Flatrès, Charlotte
Aumar, Madeleine
Ley, Delphine
Sfeir, Rony
Nicolas, Audrey
Bonnevalle, Michel
Duhamel, Alain
Gottrand, Frédéric
Article History
Received: 5 November 2020
Revised: 19 February 2021
Accepted: 21 March 2021
First Online: 16 April 2021
Competing interests
: The authors declare no competing interests.
: Data were collected from a population-based registry of esophageal atresia, which began collecting data prospectively on all infants born with esophageal atresia in France from January 1, 2007. The registry was approved by the National Informatics and Privacy Committee and was qualified by the National Committee of Register. All data were used anonymously, and the parents were informed of the aims of the registry.