Blau syndromeA rare autosomal dominant MIM186580 condition characterised by early-onset granulomatous polyarthritis, uveitis, cranial neuropathies, and a red-brown papular rash. Crohn’s disease occurs in 30% of patients.
A rare autosomal dominant disease characterized by camptodactyly and granulomatous involvement of joints, skin, and uvea.
Blau,E., 20th century U.S. pediatrician.
Blau syndrome - autosomal dominant syndrome featuring camptodactyly (flexion contracture of fingers and toes), granulomatous arthritis, uveitis, and granulomatous lesions of the skin. Synonym(s): Blau type arthrocutaneouveal granulomatosis
Blau type arthrocutaneouveal granulomatosis - Synonym(s): Blau syndrome