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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Scientific Scholar
2021
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| Materias: | |
| 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 |