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Wagner syndrome; Wagner vitreoretinopathy; erosive vitreoretinopathy
Pathology:
- vitreoretinopathy
- optically empty vitreous cavity with fibrillary condensations & a avascular preretinal membrane
- perivascular sheating
Genetics:
- dominantly inherited
- type 1 associated with defects in versican (VCAN)
Clinical manifestations:
- progressive chorioretinal atrophy
- subcapsular cataract
- myopia
- systemic manifestations are absent
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 143200
References
OMIM :accession 143200