Genetic diagnosis of autosomal dominant arteriopathy syndrome CADASIL (NOTCH3 gene)

Various mutations in the Notch3 gene are the cause of the development of the autosomal dominant arteriopathy syndrome CADASIL, in which all small cerebral arteries are affected. This pathology is characterized by subcortical strokes and leukoencephalopathy (damage to the brain's white matter).

Within 11 days. The specified time does not include the day of biomaterial collection