eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | biliary atresia |
| Comorbidity | C0023890|cirrhosis |
| Sentences | 9 |
| PubMedID- 23558067 | If untreated, congenital biliary atresia leads to liver cirrhosis, liver failure and premature death. |
| PubMedID- 20927620 | The limitations are generally related to the fact that many children with portal hypertension have cirrhosis because of biliary atresia and often have abnormal portal vein anatomy; moreover, the size of the child can lead to hepatic perforation and stent malposition. |
| PubMedID- 21762660 | We proposed that features of cirrhotic cardiomyopathy are present in infants with cirrhosis due to biliary atresia (ba) as early as the time of evaluation for liver transplant and will correlate with mortality and postoperative morbidity. |
| PubMedID- 26167250 | Children with advanced biliary cirrhosis due to congenital biliary atresia sometimes showed pathological features of tma, with a concomitant decrease of plasma adamts13 activity. |
| PubMedID- 24838399 | 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. |
| PubMedID- 21436777 | Case report: a 27-year-old female was evaluated as a donor for her 2-year-old son with cholestatic cirrhosis due to biliary atresia. |
| PubMedID- 25534776 | Objectives: recurrent cholangitis may aggravate cholestatic liver cirrhosis in biliary atresia (ba) after the kasai operation. |
| PubMedID- 23180403 | Patients with cirrhosis due to biliary atresia had rickets inspite of taking high dose of vitamin d orally. |
| PubMedID- 20677347 | A 35-year-old mother was scheduled to be the living donor for liver transplantation to her second son, who suffered from biliary atresia complicated with biliary cirrhosis at the age of 2 years. |
Page: 1