Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
MESHC563990
A hereditary autosomal recessive nonhypertensive cerebral small vessel arteriopathy characterized by alopecia, SPONDYLOSIS, and progressive motor dysfunction and DEMENTIA with onset typically in the second or third decade of life. Mutations in the HTRA1 gene have been identified. OMIM: 600142
Synonyms
- CARASIL
- Subcortical Vascular Encephalopathy, Progressive
- Cerebrovascular Disease with Thin Skin, Alopecia, and Disc Disease
- Familial Young-Adult-Onset Arteriosclerotic Leukoencephalopathy with Alopecia and Lumbago without Arterial Hypertension
- Nemoto Disease
- MAEDA Syndrome
Source last updated 2026-05-24T15:30:05.592Z