Aniridia Europe gathers people all over the continent
We want to support people with aniridia in all countries and help them to share information and build useful networks in their own countries and abroad.
What is Aniridia?
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 September 2021, the federation includes 13 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
ANA Scientific Symposium: PAX6, aniridia, and beyond. November 6-7, 2021 – University of Virginia (USA)
The newly formed Aniridia North America (ANA) announces its first event to strengthen and expand research focused on aniridia and related problems. The 2021 Aniridia North America Symposium: PAX6, Aniridia, and Beyond will bring together top researchers from North...
Aniridia North America (ANA), an umbrella organization for aniridia stakeholders and international collaboration
Aniridia Europe is very happy to welcome and congratulate Aniridia North America (ANA), a US-based nonprofit organization, recently created with the mission “to represent, serve, and support the North American community of persons affected by aniridia and their...
Webinar: A fresh look to aniridia pathophysiology with a focus on translational implications, Friday 22nd October 2021, 18.00 CET
Aniridia-Net and Aniridia Europe are happy to announce this new webinar on aniridia, recommended to an audience of professionals working in the field. The speakers, Dr. Juan Álvarez de Toledo (Centro de Oftalmología Barraquer, Barcelona, Spain) and Dr. Paolo Rama...