| Submission declined on 30 September 2024 by AlphaBetaGamma (talk). The proposed article does not have sufficient content to require an article of its own, but it could be merged into the existing article at List of diseases (V). Since anyone can edit Wikipedia, you are welcome to add that information yourself. Thank you.
Where to get help
How to improve a draft
You can also browse Wikipedia:Featured articles and Wikipedia:Good articles to find examples of Wikipedia's best writing on topics similar to your proposed article. Improving your odds of a speedy review To improve your odds of a faster review, tag your draft with relevant WikiProject tags using the button below. This will let reviewers know a new draft has been submitted in their area of interest. For instance, if you wrote about a female astronomer, you would want to add the Biography, Astronomy, and Women scientists tags. Editor resources
|  |
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
editSymptoms 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
editFewer than 1,000 people in the United States have this hereditary eye disorder.[1]
Reference list
edit- ^ a b c "Diseases - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2024-03-11.