Question
Two members of a family presented with loss of vision at night is diagnosed having retinitis pigmentosa. Which of the following is NOT true about retinitis pigmentosa?
A. |
Vision is retained till late stage
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B. |
Central vision is lost early
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C. |
Affects rods and cones
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D. |
Tunnel vision may be seen
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Show Answer
Correct Answer � B
Explanation
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- Retinitis pigmentosa (RP) represents a group of hereditary progressive retinal disorders.
- It affects approximately 1.5 million people worldwide. Retinitis pigmentosa usually affects both eyes symmetrically, although in some cases, it affects one eye more than the other.
- There are several forms of retinitis pigmentosa with different inheritance patterns, clinical signs, and visual symptoms.
- Common to all of them is progressive degeneration of the retina, specifically of the light-sensitive (photoreceptor) cells known as the rod and cone photoreceptors.
- The rods, which are largely responsible for night vision, are involved earlier in the course of the disease.
- RP affects cones, which are responsible for color and central vision, later.
- Rod-cone dystrophy and progressive pigmentary retinopathy are other names for RP.
- Difficulty with night vision, slow adaptation to the dark, and gradual loss of peripheral vision are typically the first symptoms.
- People usually retain central visual acuity is until late in the disease. Doctors commonly diagnose RP during adolescence, though symptoms may begin at any age.
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