Congenital Abnormalities Clinical Trial
Official title:
Registry of Congenital Anomalies in Nouvelle-Aquitaine, France
Regional population-based registry for the epidemiological surveillance of congenital anomalies
By systematically collecting data on congenital anomalies, the registry aims to : - provide essential epidemiological information on congenital anomalies in South West of France - Promote etiological research concerning congenital anomalies, particularly with regard to environmental risk factors (systematic questionnaire) and other teratogenic agents (drugs) - act as an information and resource center for the population, health professionals and managers regarding clusters or exposures or risk factors of concern. - evaluate the effectiveness of primary prevention - assess the impact of developments in prenatal screening - study the fate of children with congenital anomalies, particularly in terms of neurodevelopment, through the creation of cohorts. ;
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