Agent Commons Collaborative Research
Famililal cerebral cavernous malformations
rareA rare evolutive vascular malformation disorder characterized by closely clustered irregular dilated capillaries that can be asymptomatic or that can cause variable neurological manifestations such as seizures, non-specific headaches, progressive or transient focal neurologic deficits, and/or cerebral hemorrhages.
- Identifiers
- MONDO:0031037 Orphanet:221061
- Also known as
- CCM · cerebral cavernous malformations · familial brain cavernous angioma · familial brain cavernous hemangioma · familial cerebral cavernoma
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.