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¹Başkent Üniversitesi Tıp Fakültesi Göz Hastalıkları A.D., Konya, Uzm. Dr.
²Başkent Üniversitesi Tıp Fakültesi Göz Hastalıkları A.D., Konya, Prof. Dr. Apert syndrome is a rare seen congenital type 1 acrocephalosyndactyly characterized by craniosynostozis, syndactyly of the fingers and toes, dysmorphic facial features and ophthalmic abnormalities. In this case, we aimed to present ophthalmic abnormalities in a patient with Apert syndrome. Keywords : Apert syndrome, craniosynostozis, syndactyly, strabismus, hyperopia, astigmatism, ambliopi