Non-convulsive Status Epilepticus in SEMA6B-Related Progressive Myoclonic Epilepsy: A Case Report With Literature Review

Progressive myoclonic epilepsy (PME) is a group of rare diseases characterized by progressive myoclonus, cognitive impairment, ataxia, and other neurologic deficits. PME has high genetic heterogeneity, and more than 40 genes are reportedly associated with this disorder. SEMA6B encodes a member of th...

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Detalles Bibliográficos
Autores principales: Duan, Jing, Chen, Yan, Hu, Zhanqi, Ye, Yuanzhen, Zhang, Tian, Li, Cong, Zeng, Qi, Zhao, Xia, Mai, Jiahui, Sun, Yang, Liu, Chao, Zheng, Wenxin, Xiao, Yuhan, Liao, Jianxiang, Chen, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096209/
https://www.ncbi.nlm.nih.gov/pubmed/35573939
http://dx.doi.org/10.3389/fped.2022.859183

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096209/
https://www.ncbi.nlm.nih.gov/pubmed/35573939
http://dx.doi.org/10.3389/fped.2022.859183

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