Draft:Vitreoretinal degeneration

Submission declined on 30 September 2024 by AlphaBetaGamma (talk).

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Declined by AlphaBetaGamma 2 months ago. Last edited by AlphaBetaGamma 2 months ago. Reviewer: Inform author.

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Vitreoretinal degeneration, or dominant hyaloideoretinal dystrophy of Wagner, VCAN-related vitreoretinopathy, vitreoretinal degeneration, Wagner type or Wagner syndrome, is a hereditary eye disorder that soon leads to vision loss. This eye disorder is characterised by the clear thick gel (the vitrous) develops into a thin layer. Vitreoretinal degeneration is caused by genetic changes in the VCAN gene and is inherited in an autosomal manner.^[1]

Symptoms

Symptoms will presents itself as thinning of the light-sensitive tissue that lines the back of the eye (retinal detachment). Not only that but abnormalities of the blood vessels within the retina are present.^[1]

Estimation

Fewer than 1,000 people in the United States have this hereditary eye disorder.^[1]

Reference list

^ ^a ^b ^c "Diseases - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2024-03-11.

[:0-1] "Diseases - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2024-03-11.

[1]