Evidence map›Paper›PMID 42490296›Full record

ArticleEpilepsia2026

Characterizing chapeau de gendarme in pediatric epilepsy through systematic video-EEG evaluation.

Hanna Barbara Brinkmann, Lea Nakamura, Jan Schönberger, Julia Jacobs, Victoria San Antonio-Arce, Kerstin Alexandra Klotz

Abstract read
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Article in Epilepsia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hanna Barbara BrinkmannDepartment of Neuropediatrics and Muscle Disorders, Center for Pediatrics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Lea NakamuraDepartment of Neuropediatrics and Muscle Disorders, Center for Pediatrics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Jan SchönbergerDepartment of Neuropediatrics and Muscle Disorders, Center for Pediatrics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Julia JacobsDepartment of Neuropediatrics and Muscle Disorders, Center for Pediatrics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Victoria San Antonio-ArceEpilepsy Center, Medical Center, Member of the European Reference Network for Rare and Complex Epilepsies EpiCARE, Faculty of Medicine University of Freiburg, University of Freiburg, Freiburg im Breisgau, Germany.ORCID https://orcid.org/0000-0002-2780-6560
Kerstin Alexandra KlotzDepartment of Neuropediatrics and Muscle Disorders, Center for Pediatrics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.ORCID https://orcid.org/0000-0002-1601-5384

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveChapeau de gendarme (CdG) is a subtle but clinically relevant semiology that has been scarcely studied in children. Previous studies have primarily focused on its localizing value in small, surgical cohorts. This study aimed to systematically characterize frequency and clinical features of CdG across the pediatric age spectrum.

methodsWe retrospectively analyzed video-electroencephalography (EEG) monitoring of 264 children with epilepsy (0-17 years). Up to 10 seizures per type were reviewed per patient. CdG was defined as a symmetrical downward contraction of both mouth corners and chin contraction lasting ≥5 s. CdG characteristics, co-occurring semiologies, and EEG patterns were assessed and compared to the cohort without CdG.

resultsCdG was identified in 28 of 264 patients (10.6%), corresponding to 73 seizures. The median age at first observed CdG was 12.3 years (range 1.3-16.8), with a trend toward increasing frequency in older children. All but one case occurred in focal epilepsies, which were significantly more frequent in the CdG cohort than in those without CdG (p = .009). CdG appeared early in the seizure course (≤5 s in 61.6%) and more often during sleep (p < .001). Hyperkinetic behavior occurred significantly more often in CdG seizures (p < .001). Progression to bilateral tonic-clonic seizures was recorded in 20.5% of CdG seizures (17.9% of patients with CdG) and occurred more frequently in the CdG cohort than in patients without CdG (p < .001). The first ictal scalp EEG pattern most frequently involved the frontal lobe (57.7%). SIGNIFICANCE: CdG occurred in a notable proportion of pediatric patients across the entire age range, with a descriptive tendency toward higher occurrence in older children. These findings provide an essential foundation for future investigations exploring developmental and network mechanisms underlying this semiology.

Indexed as

ElectroencephalographyEpilepsySeizuresAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesVideo Recordingfocal epilepsyhyperkineticictal poutingsemiology

Identifiers

PMID42490296
PMCPMC13675766

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