Famililal cerebral cavernous malformations
MONDO:0031037A 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
1 clinical trial for this condition and its sub-types, 1 tagged with Famililal cerebral cavernous malformations itself.
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Browse by category →Sub-types of Famililal cerebral cavernous malformations
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Cerebral cavernous malformation 2 0 trials
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Cerebral cavernous malformation 3 0 trials
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Cerebral cavernous malformation 4 0 trials
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Cerebral cavernous malformations 5 0 trials