Ophthalmology · Ophthalmology / Inherited retinal disease
Wagner syndrome
also: Wagner vitreoretinopathy
Dominant vitreoretinopathy without systemic features.
- Specialty
- Ophthalmology
- Subspecialty
- Ophthalmology / Inherited retinal disease
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, from childhood
- Gene(s) involved
- VCAN
- Alternative names & eponyms
- Wagner vitreoretinopathy
Etiology & mechanism
Versican (VCAN) splicing mutations.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Wagner syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
1 shared
Cohen syndrome
myopia
1 shared
Congenital rubella syndrome
cataract
1 shared
Epstein syndrome
cataract
1 shared
Fuchs heterochromic iridocyclitis syndrome
cataract
1 shared
Knobloch syndrome
cataract
1 shared
Marshall syndrome
cataract
1 shared
Poretti–Boltshauser syndrome
myopia
1 shared
Pseudoexfoliation syndrome
cataract
1 shared
Usher syndrome
cataract
Shares genes with
None.
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