Article

Expanding the Genetic and Clinical Spectrum of SCN1A-Related Hemiplegic Migraine: Analysis of Mutations in Japanese

2025-01-20

Abstract excerpt

Familial Hemiplegic migraine (FHM) is characterized by repeated episodes of reversible localized neurological deficits, in addition to headache. The aura of HM includes visual, sensory, motor, and verbal symptoms. HM is classified into non-familial sporadic HM (SHM) and familial HM (FHM). Here, we analyzed the clinical symptoms and their relevance in four Japanese patients considered to have SCN1A mutations as a c...

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Literature Corpus work: 4f659d1f-3cb0-5e62-a7f5-621d8bb7cf16
DOI: 10.20944/preprints202501.1367.v1

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