Parents’ experiences of condition management in children born with esophageal atresia-tracheoesophageal fistula during their early childhood [PDF]
Orphanet Journal of Rare DiseasesBackground Esophageal atresia-tracheoesophageal fistula (EA-TEF) is a rare congenital malformation of the esophagus and airways. Following surgical repair, children commonly face ongoing aerodigestive morbidity.
Michaela Dellenmark-Blom +12 more
doaj +2 more sources
Successful treatment of corrosive esophageal atresia in a child using combined antegrade-retrograde dilation: a case report [PDF]
Frontiers in PediatricsCorrosive esophageal injury in children may rarely lead to complete atresia. No standardized treatment exists for pediatric corrosive esophageal atresia. This case demonstrates a novel minimally invasive approach.
Hao Wu +9 more
doaj +2 more sources
Diagnostic value of prenatal ultrasound in the typing of fetal esophageal atresia [PDF]
Frontiers in MedicineObjectiveTo investigate the prenatal ultrasound image features and diagnostic value of fetal esophageal atresia (EA).MethodsThe clinical and prenatal ultrasound data of 24 fetuses with suspected esophageal atresia diagnosed by prenatal ultrasound and/or ...
Lijun Song +6 more
doaj +2 more sources
Interleukin‐18 signaling promotes activation of hepatic stellate cells in mouse liver fibrosis
Hepatology, EarlyView., 2022 Interleukin‐18 signaling promotes activation of hepatic stellate cells in mouse liver fibrosis. Abstract Background and Aims Nucleotide‐binding oligomerization domain‐like receptor‐family pyrin domain‐containing 3 (NLRP3) inflammasome activation has been shown to result in liver fibrosis.
Jana Knorr +19 more
wiley +1 more source
Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy
Hepatology, EarlyView., 2022 Serum bile acid levels predict outcomes in patients with biliary atresia who achieve normalized bilirubin levels after Kasai portoenterostomy. Abstract Background and Aims In biliary atresia, serum bilirubin is commonly used to predict outcomes after Kasai portoenterostomy (KP).
Sanjiv Harpavat +22 more
wiley +1 more source
Esophageal atresia – gastrointestinal and nutritional complications [PDF]
Romanian Journal of Pediatrics, 2020 Esophageal atresia (EA) is one of the most common digestive malformations; 50% of the patients with EA have other congenital anomalies associated. Due to the progress regarding the surgical techniques and the treatments given in the neonatal intensive ...
Ioana-Valentina Nenciu +3 more
doaj +1 more source
PLoS ONE, 2023 BackgroundEsophageal atresia (EA) with or without tracheoesophageal fistula (TEF) is the most common congenital anomaly of the esophagus. This anomaly continues to cause considerable morbidity and mortality in Sub-Saharan Africa, presenting various ...
Natnael Moges +14 more
doaj +1 more source
Atresia of the esophagus - thoracotomy vs thoracoscopy
Journal of Education, Health and Sport, 2018 Esophageal atresia is a congenital medical condition associated with the disorder of the alimentary tract. It is usually associated with one or more fistulas to the trachea. Esophageal atresia is often associated with other congenital defects.
Robert Chudzik +4 more
doaj +3 more sources
Tantangan Dalam Diagnosis Atresia Esofagus Tipe C: Sebuah Laporan Kasus
Keluwih, 2023 —Newborn with hypersalivation and vomiting can be caused by various causes, one of which is esophageal atresia. Esophageal atresia is a rare disease, the most life-threatening congenital malformations in newborns, a congenital gastro-intestinal ...
Lucia Pudyastuti Retnaningtyas
doaj +1 more source
Dysmotility in Esophageal Atresia: Pathophysiology, Characterization, and Treatment
Frontiers in Pediatrics, 2017 Esophageal dysmotility is almost universal after esophageal atresia (EA) repair and is mainly related to the developmental anomaly of the esophagus.
Christophe Faure +1 more
doaj +1 more source