Hereditary Vitreoretinopathy Report

Hereditary VitreoretinopathyHV are a group of congenital retina and vitreous degeneration, caused by genetic mutations in more than 20 genes and is characterazed by high risk of retinal detachment, early cataract, optically empty vitreous and neovascularization. Among involved genes we can found those codying for collagen and for potassium channel.More than 20 genes analyzed It is recommended if: This report is designed for those with a family history of hereditary vitreoretinopathies or symptoms of including conditions such as early cataract and retinal detachment. List of main conditions: Familial Exudative Vitreoretinopathy Stickler Syndrome Snowflake Vitreoretinal Degeneration