Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review

Du, Y; Li, C; Duan, FJ; Zhao, C; Zhang, W

Zhang, W (corresponding author), Fourth Mil Med Univ, Tangdu Hosp, Dept Neurol, Xian 710038, Shaanxi, Peoples R China.

NEUROPEDIATRICS, 2020; 51 (3): 215

Abstract

Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant inheritance disorder caused by ATP1A2 mutation, and the clinical spectrum is heter......

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