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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Mengmeng Li, Xiangyu Zheng, Rui Zhong, Qian Zhao, Yingxue Lu, Zan Wang, Weihong Lin
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2019-11-01
Serie:Frontiers in Neurology
Ämnen:
familial hemiplegic migraine
migraine
genetic
CACNA1A gene
encephalopathy
Länkar:https://www.frontiersin.org/article/10.3389/fneur.2019.01221/full
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk