Rationale Esophageal atresia (EA) is a congenital malformation. Nowadays, its initial
prognosis is excellent thanks to improvements in neonatal and surgical management …

Objectives: Esophageal atresia (EA) is a rare malformation characterized of discontinuity of
the esophagus, concurrent with or without a tracheoesophageal fistula (TEF). We report the …

Background Esophageal atresia (EA) and tracheoesophageal fistula (TEF) represent major
therapeutic challenges, frequently associated with serious morbidities following surgical …

The treatment of esophageal atresia is not centralized in Germany. Therefore, high numbers
of departments are involved. Data on the results of esophageal atresia repair from Germany …

The aim of this study was to evaluate the medium-term outcome (health status, medical and
surgical French National Health Authority-recommended follow-up, and quality of life) of …

BACKGROUND: Clinical experiences of adults who underwent surgery for esophageal
atresia at birth is limited. There is some evidence that suggests considerable long‐term …

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 …

Out of a series of 146 patients with oesophageal atresia 9 (6.2%) underwent colon
interposition from 1963 to 1971. All eight surviving patients were seen at follow-up after a …

Progress in perinatal and postoperative techniques has reduced the prognostic role of
traditional risk factors in esophageal atresia (EA). This paper reports on 75 cases of …

While many long-term complications of esophageal atresia (EA) have been well
investigated, little is known about feeding difficulties in children after surgical correction of …