Article
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.
Cephalalgia : an international journal of headache - 1 Mar 2014
Roth Christian, Freilinger Tobias, Kirovski Georgi, Dunkel Juliane, Shah Yogesh, Wilken Bernd, Rautenstrauß Bernd, Ferbert Andreas
Abstract excerpt
INTRODUCTION: Familial hemiplegic migraine (FHM) is a rare subtype of migraine with transient hemiplegic aura. PATIENTS AND METHODS: We describe three unrelated families with familial hemiplegic migraine type II (FHM2). Retrospectively, information on 47 family members could be obtained, 15 by personal examination and 32 by indirect anamnesis from relatives. Genetic analyses were performed in 13 patients....
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