Dubin-Johnson syndrome

References

Key articles

Dubin IN, Johnson FB. Chronic idiopathic jaundice with unidentified pigment in the liver cells: a new clinicopathologic entity with report of 12 cases. Medicine. 1954 Sep;33(3):155-97. Abstract

Haimi-Cohen Y, Merlob P, Marcus-Eidlits T, et al. Dubin-Johnson syndrome as a cause of neonatal jaundice: the importance of coproporphyrins investigation. Clin Pediatr (Phil). 1998 Aug;37(8):511-3. Abstract

Paulusma CC, Kool M, Bosma PJ, et al. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome. Hepatology. 1997 Jun;25(6):1539-42.Full text  Abstract

Frank M, Doss M, de Carvalho DG. Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in Dubin-Johnson syndrome. Hepatogastroenterology. 1990 Feb;37(1):147-51. Abstract

Machida I, Wakusawa S, Sanae F, et al. Mutational analysis of the MRP2 gene and long-term follow-up of Dubin-Johnson syndrome in Japan. J Gastroenterol. 2005 Apr;40(4):366-70. Abstract

Reference articles

1. Dubin IN, Johnson FB. Chronic idiopathic jaundice with unidentified pigment in the liver cells: a new clinicopathologic entity with report of 12 cases. Medicine. 1954 Sep;33(3):155-97. Abstract

2. Sprinz H, Nelson RS. Persistent nonhemolytic hyperbilirubinemia associated with lipochrome-like pigment in liver cells: report of 4 cases. Ann Intern Med. 1954 Nov;41(5):952-62. Abstract

3. Dubin IN. Chronic idiopathic jaundice: a review of 50 cases. Am J Med. 1958 Feb;24(2):268-92. Abstract

4. Javitt NB, Kondo T, Kuchiba K. Bile acid secretion in Dubin-Johnson syndrome. Gastroenterology. 1978 Nov;75(5):931-2. Abstract

5. Rastogi A, Krishnani N, Pandey R. Dubin-Johnson syndrome: a clinicopathologic study of twenty cases. Indian J Pathol Microbiol. 2006 Oct;49(4):500-4. Abstract

6. Seligsohn U, Shani M. The Dubin-Johnson syndrome and pregnancy. Acta Hepatogastroenterol. 1977 Jun;24(3):167-9. Abstract

7. Di Zoglio JD, Cardillo E. The Dubin-Johnson syndrome and pregnancy. Obstet Gynecol. 1973 Oct;42(4):560-3. Abstract

8. Skornick YG, Klausner JM, Lelcuk S, et al. Cholelithiasis in Dubin-Johnson syndrome. Surg Gynecol Obstet. 1983 Nov;157(5):447-9. Abstract

9. Sotelo-Avila C, Danis RK, Krafcik J, et al. Cholecystitis in a 17-year-old boy with recurrent jaundice since childhood. J Pediatr. 1988 Apr;112(4):668-74. Abstract

10. Kondo T, Yagi R. Dubin-Johnson syndrome in a neonate. N Engl J Med. 1975 May 8;292(19):1028-9. Abstract

11. Nakata F, Oyanagi K, Fujiwara M, et al. Dubin-Johnson syndrome in a neonate. Eur J Paediatr. 1979;132(4):299-301. Abstract

12. Haimi-Cohen Y, Merlob P, Marcus-Eidlits T, et al. Dubin-Johnson syndrome as a cause of neonatal jaundice: the importance of coproporphyrins investigation. Clin Pediatr (Phil). 1998 Aug;37(8):511-3. Abstract

13. Tsai WH, Teng RJ, Chu JS, et al. Neonatal Dubin-Johnson syndrome. J Paediatr Gastroenterol Nutr. 1994 Feb;18(2):253-4. Abstract

14. Shani M, Seligsohn V, Gilon E, et al. Dubin-Johnson syndrome in Israel: clinical, laboratory and genetic aspects of 101 cases. Q J Med. 1970 Oct;39(156):549-67. Abstract

15. Zlotogora J. Hereditary disorders among Iranian Jews. Am J Med Genet. 1995 Jul 31;58(1):32-7. Abstract

16. Mor-Cohen R, Zivelin A, Fromovich-Amit Y, et al. Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrations. Blood Coagul Fibrinolysis. 2007 Mar;18(2):139-44. Abstract

17. Paulusma CC, Kool M, Bosma PJ, et al. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome. Hepatology. 1997 Jun;25(6):1539-42.Full text  Abstract

18. Toh S, Wada M, Uchiumi T, et al. Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/CMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome. Am J Hum Genet. 1999 Mar;64(3):739-46.Full text  Abstract

19. Van Kuijck MA, Kool M, Merkx GF, et al. Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19d2 by fluorescent in situ hybridization. Cytogenet Cell Genet. 1997;77(3-4):285-7. Abstract

20. Mor-Cohen R, Zivelin A, Rosenberg N, et al. A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients. Hepatology Res. 2005 Feb;31(2):104-11. Abstract

21. Kartenbeck J, Leuschner U, Mayer R, et al. Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome. Hepatology. 1996 May;23(5):1061-6. Abstract

22. Jedlitschky G, Hoffmann U, Kroemer HK. Structure and function of the MRP2 (ABCC2) protein and its role in drug disposition. Expert Opin Drug Metab Toxicol. 2006 Jun;2(3):351-66. Abstract

23. Varma RR, Grainger JM, Scheuer PJ. A case of Dubin-Johnson syndrome complicated by acute hepatitis. Gut. 1970 Oct;11(10):817-21. Abstract

24. Hunter FM, Sparks RD, Flinner RI. Hepatitis with resulting mobilization of hepatic pigment in a patient with Dubin-Johnson syndrome. Gastroenterology.1964 Dec;47:631-5. Abstract

25. Ware AJ, Eigenbrodtt EH, Naftalis J, et al. Dubin Johnson syndrome and viral hepatitis. Gastroenterology. 1974 Sep;67(3):560-1. Abstract

26. Ware AJ, Eigenbrodtt EH, Shorey J. Viral hepatitis complicating the Dubin-Johnson syndrome. Gastroenterology. 1972 Aug;63(2):331-9. Abstract

27. Bar-Meir S, Baron J, Seligson U, et al. 99mTc-HIDA cholescintigraphy rotor in Dubin-Johnson syndromes. Radiology. 1982 Mar;142(3):743-6. Abstract

28. The familial conjugated hyperbilirubinemias. Semin Liver Dis. 1994 Nov;14(4):386-94. Abstract

29. Frank M, Doss M, de Carvalho DG. Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in Dubin-Johnson syndrome. Hepatogastroenterology. 1990 Feb;37(1):147-51. Abstract

30. Rocchi E, Balli F, Gibertini P, et al. Coproporphyrin excretion in healthy newborn babies. J Pediatr Gastroenterol Nutr. 1984 Jun;3(3):402-7. Abstract

31. Mayatepek E, Lehmann WD. Defective hepatobilary leukotriene elimination in patients with Dubin-Johnson syndrome. Clin Chim Acta. 1996 May 30;249(1-2):37-46. Abstract

32. Lyu Y, Wei X, Xu J, et al. [Diagnosis of a patient with Dubin-Johnson syndrome by using next generation sequencing]. [in chi]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):242-245.

33. Wu L, Zhang W, Jia S, et al. Mutation analysis of the ABCC2 gene in Chinese patients with Dubin-Johnson syndrome. Exp Ther Med. 2018 Sep 3;16(5):4201-4206Full text  Abstract

34. Summerfield JA, Scott J, Berman M, et al. Benign recurrent intrahepatic cholestasis: studies of bilirubin kinetics, bile acids, and cholangiography. Gut. 1980 Feb;21(2):154-60. Abstract

35. Wareham NJ, Dickson CJ, Baskerville PA. Benign recurrent intrahepatic cholestasis. J R Soc Med. 1985 Nov;78(11):955-6.Full text  Abstract

36. Machida I, Wakusawa S, Sanae F, et al. Mutational analysis of the MRP2 gene and long-term follow-up of Dubin-Johnson syndrome in Japan. J Gastroenterol. 2005 Apr;40(4):366-70. Abstract

37. Lindberg MC. Hepatobiliary complications of oral contraceptives. J Gen Intern Med. 1992 Mar-Apr;7(2):199-209. Abstract

38. Cohen L, Lewis C, Arias IM. Pregnancy, oral contraceptives and chronic familial jaundice with predominantly conjugated hyperbilirubinemia (Dubin-Johnson syndrome). Gastroenterology. 1972 Jun;62(6):1182-90. Abstract

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