©The Author(s) 2022.
World J Gastrointest Pharmacol Ther. Jul 5, 2022; 13(4): 33-46
Published online Jul 5, 2022. doi: 10.4292/wjgpt.v13.i4.33
Published online Jul 5, 2022. doi: 10.4292/wjgpt.v13.i4.33
Table 1 Associated anomalies of embryonic or syndromic biliary atresia
| Origin of anomaly | Description |
| Splenic anomalies | Asplenia, double splen, polysplenia |
| Cardiovascular anomalies | Interrupted/absent inferior vena cava, dextrocardia, left atrial isomerism, other cardiac anomalies (pulmonary stenosis, ASD, VSD, PDA, total anomalous pulmonary venous return, coarctation of the aorta, TOF, hypoplastic left heart syndrome) |
| Portal vein and hepatic artery anomalies | Preduodenal portal vein, anomaly originated hepatic artery |
| Abdominal anomalies | Situs inversus, midgut malrotation, intestinal atresia (esophageal, duodenal or jejunal), anular pancreas, short pancreas |
| Renal anomalies | Renal agenesis, hypoplastic or polycystic kidneys |
| Other uncommon anomalies | Primary ciliary dyskinesia, caudal regression syndrome |
- Citation: Islek A, Tumgor G. Biliary atresia and congenital disorders of the extrahepatic bile ducts. World J Gastrointest Pharmacol Ther 2022; 13(4): 33-46
- URL: https://www.wjgnet.com/2150-5349/full/v13/i4/33.htm
- DOI: https://dx.doi.org/10.4292/wjgpt.v13.i4.33