Usher Syndrome

Sponsored diagnostic testing programs for Usher Syndrome

Usher syndrome combines sensorineural hearing loss with progressive retinitis pigmentosa and may include vestibular dysfunction. Severity and onset differ by subtype. Genetic testing identifies the subtype, informs prognosis, and guides hearing and vision management and family counseling.

1 program found for Usher 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