Esophageal Atresia and Tracheoesophageal Fistula

David C. Van der Zee; Maud Y. Van Herwaarden; Stefaan H. Tytgat; Michela Maffi; Mario Lima

doi:10.1007/978-3-319-93534-8_14

Esophageal Atresia and Tracheoesophageal Fistula

David C. Van der Zee, Maud Y. Van Herwaarden, Stefaan H. Tytgat, Michela Maffi, Mario Lima^*

^*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

4 Citations (Scopus)

Abstract

Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) represents a congenital developmental anomaly. It is the most common congenital malformation of the esophagus characterized by an esophageal discontinuity (the upper esophagus terminates in a blind-ending pouch) and a possible tracheoesophageal connection [1–3].

Original language	English
Title of host publication	Neonatal Surgery
Subtitle of host publication	Contemporary Strategies from Fetal Life to the First Year of Age
Publisher	Springer
Pages	187-206
Number of pages	20
ISBN (Electronic)	9783319935348
ISBN (Print)	9783319935324
DOIs	https://doi.org/10.1007/978-3-319-93534-8_14
Publication status	Published - 1 Jan 2019

Keywords

Brain perfusion
Congenital stenosis
Definition of long-gap esophageal atresia
Esophageal atresia
Long-term follow-up
Thoracoscopy

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10.1007/978-3-319-93534-8_14

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abstract = "Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) represents a congenital developmental anomaly. It is the most common congenital malformation of the esophagus characterized by an esophageal discontinuity (the upper esophagus terminates in a blind-ending pouch) and a possible tracheoesophageal connection [1–3].",

keywords = "Brain perfusion, Congenital stenosis, Definition of long-gap esophageal atresia, Esophageal atresia, Long-term follow-up, Thoracoscopy",

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AU - Van der Zee, David C.

AU - Van Herwaarden, Maud Y.

AU - Tytgat, Stefaan H.

AU - Maffi, Michela

AU - Lima, Mario

N1 - Publisher Copyright: © Springer Nature Switzerland AG 2019.

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AB - Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) represents a congenital developmental anomaly. It is the most common congenital malformation of the esophagus characterized by an esophageal discontinuity (the upper esophagus terminates in a blind-ending pouch) and a possible tracheoesophageal connection [1–3].

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KW - Congenital stenosis

KW - Definition of long-gap esophageal atresia

KW - Esophageal atresia

KW - Long-term follow-up

KW - Thoracoscopy

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ER -

Esophageal Atresia and Tracheoesophageal Fistula

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Keywords

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