Hemangioma, Cavernous, Central Nervous System
Synonyms
Angioma, Familial Cavernous
Angiomas, Familial Cavernous
Angiomatous Malformation, Cavernous
Angiomatous Malformations, Cavernous
Brain Cavernous Hemangioma
Brain Cavernous Hemangiomas
Capillary Malformation, Cerebral
Capillary Malformations, Cerebral
Cavernous Angioma, Central Nervous System
Cavernous Angioma, Familial
Cavernous Angiomas, Familial
Cavernous Angiomatous Malformation
Cavernous Angiomatous Malformations
Cavernous Hemangioma of Brain
Cavernous Hemangioma, Central Nervous System
Cavernous Hemangioma, Cerebral
Cavernous Hemangioma, Extracerebral
Cavernous Hemangioma, Intracerebral
Cavernous Hemangiomas, Cerebral
Cavernous Hemangiomas, Extracerebral
Cavernous Hemangiomas, Intracerebral
Cavernous Malformation, Cerebral
Cavernous Malformation, Familial
Cavernous Malformations, Cerebral
Cavernous Malformations, Familial
Central Nervous System Cavernous Hemangioma
Cerebral Capillary Malformation
Cerebral Capillary Malformations
Cerebral Cavernous Hemangioma
Cerebral Cavernous Hemangiomas
Cerebral Cavernous Malformation
Cerebral Cavernous Malformations
Extracerebral Cavernous Hemangioma
Extracerebral Cavernous Hemangiomas
Familial Cavernous Angioma
Familial Cavernous Angiomas
Familial Cavernous Malformation
Familial Cavernous Malformations
Hemangioma, Cerebral Cavernous
Hemangioma, Extracerebral Cavernous
Hemangioma, Intracerebral Cavernous
Hemangiomas, Cerebral Cavernous
Hemangiomas, Extracerebral Cavernous
Hemangiomas, Intracerebral Cavernous
Intracerebral Cavernous Hemangioma
Intracerebral Cavernous Hemangiomas
Malformation, Cavernous Angiomatous
Malformation, Cerebral Capillary
Malformation, Cerebral Cavernous
Malformation, Familial Cavernous
Malformations, Cavernous Angiomatous
Malformations, Cerebral Capillary
Malformations, Cerebral Cavernous
Malformations, Familial Cavernous
A vascular anomaly composed of a collection of large, thin walled tortuous VEINS that can occur in any part of the central nervous system but lack intervening nervous tissue. Familial occurrence is common and has been associated with a number of genes mapped to 7q, 7p and 3q. Clinical features include SEIZURES; HEADACHE; STROKE; and progressive neurological deficit.