Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation

Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during the aura phase. Mutations in CACNA1A, ATP1A2, SCN1A, and PRRT2 genes have been described. Methods. To describe a mutation in ATP1A2 gene in a FHM case with especially seve...

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Detalles Bibliográficos
Autores principales: Martínez, E., Moreno, R., López-Mesonero, L., Vidriales, I., Ruiz, M., Guerrero, A. L., Tellería, J. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081966/
https://www.ncbi.nlm.nih.gov/pubmed/27818813
http://dx.doi.org/10.1155/2016/3464285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081966/
https://www.ncbi.nlm.nih.gov/pubmed/27818813
http://dx.doi.org/10.1155/2016/3464285

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