| Literature DB >> 9508240 |
S Manouvrier-Hanu1, B Puech, F Piette, O Boute-Benejean, A Desbonnet, B Duquesnoy, J P Farriaux.
Abstract
Blau syndrome (MK186580) comprises granulomatous arthritis, iritis, and skin rash, and is an autosomal-dominant trait with variable expressivity. So far it was described in 5 families. We report on a sixth family with severe progression of eye involvement and discuss the nosology with similar diseases, such as early-infantile sarcoidosis.Entities:
Mesh：
Year: 1998 PMID： 9508240
Source DB: PubMed Journal: Am J Med Genet ISSN： 0148-7299