Epileptic seizures worsen the gait and motor abnormalities in adult patients with Dravet syndrome (with a case report and literature review)

Dravet syndrome (DS), previously known as severe myoclonic epilepsy in infancy (SMEI), is considered the most serious “epileptic encephalopathy.” Here, we present a man with a de novo SCN1A mutation who was diagnosed with DS at the age of 29. In addition to pharmaco‐resistant seizures and cognitive...

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Detalles Bibliográficos
Autores principales: Du, Xiaoping, Lian, Shizhong, Sun, Meizhen, Li, Ruilong, Wang, Huifang, Yang, Xiaoping, Wang, Huifen, Zhang, Xiaobin, Wang, Fengpeng, Yao, Yi, Guo, Junhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Short Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690644/
https://www.ncbi.nlm.nih.gov/pubmed/37418349
http://dx.doi.org/10.1002/epi4.12780

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690644/
https://www.ncbi.nlm.nih.gov/pubmed/37418349
http://dx.doi.org/10.1002/epi4.12780

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