JUVENILE RETINOSCHISIS: A CASE REPORT
Singh Hemendra, Srivastav Tanmay*, Kumar Abhishek Bhushan Prashant and Mishra Deepak
ABSTRACT
Juvenile retinoschisis is a hereditary macular dystrophy that is inheritated in the XR (X-linked recessive) manner. Macular folds associated with or without peripheral retinoschisis are major clinical signs, which are responsible for decreased visual acuity. A 17 year old male boy who came in OPD for a consultation for progressive diminution in visual acuity since 5 years. Visual acuity was 3/60 without correction; and the left eye at 3/60, After the myopic correction both eye achieved a 5/60 best corrected visual acuity. The fundus examination revealed supero-nasal juxtamacular radial lines with increased separation with some microcysts in both eyes. Superonasal retinal splitting with microcyst was the major examination finding in retinal periphery.
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