eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | tracheoesophageal fistula |
| Comorbidity | |esophageal atresia |
| Sentences | 101 |
| PubMedID- 23900505 | Esophageal lung diagnosed following the primary repair of esophageal atresia with tracheo-esophageal fistula in a neonate. |
| PubMedID- 22851858 | esophageal atresia (ea) with or without tracheoesophageal fistula (tef) is the most common congenital anomaly of the esophagus. |
| PubMedID- 25926795 | Vater/vacterl association refers to the non-random co-occurrence of at least three congenital anomalies: vertebral defects, anorectal malformations, cardiac defects, tracheoesophageal fistula with or without esophageal atresia, renal malformations, and limb defects; vater/vacterl-phenotype refers to the non-random co-occurrence of at least two of these congenital anomalies (hilger et al., 2013). |
| PubMedID- 24464842 | We present a case of oesophageal atresia with distal tracheo-oesophageal fistula and duodenal atresia, which later on was detected to have cystic variant of biliary atresia. |
| PubMedID- 26023379 | In addition, the diagnosis was missed in patients operated for malrotation elsewhere (n=2), imperforate anus (n=2) and esophageal atresia with tracheo-esophageal fistula (n=1). |
| PubMedID- 25493344 | After surgical correction of esophageal atresia with or without tracheoesophageal fistula, esophageal body motility dysfunction has been reported in nearly all patients. |
| PubMedID- 26294094 | The vater/vacterl association describes the combination of congenital anomalies including vertebral defects, anorectal malformations, cardiac defects, tracheoesophageal fistula with or without esophageal atresia, renal malformations, and limb defects. |
| PubMedID- 23276758 | esophageal atresia with distal tracheoesophageal fistula was diagnosed. |
| PubMedID- 25988067 | The acronym vacterl describes the non-random co-occurrence of three of the following anomalies: vertebral (v), anal (a), cardiac (c), tracheoesophageal fistula with or without oesophageal atresia (te), renal (r) and limb defects (l). |
| PubMedID- 25011995 | Purpose: esophageal atresia (ea), with or without tracheoesophageal fistula (tef), is associated with postoperative gastroesophageal reflux (ger). |
| PubMedID- 26290814 | Infantile hypertrophic pyloric stenosis in postoperative esophageal atresia with tracheoesophageal fistula. |
| PubMedID- 25638612 | Aim: we assessed the occurrence and outcome of major reoperations following repair of esophageal atresia with or without tracheoesophageal fistula (tof). |
| PubMedID- 23904729 | esophageal atresia with tracheoesophageal fistula (tef with ea) is a common disease which is associated with many other congenital abnormalities. |
| PubMedID- 23599581 | esophageal atresia with tracheo-esophageal fistula occurs in approximately 1 in 3000 live births. |
| PubMedID- 20476878 | Tar syndrome and esophageal atresia with tracheoesophageal fistula has been reported in only two cases in literature. |
| PubMedID- 24237863 | Other recognised conditions were mainly amniotic bands (n = 27, 25%), of which most of the cases had transverse reduction defects (14 upper limb, 10 lower limb) and syndactyly (9 upper limb, 4 lower limb), arthrogryposis (n = 14, 13%) and vater/vacterl association (vertebral defects, anal atresia, cardiac anomalies, tracheo-oesophageal fistula with oesophageal atresia, renal dysplasia, limb defects (n = 13, 12%)). |
| PubMedID- 22696089 | 8esophageal atresia with distal tracheoesophageal fistula. |
| PubMedID- 23964045 | The cooccurrence of congenital diaphragmatic hernia and oesophageal atresia with distal tracheo-oesophageal fistula is very rare and carries high mortality. |
| PubMedID- 25052256 | Thoracoscopic versus open repair of esophageal atresia with tracheoesophageal fistula at a single institution. |
| PubMedID- 20706657 | Abnormalities of the esophagus such as gastroesophageal reflux disease (gerd), esophageal motility disorders, esophageal duplications cysts, and tracheoesophageal fistula with esophageal atresia are rare but documented occurrences with congenital diaphragmatic hernia [1, 2]. |
| PubMedID- 25286746 | Oesophageal atresia with tracheo-oesophageal fistula in a preterm neonate in limbe, cameroon: case report & brief literature review. |
| PubMedID- 24210691 | All 3 core features (anal atresia, tracheoesophageal fistula with esophageal atresia, and costovertebral anomalies) were present in only 12% of the patients. |
| PubMedID- 23117198 | Purpose: to describe the frequency of different findings at fluoroscopic evaluation of postoperative esophagus in children following repair for esophageal atresia with or without tracheo-esophageal fistula. |
| PubMedID- 26548437 | esophageal atresia (ea) with or without tracheo-esophageal fistula (tef) is a relatively rare congenital anomaly. |
| PubMedID- 25196458 | Background: vacterl association refers to a combination of congenital anomalies that can include: vertebral anomalies, anal atresia, cardiac malformations, tracheo-esophageal fistula with esophageal atresia, renal anomalies (typically structural renal anomalies), and limb anomalies. |
| PubMedID- 25927380 | Several congenital malformations have been sporadically described such as esophageal atresia with tracheoesophageal fistula, pierre-robin sequence, cardiovascular malformation, and hemihyperplasia. |
| PubMedID- 24435793 | Emergency out-of-hospital presentation of neonatal esophageal atresia with tracheoesophageal fistula. |
| PubMedID- 21846383 | As initially described, the condition included the statistically non-random co-occurrence of a group of congenital malformations: vertebral defects, anal atresia, tracheo-esophageal fistula (tef) with esophageal atresia, and radial and renal dysplasia [1,2]. |
| PubMedID- 26055999 | Background: the vacterl association is a typically sporadic, non-random collection of congenital anomalies that includes vertebral defects, anal atresia, cardiac defects, tracheoesophageal fistula with esophageal atresia, renal anomalies, and limb abnormalities. |
| PubMedID- 26498647 | Vacterl (vertebral defects (v), anal atresia (a), cardiac malformations (c), tracheoesophageal fistula with esophageal atresia (te), renal dysplasia (r), and limb anomalies (l)) was defined as at least three components present. |
| PubMedID- 20610191 | Congenital malformations of the esophagus are frequently encountered by pediatric surgeons, especially esophageal atresia with or without tracheo-esophageal fistula. |
| PubMedID- 21922362 | Management of esophageal atresia with a tracheoesophageal fistula complicated by gastric perforation. |
| PubMedID- 25960363 | He had esophageal atresia with distal tracheoesophageal fistula. |
| PubMedID- 23377222 | esophageal atresia with double tracheoesophageal fistula. |
| PubMedID- 24647291 | Background: management of long gap oesophageal atresia with tracheoesophageal fistula (oa tef) is challenging. |
| PubMedID- 21238638 | Background/purpose: congenital diaphragmatic hernia (cdh) and esophageal atresia with tracheoesophageal fistula (ea/tof) can be repaired thoracoscopically, but this may cause hypercapnia, acidosis, and reduced cerebral oxygenation. |
| PubMedID- 21430849 | esophageal atresia with tracheo-esophageal fistula: making anastomosis easy. |
| PubMedID- 24851754 | Background: esophageal atresia (ea), with or without tracheoesophageal fistula (tef), is commonly associated with gastroesophageal reflux (ger) after surgical repair. |
| PubMedID- 25169923 | The first thoracoscopic esophageal atresia with tracheo-esophageal fistula (eatef) repair was performed in march of 2000. |
| PubMedID- 26309244 | Feeding and swallowing disorders are commonly seen in clinical practice in infants and children treated for esophageal atresia with or without tracheoesophageal fistula. |
| PubMedID- 25148734 | Aims: oesophageal atresia (oa) with or without tracheoesophageal fistula (tof) is the most common congenital anomaly of the oesophagus. |
| PubMedID- 24239950 | Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12. |
| PubMedID- 20676578 | esophageal atresia with tracheoesophageal fistula and imperforate anus were detected during the neonatal period. |
| PubMedID- 22066071 | Associate anomalies were combined in 3 patients, 1 patient combined the vertebral, anorectal, cardiac, esophageal atresia with tracheoesophageal fistula, renal and radial and limb anomalies (vacter) syndrome. |
| PubMedID- 25755969 | On contrast, chest x-ray performed directly after birth the presence of congenital defect—esophageal atresia with tracheoesophageal fistula—was confirmed (the upper end of esophagus visible at the level of th4–5, dilated intestinal loops filled with air). |
| PubMedID- 26023532 | Out of five patients, four patients had tracheo-esophageal fistula with long gap esophageal atresia and one patient had isolated esophageal atresia. |
| PubMedID- 25131394 | Background: the acronym vater/vacterl association describes the combination of at least three of the following cardinal features: vertebral defects, anorectal malformations, cardiac defects, tracheoesophageal fistula with or without esophageal atresia, renal malformations, and limb defects. |
| PubMedID- 25402321 | Results: in an 18-month period from 1947 to 1948, in new plymouth small provincial hospital, henry barrett successfully completed the first primary repair of an oesophageal atresia with distal tracheoesophageal fistula in the southern hemisphere and the second and third successful ligations of patent ductus arteriosus in new zealand. |
| PubMedID- 24274029 | Gli2–/–,gli3+/– mutants displayed esophageal atresia with tracheo-esophageal fistula and a severe lung phenotype [20]. |
| PubMedID- 20849991 | The non-random association of vertebral defects (v), anorectal malformations (a), cardiac defects (c), tracheoesophageal fistula with esophageal atresia (te), renal malformations (r), and limb defects (l) is termed vacterl association. |