Esophageal atresia (EA) is one of the most common congenital digestive malformations and
requires surgical correction early in life. Dedicated centers have reported survival rates up to …

Esophageal atresia (EA) is a rare congenital anomaly. Enhanced operative techniques and
intensive care treatment have improved survival among children with repaired EA (range, 93 …

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: Currently, no recommendations exist for the endoscopic screening of
patients in adulthood, with surgically corrected esophageal atresia (EA), for the development …

Background & Aims Esophageal atresia is rare, but improved surgical and intensive care
techniques have increased rates of survival in children, so there are now many adults with …

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

OBJECTIVE: Esophageal atresia (EA) predisposes to gastroesophageal reflux that is
associated with intestinal metaplasia and may result in development of adenocarcinoma of …

Background Endoscopic surveillance of adults with esophageal atresia is advocated, but the
optimal surveillance strategy remains uncertain. This study aimed to provide …

Esophageal atresia (EA) is the most common congenital anomaly of the esophagus. With
the progress of surgical and anesthetic techniques, the survival is now more than 90% and …

Objectives: Patients with esophageal atresia/tracheoesophageal fistula (EA-TEF) can
develop Barrett esophagus as a long-term consequence of their condition. Intestinal …