Early and Late-Onset Retinal Degeneration

Sponsored diagnostic testing programs for Early and Late-Onset Retinal Degeneration

Early and late-onset retinal degenerations comprise a group of inherited disorders causing progressive loss of photoreceptors, leading to night blindness, visual field constriction, and eventual central vision loss. Age at onset and rate of progression vary by genetic cause. Genetic testing helps identify the specific subtype and informs prognosis and counseling.

1 program found for Early and Late-Onset Retinal Degeneration

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