Juvenile Retinoschisis

Sponsored diagnostic testing programs for Juvenile Retinoschisis

X-linked juvenile retinoschisis is a retinal disorder characterized by splitting of the retinal layers, leading to reduced central vision, foveal schisis, and sometimes peripheral schisis with risk of retinal detachment. Symptoms often begin in childhood. Genetic testing confirms the diagnosis and supports monitoring and counseling of at-risk males.

1 program found for Juvenile Retinoschisis

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