WordNet

an abnormal condition in which a normal opening or tube in the body (as the urethra) is closed or absent
relating to the bile ducts or the gallbladder

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1. 胆道閉鎖症 biliary atresia
2. 新生児や乳幼児に生じる胆汁うっ滞の原因 causes of cholestasis in neonates and young infants
3. 抱合型高ビリルビン血症関連の遺伝性疾患 inherited disorders associated with conjugated hyperbilirubinemia
4. 新生児や乳児の胆汁うっ滞への評価アプローチ approach to evaluation of cholestasis in neonates and young infants
5. 肝内胆管の消失および胆管消失症候群 hepatic ductopenia and vanishing bile duct syndrome

Hepatocytes buried in the cirrhotic livers of patients with biliary atresia proliferate and function in the livers of uPA-NOG mice.

Suemizu H1, Nakamura K, Kawai K, Higuchi Y, Kasahara M, Fujimoto J, Tanoue A, Nakamura M.
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.Liver Transpl.2014 May 18. doi: 10.1002/lt.23916. [Epub ahead of print]
The pathogenesis of biliary atresia (BA), which leads to end-stage cirrhosis in most patients, has been thought to inflame and obstruct the intrahepatic and extrahepatic bile ducts. BA is not believed to be caused by abnormalities in parenchymal hepatocytes. However, there has been no report of a de
PMID 24838399

Expansion of PROMININ-1-expressing cells in association with fibrosis of biliary atresia.

Mavila N1, James D, Shivakumar P, Nguyen MV, Utley S, Mak K, Wu A, Zhou S, Wang L, Vendyres C, Groff M, Asahina K, Wang KS.
Hepatology (Baltimore, Md.).Hepatology.2014 May 3. doi: 10.1002/hep.27203. [Epub ahead of print]
Biliary atresia (BA), the most common cause of end-stage liver disease and the leading indication for pediatric liver transplantation, is associated with intrahepatic ductular reactions within regions of rapidly expanding periportal biliary fibrosis. While the extent of such biliary fibrosis is a ne
PMID 24798639

Saito T1, Terui K, Mitsunaga T, Nakata M, Kuriyama Y, Higashimoto Y, Onuma N, Takahashi H, Yoshida H.
Journal of pediatric gastroenterology and nutrition.J Pediatr Gastroenterol Nutr.2014 Apr 23. [Epub ahead of print]
BACKGROUND:: The significance of pediatric ERCP according to age or disease variation is inconclusive. This study aimed to evaluate the usefulness of pediatric ERCP in diagnosing or treating small children with pancreaticobiliary disorders including choledochal cyst (CC) and biliary atresia (BA).MET
PMID 24762457