Wagner Syndrome

Sponsored diagnostic testing programs for Wagner Syndrome

Wagner syndrome is a hereditary vitreoretinopathy characterized by vitreous degeneration, retinal detachment risk, cataracts, and progressive vision loss. Systemic features are uncommon. Genetic testing confirms the diagnosis and guides ophthalmologic monitoring and counseling.

1 program found for Wagner Syndrome

Programs

1 program
Invitae Unlock™

Invitae Inherited Retinal Disorders Panel

This program offers U.S. clinicians access to comprehensive genetic testing for patients with suspected inherited retinal diseases, including RP, CRD, LCA, Stargardt disease, and other IRDs. Testing is also appropriate for asymptomatic individuals with a family history of IRD or a known pathogenic variant in a relevant gene, supporting diagnosis, risk assessment, and patient management.

Ophthalmology
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Performing labInvitae | Labcorp