The APS Type 1 (APECED) Registry Launches on Rare Disease Day 2019

In celebration of World Rare Disease Day 2019, the APS Type 1 Foundation is thrilled to announce the official launch of the APS Type 1 (APECED) Registry.  We hope the information collected in this registry will help researchers better understand APS Type 1 and help clinicians be able to better diagnose and treat the conditions caused by APS Type 1.  Help us reach our goal of enrolling 100 families this year!