European Reference Network on Rare Endocrine Conditions (Endo-ERN)
The European Society of Endocrinology (ESE) in collaboration with the European Society for Paediatric Endocrinology (ESPE) worked together to establish Endo-ERN. The objective of Endo-ERN and all European Reference Networks (ERNs) is to ensure that it is the medical knowledge and expertise that travel, rather than the patients.
Endo-ERN is a network of 100+ Reference Centres (RCs) in 28 countries that offer access to clinical experts for patient rare endocrine conditions.
Endo-ERN offers:
- Secure virtual consultations
- Rare disease registries (EuRRECa)
- Patient information endorsed by European Patient Advocacy Groups (ePAGs)
- Rare disease research & guidelines
- Training & Education
Register for the Endo-ERN newsletter to be kept up-to-date.