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Fırat Ünv. Tıp Fak. Göz Hast. A.D., Elazığ Purpose: Congenital hereditary retinoschisis, or juvenile Xlinked retinoschisis, is a bilateral vitreoretinal dystrophy that devolops early in life. It is a relatively rare disease. It is seen between the ages of 5-10, predominantly in males. In this report, we examined the clinical features and the characteristical findings in two cases of congenital retinoschisis.

Keywords : Congenital retinoschisis, foveal schisis, peripheral retinoschisis.