Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report

Familial hemiplegic migraine (FHM) is a rare, monogenic, autosomal dominant subtype of migraine, in which three genes, CACNA1A, ATP1A2, and SCN1A, are currently known to be involved. The familial hemiplegic migraine type 3 (FHM3) is seldom caused by mutations in SCN1A. Here, we report a rare case of...

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Detalles Bibliográficos
Autores principales: Shao, Na, Zhang, Haining, Wang, Xue, Zhang, Wuqiong, Yu, Miaomiao, Meng, Hongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249337/
https://www.ncbi.nlm.nih.gov/pubmed/30498473
http://dx.doi.org/10.3389/fneur.2018.00976

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249337/
https://www.ncbi.nlm.nih.gov/pubmed/30498473
http://dx.doi.org/10.3389/fneur.2018.00976

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