Extensive radial lattice degeneration is noted in this patient with molecularly confirmed Stickler's syndrome (COL2A1 mutation), a condition with autosomal dominant inheritance. The patient has had a retinal detachment in this eye with repair via scleral buckle and cryotherapy, seen on the temporal aspect in this photo.
Ophthalmic Atlas Images by EyeRounds.org, The University of Iowa are licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
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