Corpus callosotomy for drug-resistant epilepsy in a pediatric patient with Waardenburg syndrome Type I

BACKGROUND: Waardenburg syndrome (WS) is caused by autosomal dominant mutations. Since the coexistence of epilepsy and WS type I is rare, the detailed clinical features and treatment of epilepsy, including surgery, have not been fully reported for these patients. We report the first case of an indiv...

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Detalles Bibliográficos
Autores principales: Shimogawa, Takafumi, Mukae, Nobutaka, Morioka, Takato, Sakata, Ayumi, Sakai, Yasunari, Matsumoto, Nozomu, Mizoguchi, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168647/
https://www.ncbi.nlm.nih.gov/pubmed/34084644
http://dx.doi.org/10.25259/SNI_228_2021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168647/
https://www.ncbi.nlm.nih.gov/pubmed/34084644
http://dx.doi.org/10.25259/SNI_228_2021

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