Current developments in pediatric liver transplantation

Table 1 Diseases indicating pediatric liver transplantation (modified after[7])

Cholestatic disorders	Extrahepatic biliary atresia
	Intrahepatic biliary hypoplasia (Alagille disease, other)
	Progressive familial intrahepatic cholestasis
	Sclerosing cholangitis (primary, neonatal, secondary)
	Nutritive-toxic cirrhosis
	Caroli disease
	Cholangiodysplasia
	Congenital liver fibrosis
	Langerhans cell histiocytosis
Acute liver failure
Metabolic, with cirrhosis	Alpha 1-antitrypsin deficiency
	Wilson's disease
	Tyrosinemia
	Galactosemia
	Neonatal hemochromatosis
	Cystic fibrosis
	Glycogenosis type IV
	Metabolic bile acid dysfunction
	Niemann-Pick's disease
	Gaucher's disease
Metabolic, without cirrhosis	Hyperoxaluria
	Crigler-Najjar syndrome
	Urea cycle disorders
	Familial hypercholesteremia type IIA
	Glycogenosis type IA
	Hemophilia type A, type B
	Protein C deficiency
	Wolman's disease
	Organic acidemia
Hepatitis	Hepatitis B
	Hepatitis C
	Hepatitis non-ABC
	Autoimmune hepatitis
	Neonatal hepatitis
Liver tumors	Hepatoblastoma
	Hepatocellular carcinoma
	Fibrolamellar carcinoma
	Hemangioendothelioma
Various	Budd-Chiari syndrome
	Cryptogenic liver cirrhosis
	Infantile copper overload