Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Sarah GutermanClaire BeneteauSylvia RedonCéline DupontChantal MissirianPauline JaegerBerenice HerveClémence JacquinNathalie Douet-GuilbertMarianne TillAnne-Claude TabetKamran MoradkhaniValérie MalanMartine Doco-FenzyFrançois VialardPublished in: Prenatal diagnosis (2019)
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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