Phenotype #0000308687

Individual ID 00417177
Associated disease EVR1
Phenotype details 4y: peripheral retinal fold in the left eye associated with retinal traction; left eye: areas of preretinal fibrosis, both eyes: characteristic deficient vascularization of the peripheral retina; poor vision: best corrected visual acuity right, left eye: 6/48, 2/58
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite familial exudative vitreoretinopathy
Age/Examination 4y (4 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset 8m
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-09-13 15:10:40 +02:00 (CEST)
Date last edited N/A

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