Fig. 4From: Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseasesDistributions of final diagnosis of intrahepatic cholestasis in infancy in 135 Taiwanese infants 2000–2012. (Adapted from Lu FT et al., J Pediatr Gastroenterol Nutr 2014;59: 695–701). ALG, Alagille syndrome; GGT, gamma-glutamyl transpeptidase; IEBAM, inborn error of bile acid metabolism; NH, neonatal hepatitis; NICCD, neonatal intrahepatic cholestasis caused by citrin deficiency; PFIC, progressive familial intrahepatic cholestasisBack to article page