Retinitis Pigmentosa (RP)

Sponsored diagnostic testing programs for Retinitis Pigmentosa (RP)

Retinitis pigmentosa is a group of hereditary retinal dystrophies causing progressive night blindness, peripheral vision loss, and eventual central vision decline. Onset and progression vary widely. Genetic testing identifies the causative gene and informs prognosis, trial eligibility, and family counseling.

1 program found for Retinitis Pigmentosa (RP)

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