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An autosomal dominant inflammatory disorder characterized by the formation of immune granulomas invading the skin, joints and eye. Other organs may be involved. Clinical manifestations are variable and include early-onset granulomatous arthritis, uveitis and skin rash. Blindness, joint destruction and visceral involvement have been reported in severe cases.




Arthrocutaneouveal granulomatosis
Familial granulomatosis blau type
Familial granulomatous inflammatory arthritis dermatitis and uveitis
Familial juvenile systemic granulomatosis
Jabs syndrome
Sarcoidosis, early-onset


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