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Fig. 5 | BMC Gastroenterology

Fig. 5

From: Role of percutaneous liver biopsy in infantile cholestasis: cohort from Arabs

Fig. 5

Differential diagnosis of liver biopsy driven infantile cholestasis. INH ideopathic neonatal hepatitis; BA biliary atresia; PFIC progressive familial intrahepatic cholestasis; NSC neonatal sclerosing cholangitis; BASD bile acid synthesis disorder; CMV cytomegalovirus. Miscellaneous causes include, one case each: Dubin-Johnson syndrome, Tight junction (TJP) mutation (USP53), Multifactorial: prematurity and total parenteral nutrition (TPN), Spino-cerebellar ataxia type XXI, Down syndrome, Progressive familial intrahepatic cholestasis 1 (PFIC 1), Bile duct paucity (FOXA1 gene mutation), Gaucher disease, Ciliopathy WDR 19 mutation, Ciliopathy TTC 26 gene mutation, Hepatitis B virus cholestasis (HBV), Panhypopituitarism, Zellweger syndrome, IARS mutation = Infantile hepatopathy steatosis and portal-tract fibrosis, intellectual disability, muscular hypotonia and growth retardation syndrome

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