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A 13-year-old-male patient presented with a complaint of progressive visual. His symptoms started 3 years ago and worsened within the past 2 years. There was no one with a family history of similar complaints. He had no previous history of trauma, inflammatory or infectious ocular disease. He had a best-corrected visual acuity of 0.3 in both eyes. Refraction was +2.50 diopters in both eyes. The foveal sections examined with high-resolution optical coherence tomography (OCT) demonstrated wide hyporeflective cystoid spaces that split the neurosensory retina at the center of the fovea and small cystic space that formed bridges between the outer and inner retinal layers in perifoveal area bilaterally. In our study high-resolution OCT findings in patient diagnosed with congenital retinoschisis were analyzed. Also, the current developments related to management of the disease were presented.

High-Resolution Optical Coherence Tomography In Diagnosis of Congenital Hereditary Retinoschisis