Article
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.
Cephalalgia : an international journal of headache - 1 Jul 2017
Pelzer N, Blom D E, Stam A H, Vijfhuizen L S, Hageman Atm, van Vliet J A, Ferrari M D, van den Maagdenberg Amjm, Haan J, Terwindt G M
Abstract excerpt
Background Familial hemiplegic migraine (FHM) is a rare monogenic migraine subtype characterised by attacks associated with transient motor weakness. Clinical information is mainly based on reports of small families with only short follow-up. Here, we document a prospective 15-year follow-up of an extended family with FHM type 2. Patients and methods After diagnosing FHM in a patient with severe attacks...
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