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.
No takes yet. Share an insight, caveat, or question.
Manouvrier‐Hanu et al. (1998) studied this question.
Synapse has enriched one closely related paper. Consider it for comparative context: