Cone-Rod Dystrophy (CRD)

Sponsored diagnostic testing programs for Cone-Rod Dystrophy (CRD)

Cone-rod dystrophy is a group of inherited retinal disorders in which cone dysfunction precedes rod involvement, leading to early loss of visual acuity, color vision defects, and light sensitivity followed by night blindness and visual field loss. Genetic testing clarifies the subtype and informs prognosis and counseling.

1 program found for Cone-Rod Dystrophy (CRD)

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