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