Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions
- PMID: 9738733
- DOI: 10.1016/s0022-3476(98)70286-0
Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions
Abstract
Blau syndrome is a granulomatous disease of the skin, eyes, and joints, usually without visceral involvement. It is inherited in a autosomal dominant manner. The Blau susceptibility locus has been mapped to chromosome 16 p 12-q21. A recent report has added liver granulomata. We describe a family with Blau syndrome in whom 1 member had renal interstitial granulomata.
Comment in
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Autosomal dominant granulomatous disease of childhood: the naming of things.J Pediatr. 1998 Sep;133(3):322-3. doi: 10.1016/s0022-3476(98)70263-x. J Pediatr. 1998. PMID: 9738710 No abstract available.
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Autosomal dominant granulomatous disease of childhood.J Pediatr. 1999 May;134(5):663-4. doi: 10.1016/s0022-3476(99)70269-6. J Pediatr. 1999. PMID: 10228311 No abstract available.
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