Efficacy of Antiseizure Medications in Wolf-Hirschhorn Syndrome.


Journal

Neuropediatrics
ISSN: 1439-1899
Titre abrégé: Neuropediatrics
Pays: Germany
ID NLM: 8101187

Informations de publication

Date de publication:
10 2023
Historique:
medline: 21 9 2023
pubmed: 20 4 2023
entrez: 19 04 2023
Statut: ppublish

Résumé

Wolf-Hirschhorn syndrome (WHS) is caused by deletion of the terminal region of chromosome 4 short arm and is frequently associated with intractable epilepsy. This article evaluates the clinical features of epileptic seizures in WHS and the therapeutic efficacy of oral antiseizure medications (ASMs). Patients with WHS who were treated for epilepsy at the Saitama Children's Medical Center under 5 years of age were included. WHS was diagnosed based on genetic tests and clinical symptoms. Medical records regarding the age of onset of epilepsy, seizure type, treatment of status epilepticus (SE), and effectiveness of ASMs were retrospectively reviewed. Oral ASMs were considered effective when seizures were reduced by at least 50% compared with the premedication level. Eleven patients were included in the study. The median age at the onset of epilepsy was 9 months (range: 5-32 months). Unknown-onset bilateral tonic-clonic seizure was the most common type of seizure, occurring in 10 patients. Focal clonic seizures occurred in four patients. Ten patients exhibited recurrent episodes of SE, and its frequency during infancy was monthly in eight patients and yearly in two. SE occurrence peaked at 1 year of age and decreased after 3 years of age. The most effective ASM was levetiracetam. Although WHS-associated epilepsy is intractable with frequent SE occurrence during infancy, improvement in seizure control is expected with age. Levetiracetam may be a novel ASM for WHS.

Identifiants

pubmed: 37075791
doi: 10.1055/a-2077-1988
doi:

Substances chimiques

Levetiracetam 44YRR34555
Anticonvulsants 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

339-343

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

S.H. received funding for travel and speaker honoraria from UCB Japan Co. Ltd, Daiichi Sankyo Co. Ltd., and Eisai Co. Ltd., and received research funds from Syneos Health Clinical Co. Ltd for the clinical trial of Zogenix. K.K. received research funds from Syneos Health Clinical Co. Ltd. for the clinical trial of Zogenix. Atsuro Daida received grant funding to research abroad from SENSHIN Medical Research Foundation. The other authors have no conflicts of interest to declare.

Auteurs

Ayumi Horiguchi (A)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Reiko Koichihara (R)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Kenjiro Kikuchi (K)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Hazuki Nonoyama (H)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Atsuro Daida (A)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Daiju Oba (D)

Division of Medical Genetics, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Yuko Hirata (Y)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Ryuki Matsuura (R)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Hirofumi Ohashi (H)

Division of Medical Genetics, Saitama Children's Medical Center, Saitama, Saitama, Japan.

Shin-Ichiro Hamano (SI)

Division of Neurology, Saitama Children's Medical Center, Saitama, Saitama, Japan.

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Classifications MeSH