Diagnostic Process for Inherited Retinal Diseases (IRDs)
Navigating the Diagnostic Process for IRDs
In Episode 2 of the EURETINA Independent Medical Education (IME) Video Interview Series on Genetic Diagnosis Awareness of Inherited Retinal Diseases (IRDs), Professors Omar Mahroo and Dominik Fischer return to discuss the step-by-step process of diagnosing IRDs and the role of genetic testing within that pathway.
The episode highlights the essential clinical investigations that can guide a diagnosis, including when to initiate genetic testing and how to determine the most appropriate type of genetic test. The discussion also addresses next steps when initial testing—such as whole genome sequencing—does not yield conclusive results.
This conversation offers a practical, experience-based perspective on diagnostic strategy and is an important resource for clinicians involved in the care of patients with suspected inherited retinal diseases.
👉 Watch Now to view Episode 2 and continue exploring the EURETINA IME Video Interview Series on IRD genetic diagnosis awareness.

This Independent Medical Education (IME) activity is supported by Johnson & Johnson Vision and Neurotech.
