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C. De Vigan

Researcher at French Institute of Health and Medical Research

Publications -  21
Citations -  848

C. De Vigan is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Prenatal diagnosis & Pregnancy. The author has an hindex of 14, co-authored 21 publications receiving 816 citations. Previous affiliations of C. De Vigan include Pierre-and-Marie-Curie University.

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Journal ArticleDOI

Prenatal diagnosis of severe structural congenital malformations in Europe

TL;DR: To assess at a population‐based level the frequency with which severe structural congenital malformations are detected prenatally in Europe and the gestational age at detection, and to describe regional variation in these indicators.
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Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999

TL;DR: In this article, the authors examined trends in the live birth prevalence of Down syndrome in Europe in the light of trends in maternal age and in prenatal diagnosis, finding that the proportion of births to mothers of 35 years of age and over has risen quite dramatically from 8 to 14% for the European Union as a whole, with steeper rises in some regions.
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Turner syndrome: evaluation of prenatal diagnosis in 19 European registries.

TL;DR: Prenatal detection of Turner syndrome by ultrasound examination was high in this unselected population and prenatal counseling for 45,X mosaicism should take into account the expectation of a milder phenotype.
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Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe.

TL;DR: It is shown that ultrasound screening is an important tool in the prenatal detection of chromosomal abnormalities in Europe, leading to a significant reduction in the prevalence of livebirth children with chromosomal anomalies.
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[Prevalence and prenatal diagnosis of congenital malformations in the Parisian population: twenty years of surveillance by the Paris Registry of congenital malformations].

TL;DR: The Paris Registry of Congenital Malformations, which includes all births and pregnancy terminations with structural birth defects or chromosomal anomalies, provides population-based data on the prevalence of malforms and their associations with other anomalies.