Abstract
Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during aura phase. Mutations in CACNA1A, ATP1A2, SCN1A and PRRT2 genes have been described.
Highlights
Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during aura phase
Aim To describe a novel mutation in ATP1A2 gene in a FHM case with especially severe and prolonged symptoms
Her mother was diagnosed as hemiplegic migraine without genetic confirmation
Summary
Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during aura phase. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks E Martínez1*, R Moreno2, L López-Mesonero3, M Ruiz3, I Vidriales2, P Mulero3, N Téllez3, A Guerrero1, JJ Tellería4 From 4th European Headache and Migraine Trust International Congress: EHMTIC 2014 Copenhagen, Denmark. Introduction Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during aura phase.
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