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Pigmentary retinopathy
- ... that is not present in other family members. Pigmentary retinopathy Rod-cone dystrophy RP Tapetoretinal degeneration Genetic Testing ...
- Neuropathy, ataxia, and retinitis pigmentosa (NARP) is a condition that causes a variety of signs and symptoms that mainly affect the nervous system. The ... the vision loss results from a condition called retinitis pigmentosa. This eye disease causes the light-sensing cells ...
- Retinitis pigmentosa is an eye disease in which there is damage to the retina . The retina is the ... Retinitis pigmentosa can run in families. The disorder can be caused by several genetic defects. The cells controlling ...
- Usher Syndrome (National Library of Medicine)... inherited disease that causes serious hearing loss and retinitis pigmentosa, an eye disorder that causes your vision to ...
- ... found to cause the X-linked form of retinitis pigmentosa. This condition primarily affects males, causing night blindness ... 70 percent of all cases of X-linked retinitis pigmentosa.Most of the mutations responsible for X-linked ...
- ... vision is caused by an eye disease called retinitis pigmentosa (RP), which affects the layer of light-sensitive ... of the eye (cataracts). However, many people with retinitis pigmentosa retain some central vision throughout their lives.Researchers ...
- ... Affected individuals also have an eye condition called pigmentary retinopathy, which results from breakdown (degeneration) of the light- ...
- Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among ...
- ... light that remains stable (stationary) over time. Unlike retinitis pigmentosa (described below), autosomal dominant congenital stationary night blindness ...
- ... in people with the X-linked form of retinitis pigmentosa. This condition primarily affects males, causing night blindness ... 15 percent of all cases of X-linked retinitis pigmentosa.Most mutations in the RP2 gene lead to ...