Loterre: Human diseases: CADASIL syndrome

disease > genetic disease > hereditary disease > CADASIL syndrome

disease > cardiovascular disease > vascular disease > arterial disease > CADASIL syndrome

disease > cardiovascular disease > vascular dementia > CADASIL syndrome

... > central nervous system diseases > cerebral disorder > cerebrovascular disease > vascular dementia > CADASIL syndrome

... > cardiovascular disease > vascular disease > cerebrovascular disease > vascular dementia > CADASIL syndrome

... > central nervous system diseases > cerebral disorder > dementia > vascular dementia > CADASIL syndrome

disease > degenerative disease > dementia > vascular dementia > CADASIL syndrome

CADASIL syndrome

CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder, and is thought to be caused by mutations of the Notch 3 gene on chromosome 19. The disease belongs to a family of disorders called the leukodystrophies. (Wikipedia)

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