Cerebral Amyloid Angiopathy [mozková amyloidní angiopatie]
- Terms
-
amyloidní angiopatie mozku
cerebrální amyloidní angiopatie
cerebrální amyloidová angiopatie
kongofilní cerebrální angiopatie
mozek - angiopatie amyloidní
mozková amyloidová angiopatie
sporadická cerebrální amyloidová angiopatie
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Amyloid Angiopathy, Cerebral
Congophilic Angiopathy
Sporadic Cerebral Amyloid Angiopathy
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)
- Annotation
- /genet:consider also CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL
- DUI
- D016657 MeSH Browser
- CUI
- M0025384
- Previous indexing
- Amyloidosis (1974-1991); Cerebrovascular Disorders (1974-1991)
- History note
- 1992
- Public note
- 1992
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
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- CL
- classification 1
- CO
- complications 4
- CN
- congenital 0
- DI
- diagnosis 7
- DG
- diagnostic imaging 0
- DH
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- DT
- drug therapy 0
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- embryology 0
- EN
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- EP
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- EH
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- ET
- etiology 1
- GE
- genetics 1
- HI
- history 0
- IM
- immunology 0
- ME
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- MI
- microbiology 0
- MO
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- NU
- nursing 0
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- parasitology 0
- PA
- pathology 1
- PP
- physiopathology 2
- PC
- prevention & control 0
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- psychology 0
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- TH
- therapy 3
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- urine 0
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- veterinary 0
- VI
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