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Retinoschisis is a rare disease of the nerve tissue in the eye. The retina, which consists of multiple layers of interconnected nerve and pigment cells, separates into separate layers resulting in a loss of vision in the corresponding visual field.
It is estimated that retinoschisis affects one in 5,000 to 25,000 individuals, primarily young males. "Schisis" is derived from the Latin word meaning "splitting," describing the splitting of the retinal layers from each other. If the retinoschisis involves the macula, then the high-resolution central area of vision used to view detail is lost, and this one form of macular degeneration. Treatment is often aimed at restricting any worsening of the separation so that it does not encroach on the macula.
Retinoschisis can be caused by an X-linked genetic defect, affecting the vision of men who inherit the disease from their unaffected carrier mothers. The genetic form of this disease usually starts during childhood and is called Juvenile X-linked Retinoschisis. Affected males are usually identified in grade school, but occasionally are identified as young infants. Senile retinoschisis, on the other hand, is the splitting of the retina as a result of aging. It can affect both men and women and is not a genetic condition.
Very few affected individuals go completely blind from retinoschisis, but some sufferers have very limited reading vision and are "legally blind". Visual acuity can be reduced to less than 20/200 in both eyes.
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