Abstract Background In 10–15% of children with esophageal atresia (EA) delayed
reconstruction of esophageal atresia (DREA) is necessary due to long-gap EA and/or …

Aim To perform a definitive procedure in pure esophageal atresia by gastric pull-up in the
newborn. Patients/methods A primary gastric pull-up was performed in six newborns with …

Background The early outcomes of using jejunal interpositions to establish esophageal
continuity in patients who have had a failed repair of esophageal atresia (EA) were …

Background Esophageal atresia is a major congenital foregut anomaly. Affected patients
often suffer from respiratory and gastro-intestinal morbidity. The objective of this study is to …

Introduction We present the short-and long-term outcomes in the management of pure long-
gap esophageal atresia (LGEA) using the Foker technique (FT) of esophageal elongation by …

Objective The aim of this study was to evaluate the outcome of patients with oesophageal
atresia type III (EA), focusing on the presence of late sequelae and quality of life. Methods …

The management of long-gap esophageal atresia remains challenging with limited
consensus on the definition, evaluation, and surgical approach to treatment. Efforts to …

Background Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF)
remains one of the most common gastrointestinal neonatal malformations. Even though …

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

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 …