Wagner syndrome

Also known as: Wagner vitreoretinopathy

Dominant vitreoretinopathy without systemic features.

Medical specialty: Ophthalmology
Subspecialty: Ophthalmology / Inherited retinal disease
Sex & age distribution: Male: affected; Female: affected, equal; Children: yes, from childhood
Gene(s) involved: VCAN

Etiology & mechanism

Versican (VCAN) splicing mutations.

Gene(s) involved (1)

VCAN

Symptoms & signs (5)

cataractmyopiaoptically empty vitreousperipheral chorioretinal atrophyretinal detachment risk

SyndromeScope — educational reference. Content is model-generated and not clinically verified; always confirm against OMIM, Orphanet and GeneReviews before clinical use.