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Fig. 2 | Pediatric Rheumatology

Fig. 2

From: Blau syndrome: a case report from Palestine

Fig. 2

Pedigree 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 (+)

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