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CADASIL MeSH Descriptor Data 2023


MeSH Heading
CADASIL
Tree Number(s)
C10.228.140.300.150.477.200.100
C10.228.140.300.275.249
C10.228.140.300.400.203
C10.228.140.300.510.200.175
C10.228.140.300.775.200.200.100
C10.228.140.380.230.124
C14.907.253.092.477.200.100
C14.907.253.329.249
C14.907.253.560.200.175
C14.907.253.855.200.200.100
C16.320.129
C23.550.513.355.250.200.100
C23.550.717.489.250.200.100
Unique ID
D046589
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D046589
Scope Note
A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146)
Entry Term(s)
CADASILM
Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Dementia, Hereditary Multi-Infarct Type
Previous Indexing
Cerebrovascular Disorders (1994-2004)
Dementia, Multi-Infarct (1994-2004)
Public MeSH Note
2005; see DEMENTIA, MULTI-INFARCT 2000-2004
History Note
2005; use DEMENTIA, MULTI-INFARCT 2000-2004
Date Established
2005/01/01
Date of Entry
2004/07/07
Revision Date
2019/07/01
CADASIL Preferred
CADASILM Related
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