Oculoauricular Syndrome

Sponsored diagnostic testing programs for Oculoauricular Syndrome

Oculoauricular syndrome is characterized by structural eye anomalies and external ear malformations, sometimes with associated hearing loss or developmental delay. Ocular findings may include coloboma or microphthalmia. Genetic testing clarifies the diagnosis and guides hearing and vision surveillance and counseling.

1 program found for Oculoauricular Syndrome

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