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PedAM

Pediatric Disease Annotations & Medicines




Disease esophageal atresia
Symptom C0016169|fistula
Sentences 85
PubMedID- 25286746 Oesophageal atresia with tracheo-oesophageal fistula in a preterm neonate in limbe, cameroon: case report & brief literature review.
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- 21129543 Tracheoesophageal fistula after primary repair of type c esophageal atresia in the neonatal period: recurrent or missed second congenital fistula.
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- 21922362 Management of esophageal atresia with a tracheoesophageal fistula complicated by gastric perforation.
PubMedID- 25169923 The first thoracoscopic esophageal atresia with tracheo-esophageal fistula (eatef) repair was performed in march of 2000.
PubMedID- 24647291 Background: management of long gap oesophageal atresia with tracheoesophageal fistula (oa tef) is challenging.
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- 25177126 esophageal atresia with tracheoesophageal fistula associated with situs inversus totalis.
PubMedID- 24732499 We have developed low-cost, portable simulators for esophageal atresia with tracheoesophageal fistula (ea/tef) and duodenal atresia (da) that recreate the 3-dimensional challenges for minimally invasive repair.
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- 22878767 Combined oesophageal atresia with upper pouch fistula and meconium peritonitis.
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- 24274029 Gli2–/–,gli3+/– mutants displayed esophageal atresia with tracheo-esophageal fistula and a severe lung phenotype .
PubMedID- 20706657 These associations include tracheoesophageal fistula with esophageal atresia, gerd, esophageal dysmotility, esophageal duplication cysts, and esophageal ectasia .
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- 23679024 The first thoracoscopic esophageal atresia with tracheoesophageal fistula (eatef) repair was performed in march of 2000.
PubMedID- 21651769 Extracranial anomalies comprised esophageal atresia with tracheoesophageal fistula that was corrected at birth, ventricular septal defect, multiple thoracic hemivertebrae, and partial fusion of ribs 4-5 on the right side.
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 .
PubMedID- 26023460 These included epidermolysis bullosa (eb) in two, esophageal atresia with distal trachea-esophageal fistula in one, colonic atresia in one, sensori-neural deafness and multicystic dysplastic kidney (mckd) in one patient.
PubMedID- 23646058 We experienced a case of lung torsion following esophageal atresia with tracheoesophageal fistula (tef) repair that required repeated detorsion and lobectomy surgeries.
PubMedID- 20476878 Tar syndrome and esophageal atresia with tracheoesophageal fistula has been reported in only two cases in literature.
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- 24634808 Isolated esophageal atresia without tracheoesophageal fistula comprise approximately 6 to 8% of cases (laberge and puligandla 2008), with the remainder associated with fistula between the esophagus and trachea.
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 .
PubMedID- 20438916 Three babies had esophageal atresia without fistula, and 2 had the common type with proximal atresia and distal tracheoesophageal fistula.
PubMedID- 24210691 Vacterl (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement.
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- 23400141 Thoracoscopic repair of esophageal atresia with tracheoesophageal fistula (ea/tef) is a technically challenging surgical procedure.
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 .
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- 24596059 Twenty-seven were cases of esophageal atresia with trachea-esophageal fistula (eatef), nine pulmonary metastasis from abdominal solid tumors, six mediastinal masses, three hydatid cyst, three eventration of diaphragm, two bronchiectasis, and one each of h-type tef and congenital esophageal stenosis.
PubMedID- 23904729 esophageal atresia with tracheoesophageal fistula (tef with ea) is a common disease which is associated with many other congenital abnormalities.
PubMedID- 20676578 esophageal atresia with tracheoesophageal fistula and imperforate anus were detected during the neonatal period.
PubMedID- 24765498 Vacterl (vertebral defects, anal atresia, cardiovascular malformation, tracheo-esophageal fistula with esophageal atresia, radial/renal dysplasia and limb anomalies) is a non-random and typically sporadic association of malformations in structures derived from the embryonic mesoderm.
PubMedID- 22953298 Brookes et al reported seven patients of h-type tef and one patient with a missed proximal h-type fistula associated with esophageal atresia.
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- 25448787 Oesophageal atresia with tracheo-oesophageal fistula is a relatively common congenital anomaly occurring in around 1:2500 births.
PubMedID- 22008350 esophageal atresia with distal fistula and long overlapping upper esophageal pouch.
PubMedID- 24630317 Recurrent tracheoesophageal fistula in children with repaired esophageal atresia and the usefulness of flexible bronchoscopy.
PubMedID- 22991204 Introduction: vacterl is a rare, non-random association comprising at least three major component features defined by the acronym, and including vertebral anomalies, anorectal malformations, cardiac defects, tracheo-oesophageal fistula with or without oesophageal atresia (tof/oa), renal abnormalities and limb anomalies.
PubMedID- 21058245 Indications for esophageal replacement included esophageal atresia with or without fistula (10) and caustic injury (6).
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).
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- 21810502 Background: a recent series detailing thoracoscopic repair of esophageal atresia with tracheoesophageal fistula (ea/tef) reported lower complication rates compared with historic controls.
PubMedID- 23172569 Introduction: the thoracoscopic approach to esophageal atresia (ea) with tracheoesophageal fistula (tof) represents a challenging procedure whose real benefits remains unclear.
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.
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- 23088440 Gastrointestinal malformations, such as esophageal atresia with tracheo-esophageal fistula, occur with increased frequency but are not a common feature in trisomy 18; pyloric stenosis has been reported and should be considered in the older infant with vomiting.
PubMedID- 26392058 Background/purpose: the purpose of this study was to investigate the rates of vocal cord paresis/paralysis (vcp) in patients treated for esophageal atresia (ea) with and without fistula performed thoracoscopically versus open.

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