Article
The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China.
The journal of headache and pain - 1 Jan 2016
He Dan, Chen Daiqi, Li Xuefei, Hu Zheng, Yu Zhiyuan, Wang Wei, Luo Xiang
Abstract excerpt
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common form of hereditary stroke disorder caused by mutations in the NOTCH3 gene. Although CADASIL scale is a widely used tool to screen clinically suspected CADASIL patients, the differential effects of this scale in various populations remain unknown. METHODS: 92 CADASIL-like patients and...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.