Abstract
Biliary atresia (BA) is characterised by fibro-obliteration of the biliary tree, presenting in infancy with obstructive jaundice. The Kasai portoenterostomy (‘Kasai’) surgery aims to re-establish bile flow by creating a bilioenteric conduit. However, liver transplantation (LT) is often required; BA remains the lead indication for LT in paediatrics.
| Original language | English |
|---|---|
| Pages (from-to) | 581 |
| Number of pages | 1 |
| Journal | Archives of Disease in Childhood |
| Volume | 110 |
| Issue number | 7 |
| Early online date | 19 Jan 2025 |
| DOIs | |
| Publication status | Published - Jul 2025 |
Keywords
- Gastroenterology
- Jaundice
- Microbiology
- Paediatrics
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