| Descriptor English: | Cerebral Amyloid Angiopathy | ||||||
| Descriptor Spanish: |
Angiopatía Amiloide Cerebral
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| Descriptor Portuguese: | Angiopatia Amiloide Cerebral | ||||||
| Descriptor French: | Angiopathie amyloïde cérébrale | ||||||
| Entry term(s): |
Amyloid Angiopathy, Cerebral Angiopathy, Cerebral Amyloid Angiopathy, Congophilic Cerebral Amyloid Angiopathies Congophilic Angiopathies Congophilic Angiopathy Sporadic Cerebral Amyloid Angiopathy |
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| Tree number(s): |
C10.228.140.300.510.200.200 C14.907.253.560.200.200 C18.452.845.500.100 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016657 | ||||||
| Scope note: | A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. Clinical features include multiple, small lobar CEREBRAL HEMORRHAGE; cerebral ischemia (BRAIN ISCHEMIA); and CEREBRAL INFARCTION. Cerebral amyloid angiopathy is unrelated to generalized AMYLOIDOSIS. Amyloidogenic peptides in this condition are nearly always the same ones found in ALZHEIMER DISEASE. (from Kumar: Robbins and Cotran: Pathologic Basis of Disease, 7th ed., 2005) |
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| Annotation: | /genet:consider also CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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: |
Amyloidosis (1974-1991) Cerebrovascular Disorders (1974-1991) |
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| Public MeSH Note: | 1992 |
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| History Note: | 1992 |
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| DeCS ID: | 30198 | ||||||
| Unique ID: | D016657 | ||||||
| NLM Classification: | WL 355 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1992/01/01 | ||||||
| Date of Entry: | 1991/01/24 | ||||||
| Revision Date: | 2009/07/06 |
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Cerebral Amyloid Angiopathy
- Preferred
Sporadic Cerebral Amyloid Angiopathy
- Narrower
| Concept UI |
M0025384 |
| Scope note | A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. Clinical features include multiple, small lobar CEREBRAL HEMORRHAGE; cerebral ischemia (BRAIN ISCHEMIA); and CEREBRAL INFARCTION. Cerebral amyloid angiopathy is unrelated to generalized AMYLOIDOSIS. Amyloidogenic peptides in this condition are nearly always the same ones found in ALZHEIMER DISEASE. (from Kumar: Robbins and Cotran: Pathologic Basis of Disease, 7th ed., 2005) |
| Preferred term | Cerebral Amyloid Angiopathy |
| Entry term(s) |
Amyloid Angiopathy, Cerebral Angiopathy, Cerebral Amyloid Angiopathy, Congophilic Cerebral Amyloid Angiopathies Congophilic Angiopathies Congophilic Angiopathy |
| Concept UI |
M0334467 |
| Preferred term | Sporadic Cerebral Amyloid Angiopathy |
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