Sveinsson Chorioretinal Atrophy (SCRA)

Sponsored diagnostic testing programs for Sveinsson Chorioretinal Atrophy (SCRA)

SCRA is an inherited retinal degeneration marked by expanding chorioretinal atrophy and progressive vision loss, often beginning in childhood or young adulthood. The disease course is gradual but relentless. Genetic testing confirms the diagnosis and supports monitoring and family risk assessment.

1 program found for Sveinsson Chorioretinal Atrophy (SCRA)

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