaviorThree sub-lobar language patternstime from SEEG seizure onset to ICA onset and epileptogenic zonetime from SEEG seizure onset to ICA onset and seizure onset zoneTIRDA (Temporal Intermittent Rhythmic Delta Activity) - scalp EEG interictaltonic face or neck posturingtonic neck posturingtotal time of peri-ictal respiratory alterationTuxhorn cited sensory-aura localization observationtypes of evoked sensationsTypical dialeptic seizureunilateral hypometabolism on PET/MRI coregistrationusual seizure semiologyversion interobserver agreementVestibular / vertiginous aura (PIVC component)vestibular stimulation responses versus vestibular ictal symptomsvideo-EEG event count and concordancevisual seizuresVocal automatismsWhole-group occurrence of ictal signsWilliamson cited occipital seizure spread patterns“Pure” premotor seizures
Reviewed Evidence Library4,120 findings · 4,518 reported results · 73 manuscripts
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Source Library — 73 Manuscripts
alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf
193 findings · 92 reported results · 1 reviewed source file
Reviewed source files
  • alim-marvasti-probabilistic-landscape-seizure-semiology-localizing-values-2022.pdf15 pages · CANONICAL REVIEWED VERSION
alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf
105 findings · 71 reported results · 1 reviewed source file
Reviewed source files
  • alkawadri-cingulate-epilepsy-three-electroclinical-subtypes-surgical-outcomes-2013.pdf8 pages · CANONICAL REVIEWED VERSION
aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf
24 findings · 29 reported results · 1 reviewed source file
Reviewed source files
  • aron-jonas-language-mapping-stereo-electroencephalography-review-expert-opinion-2021.pdf12 pages · CANONICAL REVIEWED VERSION
asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf
97 findings · 91 reported results · 1 reviewed source file
Reviewed source files
  • asadollahi-drug-resistant-parietal-lobe-epilepsy-clinical-manifestations-surgery-outcome-2017.pdf5 pages · CANONICAL REVIEWED VERSION
barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf
86 findings · 285 reported results · 1 reviewed source file
Reviewed source files
  • barba-temporal-plus-epilepsy-clinical-scalp-eeg-2007.pdf11 pages · CANONICAL REVIEWED VERSION
bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf
143 findings · 99 reported results · 1 reviewed source file
Reviewed source files
  • bartolomei-clinical-anatomical-characteristics-basal-temporal-seizures-systematic-review-2025.pdf11 pages · CANONICAL REVIEWED VERSION
blair-temporal-lobe-epilepsy-semiology-2012.pdf
66 findings · 11 reported results · 1 reviewed source file
Reviewed source files
  • blair-temporal-lobe-epilepsy-semiology-2012.pdf10 pages · CANONICAL REVIEWED VERSION
bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf
28 findings · 124 reported results · 2 reviewed source files
Reviewed source files
  • bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-46edb4.pdf14 pages · ALTERNATE REVIEWED VERSION
  • bonini-frontal-lobe-seizures-clinical-semiology-localization-2014-838eb8.pdf14 pages · CANONICAL REVIEWED VERSION
buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf
50 findings · 18 reported results · 1 reviewed source file
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  • buonocore-ictal-semiology-sma-pre-sma-systematic-review-meta-analysis-2025.pdf10 pages · CANONICAL REVIEWED VERSION
chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf
319 findings · 268 reported results · 1 reviewed source file
Reviewed source files
  • chassoux-ictal-semiology-anterior-cingulate-epilepsy-systematic-review-2025.pdf18 pages · CANONICAL REVIEWED VERSION
chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf
30 findings · 9 reported results · 1 reviewed source file
Reviewed source files
  • chauvel-mcgonigal-emergence-semiology-epileptic-seizures-2014.pdf10 pages · CANONICAL REVIEWED VERSION
chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf
105 findings · 40 reported results · 2 reviewed source files
Reviewed source files
  • chowdhury-localisation-focal-epilepsy-practical-guide-2021.pdf12 pages · CANONICAL REVIEWED VERSION
  • chowdhury-localisation-in-focal-epilepsy-practical-guide-2021.pdf12 pages · ALTERNATE REVIEWED VERSION
cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf
22 findings · 137 reported results · 1 reviewed source file
Reviewed source files
  • cossette-roberge-localizing-lateralizing-auditory-phenomena-seizures-2023.pdf12 pages · CANONICAL REVIEWED VERSION
despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf
111 findings · 89 reported results · 1 reviewed source file
Reviewed source files
  • despins-semiology-seizures-involving-orbitofrontal-cortex-2025.pdf8 pages · CANONICAL REVIEWED VERSION
doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf
318 findings · 114 reported results · 1 reviewed source file
Reviewed source files
  • doerrfuss-ictal-semiology-lateral-temporal-epilepsy-systematic-review-meta-analysis-2026.pdf12 pages · CANONICAL REVIEWED VERSION
e236615-full.pdf
28 findings · 47 reported results · 1 reviewed source file
Reviewed source files
  • e236615-full.pdf5 pages · CANONICAL REVIEWED VERSION
elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf
32 findings · 192 reported results · 1 reviewed source file
Reviewed source files
  • elwan-kotagal-lateralizing-localizing-seizure-semiology-2018.pdf6 pages · CANONICAL REVIEWED VERSION
enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf
32 findings · 16 reported results · 1 reviewed source file
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  • enatsu-posterior-cingulate-epilepsy-clinical-neurophysiological-analysis-2014.pdf7 pages · CANONICAL REVIEWED VERSION
epilepsy-fellowship-handbook-semiologyreferences.pdf
24 findings · 0 reported results · 1 reviewed source file
Reviewed source files
  • epilepsy-fellowship-handbook-semiologyreferences.pdf3 pages · CANONICAL REVIEWED VERSION
fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf
34 findings · 72 reported results · 1 reviewed source file
Reviewed source files
  • fakhoury-right-left-temporal-lobe-clinical-features-1994.pdf7 pages · CANONICAL REVIEWED VERSION
foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf
34 findings · 65 reported results · 1 reviewed source file
Reviewed source files
  • foldvary-focal-epilepsy-surgical-evaluation-comprehensive-clinical-neurophysiology-2000.pdf16 pages · CANONICAL REVIEWED VERSION
foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf
62 findings · 43 reported results · 1 reviewed source file
Reviewed source files
  • foldvary-schaefer-localizing-lateralizing-auras-seizures-2011.pdf7 pages · CANONICAL REVIEWED VERSION
frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf
47 findings · 34 reported results · 1 reviewed source file
Reviewed source files
  • frazzini-cousyn-navarro-semiology-eeg-neuroimaging-temporal-lobe-epilepsies-2022.pdf30 pages · CANONICAL REVIEWED VERSION
gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf
28 findings · 90 reported results · 1 reviewed source file
Reviewed source files
  • gabr-speech-manifestations-lateralization-temporal-lobe-seizures-1989.pdf6 pages · CANONICAL REVIEWED VERSION
gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf
20 findings · 63 reported results · 1 reviewed source file
Reviewed source files
  • gibbs-clinical-features-sleep-related-hypermotor-epilepsy-2019.pdf11 pages · CANONICAL REVIEWED VERSION
gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf
142 findings · 92 reported results · 1 reviewed source file
Reviewed source files
  • gokce-samar-ictal-semiology-fronto-opercular-epilepsy-systematic-review-2026.pdf11 pages · CANONICAL REVIEWED VERSION
hauser-incidence-epilepsy-unprovoked-seizures-rochester-1935-1984-1993.pdf
0 findings · 0 reported results · 1 reviewed source file
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  • hauser-incidence-epilepsy-unprovoked-seizures-rochester-1935-1984-1993.pdf16 pages · CANONICAL REVIEWED VERSION
hickok-poeppel-cortical-organization-speech-processing-2007.pdf
16 findings · 2 reported results · 1 reviewed source file
Reviewed source files
  • hickok-poeppel-cortical-organization-speech-processing-2007.pdf10 pages · CANONICAL REVIEWED VERSION
hwang-painful-seizures-review-ictal-pain-2019.pdf
40 findings · 37 reported results · 1 reviewed source file
Reviewed source files
  • hwang-painful-seizures-review-ictal-pain-2019.pdf7 pages · CANONICAL REVIEWED VERSION
ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf
15 findings · 10 reported results · 1 reviewed source file
Reviewed source files
  • ictal-paraphasia-atypical-temporal-lobe-epilepsy.pdf5 pages · CANONICAL REVIEWED VERSION
ictal-speech-disturbance-cerebral-dominance.pdf
18 findings · 50 reported results · 1 reviewed source file
Reviewed source files
  • ictal-speech-disturbance-cerebral-dominance.pdf6 pages · CANONICAL REVIEWED VERSION
isnard-french-guidelines-stereoelectroencephalography-2018.pdf
30 findings · 13 reported results · 1 reviewed source file
Reviewed source files
  • isnard-french-guidelines-stereoelectroencephalography-2018.pdf9 pages · CANONICAL REVIEWED VERSION
jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdf
9 findings · 10 reported results · 1 reviewed source file
Reviewed source files
  • jain-bottom-of-sulcus-dysplasia-surgical-outcomes-2021.pdf11 pages · CANONICAL REVIEWED VERSION
jobst-insula-and-its-epilepsies-2019.pdf
155 findings · 28 reported results · 1 reviewed source file
Reviewed source files
  • jobst-insula-and-its-epilepsies-2019.pdf11 pages · CANONICAL REVIEWED VERSION
khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf
54 findings · 108 reported results · 1 reviewed source file
Reviewed source files
  • khoo-semiology-epileptogenic-zone-frontal-surgery-2023.pdf7 pages · CANONICAL REVIEWED VERSION
kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf
79 findings · 21 reported results · 1 reviewed source file
Reviewed source files
  • kinney-structured-testing-ictal-postictal-video-eeg-2019.pdf10 pages · CANONICAL REVIEWED VERSION
kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf
34 findings · 65 reported results · 1 reviewed source file
Reviewed source files
  • kotagal-asymmetric-tonic-limb-posturing-secondarily-generalized.pdf6 pages · CANONICAL REVIEWED VERSION
lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdf
29 findings · 100 reported results · 1 reviewed source file
Reviewed source files
  • lacuey-ictal-central-apnea-predictive-mesial-temporal-seizure-onset-2024.pdf23 pages · CANONICAL REVIEWED VERSION
laoprasert-stereoelectroencephalography-seeg-mset-2018.pdf
38 findings · 85 reported results · 1 reviewed source file
Reviewed source files
  • laoprasert-stereoelectroencephalography-seeg-mset-2018.pdf93 pages · CANONICAL REVIEWED VERSION
loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdf
10 findings · 10 reported results · 1 reviewed source file
Reviewed source files
  • loddenkemper-five-dimensional-patient-oriented-epilepsy-classification-2005.pdf9 pages · CANONICAL REVIEWED VERSION
loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf
117 findings · 232 reported results · 1 reviewed source file
Reviewed source files
  • loddenkemper-lateralizing-signs-during-seizures-in-focal-epilepsy-2005.pdf17 pages · CANONICAL REVIEWED VERSION
luders-semiological-seizure-classification-1998.pdf
68 findings · 13 reported results · 2 reviewed source files
Reviewed source files
  • luders-semiological-seizure-classification-1998.pdf8 pages · ALTERNATE REVIEWED VERSION
  • luders-semiological-seizure-classification-1998.pdf8 pages · CANONICAL REVIEWED VERSION
maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf
58 findings · 164 reported results · 1 reviewed source file
Reviewed source files
  • maillard-semiologic-electrophysiologic-temporal-seizure-subtypes-2004.pdf10 pages · CANONICAL REVIEWED VERSION
marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf
12 findings · 99 reported results · 1 reviewed source file
Reviewed source files
  • marashly-ictal-motor-sequences-lateralization-localization-values-2016.pdf23 pages · CANONICAL REVIEWED VERSION
mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf
36 findings · 145 reported results · 1 reviewed source file
Reviewed source files
  • mazzola-electrical-stimulation-human-insula-ictal-semiology-2017.pdf8 pages · CANONICAL REVIEWED VERSION
mcgonigal-frontal-lobe-seizures-overview-update-2022.pdf
16 findings · 4 reported results · 1 reviewed source file
Reviewed source files
  • mcgonigal-frontal-lobe-seizures-overview-update-2022.pdf9 pages · CANONICAL REVIEWED VERSION
mcgonigal-on-seizure-semiology-2021-5ba29d.pdf
55 findings · 71 reported results · 2 reviewed source files
Reviewed source files
  • mcgonigal-on-seizure-semiology-2021-5ba29d.pdf17 pages · ALTERNATE REVIEWED VERSION
  • mcgonigal-on-seizure-semiology-2021-9127f2.pdf17 pages · CANONICAL REVIEWED VERSION
meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf
30 findings · 98 reported results · 1 reviewed source file
Reviewed source files
  • meletti-persistent-postictal-central-apnea-focal-seizures-2025.pdf12 pages · CANONICAL REVIEWED VERSION
misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf
38 findings · 30 reported results · 1 reviewed source file
Reviewed source files
  • misulis-sonmezturk-ess-abou-khalil-atlas-eeg-seizure-semiology-management-3e-2022.pdf473 pages · CANONICAL REVIEWED VERSION
montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf
14 findings · 8 reported results · 1 reviewed source file
Reviewed source files
  • montavont-ictal-dysprosody-nondominant-frontal-operculum-2005.pdf5 pages · CANONICAL REVIEWED VERSION
moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf
93 findings · 63 reported results · 1 reviewed source file
Reviewed source files
  • moser-chapeau-de-gendarme-sign-focal-epilepsy-systematic-review-2025.pdf16 pages · CANONICAL REVIEWED VERSION
oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf
113 findings · 81 reported results · 1 reviewed source file
Reviewed source files
  • oane-ictal-semiology-temporo-frontal-epilepsy-systematic-review-meta-analysis-2025.pdf16 pages · CANONICAL REVIEWED VERSION
ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf
17 findings · 75 reported results · 1 reviewed source file
Reviewed source files
  • ochoa-urrea-sudep-risk-markers-prospective-cohort-2025.pdf11 pages · CANONICAL REVIEWED VERSION
palinacousis-seven-new-cases.pdf
18 findings · 16 reported results · 1 reviewed source file
Reviewed source files
  • palinacousis-seven-new-cases.pdf4 pages · CANONICAL REVIEWED VERSION
pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf
22 findings · 12 reported results · 1 reviewed source file
Reviewed source files
  • pana-nguyen-operculo-insular-epilepsy-stereo-eeg-2020.pdf18 pages · CANONICAL REVIEWED VERSION
pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf
13 findings · 14 reported results · 1 reviewed source file
Reviewed source files
  • pitkaniemi-hodological-organization-spoken-language-production-singing-2023.pdf12 pages · CANONICAL REVIEWED VERSION
popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf
16 findings · 23 reported results · 1 reviewed source file
Reviewed source files
  • popa-illusory-own-body-perceptions-cingulate-cortex-intracranial-stimulation-2019.pdf14 pages · CANONICAL REVIEWED VERSION
roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf
26 findings · 69 reported results · 1 reviewed source file
Reviewed source files
  • roh-lateralizing-value-ictal-behaviors-temporal-lobe-epilepsy-1996.pdf8 pages · CANONICAL REVIEWED VERSION
salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf
110 findings · 65 reported results · 1 reviewed source file
Reviewed source files
  • salanova-occipital-lobe-epilepsy-electroclinical-manifestations-42-patients-1992.pdf26 pages · CANONICAL REVIEWED VERSION
salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf
108 findings · 90 reported results · 1 reviewed source file
Reviewed source files
  • salanova-parietal-lobe-epilepsy-clinical-manifestations-outcome-1995.pdf21 pages · CANONICAL REVIEWED VERSION
schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf
55 findings · 25 reported results · 1 reviewed source file
Reviewed source files
  • schulze-bonhage-semiology-temporo-polar-mediolateral-temporal-origin-systematic-review-2025.pdf9 pages · CANONICAL REVIEWED VERSION
serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf
20 findings · 73 reported results · 1 reviewed source file
Reviewed source files
  • serafetinides-falconer-speech-disturbances-temporal-lobe-seizures-100-patients-1963.pdf14 pages · CANONICAL REVIEWED VERSION
simone-anatomo-functional-organization-insular-networks-2025.pdf
4 findings · 0 reported results · 1 reviewed source file
Reviewed source files
  • simone-anatomo-functional-organization-insular-networks-2025.pdf22 pages · CANONICAL REVIEWED VERSION
sisodiya-malformations-cortical-development-epilepsy-2004.pdf
9 findings · 1 reported result · 1 reviewed source file
Reviewed source files
  • sisodiya-malformations-cortical-development-epilepsy-2004.pdf10 pages · CANONICAL REVIEWED VERSION
suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf
23 findings · 9 reported results · 1 reviewed source file
Reviewed source files
  • suzuki-sensory-motor-networks-reflex-seizure-case-report-2017.pdf4 pages · CANONICAL REVIEWED VERSION
trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf
28 findings · 11 reported results · 1 reviewed source file
Reviewed source files
  • trebuchon-drane-electrical-stimulation-functional-mapping-seeg-2025.pdf25 pages · CANONICAL REVIEWED VERSION
tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf
43 findings · 13 reported results · 1 reviewed source file
Reviewed source files
  • tufenkjian-luders-seizure-semiology-localizing-epileptogenic-zone-2012.pdf8 pages · CANONICAL REVIEWED VERSION
unterberger-epileptic-aphasia-critical-appraisal-2021.pdf
29 findings · 10 reported results · 1 reviewed source file
Reviewed source files
  • unterberger-epileptic-aphasia-critical-appraisal-2021.pdf8 pages · CANONICAL REVIEWED VERSION
wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf
25 findings · 65 reported results · 1 reviewed source file
Reviewed source files
  • wang-electroclinical-insulo-opercular-epilepsy-seeg-pet-2019.pdf13 pages · CANONICAL REVIEWED VERSION
wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf
66 findings · 29 reported results · 1 reviewed source file
Reviewed source files
  • wang-hypermotor-seizures-temporal-pole-lesions-2008.pdf6 pages · CANONICAL REVIEWED VERSION
wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf
105 findings · 21 reported results · 1 reviewed source file
Reviewed source files
  • wang-phenotypic-spectrum-occipital-lobe-epilepsy-seeg-network-classification-2026.pdf17 pages · CANONICAL REVIEWED VERSION
wyllie1986.pdf
16 findings · 154 reported results · 1 reviewed source file
Reviewed source files
  • wyllie1986.pdf7 pages · CANONICAL REVIEWED VERSION
zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf
10 findings · 5 reported results · 1 reviewed source file
Reviewed source files
  • zhang-ipsiversive-ictal-eye-deviation-temporal-epilepsy-2017.pdf10 pages · CANONICAL REVIEWED VERSION
Abbreviations and Terminology
EZ = Epileptogenic Zone
MTLE = Mesial Temporal Lobe Epilepsy
NFLE = Nocturnal Frontal Lobe Epilepsy
SEEG = Stereoelectroencephalography
SDE = Subdural Electrode (grid/strip)
OFC = Orbitofrontal Cortex
ACC = Anterior Cingulate Cortex
SMA = Supplementary Motor Area
SSMA = Supplementary Sensorimotor Area
FEF = Frontal Eye Field (BA 8)
TPJ = Temporo-Parietal Junction
PIVC = Parieto-Insular Vestibular Cortex
STG/MTG/ITG = Sup./Mid./Inf. Temporal Gyrus
SPL/IPL = Sup./Inf. Parietal Lobule
S1/S2 = 1°/2° Somatosensory Cortex
M1 = Primary Motor Cortex
V1-V5 = Visual areas (calcarine→MT/V5)
BATS = Bilateral Asymmetric Tonic Seizure
AP sign = Automatism + Posturing (temporal)
M2E = Mouth-to-hand automatism (SMA)
AAPR = Automatism w/ preserved responsiveness
TIRDA = Temporal Intermittent Rhythmic Delta
SUDEP = Sudden Unexplained Death in Epilepsy
PPV = Positive Predictive Value
OBE = Out-of-Body Experience
GTCS = Generalized Tonic-Clonic Seizure
BG = Basal Ganglia
Publication changelog
v1.4.8 data
  • Corrected relationships among equivalent semiology terms and clinical classifications.
  • Corrected links among lateralization, localization, anatomical regions, Brodmann areas, and supporting publications.
  • Aligned regional browsing, weighted evidence summaries, reviewed evidence, and source views so they use the same reviewed relationships.
  • Applied active search, controlled Phase of Seizure categories (including Stimulation induced), lateralization, evidence filters, and non-region organization to Brodmann-map signs, counts, density, and highlighted signs; a small filter indicator names the active constraints and confirms Brain Region is not applied. On mobile, a visible Clear control resets the search and map selection, and the page header and persistent controls remain below the device status area.
  • v1.4 Consolidated regional, classification, reviewed-evidence, study-result, weighted-evidence, and source views.
  • v1.0–1.3 Published the atlas, expanded source coverage and evidence summaries, and introduced search tools and interactive Brodmann maps.