cerebral arteriovenous malformation
MIM.108010
Predisposition syndromes
autosomal dominant familial cerebral arteriovenous malformation
hereditary hemorrhagic telangiectasia (HHT) (MIM.187300)
hereditary neurocutaneous angioma (MIM.106070)
Differential diagnosis
cerebral cavernous malformations (MIM.116860) which are venous and usually arteriographically 'silent'.
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