Biliary atresia

Summary Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. Good outcomes for infants depend on early referral and timely Kasai portoente...

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Veröffentlicht in:	The Lancet (British edition) 2009-11, Vol.374 (9702), p.1704-1713
Hauptverfasser:	Hartley, Jane L, Dr, Davenport, Mark, Prof, Kelly, Deirdre A, Prof
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - epidemiology Abnormalities, Multiple - genetics Alcohol use Algorithms Biliary Atresia - diagnosis Biliary Atresia - epidemiology Biliary Atresia - etiology Biliary Atresia - surgery Biological and medical sciences Changes Children & youth Data collection Diagnosis, Differential Disease Progression Early Diagnosis General aspects Genes Genetic Predisposition to Disease - epidemiology Genetic Predisposition to Disease - genetics Humans Infant, Newborn Infants Internal Medicine Jaundice, Neonatal - etiology Liver Liver cirrhosis Liver diseases Liver Transplantation Medical sciences Neonatal Screening Palliative Care Patient Selection Portoenterostomy, Hepatic Prognosis Quality of life Rare Diseases Referral and Consultation Risk Factors Studies Transplants & implants Treatment Outcome
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