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Jabs Syndrome (Synovitis, Granulomatous Uveitis, and Cranial Neuropathies)
General: Autosomal dominant.
Ocular: Granulomatous uveitis; iritis; sixth nerve palsy.
Clinical: Granulomatous synovitis; corticosteroid responsive hearing loss; boggy polysynovitis; boutonneuse deformities; granulomatous arthritis; skin involvement; fever; hypertension; large-vessel vasculitis.
Blau EB. Familial granulomatous arthritis, iritis, and rash. J Pediatr
Jabs DA, et al. Familial granulomatous, synovitis, uveitis, and cranial neuropathies. Am J Med 1985; 78:801-804.
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