Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) is the most
common congenital anomaly of the esophagus. The improvement of survival observed over …

Esophageal atresia (EA) affects one in 2,840 newborns, and over half have associated
anomalies that typically affect the midline. After EA repair in infancy, gastroesophageal reflux …

Purpose A prospective national register was established in 2008 to record all new cases of
live-birth newborns with esophageal atresia (EA). This epidemiological survey was …

Background Esophageal atresia (EA) is a rare congenital anomaly with high infantile
survival rates. The aim of this study was to outline the prevalence of common long-term …

Purpose Management of newborns with long-gap esophageal atresia (LGEA) remains a
challenge for pediatric surgeons. Since spontaneous growth of the esophageal segments …

The successful operative management of oesophageal atresia and tracheo-oesophageal
atresia has been available for approximately 70 years. During this time neonatal intensive …

We report Down syndrome (DS)‐associated congenital gastrointestinal (GI) defects
identified during a 15 year, population‐based study of the etiology and phenotypic …

Objective: This systematic review with meta-analysis compares health-and provider-based
outcomes of thoracoscopic to thoracotomy repair of esophageal atresia. Summary of …

Survivors of esophageal atresia are reaching their adulthood in large numbers for the first
time enabling assessment of true long-term outcome among this group of patients. This …

Although after oesophageal atresia (OA) repair in infancy, respiratory problems are
common, their natural history remains unclear. We assessed morbidity, pulmonary function …