Congenital Stationary Night Blindness (CSNB)

Sponsored diagnostic testing programs for Congenital Stationary Night Blindness (CSNB)

Congenital stationary night blindness is a non-progressive retinal disorder characterized by impaired night vision, sometimes with decreased visual acuity, myopia, or nystagmus. Symptoms typically present in childhood and remain relatively stable over time. Genetic testing confirms the diagnosis and distinguishes CSNB from progressive dystrophies.

1 program found for Congenital Stationary Night Blindness (CSNB)

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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