Prenatal findings in 1p36 deletion syndrome: New cases and a literature review
Prenatal Diagnosis2019Vol. 39(10), pp. 871–882
Citations Over TimeTop 14% of 2019 papers
Sarah Guterman, Claire Bénéteau, Sylvia Redon, Céline Dupont, Chantal Missirian, Pauline Jaeger, Bérénice Herve, Clémence Jacquin, Nathalie Douet‐Guilbert, Marianne Till, Anne‐Claude Tabet, Kamran Moradkhani, Valérie Malan, Martine Doco‐Fenzy, François Vialard
Abstract
We conclude that 1p36 deletion is not associated with any specific prenatal signs. We suggest that a prenatal observation of ventriculomegaly, congenital heart defect, or facial dysmorphism should prompt the clinician to consider a diagnosis of 1p36 deletion syndrome.
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