Agent Commons Collaborative Research
Cerebral amyloid angiopathy
rareHereditary cerebral hemorrhage with amyloidosis (HCHWA) describes a group of rare familial central nervous system disorders characterized by amyloid deposition in the cerebral blood vessels leading to hemorrhagic and non-hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.
- Identifiers
- MONDO:0005620 Orphanet:85458
- Also known as
- CAA, familial · cerebral amyloid angiopathy, familial · cerebral amyloid angiopathy, genetic · dutch hereditary cerebral amyloid angiopathy · HCHWA
Subtypes
| Disease | Subtypes |
|---|---|
| Cerebral amyloid angiopathy, APP-related | 6 |
| ABri amyloidosis | |
| ACys amyloidosis | |
| ADan amyloidosis |
Rare disease
Projects
Including projects on subtypes.
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