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PedAM

Pediatric Disease Annotations & Medicines




Disease tracheoesophageal fistula
Phenotype |esophageal atresia
Sentences 80
PubMedID- 20476878 Tar syndrome and esophageal atresia with tracheoesophageal fistula has been reported in only two cases in literature.
PubMedID- 22028963 Fowler reported subclavian artery occlusion in a premature baby who had (r) closed tube thoracostomy drainage after thoracotomy for repair of tracheoesophageal fistula with oesophageal atresia [65].
PubMedID- 20706657 tracheoesophageal fistula with esophageal atresia is a known association of cdh, albeit a rare one with an incidence of 0.005 per 1000 births [4].
PubMedID- 24631216 esophageal atresia with tracheoesophageal fistula (ea/tef) is a serious human birth defect, in which the esophagus ends before reaching the stomach, and is aberrantly connected with the trachea.
PubMedID- 22696089 8esophageal atresia with distal tracheoesophageal fistula.
PubMedID- 21504909 A specific set of the malformations that are typical of cd forms the vacterl association (omim 192350; acronym of vertebral anomalies, anal atresia, cardiac defect, tracheoesophageal fistula with esophageal atresia, renal abnormalities and limb abnormalities).
PubMedID- 24152966 The acronym “vacterl” describes the combination of at least three of the following congenital anomalies: vertebral defects (v), anorectal malformations (a), cardiac defects (c), tracheoesophageal fistula with or without esophageal atresia (te), renal malformations (r), and limb defects (l).
PubMedID- 25032210 We had an uncommon situation where a nasogastric tube reached the stomach through the trachea and tracheo-esophageal fistula, leading to misdiagnosis in a case of esophageal atresia with tracheoesophageal fistula.
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- 23679034 Long-term respiratory complications of congenital esophageal atresia with or without tracheoesophageal fistula: an update.
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- 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- 26023409 In standard technique for repair of esophageal atresia with tracheoesophageal fistula (ea/tef), the azygos vein is ligated and divided before the mobilization of esophageal pouches [1-3].
PubMedID- 24630317 Recurrent tracheoesophageal fistula in children with repaired esophageal atresia and the usefulness of flexible bronchoscopy.
PubMedID- 24482727 A 3-day-old neonate, given a diagnosis of esophageal atresia (ea) with tracheoesophageal fistula (tef), which is large and just above the carina, was scheduled for tef repair.
PubMedID- 25927380 Several congenital malformations have been sporadically described such as esophageal atresia with tracheoesophageal fistula, pierre-robin sequence, cardiovascular malformation, and hemihyperplasia.
PubMedID- 23084209 esophageal atresia with tracheoesophageal fistula (ea-tef) associated with a right aortic arch poses a dilemma to the pediatric surgeon, often necessitating an operative approach via a left thoracotomy.
PubMedID- 24741218 The association of pyloric stenosis and esophageal atresia with tracheoesophageal fistula, although rare, is well documented.
PubMedID- 24829898 Progress in surgical techniques and perinatal care allowed dramatic improvement of survival in the decades elapsed since the first successful primary repair of esophageal atresia with tracheoesophageal fistula (ea ± tef) in 1941 (1).
PubMedID- 20676578 esophageal atresia with tracheoesophageal fistula and imperforate anus were detected during the neonatal period.
PubMedID- 22851858 esophageal atresia (ea) with or without tracheoesophageal fistula (tef) is the most common congenital anomaly of the esophagus.
PubMedID- 24311518 Although esophageal atresia (ea) with tracheoesophageal fistula (tef) is a potentially fatal complication that can only be rescued through surgical correction, no reports have addressed the efficacy of surgical intervention for ea in patients with trisomy 18.
PubMedID- 23904729 tracheoesophageal fistula with esophageal atresia with absent external ear: a unusual association.
PubMedID- 24363086 Purpose: gastrointestinal malformations such as esophageal atresia with tracheoesophageal fistula (ea/tef) and duodenal atresia (da) have been reported in infants born to hyperthyroid mothers or with congenital hypothyroidism.
PubMedID- 23549274 The acronym vater/vacterl association describes the combination of at least three of the following congenital anomalies: vertebral defects (v), anorectal malformations (a), cardiac defects (c), tracheoesophageal fistula with or without esophageal atresia (te), renal malformations (r), and limb defects (l).
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- 23845651 Aim of the study: this retrospective study was performed to compare the relative incidence of esophageal atresia (ea) with proximal tracheoesophageal fistula (ptef) at our institution with those reported in literature and to test the hypothesis that our higher relative incidence is caused by the routine use of tracheoscopy.
PubMedID- 24435793 Emergency out-of-hospital presentation of neonatal esophageal atresia with tracheoesophageal fistula.
PubMedID- 21238630 A term female newborn underwent uncomplicated repair of esophageal atresia with tracheoesophageal fistula (type c) then coarctation of the aorta.
PubMedID- 25161763 Results: among the nine patients, three (33.3%) were preterm babies and five (55.5%) had associated anomalies, which included diaphragmatic eventration (n = 2), congenital diaphragmatic hernia, esophageal atresia with tracheoesophageal fistula, and antral web.
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- 25475795 Background/purpose: we describe our initial experience of thoracoscopic esophageal atresia with distal tracheoesophageal fistula (ea/tef) repair.
PubMedID- 26123147 He had esophageal atresia with distal tracheoesophageal fistula.
PubMedID- 25011995 Purpose: esophageal atresia (ea), with or without tracheoesophageal fistula (tef), is associated with postoperative gastroesophageal reflux (ger).
PubMedID- 21516499 We present a case of a neonate who underwent surgery for esophageal atresia (ea) with tracheoesophageal fistula (tef) with an unusual finding on postoperative chest radiographs.
PubMedID- 23407700 Miscellaneous cases consisted of esophageal atresia with tracheoesophageal fistula bypassing gastric vomitus (n = 1), hypertrophic pyloric stenosis with initial impression of bilious vomiting (n = 1), hirschprung disease (n = 1) and adhesion band (n = 1).
PubMedID- 25988067 The acronym ‘vater/vacterl’ association describes the combination of at least three of the following congenital anomalies: vertebral defects (v), anorectal malformations (a), cardiac defects (c), tracheoesophageal fistula with or without oesophageal atresia (te), renal malformations (r) and limb defects (l) [1].
PubMedID- 22005378 Multiple anastomotic complications following repair of oesophageal atresia with tracheoesophageal fistula: a report of two cases.
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- 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- 22722826 Results: all the 30 cases had type-c esophageal atresia with tracheoesophageal fistula as per gross classification.
PubMedID- 23044311 Comparison of neonatal tolerance to thoracoscopic and open repair of esophageal atresia with tracheoesophageal fistula.
PubMedID- 23679024 The first thoracoscopic esophageal atresia with tracheoesophageal fistula (eatef) repair was performed in march of 2000.
PubMedID- 24239950 Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12.
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- 24634808 Delayed diagnosis of high proximal tracheoesophageal fistula in esophageal atresia and a novel approach to the treatment of tracheomalacia by submanubrial tracheopexy.
PubMedID- 20056230 Diagnosis of esophageal atresia with tracheoesophageal fistula: is there a need for gastrointestinal contrast.
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.
PubMedID- 24851754 Background: esophageal atresia (ea), with or without tracheoesophageal fistula (tef), is commonly associated with gastroesophageal reflux (ger) after surgical repair.
PubMedID- 23604057 Background: congenital diaphragmatic hernia (cdh) and esophageal atresia with tracheoesophageal fistula (ea/tef) can be repaired thoracoscopically, but this may cause hypercapnia and acidosis, which are potentially harmful.

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