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Article

Genetic diagnosis and acetazolamide treatment of familial hemiplegic migraine.

Brain & development - 1 Apr 2011

Omata Taku, Takanashi Jun-ichi, Wada Takahito, Arai Hidee, Tanabe Yuzo

Abstract excerpt

A female patient presented with horizontal gaze nystagmus, mild cerebellar ataxia, recurrent headache and hemiplegia since childhood with cerebellar atrophy on magnetic resonance imaging. Genetic analysis revealed a CACNA1A gene mutation, leading to a diagnosis of familial hemiplegic migraine (FHM1). FHM is very rare, but should be considered as a differential diagnosis for childhood cerebellar symptoms and/or...

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Identifiers

PMID: 20542393
DOI: 10.1016/j.braindev.2010.05.006

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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