Fig. 2From: Blau syndrome: a case report from PalestinePedigree of the family. The arrow (►) points to the proband. The asterisks (*) indicates the individuals who had undergone clinical and genetic testing. Those with Blau syndrome manifestations are colored, and those who are carriers for the heterozygous mutation in CARD15/NOD2 (p.R334Q) are marked with a plus sign (+)Back to article page