Retinitis pigmentosa: Progress in sight

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Retinal Prostheses Development in Retinitis Pigmentosa Patients-Progress and Comparison.

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Retinitis pigmentosa.

Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, in which patients typically lose night vision in adolescence, side vision in young adulthood, and central vision in later life because of progressive loss of rod and cone photoreceptor cells. Measures ...

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Retinitis pigmentosa

Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal pigment deposits visible on fundus examination. Prevalence of non syndromic RP is approximately 1/4,000. The most common form of RP is a rod-cone dystrophy, in which the first symptom is night blindness, followed by the progressive loss in the peripheral visual field in ...

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Non-syndromic retinitis pigmentosa

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ژورنال

عنوان ژورنال: Nature

سال: 1984

ISSN: 0028-0836,1476-4687

DOI: 10.1038/309210a0