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Article

CADASIL in Arabs: clinical and genetic findings

9 Nov 2007

Abstract excerpt

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is increasingly recognized as an inherited arterial disease leading to a step-wise decline and eventually to dementia. CADASIL is caused by mutations in NOTCH3 epidermal growth factor-like repeat that maps to chromosome 19. CADASIL cases have been identified in most countries of Western and Central...

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Share to Cerebrovascular and genetic disorders
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PMID: 17996090
DOI: 10.1186/1471-2350-8-67

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