Aniridia is a very rare disease and every family affected is often alone to face the diagnosis. Aniridia Europe, the federation of European aniridia associations and representatives, has been founded to change this situation.
Our objectives are:
- collaborate in spreading proper and correct information on aniridia and the best available treatments
- support and inspire research by creating scientific interest on aniridia and associated illnesses and connecting professionals both at local and international level
- promote the development of national and international guidelines on aniridia
- encourage people affected by aniridia to create associations in other countries