It is our pleasure to share with you the 2020 ERKReg registry annual report.
This report is based on patient data submitted to www.registry.erknet.org by ERKNet members, Affiliated Partners, and external centers participating in the registry.
In this report, we present demographics of rare kidney disease patients, the characteristics of the adult and pediatric populations, and information on the clinical quality of care provided by ERKNet centers.
The ERKReg project office would like to thank all its contributors for their dedication and support!
