Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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

19 clinical trials for this condition and its sub-types, 19 tagged with Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by