Optic Atrophy

Sponsored diagnostic testing programs for Optic Atrophy

Hereditary optic atrophy refers to progressive degeneration of the optic nerve, resulting in bilateral vision loss, color vision deficits, and central scotomas. Onset may occur in childhood or adulthood depending on the genetic subtype. Genetic testing clarifies the cause, guides prognosis, and supports counseling and family screening.

1 program found for Optic Atrophy

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