neonatal cholestasis
Etiology
biliary diseases
- biliary atresia
- biliary duct paucity
- Aagenaes syndrome (norwegian)
- north american indian cirrhosis (north american indian cholestasis)
- Greenland eskimo cholestasis
- bile acide synthetic diseases
- 3beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency
- delta4-3-oxosteroid-5beta-reductase deficiency
- familial intrahepatic cholestasis syndromes (FIHC)
- Byler diseases
- bile anomalies
- cystic fibrosis
metabolic diseases
- alpha-1-antitrypsin deficiency
- Niemann-Pick diseases type C
References
Bove KE, Heubi JE, Balistreri WF, Setchell KD. Bile acid synthetic defects and liver disease: a comprehensive review. Pediatr Dev Pathol. 2004 Jul-Aug;7(4):315-34. PMID: 15383928
Knisely AS. Progressive familial intrahepatic cholestasis: an update. Pediatr Dev Pathol. 2004 Jul-Aug;7(4):309-14. PMID: 15383927
Knisely AS. Progressive familial intrahepatic cholestasis: a personal perspective. Pediatr Dev Pathol. 2000 Mar-Apr;3(2):113-25. PMID: 10679031
Jevon GP, Dimmick JE. Histopathologic approach to metabolic liver disease: Part 1. Pediatr Dev Pathol. 1998 May-Jun;1(3):179-99. PMID: 10463278
P.S.
Histopathological diagnosis of intra- and extrahepatic neonatal cholestasis, Braz J Med Biol Res, July 1998, Volume 31(7) 911-919