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Fig. 4 | Journal of Biomedical Science

Fig. 4

From: Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases

Fig. 4

Distributions 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 cholestasis

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