EUROCAT is a network of population-based registries for the epidemiological surveillance of congenital anomalies, covering 1.7 million births in 21 countries of Europe
Announcements [Archive Announcements]
Meetings & Events
12th EUROCAT European Symposium and 28th Registry Leaders Meeting 12-14 June 2013Once again we had a very successful and informative meeting. Many thanks to all those who contributed and helped to organise the Symposium and Registry Leaders MeetingThe next Registry Leaders Meeting will be held in Belfast, UK on 26-27 June 2014. Further details to follow.
CHW Wijers, IALM van Rooij, MK Bakker, CLM Marcelis, MC Addor, I Barisic, J Beres, S Bianca, F Bianchi, E Calzolari, R Greenlees, N Lelong, A Latos-Bielenska, CM Dias, R McDonnell, C Mullaney, V Nelen, M O'Mahony, A Queisser-Luft, J Rankin, N Zymak-Zakutnia, I de Blaauw, N Roeleveld, HEK de Walle (2013). Anorectal Malformations and Pregnancy-Related Disorders: A Registry-Based Case-Control Study in 17 European Regions, BJOG [link]
EUROCAT's Position on the Commission's Proposed EU Regulation on Data Protection[read more]EUROCAT/EUROPLAN Recommendations on Policies to be Considered for the Primary Prevention of Congenital Anomalies in National Plans and Strategies on Rare Diseases [pdf]