NEUROD1-Related Early-Onset Diabetes

Sponsored diagnostic testing programs for NEUROD1-Related Early-Onset Diabetes

NEUROD1-related early-onset diabetes is a form of monogenic diabetes presenting in adolescence or early adulthood, sometimes associated with mild neurodevelopmental features or sensorineural hearing loss. Affected individuals often respond well to tailored therapy based on the genetic etiology. Genetic testing confirms the diagnosis and informs treatment and family risk.

1 program found for NEUROD1-Related Early-Onset Diabetes

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