PedAM
Pediatric Disease Annotations & Medicines
| Disease | liver disease |
| Phenotype | C0005411|biliary atresia |
| Sentences | 5 |
| PubMedID- 23696064 | Therefore, severe liver disease in infants with biliary atresia cannot be excluded only on the basis of ultrasound findings. |
| PubMedID- 20870622 | Three infants were identified as having significant liver disease, including one with biliary atresia. |
| PubMedID- 20422055 | The patients with liver cirrhosis due to tyrosinemia and biliary atresia had evidence of liver disease from the early days after being born. |
| PubMedID- 21998045 | Purpose: to evaluate the efficacy of ultrasonographically (us)-guided percutaneous cholecystocholangiography (pcc) for early diagnosis and characterization of biliary atresia in infants with cholestatic liver disease. |
| PubMedID- 22886419 | Chronic cholelithiasis, primary sclerosing cholangitis (psc), primary biliary cirrhosis (pbc), and biliary atresia are examples of cholestatic human liver diseases, as reviewed elsewhere.1, 2 cholestasis results in bile duct injury caused by the accumulation of toxic hydrophobic bile acids, which also damages the periportal hepatocytes.3 in response to injury, both biliary epithelial cells (becs) and hepatocytes will proliferate to compensate for their respective loss. |
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