Article
Familial Hemiplegic Migraine With Asymmetric Encephalopathy Secondary to ATP1A2 Mutation: A Case Series.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society - 1 Jan 2018
Murphy Olwen C, Merwick Aine, OʼMahony Olivia, Ryan Aisling M, McNamara Brian
Abstract excerpt
INTRODUCTION: Familial hemiplegic migraine (FHM) is a genetic disease with a variable clinical phenotype. The imaging and electroencephalogram (EEG) correlates of FHM are not well described. CASE SERIES: We describe a case series of five young women aged 12 to 32 years. Each case presented with headache, encephalopathy, and hemiparesis of varying severity. One patient developed seizures. All patients improved...
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