Apert's syndrome: ophthalmic importance and clinical findings.

Caça I.Caça F.N.Sakalar Y.B.Erdem S.Alakus F.Ciftci S.Dogan E.2024-04-242024-04-2420091530-4086https://hdl.handle.net/11468/24720Apert's syndrome is a rare form of craniosynostosis that exhibits with many ocular manifestations. We present two cases of Apert's syndrome. Our first case is a 10-year-old girl admitted with exotropia, V pattern and proptosis on examination. Investigations revealed coronal craniosynostosis, cleft palate, vaginal atresia and syndactyly of the hands and feet. The second case is a 5-year-old boy presented with hypertelorism, exotropia, dissociated vertical deviation and proptosis. Investigations revealed coronal craniosynostosis, bifid uvula and syndactyly of the hands and feet.eninfo:eu-repo/semantics/closedAccessApert's syndrome: ophthalmic importance and clinical findings.Apert's syndrome: ophthalmic importance and clinical findings.Article41144462-s2.0-6614914385919413227N/A