CADASIL

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CADASILct.jpg

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)


  • Subcortical lacunar infarcts and leukoencephalopathy in young adults
  • Anterior temporal pole and external capsule have higher sensitivity and specificity
  • Hereditary small-vessel disease due to mutations in Notch3 gene on chromosome 19