Familial Hemiplegic Migraine Type 1 Associated with Parkinsonism: A Case Report

Familial Hemiplegic Migraine Type 1 Associated with Parkinsonism: A Case Report

Familial hemiplegic migraine type 1 (FHM1), episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) are allelic disorders caused by mutations in the CACNA1A gene on chromosome 19p13. It is well described that FHM1 can present with cerebellar signs, but parkinsonism has not previously b...

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Bibliographic Details
Main Authors: Marie Bruun, Lena Elisabeth Hjermind, Carsten Thomsen, Else Danielsen, Lise Lykke Thomsen, Lars Hageman Pinborg, Nastaran Khabbazbavani, Joergen Erik Nielsen
Format: Article
Language:English
Published: Karger Publishers 2015-04-01
Series:Case Reports in Neurology
Subjects:
Familial hemiplegic migraine type 1
Parkinsonism
CACNA1A
Spinocerebellar ataxia type 6
Episodic ataxia type 2
Online Access:http://www.karger.com/Article/FullText/381827

Internet

http://www.karger.com/Article/FullText/381827

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