Descriptor English: | CADASIL | ||||||
Descriptor Spanish: |
CADASIL
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Descriptor Portuguese: | CADASIL | ||||||
Descriptor French: | CADASIL | ||||||
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 Dementia, Hereditary Multi-Infarct Type |
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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 |
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RDF Unique Identifier: | https://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) |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Previous Indexing: |
Cerebrovascular Disorders (1994-2004) Dementia, Multi-Infarct (1994-2004) |
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Public MeSH Note: | 2005; see DEMENTIA, MULTI-INFARCT 2000-2004 |
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History Note: | 2005; use DEMENTIA, MULTI-INFARCT 2000-2004 |
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DeCS ID: | 38632 | ||||||
Unique ID: | D046589 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2005/01/01 | ||||||
Date of Entry: | 2004/07/07 | ||||||
Revision Date: | 2013/07/08 |
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CADASIL
- Preferred
CADASILM
- Related but not broader or narrower
Concept UI |
M0334725 |
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) |
Preferred term | CADASIL |
Entry term(s) |
Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Dementia, Hereditary Multi Infarct Type Dementia, Hereditary Multi-Infarct Type |
Concept UI |
M0454809 |
Scope note | A subvariety of CADASIL characterized by the high frequency of MIGRAINE. The acronym stands for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts, Leukoencephalopathy, and Migraine. |
Preferred term | CADASILM |
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