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Published online 2016 Mar 21. doi: 10.5334/jbr-btr.938
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Table 1

Diagnostic criteria of familial cerebral cavernous malformation (FCCM) [1,2].

Diagnostic Criteria of FCCM (At Least 1 of the Following Criteria):
– the presence of multiple CCM (typically 5 or more)
– the occurrence of CCM in at least two members of a family
– the presence of a mutation in one of the three genes causing FCCM.