Abstract

A 13-year-old male with a complaint of progressive visual decrease has been referred. The symptom started 3 years ago and worsened in 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 dioptrics in the both eyes. The foveal sections examined with high-resolution optical coherence tomography (OCT) that 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 was examined high-resolution OCT findings in patient diagnosed with congenital retinoschisis. Also, the current developments related to management of the disease were presented.