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To stent or not to stent? A meta‐analysis of endonasal congenital bilateral choanal atresia repair
The Laryngoscope, 2016The use of nasal stents as a postoperative adjunct following repair of choanal atresia remains controversial. The study objective was to systematically review the literature regarding the efficacy and safety of stenting following transnasal endoscopic ...
J. Strychowsky +4 more
semanticscholar +1 more source
Oesophageal atresia and biliary atresia: a rare association
Pediatric Surgery International, 2004Oesophageal atresia is known to be associated with cardiovascular, gastrointestinal, genitourinary and skeletal anomalies. Its association with biliary atresia is very rare and only a few cases have been reported in the literature. Although biliary atresia could be part of a multiple anomaly syndrome, its isolated occurrence is even rare.
M. Srinivasa Rao +4 more
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Neonatal diagnosis of biliary atresia: a practical review and update
Pediatric Radiology, 2021D. Brahee, B. Lampl
semanticscholar +1 more source
Esophageal atresia and tracheo-esophageal fistula.
Seminars in Pediatric Surgery, 2017Management of esophageal atresia has merged from correction of the anomaly to the complete spectrum of management of esophageal atresia and all its sequelae.
D. van der Zee +2 more
semanticscholar +1 more source
Seminars in Neonatology, 2003
Biliary atresia (BA) is a congenital obliterative cholangiopathy of unknown aetiology, affecting both the intra- and extrahepatic bile ducts. Although relatively rare, BA must be excluded in any infant with conjugated hyperbilirubinaemia since the prognosis is improved by early diagnosis and prompt surgery.
Hiroyuki, Kobayashi, Mark D, Stringer
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Biliary atresia (BA) is a congenital obliterative cholangiopathy of unknown aetiology, affecting both the intra- and extrahepatic bile ducts. Although relatively rare, BA must be excluded in any infant with conjugated hyperbilirubinaemia since the prognosis is improved by early diagnosis and prompt surgery.
Hiroyuki, Kobayashi, Mark D, Stringer
openaire +2 more sources
The endoscopic transseptal approach for choanal atresia repair
International Forum of Allergy and Rhinology, 2016There are many standard repair options for choanal atresia including puncture, dilatation and drilling of the atretic plate. Most of these techniques involve postoperative stenting, which may promote granulation and scarring, with possible progression to
P. Wormald +7 more
semanticscholar +1 more source
Biliary Atresia: Clinical Lessons Learned
Journal of Pediatric Gastroenterology and Nutrition - JPGN, 2015Biliary atresia is a rare disease of unclear etiology, in which obstruction of the biliary tree causes severe cholestasis leading to cirrhosis and ultimately death if left untreated.
Amy G. Feldman, C. Mack
semanticscholar +1 more source
Nature Reviews Disease Primers
Biliary atresia (BA) is a progressive inflammatory fibrosclerosing disease of the biliary system and a major cause of neonatal cholestasis. It affects 1:5,000-20,000 live births, with the highest incidence in Asia. The pathogenesis is still unknown, but emerging research suggests a role for ciliary dysfunction, redox stress and hypoxia.
Paul K. H. Tam +9 more
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Biliary atresia (BA) is a progressive inflammatory fibrosclerosing disease of the biliary system and a major cause of neonatal cholestasis. It affects 1:5,000-20,000 live births, with the highest incidence in Asia. The pathogenesis is still unknown, but emerging research suggests a role for ciliary dysfunction, redox stress and hypoxia.
Paul K. H. Tam +9 more
openaire +2 more sources
Pediatrics, 1981
Since Kasai et al1 demonstrated convincingly that biliary atresia was a treatable, and in some instances curable condition, the approach to the jaundiced infant has changed dramatically. Efforts to identify infants with this disease were greatly accelerated as the "hands off" philosophy, predicated on the assumption that attempts to correct biliary ...
openaire +2 more sources
Since Kasai et al1 demonstrated convincingly that biliary atresia was a treatable, and in some instances curable condition, the approach to the jaundiced infant has changed dramatically. Efforts to identify infants with this disease were greatly accelerated as the "hands off" philosophy, predicated on the assumption that attempts to correct biliary ...
openaire +2 more sources