Bradyopsia

Sponsored diagnostic testing programs for Bradyopsia

Bradyopsia is a rare cone system disorder characterized by difficulty adapting to changes in light levels and delayed visual processing of moving images. Visual acuity may be mildly reduced, but structural retinal abnormalities can be subtle. Genetic testing confirms the diagnosis and distinguishes it from other retinal dystrophies.

1 program found for Bradyopsia

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