“…Biliary atresia is a congenital biliary disorder, commonly causing progressive and obstructive pathological changes in the intra and extrahepatic ducts, secondary to inflammation, and often causing progressive fibrosis and liver damage, resulting in cirrhosis of the liver and consequent liver failure [2,3,4,5] It is characterized by absence or severe deficiency of the extra-hepatic biliary tree [6], and accounts for over half of children who undergo liver transplantation [5]. It is thought to affect 1 in 10,000 -15,000 newborn infants, with a recognized male preponderance [3,5].…”