Congenital Nystagmus Type 1

Sponsored diagnostic testing programs for Congenital Nystagmus Type 1

Congenital nystagmus type 1 is a hereditary eye movement disorder characterized by involuntary, rhythmic oscillations of the eyes beginning in infancy. Visual acuity can be variably affected, and some individuals adopt a head posture to improve vision. Genetic testing can identify the underlying cause and support counseling.

1 program found for Congenital Nystagmus Type 1

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