Phenotype #0000315273

Individual ID 00424065
Associated disease WGVRP
Phenotype details ophtalmological examinations right, left eye: best corrected visual acuity: 20/20, 20/32; recent refraction spherical equivalent: not available, -1; past (presurgical) refraction spherical equivalent: (age 14 y) -1.00 + 1.00 x 90, (age 14 y) -1.00 + 2.00 x 90; axial length, mm: 24.56, 25.07; lens status: Clear, Clear; retinal detachment age, y:not available; surgery: none, scleral buckle/pars plana vitrectomy; optically empty vitreous: yes, yes; vitreal avascular membranes: yes, yes; retinal traction: severe, severe; chorioretinal atrophy: none, none; retinal pigmentary changes: none, none; ocular alignment: orthophoria, orthophoria; visual field: enlarged blind spot, paracentral scotoma
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Age/Examination 16y (16 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-11-16 15:54:07 +01:00 (CET)
Date last edited N/A

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