Familial hemiplegic migraine with a PRRT2 mutation: Phenotypic variations and carbamazepine efficacy

To understand the clinical characteristics of familial hemiplegic migraine (FHM) caused by a PRRT2 mutation and to examine the efficacy of preventive treatment.

Source: Brain and Development - January 1, 2020 Category: Neurology Authors: Sato Suzuki-Muromoto, Rika Kosaki, Kenjiro Kosaki, Masaya Kubota Tags: Case Report Source Type: research