Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
Definition
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 autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1, CADASIL, CADASIL syndrome, CADASIL type 1, CADASIL1, CASIL, cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1, dementia, hereditary multi-infarct type, hereditary multi-infarct dementia — per MONDO