Stargardt Disease

Sponsored diagnostic testing programs for Stargardt Disease

Stargardt disease is an inherited macular dystrophy characterized by progressive central vision loss due to accumulation of lipofuscin in the retinal pigment epithelium. Symptoms typically begin in childhood or adolescence. Genetic testing confirms the diagnosis and informs prognosis, counseling, and eligibility for clinical trials.

1 program found for Stargardt Disease

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