Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome.

doi:10.1002/pd.6302

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Article

Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome.

Prenatal diagnosis - 1 Feb 2023

Bedei Ivonne, Gloning Karl-Philipp, Joyeux Luc, Meyer-Wittkopf Matthias, Willner Daria, Krapp Martin, Scharf Alexander, Degenhardt Jan, Heling Kai-Sven, Kozlowski Peter, Trautmann Kathrin, Jahns Kai M, Geipel Annegret, Tekesin Ismail, Elsässer Michael, Wilhelm Lucas, Gottschalk Ingo, Baumüller Jan-Erik, Birdir Cahit, Schröer Andreas, Zöllner Felix, Wolter Aline, Schenk Johanna, Gehrke Tascha, Spaeth Alicia, Axt-Fliedner Roland

Abstract excerpt

OBJECTIVE: Omphalocele is known to be associated with genetic anomalies like trisomy 13, 18 and Beckwith-Wiedemann syndrome, but not with Turner syndrome (TS). Our aim was to assess the incidence of omphalocele in fetuses with TS, the phenotype of this association with other anomalies, their karyotype, and the fetal outcomes. METHOD: Retrospective multicenter study of fetuses with confirmed diagnosis of TS. Data...

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PMID: 36600414
DOI: 10.1002/pd.6302

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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