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Genetic and Rare Diseases Information Center (GARD)

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Familial exudative vitreoretinopathy


Other Names for this Disease

  • Criswick-Schepens syndrome
  • Exudative vitreoretinopathy, familial
  • FEVR
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Overview

Familial exudative vitreoretinopathy (FEVR) is a hereditary disorder that can cause progressive vision loss. This condition affects the retina, the light-sensitive tissue that lines the back of the eye, by preventing blood vessels from forming at the edges of the retina. This reduces the blood supply to retina. The signs and symptoms include vision loss or blindness, retinal detachment, strabismus, and a visible whiteness (leukocoria) in the normally black pupil. The severity of FEVR varies widely, even within the same family. Many people with this condition do not experience any vision problems.[1]

FEVR has different inheritance patterns depending on the gene involved. Most individuals have the autosomal dominant form of this condition, caused by mutations in the FZD4 or LRP5 gene. FEVR caused by LRP5 gene mutations can also have an autosomal recessive inheritance. When this condition is caused by mutations in the NDP gene, it has an X-linked pattern of inheritance.[1]
Last updated: 3/4/2011

References

  1. Familial exudative vitreoretinopathy. Genetics Home Reference. February 2009; http://ghr.nlm.nih.gov/condition/familial-exudative-vitreoretinopathy. Accessed 3/3/2011.
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Basic Information

  • Genetics Home Reference (GHR) contains information on Familial exudative vitreoretinopathy. This website is maintained by the National Library of Medicine.

In Depth Information

Other Names for this Disease
  • Criswick-Schepens syndrome
  • Exudative vitreoretinopathy, familial
  • FEVR
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.