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 Day 2021 is coming!!!
- Aniridia-Net webinar. Managing aniridia: dos and don’ts from infancy to adulthood
- Report on Aniridia-Net webinar: Eyes open on stem cells dynamics, signature and niche by Ruby Shalom Feuerstein and Daniel Aberdam