Explosive‐Onset Epilepsia Partialis Continua and Chorea

This 2-year-old neurodevelopmentally normal boy presented with abrupt onset of multiple leg clonic seizures with retained awareness (Video 1). Video-electroencephalography confirmed epileptic spikes and ictal onset arising from the vertex region, with an otherwise normal background. Initially controlled with levetiracetam, the seizures evolved to right leg epilepsia partialis continua (EPC). Two weeks later, he developed a hyperkinetic movement disorder reminiscent of chorea-ballismus. One week later, he exhibited developmental regression with encephalopathy, mutism, and insomnia. Anti-N-methyl-d-aspartate receptor (anti-NMDAR) antibody was positive in serum and cerebrospinal fluid, and oligoclonal bands were present. He received intravenous high-dose steroids and intravenous immune globulin and had incremental improvement. By 9 weeks from presentation he had made a remarkable recovery with almost complete symptom resolution. The vast majority (95%) of children with anti-NMDAR encephalitis will develop a movement disorder, most commonly orofacial-lingual dyskinesias, but these may manifest broadly as chorea, athetosis, ballismus, dystonia, stereotypies, opisthotonus, oculogyric crisis, or bradykinesia [1]. Compared with adults, EPC and movement disorders occur more often as the initial presenting manifestation in children [2]. A diagnosis of anti-NMDAR encephalitis should be considered in young children with new-onset movement disorders and seizures (in particular, EPC), even in the absence of classically associated psychiatric or cognitive symptoms. Peter F. Sarnacki: conceptualization, investigation, writing–original draft, methodology, visualization, writing–review and editing, formal analysis, project administration, data curation. Gary Hsich: investigation, visualization, supervision, writing–review and editing. Aaron Abrams: conceptualization, writing–review and editing, visualization, supervision. Sumit Parikh: conceptualization, writing–review and editing, visualization, supervision. The authors declare no conflicts of interest.

Authors

Institutions

Publication Details

Journal
Annals of the Child Neurology Society
Published
2025-02-20
DOI
https://doi.org/10.1002/cns3.20106
Primary Topic
Autoimmune Neurological Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Explosive‐Onset Epilepsia Partialis Continua and Chorea

Sumit Parikh, Gary Hsich, Aaron Abrams, Peter F. Sarnacki
Annals of the Child Neurology Society
Autoimmune Neurological Disorders and Treatments
article

Explosive‐Onset Epilepsia Partialis Continua and Chorea

Sumit Parikh, Gary Hsich, Aaron Abrams, Peter F. Sarnacki
article en

Abstract

This 2-year-old neurodevelopmentally normal boy presented with abrupt onset of multiple leg clonic seizures with retained awareness (Video 1). Video-electroencephalography confirmed epileptic spikes and ictal onset arising from the vertex region, with an otherwise normal background. Initially controlled with levetiracetam, the seizures evolved to right leg epilepsia partialis continua (EPC). Two weeks later, he developed a hyperkinetic movement disorder reminiscent of chorea-ballismus. One week later, he exhibited developmental regression with encephalopathy, mutism, and insomnia. Anti-N-methyl-d-aspartate receptor (anti-NMDAR) antibody was positive in serum and cerebrospinal fluid, and oligoclonal bands were present. He received intravenous high-dose steroids and intravenous immune globulin and had incremental improvement. By 9 weeks from presentation he had made a remarkable recovery with almost complete symptom resolution. The vast majority (95%) of children with anti-NMDAR encephalitis will develop a movement disorder, most commonly orofacial-lingual dyskinesias, but these may manifest broadly as chorea, athetosis, ballismus, dystonia, stereotypies, opisthotonus, oculogyric crisis, or bradykinesia [1]. Compared with adults, EPC and movement disorders occur more often as the initial presenting manifestation in children [2]. A diagnosis of anti-NMDAR encephalitis should be considered in young children with new-onset movement disorders and seizures (in particular, EPC), even in the absence of classically associated psychiatric or cognitive symptoms. Peter F. Sarnacki: conceptualization, investigation, writing–original draft, methodology, visualization, writing–review and editing, formal analysis, project administration, data curation. Gary Hsich: investigation, visualization, supervision, writing–review and editing. Aaron Abrams: conceptualization, writing–review and editing, visualization, supervision. Sumit Parikh: conceptualization, writing–review and editing, visualization, supervision. The authors declare no conflicts of interest.

Annals of the Child Neurology SocietyVol. 3(1)
Cleveland Clinic (US)
Openalex Percentile: Top 95%
Autoimmune Neurological Disorders and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Explosive‐Onset Epilepsia Partialis Continua and Chorea — Sumit Parikh, Gary Hsich, et al. · Annals of the Child Neurology Society (2025) | TGRS Research Map | TGRS