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Article

Autosomal dominant migraine with MRI white‐matter abnormalities mapping to the CADASIL locus

1 Jun 1995

Abstract excerpt

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant cerebral arteriopathy mapped to chromosome 19 and characterized mainly by recurrent subcortical ischemic strokes and extensive white-matter signal abnormalities (WMAs) on magnetic resonance imaging. Other clinical features include migraine attacks and progressive subcortical dementia....

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Identifiers

PMID: 7783868
DOI: 10.1212/wnl.45.6.1086

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Autosomal dominant migraine with MRI white‐matter abnormalities mapping to the CADASIL locusPMID 7783868Read ↗

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SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only.Semantic proximity Read ↗

CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.Semantic proximity Read ↗

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12Semantic proximity Read ↗

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple different onset forms of frequent recurrent attacks: A case report and literature review.Semantic proximity Read ↗

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