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Article

Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation.

Headache - 1 Jan 2000

Carreño Oriel, García-Silva María Teresa, García-Campos Óscar, Martínez-de Aragón Ana, Cormand Bru, Macaya Alfons

Abstract excerpt

We report the case of a 9-year-old girl with early-onset developmental delay, chronic ataxia and prolonged hemiplegic migraine episodes bringing about progressive deterioration. Two days into one episode, diffusion-weighted magnetic resonance imaging disclosed unilateral striatal abnormal signal consistent with cytotoxic edema, which evolved into atrophy on follow-up scans. Mutational screen of CACNA1A gene...

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Identifiers

PMID: 22082423
DOI: 10.1111/j.1526-4610.2011.02014.x

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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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