Phenotype #0000315270

Individual ID 00424062
Associated disease WGVRP
Phenotype details ophtalmological examinations right, left eye (no view of fundus because of opacity of anterior ocular media): best corrected visual acuity: hand movement, 20/25; recent refraction spherical equivalent: -0.875, 0.25; past (presurgical) refraction spherical equivalent: not available, not available; axial length, mm: not available, 23.44; lens status: anterior chamber intraocular lens pupillary membrane, anterior chamber intraocular lens; retinal detachment age, y:not available; surgery: cataract extraction/intraocular lens tube shunt, cataract extraction/intraocular lens; optically empty vitreous: not available, yes; vitreal avascular membranes: not available, yes; retinal traction: not available, none; chorioretinal atrophy: not available, mild; retinal pigmentary changes: not available, mild; ocular alignment: orthophoria, orthophoria; visual field: not available, paracentral scotoma
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Age/Examination 60y (60 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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