Esophageal atresia with or without tracheoesophageal fistula (EA/TEF): association of different EA/TEF subtypes with specific co-occurring congenital anomalies and implications for diagnostic workup

Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) represents the most common developmental malformation of the upper digestive tract. It is classified into six subtypes according to the classification of Vogt, depending on anatomical variation of this malformation. Around 50% of...

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Hauptverfasser: Bogs, Thomas Karl-Peter (VerfasserIn) , Zwink, Nadine (VerfasserIn) , Chonitzki, Vera (VerfasserIn) , Hölscher, Alice (VerfasserIn) , Boemers, Thomas M. (VerfasserIn) , Muensterer, Oliver (VerfasserIn) , Kurz, Ralf (VerfasserIn) , Heydweiller, Andreas (VerfasserIn) , Pauly, Marcus (VerfasserIn) , Leutner, Andreas (VerfasserIn) , Ure, Benno M. (VerfasserIn) , Lacher, Martin (VerfasserIn) , Deffaa, Oliver Johannes (VerfasserIn) , Thiele, Holger (VerfasserIn) , Bagci, Soyhan (VerfasserIn) , Jenetzky, Ekkehart (VerfasserIn) , Schumacher, Johannes (VerfasserIn) , Reutter, Heiko (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2018
In: European journal of pediatric surgery
Year: 2017, Jahrgang: 28, Heft: 02, Pages: 176-182
ISSN:1439-359X
DOI:10.1055/s-0036-1597946
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1055/s-0036-1597946
Verlag, lizenzpflichtig, Volltext: http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1597946
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Verfasserangaben:Thomas Bogs, Nadine Zwink, Vera Chonitzki, Alice Hölscher, Thomas M. Boemers, Oliver Münsterer, Ralf Kurz, Andreas Heydweiller, Marcus Pauly, Andreas Leutner, Benno M. Ure, Martin Lacher, Oliver Johannes Deffaa, Holger Thiele, Soyhan Bagci, Ekkehart Jenetzky, Johannes Schumacher, Heiko Reutter
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Zusammenfassung:Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) represents the most common developmental malformation of the upper digestive tract. It is classified into six subtypes according to the classification of Vogt, depending on anatomical variation of this malformation. Around 50% of the patients with EA/TEF present additional anomalies, which often influence, next to the EA/TEF subtype, the overall prognosis of EA/TEF newborns. Here, we investigated the association of the different EA/TEF subtypes with co-occurring congenital anomalies in EA/TEF patients and demonstrate their implications for postnatal diagnostic workup.
Beschreibung:Publikationsdatum: 06. Januar 2017 (online)
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Beschreibung:Online Resource
ISSN:1439-359X
DOI:10.1055/s-0036-1597946