Oesophageal atresia–tracheoesophageal fistula (EA-TEF) is a common congenital digestive
disease. Patients with EA-TEF face gastrointestinal, surgical, respiratory, otolaryngological …

Abstract Trachea-esophageal defects (TEDs), including esophageal atresia (EA),
tracheoesophageal fistula (TEF), and laryngeal-tracheoesophageal clefts (LTEC), are a …

Introduction Evidence supporting best practice for long-gap esophageal atresia is limited.
The European Reference Network for Rare Inherited Congenital Anomalies (ERNICA) …

Background: After repair of esophageal atresia (EA), children risk digestive and respiratory
morbidity, but knowledge of their health-related quality of life (HRQOL) in China is lacking …

The operative management of patients born with long-gap esophageal atresia (LGEA)
remains a major challenge for most pediatric surgeons, due to the rarity and complex nature …

Background Esophageal atresia (EA) is a rare congenital anomaly characterized by a
discontinuity of the esophagus. Following surgical repair, survival rates have improved …

Objectives: Esophageal dysmotility is common in patients with esophageal atresia (EA).
High-resolution impedance manometry and pressure flow analysis (PFA) allow …

Monitoring the body temperatures and evaluating the thermal asymmetry of newborns give
an idea about neonatal diseases. Infrared thermography is a non-invasive, non-harmful, and …

Standard surgical repair of esophageal atresia/tracheoesophageal fistula (EA/TEF) is via a
right posterolateral thoracotomy. A recognized complication is the later development of …

Œsophageal atresia is a rare neonatal malformation consisting in an interruption of the
continuity of the œsophagus, with or without a tracheo-œsophageal fistula. Although …