Familial Hemiplegic Migraine With Progressive Cerebellar Ataxia Caused by a p.Thr666Met CACNA1A Gene Mutation in a Chinese Family

Here, we describe the first case of familial hemiplegic migraine type 1 (FHM1) resulting from a T666M mutation in the CACNA1A gene of a Chinese individual. A 54-year-old female patient demonstrated extensive clinical manifestations, including transient paropsia, hemianesthesia, logaphasia, hemiplegi...

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Detalles Bibliográficos
Autores principales: Li, Mengmeng, Zheng, Xiangyu, Zhong, Rui, Zhao, Qian, Lu, Yingxue, Wang, Zan, Lin, Weihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882281/
https://www.ncbi.nlm.nih.gov/pubmed/31824404
http://dx.doi.org/10.3389/fneur.2019.01221

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