cerebral cavernous malformations

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Autosomal dominant disorders characterized by venous sinusoids that predispose to intracranial haemorrhage. Cerebral cavernous malformation type 1 (CCM1) can be caused by mutation in the KRIT1 gene, CCM2 by mutation in the CCM2 gene encoding malcaverin, and CCM3 by mutation in the PDCD10 gene (programmed cell death 10).

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