Aniridia is a very rare disease and every family affected is often alone to face the diagnosis. Even nationally, there’s often only a small group of individuals. Get to know aniridia.
Aniridia Europe, the federation of European aniridia associations and representatives, has been founded to change this situation. Read our mission objectives.
As of March 2019, the federation includes 12 national associations as well as support groups and contact persons in 20 other European countries.
Get in touch with someone in your country.
News & events
- Aniridia Europe and Aniridia-Net working together to promote knowledge on Aniridia and collaboration among scientists and with patients
- Webinar: Digital rebels against distance, Saturday 24th April 2021, 11.00 a.m. CEST
- Report on the webinar “News from the frontier”, 27th February 2021