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 …

Background: Esophageal atresia (EA) is one of the most common congenital digestive
anomalies. With improvements in surgical techniques and intensive care treatments, the …

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 …

Objective: We assessed esophageal morbidity and relationships between surgical
complications, symptoms, endoscopic findings, immunohistochemistry, and esophageal …

Background. Little is known about how chronic conditions other than prematurity, heart
disease, and Down syndrome affect the risk and severity of hospitalization for respiratory …

Purpose Esophageal atresia (EA) is one of the most frequent congenital alimentary tract
anomalies with a considerable morbidity throughout childhood. This study evaluates the …

Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) is a rare congenital
malformation. Digestive and nutritional problems remain frequent in children with EA both in …

Background and Aims Gastroesophageal reflux (GER) is extremely frequent in patients with
esophageal atresia and tracheoesophageal fistula (EA/TEF). It is often refractory to antireflux …

After repair of esophageal atresia (EA) in a newborn, esophageal dysmotility presenting as
dysphagia and symptomatic gastroesophageal reflux are common. Significant esophageal …

The evaluation and management of an infant with esophageal atresia (EA) and
tracheoesophageal fistula (TEF) are one of the most challenging but rewarding scenarios in …