Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions - 09/09/11
Doi : 10.1016/S0022-3476(98)70286-0
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-q2 1. A recent report has added liver granulomata. We describe a family with Blau syndrome in whom 1 member had renal interstitial granulomata. (J Pediatr 1998;133:450-2)
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 | From the Department of Immunology/Allergy, Sydney Children’s Hospital, Australia Consultant Nephrologist, Nepean Hospital, Australia. |
| Reprint requests: Suk See Ting, FRACP, Department of Immunology/Allergy, Sydney Children’s Hospital, High St, Randwick, NSW 203 1, Australia. |
 | 0022-3476/98/$5.00 + 0 9/22/92091 |
© 1998
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Vol 133 - N° 3
P. 450-452 - septembre 1998 Retour au numéro
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