Familial Exudative Vitreoretinopathies

A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by FLUORESCEIN ANGIOGRAPHY. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene.

Year introduced: 2020(2014)

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Tree Number(s): C11.250.345, C11.270.238, C11.768.337, C16.131.384.424, C16.320.290.352

MeSH Unique ID: D000080345

Entry Terms:

• Exudative Vitreoretinopathy, Familial
• Vitreoretinopathy, Familial Exudative
• Familial Exudative Vitreoretinopathy
• X-Linked Familial Exudative Vitreoretinopathy
• X Linked Familial Exudative Vitreoretinopathy
• XL-FEVR

All MeSH Categories
Diseases Category
Eye Diseases
Eye Abnormalities
Familial Exudative Vitreoretinopathies

All MeSH Categories
Diseases Category
Eye Diseases
Eye Diseases, Hereditary
Familial Exudative Vitreoretinopathies

All MeSH Categories
Diseases Category
Eye Diseases
Retinal Diseases
Familial Exudative Vitreoretinopathies

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Familial Exudative Vitreoretinopathies

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Familial Exudative Vitreoretinopathies