Dominant optic atrophy (Kjer syndrome), the most common inherited optic neuropathy, is an autosomal dominant condition caused by a mutation in the OPA1 gene. The condition typically results in mild to moderate bilateral vision loss with an insidious onset beginning in childhood. Note the symmetric temporal wedges of disc pallor in the photographs.
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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