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ERN-EYE, a European Reference Network dedicated to Rare Eye Diseases
Rare Eye Diseases display major heterogeneity and represent the leading cause of visual impairment/visual loss in children & young adults. Significant barriers remain for early diagnosis, patient management & research. EU experts decided to join forces in a European Reference Network.
I am a patient :
Where can I find an expert center?
Who are the patient representatives?
I am a professional :
Where can I find an expert center?
What is the virtual clinic (CPMS)?
What is ERN-EYE? Find out in video!
Map of the ERN-EYE members across Europe (click here to read it)
RECENT NEWS
Read now the ERN-EYE position statement published in Orphanet Journal of Rare Diseases (Open Access) on the need for widely available genomic testing in rare eye diseases.
The ERN Research Mobility Fellowship funding opportunity opening on March 15th, allow you to get new competences and knowledge in an institution outside of your country.
The first GREET will take place on 26th March 2021 about Medical Retina (including pediatric cases).
Disclaimer
ERN-EYE is a European Reference Network (ERN) approved by the ERN Board of Member States. The ERNs are supported by the European Commission. For more information about the ERNs and the EU health strategy, please visit http://ec.europa.eu/health/ern The content on this website represents the views of the network and is its sole responsibility; it can in no way be taken to reflect the views of the European Commission or any other body of the European Union.
This ERN is supported by:
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