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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Bibliographic Details
Main Authors: Yasunobu Nosaki, Ken Ohyama, Maki Watanabe, Takamasa Yokoi, Yosuke Kobayashi, Mie Inaba, Nobuaki Wakamatsu, Katsushige Iwai
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:Epilepsy & Behavior Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589986420300587