Oguchi Disease

Sponsored diagnostic testing programs for Oguchi Disease

Oguchi disease is a rare form of congenital stationary night blindness characterized by markedly impaired dark adaptation and a distinctive golden-gray discoloration of the fundus that normalizes after prolonged dark adaptation. Visual acuity is often near normal. Genetic testing confirms the diagnosis and differentiates it from progressive retinal dystrophies.

1 program found for Oguchi 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