Monocular Epileptic Opsoclonus in a Patient with Alternating Hemiplegia of Childhood and ATP1A3 Mutation (P11-9.015)

To present a novel case of monocular epileptic opsoclonus (MEO) in an 18-year-old male with a confirmed ATP1A3 gene mutation and Alternating Hemiplegia of Childhood (AHC).

Authors

Osman Farooq (ORCID: https://orcid.org/0000-0001-7668-0098)
H. Foster
Ping Li (ORCID: https://orcid.org/0000-0001-8490-6640)
Alexus Ludwig (ORCID: https://orcid.org/0009-0007-5869-3355)
Margil Ranpariya (ORCID: https://orcid.org/0009-0008-7576-1142)

Institutions

University at Buffalo, State University of New York (US)

Publication Details

Journal: Neurology
Published: 2025-04-07
DOI: https://doi.org/10.1212/wnl.0000000000211291
Primary Topic: Epilepsy research and treatment
Type: article
Field-Weighted Citation Impact: 0.00

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article

Monocular Epileptic Opsoclonus in a Patient with Alternating Hemiplegia of Childhood and ATP1A3 Mutation (P11-9.015)

Osman Farooq, H. Foster, Ping Li, Alexus Ludwig et al.

Apr 7, 2025

Neurology

Epilepsy research and treatment

article

Monocular Epileptic Opsoclonus in a Patient with Alternating Hemiplegia of Childhood and ATP1A3 Mutation (P11-9.015)

Osman Farooq, H. Foster, Ping Li, Alexus Ludwig, Margil Ranpariya

April 7, 2025article en

Abstract

To present a novel case of monocular epileptic opsoclonus (MEO) in an 18-year-old male with a confirmed ATP1A3 gene mutation and Alternating Hemiplegia of Childhood (AHC).

NeurologyVol. 104(7_Supplement_1)

University at Buffalo, State University of New York (US)

Good health and well-being

Openalex Percentile: Top 91%

Epilepsy research and treatment

DOI Source OpenAlex

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Monocular Epileptic Opsoclonus in a Patient with Alternating Hemiplegia of Childhood and ATP1A3 Mutation (P11-9.015) — Osman Farooq, H. Foster, et al. · Neurology (2025) | TGRS Research Map | TGRS