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Cerebral Amyloid Angiopathy

More information in Books or onNLM PubMed
Definition: 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)  /genet:consider also CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL   
Examples Cerebral Amyloid Angiopathy, Familial
Other names Sporadic Cerebral Amyloid Angiopathy; Congophilic Angiopathy; Amyloid Angiopathy, Cerebral; Congophilic Angiopathies; Cerebral Amyloid Angiopathies; Angiopathy, Congophilic; Angiopathy, Cerebral Amyloid
 
SubstanceCAS Registry & nameCategoriesSource
Amyloid angiopathy  0   *Cerebral Amyloid Angiopathy.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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