Successful treatment of drug-resistant status epilepticus in an adult patient with Mowat-Wilson syndrome: A case report

Mowat-Wilson syndrome (MWS) is a rare genetic disorder characterized by intellectual disability, distinctive facial features, epilepsy, and multiple anomalies caused by heterozygous loss-of-function mutations in the zinc finger E-box-binding homeobox-2 gene (ZEB2). Treatment choice is very important...

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Detalles Bibliográficos
Autores principales: Nosaki, Yasunobu, Ohyama, Ken, Watanabe, Maki, Yokoi, Takamasa, Kobayashi, Yosuke, Inaba, Mie, Wakamatsu, Nobuaki, Iwai, Katsushige
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736901/
https://www.ncbi.nlm.nih.gov/pubmed/33344924
http://dx.doi.org/10.1016/j.ebr.2020.100410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736901/
https://www.ncbi.nlm.nih.gov/pubmed/33344924
http://dx.doi.org/10.1016/j.ebr.2020.100410

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