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Esophageal Atresia and Tracheoesophageal Fistula

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978-3-319-93534-8_14.pdf (1.35 MB)

Publication date

2019-01-01

Authors

Van Der Zee, D. C.ORCID 0000-0001-7627-2932ISNI 0000000396224473
Lindeboom, Maud Y AISNI 0000000140752600
Tytgat, Stefaan H A JORCID 0000-0001-5486-3766ISNI 0000000116053973
Maffi, Michela
Lima, Mario

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DOI

https://doi.org/10.1007/978-3-319-93534-8_14

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Part of book

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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, Taverne, General Medicine

Citation

Van der Zee, D C, Van Herwaarden, M Y, Tytgat, S H, Maffi, M & Lima, M 2019, Esophageal Atresia and Tracheoesophageal Fistula. in Neonatal Surgery : Contemporary Strategies from Fetal Life to the First Year of Age. Springer, pp. 187-206. https://doi.org/10.1007/978-3-319-93534-8_14

URI

https://dspace.library.uu.nl/handle/1874/457182