Phenotype #0000315274
| Individual ID |
00424066 |
| 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: no light perception, 20/160; recent refraction spherical equivalent: not available, -0.25; past (presurgical) refraction spherical equivalent: (age 4 y) +2.50 sph, (age 4 y) +2.50 sph; axial length, mm: not available, 22.18; lens status: Dense nuclear sclerotic cataract, Clear; retinal detachment age, y:9; surgery: scleral buckle/pars plana vitrectomy, none; optically empty vitreous: not available, yes; vitreal avascular membranes: not available, yes; retinal traction: not available, moderate; chorioretinal atrophy: not available, severe; retinal pigmentary changes: not available, severe; ocular alignment: orthophoria, orthophoria; visual field: not available, moderate constriction |
| 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 International |
| Created by |
Anna Tracewska |
| Date created |
2022-11-16 15:54:07 +01:00 (CET) |
| Date last edited |
N/A |
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