Establishing a linked European Cohort of Children with Congenital Anomalies
EUROlinkCAT will use the EUROCAT infrastructure to support 21 EUROCAT registries in 13 European countries to link their congenital abnormalities data to mortality, hospital discharge, prescription and educational databases. And hypotheses on their health has to be investigated at an EU level from standardised summary data and analyses on an estimated 200,000 children with a CA born from 1995 to 2014 up to age 10. This enhanced information will allow optimisation of personalised care and treatment decisions for children with rare CAs.
INTERNATIONAL CHARITABLE FUND OMNI-NET FOR CHILDREN