Familial Hemiplegic Migraine with Prolonged Coma and Cerebellar Atrophy: CACNA1A T666M Mutation in a Korean Family

We report the first Korean patient with familial hemiplegic migraine type 1, with clinical and multimodal imaging findings. A 43-yr-old man was admitted for right hemianopia and aphasia, followed by coma. MRI showed only cerebellar atrophy. CT angiography showed mild vasodilation of intracranial blo...

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Detalhes bibliográficos
Main Authors: Choi, Kyung-Ho, Kim, Jang Su, Lee, Seo-Young, Ryu, Suk-won, Kim, Sam Su, Lee, Seung-hwan, Kim, Sunghun, Park, Hee-Kwon
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Academy of Medical Sciences 2012
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3429835/
https://ncbi.nlm.nih.gov/pubmed/22969264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2012.27.9.1124
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