8B22.3 Isolated cerebral amyloid angiopathy
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Cerebral amyloid angiopathy is characterised by the progressive accumulation of amyloid protein in the walls of small-to-medium-sized arteries and arterioles predominantly located in the leptomeningeal space, the cortex, and, to a lesser extent, also in the capillaries and veins.
synonyms
- Isolated cerebral amyloid angiopathy
- CAA - [cerebral amyloid angiopathy]
- cerebrum amyloid angiopathy
- congophilic angiopathy
- Familial dementia, British type
- Familial dementia, Danish type
- Hereditary amyloid precursor protein angiopathy
- Hereditary cerebral haemorrhage with amyloidosis, Dutch type
- Hereditary cerebral haemorrhage with amyloidosis, Icelandic type
- Hereditary cystatin C amyloid angiopathy
- Sporadic amyloid angiopathy
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