MeSH Browser

MeSH Supplementary: Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Unique ID: C563990
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563990
Entry Term(s): CARASIL; Cerebrovascular Disease with Thin Skin, Alopecia, and Disc Disease; Familial Young-Adult-Onset Arteriosclerotic Leukoencephalopathy with Alopecia and Lumbago without Arterial Hypertension; MAEDA Syndrome; Nemoto Disease; Subcortical Vascular Encephalopathy, Progressive
Registry Number: 0
Heading Mapped to: *Alopecia; *Cerebral Infarction; *Spinal Diseases; *Leukoencephalopathies
Frequency: 51
Note: 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
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy MeSH Supplementary Concept Data 2024