Diagnostic des cholestases du nouveau-né

Medecine Therapeutique Pediatrie

Volumn 1, Issue 4, 1998, Pages 357-364

  Jacquemin, Emmanuel ^a   Bernard, Olivier ^a  

^a BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0004307954     PISSN: 12865494     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. Psacharopoulos HT., Mowat A.P. 1978. Incidence and early history of obstructive jaundice in infancy in Southeast England. In : Javitt N.B., ed. Neonatal hepatitis and biliary afresia. Washington DC : US Department of Health, Education and Welfare Publications, 167-175.
2. Mieli-Vergani G., Howard E.R., Portmann B., Mowat A.P. 1989. Late referral for biliary atresia-missed opportunities for effective surgery. Lancet i : 421-423.
3. Bernard O., Gauthier F 1991. Progrès récents en hépatologie pédiatrique. Arch Fr Pediatr 48 : 53-56.
4. Schroeder D., Smith L., Prain H.C. 1989. Antenatal diagnosis of choledocal cyst at 15 weeks' gestation : etiologic implications and management. J Pediatr Surg 24 : 936-938.
5. Mowat AP 1994. Liver disorders in child hood. Newton : Butterworth-Heinemann Publishers.
6. Debray D., Pariente D., Gauthier F., Myara A., Bernard O. 1993. Cholelithiasis in infancy . a study of 40 cases. J Pediatr 122 : 385-391.
7. Davenport M., Heaton N.D., Howard E.R. 1991. Spontaneous perforation of the bile ducts in infants. Br J Surg 78 : 1068-1070.
8. Laurent J., Gauthier F., Hadchouel M. 1993. Atrésie des voies biliaires Encyclopédie Médicale et Chirurgicale série Hépatologie 7.070.A.10, 2 p.
9. Debray D., Pariente D., Urvoas E., Hadchouel M., Bernard O. 1994. Sclerosing cholangitis in children. J Pediatr 124 : 49-56.
10. Alagille D., et al. 1987. Syndromic paucity of interlobular bile ducts (Alagille's syndrome or arteriohepatic dysplasia) : review of 80 cases. J Pediatr 110 : 195-200.
11. Deleuze J.F., Dhorne-Pollet S., Pollet N., Meunier-Rotival M., Hadchouel M. 1995. Le syndrome d'Alagitle en 1995 : données cliniques et génétiques. Gastroenterol Clin Biol 19 : 587-596.
12. Teckman J.H., Qu D., Perlmutter D.H. 1996. Molecular pathogenesis of liver disease in α1-antitrypsin deficiency. Hepatology 24 : 1504-1516.
13. Clayton R.J., Iber F.L, Ruebner B.H., Mc KusickV. 1969 Byler's disease. Fatal familial intrahepatic cholestasis in an Amish kindred. Am J Dis Child 117 . 112-124.
14. Maggiore C., Bernard O., Riely C., Hadchouel M., Lemonnier A., Alagille D. 1987. Normal serum γ-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosis. J Pediatr 111 : 251-252.
15. Whitington P.F., Freese D.K., Alonso E.M., Schwarzenberg S.J., Sharp H.L. 1994. Clinical and biochemical findings in progressive familial intrahepatic cholestasis. J Pediatr Gastroenterol Nutr 18 : 134-141.
16. 2--steroid dehydrogenase/ isomerase deficiency. J Pediatr 125 : 379-384.
17. 4-3 oxosteroid 5β-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis. J Clin Invest 82 : 2148-2157.
18. Vanier M T., Pentchev P , Rodriguez-Lafrasse C., Rousson R. 1991. Niemann-Pick disease type C : an update. J Inher Metab Dis 14 : 580-595.
19. Wanders R.J.A., et al. 1990. The inborn errors of peroxisomal beta-oxidation. A review. J Inher Metab Dis 13 : 411-418.
20. Leblanc A., Odievre M., Hadchouel M., Gendrel D., Chaussain J.L., Rappaport R. 1981. Neonatal cholestasis and hypoglycemia : possible role of cortisol deficiency. J Pediatr 99 : 577-580.
21. Rintala R., Lindahl H., Pohjavuori M., Saxen H., Sariola H. 1993. Surgical treatment of intractable cholestasis associated with total parenteral nutrition in premature infants. J Pediatr Surg 28 : 716-719.
22. Jacquemin E., Maurage C., Borderon J.C., Gold F., Laugier J., Rolland J.C 1995. Early cholestasis in premature infants receiving total parenteral nutrition : a possible consequence of shock and hypoxia. Eur J Pediatr Surg 5 : 259-261.
23. Alagille D. Cholestasis in the first 3 months of life 1979. Progress in liver diseases 6 : 471-485.
24. Rotig A , Cormier V., Rustin P., Munnich A. 1995. Présentation clinique des maladies mitochondriales. médecine thérapeutique 1 : 465-475.
25. Lykavieris P., Bernard O., Hadchouel M. 1996. Neonatal cholestasis as the presenting feature in cystic fibrosis. Arch Dis Child 75 : 67-70.
26. Goncalves I., et al. 1995. Mitochondrial respiratory chain defect : a new etiology for neonatal cholestasis and early liver insufficiency. J Hepatology 23 : 290-294.
27. OdaT., et al. 1997. Mutations in the human Jagged 1 gene are responsible for Alagille syndrome. Nature Genet 16 : 235-242.
28. Carlton V E.H., Knisely AS, Freimer N.B. 1995. Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region. Hum Mol Genet 4 : 1049-1053.
29. Deleuze J.F., et al. 1996. Defect of multidrug resistance 3 (MDR3) gene expression in a subtype of progressive familial intrahepatic cholestasis. Hepatology 23 : 904-906.
30. Jacquemin E., et al. 1997. Ursodeoxycholic therapy in pediatric patients with progressive familial intrahepatic cholestasis. Hepatology 25 : 519-523
31. Whitington P.F., Whitington G.C. 1988. Partial external diversion of bile for the treatment of intractable pruritus associated with intrahepatic cholestasis. Gastroenterology 95 : 130-136.
32. Hadchouel M., Fabre M. 1995. Diagnostic histologique d'une cholestase néonatale. Ann Pathol 15 : 357-364.
33. Treem W.R., Grant E.E., Barth K.H., Kremers P.W. 1988. Ultrasound guided percutaneous cholecystocholangiography for early differentiation of cholestatic liver disease in infants. J Pediatr Gastroenterol Nutr 7 : 347-352.
34. Wilkinson M.K., Mieli-Vergani G., Ball C., Portmann B., Mowat A.P 1991 Endoscopic retrograde cholangiopancreatography in infantile cholestasis. Arch Dis Childh 66 : 121-123.