Famililal cerebral cavernous malformations

A 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.

Also known as: familial brain cavernous angioma, familial brain cavernous hemangioma, familial cerebral cavernoma, familial cerebral cavernous malformation, famililal cerebral cavernous malformations, hereditary brain cavernous angioma, hereditary brain cavernous hemangioma, hereditary cerebral cavernoma

0 clinical trials for this condition and its sub-types.