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  2. European Platform on Rare Disease Registration
  3. EUROCAT

EUROCAT

European network of population-based registries for the epidemiological surveillance of congenital anomalies

  • List item: EUROCAT Network
     

    EUROCAT Network

    Overview of the EUROCAT network, its organisation and committees

     
     
  • List item: Member Registries
     

    EUROCAT Members

    Information about the EUROCAT member registries, coverage and how to apply for membership

  • List item: EUROCAT Data
     

    Data and surveillance

    Prevalence tables, prenatal detection rates and reports on statistical monitoring of congenital anomalies

  • List item: Data Collection
     

    Data Collection

    Data collection guidelines, data quality indicators and procedures for requesting EUROCAT data
     

  • List item: Prevention and risk factors
     

    Prevention and risk factors

    EUROCAT studies and recommendations for primary prevention of congenital anomalies
     

  • List item: Research
     

    Research

    Active, ongoing studies of the causes, prevention, treatment and care of affected children. See the list for more details.

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