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PedAM

Pediatric Disease Annotations & Medicines




Disease esophageal atresia
Symptom |fistula
Sentences 85
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- 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- 25052256 Thoracoscopic versus open repair of esophageal atresia with tracheoesophageal fistula at a single institution.
PubMedID- 22722826 Results: all the 30 cases had type-c esophageal atresia with tracheoesophageal fistula as per gross classification.
PubMedID- 21180508 Many years ago, i had diagnosed esophageal atresia with tracheo-esophageal fistula in the emergency room and had sent the baby to the ward.
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- 25475795 Background/purpose: we describe our initial experience of thoracoscopic esophageal atresia with distal tracheoesophageal fistula (ea/tef) repair.
PubMedID- 23599581 esophageal atresia with tracheo-esophageal fistula occurs in approximately 1 in 3000 live births.
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- 25960794 Thoracoscopic repair of esophageal atresia with a distal fistula - lessons from the first 10 operations.
PubMedID- 23276758 However, few cases of esophageal atresia with distal tracheoesophageal fistula in extremely low birth weights infants have been reported.
PubMedID- 22759370 Diagnosis of esophageal atresia (ea) with tracheo-esophageal fistula (tef) can be easily done in newborns with symptoms of excessive salivation and failure to pass infant-feeding tube (ift) into the stomach.
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- 23061032 We report a newborn who developed right sided chylothorax after repair of an esophageal atresia (ea) with tracheo-esophageal fistula (tef).
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- 23407700 There was one interesting case of esophageal atresia with tracheoesophageal fistula which bypassed the gastric contents to the proximal esophagus.
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- 26023467 A clinical diagnosis of esophageal atresia with distal tracheo-esophageal fistula (vogt type iii) was made.
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- 25032210 esophageal atresia with tracheo-oesophageal fistula (tef) occurs in 1 in 3500 live births.
PubMedID- 24239950 Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12.
PubMedID- 23365480 Three cases of recurrent tracheoesophageal atresia with fistula were treated by bronchoscpic glue injection.
PubMedID- 25287747 Besides the common features, the two boys show anomalies not previously described, such as retinal coloboma, esophageal atresia with esophageal fistula, long fingers, camptodactyly, clinodactyly, and long broad toes.
PubMedID- 23044311 Background: advances in minimally invasive surgical techniques and neonatal intensive care for neonates have allowed for repair of the neonatal esophageal atresia with tracheoesophageal fistula (ea/tef) to be approached endoscopically.
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- 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- 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- 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- 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- 24741218 The association of pyloric stenosis and esophageal atresia with tracheoesophageal fistula, although rare, is well documented.
PubMedID- 22422375 The acronym vater/vacterl association is used to describe the non-random co-occurrence of vertebral defects (v), anorectal malformations (a), cardiac defects (c), tracheo-esophageal fistula with or without esophageal atresia (te), renal malformations (r), and limb defects (l).
PubMedID- 21238630 A term female newborn underwent uncomplicated repair of esophageal atresia with tracheoesophageal fistula (type c) then coarctation of the aorta.
PubMedID- 23980565 The present study was designed to evaluate the accuracy of preoperative ultrasonography (us) in depicting the structure of esophageal atresia with distal fistula (ea-df) and to determine its role in planning the surgical strategy by digitally measuring the interpouch distance (id).
PubMedID- 23900505 Esophageal lung diagnosed following the primary repair of esophageal atresia with tracheo-esophageal fistula in a neonate.

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