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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease tracheoesophageal fistula
Symptom |esophageal atresia
Sentences 78
PubMedID- 24398799 esophageal atresia with or without tracheoesophageal fistula (ea/tef) is a relatively common birth defect often associated with additional congenital anomalies such as vertebral, anal, cardiovascular, renal and limb defects, the so-called vacterl association.
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- 25177126 esophageal atresia with tracheoesophageal fistula associated with situs inversus totalis.
PubMedID- 21922362 Management of esophageal atresia with a tracheoesophageal fistula complicated by gastric perforation.
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- 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- 21180502 A report of two neonates of esophageal atresia with tracheoesophageal fistula who had acute gastric volvulus in the postoperative period and required gastropexy after correction of the volvulus.
PubMedID- 21238630 A term female newborn underwent uncomplicated repair of esophageal atresia with tracheoesophageal fistula (type c) then coarctation of the aorta.
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- 26023409 Esophageal anastomosis medial to preserved azygos vein in esophageal atresia with tracheoesophageal fistula: restoration of normal mediastinal anatomy.
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- 24741218 The association of pyloric stenosis and esophageal atresia with tracheoesophageal fistula, although rare, is well documented.
PubMedID- 20056230 Diagnosis of esophageal atresia with tracheoesophageal fistula: is there a need for gastrointestinal contrast.
PubMedID- 20960892 Comparison of thoracoscopic and open repair of esophageal atresia with tracheoesophageal fistula.
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- 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- 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- 23679024 The first thoracoscopic esophageal atresia with tracheoesophageal fistula (eatef) repair was performed in march of 2000.
PubMedID- 24469481 Background: the objective of this study was to assess effect of number of associated anomalies on outcome in oesophageal atresia with or without tracheoesophageal fistula patients.
PubMedID- 22851858 esophageal atresia (ea) with or without tracheoesophageal fistula (tef) is the most common congenital anomaly of the esophagus.
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- 24435793 Emergency out-of-hospital presentation of neonatal esophageal atresia with tracheoesophageal fistula.
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- 25493344 After surgical correction of esophageal atresia with or without tracheoesophageal fistula, esophageal body motility dysfunction has been reported in nearly all patients.
PubMedID- 22696089 8esophageal atresia with distal tracheoesophageal fistula.
PubMedID- 24630317 Recurrent tracheoesophageal fistula in children with repaired esophageal atresia and the usefulness of flexible bronchoscopy.
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- 24107708 Two patients who had persistent lsvc also had vacterl syndrome (vertebral defects, anal atresia, cardiac malformations, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, and limb anomalies).

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