Blau Syndrome 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 848d36i ; 153
General: Rare, autosomal dominant Iris bombe, uveitis, secondary angle closure glaucoma
Clinical: Skin rash, camptodactyly, early-onset granulomatous arthritis, flexion deformity
Kurokawa T, Kikuchi T, Ohta K, et al. Ocular manifestations in Blau syndrome associated with CARD 15/Nod 2 mutation. Ophthalmology 2003; 110: 2040-2044.
Latkany P. Blau syndrome. Ophthalmology 2004; 111: 853-854.
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