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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2020
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| Materias: | |
| 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 |