Retinitis pigmentosa (RP) is the name given to a group of hereditary eye diseases that affect the retina. Retinitis pigmentosa causes the degeneration of photoreceptor cells in the retina. These are cells that capture and process light that helps us to see. As these cells degenerate and die, patients experience progressive vision loss.
Retinitis pigmentosa (RP) is the name given to a group of hereditary eye diseases that affect the retina. Retinitis pigmentosa causes the degeneration of photoreceptor cells in the retina. These are cells that capture and process light that helps us to see. As these cells degenerate and die, patients experience progressive vision loss.
There are special tests that can be used to detect RP:
Recent research findings suggest that in some forms of RP, those who have prolonged, unprotected exposure to sunlight may experience accelerated vision loss.
As yet, there is no known cure for RP. However, intensive research is currently ongoing to discover the cause, prevention, and treatment of RP.
Reducing your exposure to sunlight is important for keeping the eye protected. However, since RP is an inherited disorder that runs in families, the disease is not preventable. If someone in your family is diagnosed with retinal degeneration, it is strongly advised that all members of the family contact an eye care professional.
This document is provided for informational purposes only. Please consult an eye care professional about symptoms that may require medical attention and may or may not be covered by your medical plan and/or routine vision plan.
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