Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1

MONDO:0000914

A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.

Also known as: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, CADASIL, CADASIL syndrome, CADASIL type 1, CADASIL1, CASIL, autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1, cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1

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