Conditions / Genetic
CST3-related cerebral amyloid angiopathy
info · Genetic
A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21.
Signs and symptoms
- Cerebral hemorrhage
- Stroke
- Dementia
- Intracranial hemorrhage
- Generalized amyloid deposition
Also known as: Amyloidosis VI; Amyloidosis, Cerebroarterial, Icelandic Type; Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant; HCHWA; Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant