Related MeSH Hierarchy (5)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Familial Exudative Vitreoretinopathies
Diseases [C] » Eye Diseases [C11] » Eye Abnormalities » Familial Exudative Vitreoretinopathies
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Familial Exudative Vitreoretinopathies
Diseases [C] » Eye Diseases [C11] » Retinal Diseases » Familial Exudative Vitreoretinopathies
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Eye Abnormalities » Familial Exudative Vitreoretinopathies
Description
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. MeSH
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