Retinitis pigmentosa (RP) is a group of inherited disorders in which abnormalities in the photoreceptors of the retina lead to the progressive visual loss. Affected individuals first experience “night blindness” followed by loss of visual fields, often culminating in complete blindness late in the course of the disease. RP affects approximately 1 in 3,200 people, with an estimated 1.5 million affected worldwide.
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