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Article

Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.

Cephalalgia : an international journal of headache - 1 Feb 2018

Prontera P, Sarchielli P, Caproni S, Bedetti C, Cupini L M, Calabresi P, Costa C

Abstract excerpt

Objective We performed a systematic review on the comorbidities of familial/sporadic hemiplegic migraine (F/SHM) with seizure/epilepsy in patients with CACNA1A, ATP1A2 or SCN1A mutations, to identify the genotypes associated and investigate for the presence of mutational hot spots. Methods We performed a search in MEDLINE and in the Human Gene Mutation and Leiden Open Variation Databases for mutations in the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28058944
DOI: 10.1177/0333102416686347

Genes

ATP1A2
CACNA1A
SCN1A

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

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