Fundus Albipunctatus (FA)

Sponsored diagnostic testing programs for Fundus Albipunctatus (FA)

Fundus albipunctatus is a rare form of congenital stationary night blindness characterized by multiple small white dots in the retina and markedly delayed dark adaptation. Central visual acuity is often preserved. Genetic testing confirms the diagnosis and helps differentiate it from progressive retinal dystrophies.

1 program found for Fundus Albipunctatus (FA)

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
ViewOrder
Performing labInvitae | Labcorp