Spectrum of ocular manifestations in apert syndrome

Apert syndrome is a congenital type 1 acrocephalosyndactyly characterized by craniosynostosis, dysmorphic facial features and symmetrical syndactyly. There premature fusion of cranial sutures which leads to restriction intracranial orbital space expansion giving characteristic appearance. We are reporting two cases different age groups from ophthalmic point view, with sets ocular manifestation. Of the cases, one who presented early had better visual prognosis. Syndrome has social stigma patients often suffers psychological disturbances. Patient counselling, timely management multidisciplinary approach regular follow ups an important aspect can offer quality life.