Phenotype #0000315275
| Individual ID |
00424067 |
| Associated disease |
WGVRP |
| Phenotype details |
ophtalmological examinations right, left eye: best corrected visual acuity: 20/200, 20/50; recent refraction spherical equivalent: -3.25, 0.75; past (presurgical) refraction spherical equivalent: (age 2.5 y) 1.25 + 3.00 x 90, (age 2.5 y) -1.50+ 4.25 x 95; axial length, mm: 23.62, 22.85; lens status: posterior subcapsular cataract, Clear; retinal detachment age, y:8; surgery: scleral buckle/pars plana vitrectomy, none; optically empty vitreous: not availabled, yes; vitreal avascular membranes: not availabled, yes; retinal traction: none, none; chorioretinal atrophy: moderate, moderate; retinal pigmentary changes: none, none; ocular alignment: exotropia, exotropia; visual field: nasal scotoma, superior scotoma |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome) |
| Age/Examination |
11y (11 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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