Clinical features of Dubin-Johnson syndrome: An analysis of 10 cases

Yongle WU; Hui LIU; Xinye QIU; Yanan SUN; Qinghuan ZENG; Yuanzhi LIU; Peng LI; Shibin ZHANG

doi:10.3969/j.issn.1001-5256.2021.02.029

Volume 37 Issue 2

Mar. 2021

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Article Navigation > Journal of Clinical Hepatology > 2021 > 37(2): 396-399

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Clinical features of Dubin-Johnson syndrome: An analysis of 10 cases

DOI: 10.3969/j.issn.1001-5256.2021.02.029

a.
Center of Hepatic and Digestive Disease, Beijing YouAn Hospital, Capital Medical University, Beijing 100069, China
b.
Department of Pathology, Beijing YouAn Hospital, Capital Medical University, Beijing 100069, China

Received Date: 2020-08-19
Accepted Date: 2020-10-28
Published Date: 2021-02-20

Abstract

- Jaundice, Chronic Idiopathic,
- Signs and Symptoms,
- Diagnosis

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References(16)

References

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[2]	DUBIN IN, JOHNSON FB. Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases[J]. Medicine (Baltimore), 1954, 33(3): 155-197. DOI: 10.1097/00005792-195409000-00001
[3]	KIM KY, KIM TH, SEONG MW, et al. Mutation spectrum and biochemical features in infants with neonatal Dubin-Johnson syndrome[J]. BMC Pediatr, 2020, 20(1): 369. DOI: 10.1186/s12887-020-02260-0
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[5]	WU L, LI Y, SONG Y, et al. A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China[J]. Orphanet J Rare Dis, 2020, 15(1): 74. DOI: 10.1186/s13023-020-1346-4
[6]	BAI J, ZHENG SJ, DUAN ZP. Clinical features and diagnosis of four common types of congenital hyperbilirubinemia[J]. J Clin Hepatol, 2019, 35(8): 1680-1683. (in Chinese) DOI: 10.3969/j.issn.1001-5256.2019.08.005 白洁, 郑素军, 段钟平. 4种常见先天性高胆红素血症的临床特征及诊断思路[J]. 临床肝胆病杂志, 2019, 35(8): 1680-1683. DOI: 10.3969/j.issn.1001-5256.2019.08.005
[7]	STRASSBURG CP. Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome)[J]. Best Pract Res Clin Gastroenterol, 2010, 24(5): 555-571. DOI: 10.1016/j.bpg.2010.07.007
[8]	LEE JH, CHEN HL, CHEN HL, et al. Neonatal Dubin-Johnson syndrome: Long-term follow-up and MRP2 mutations study[J]. Pediatr Res, 2006, 59(4 Pt 1): 584-589.
[9]	SUN YL, ZHAO JM, XIN SJ, et al. Clinical and pathological features of patients with hereditary disorders of bilirubin metabolism[J]. Infect Dis Info, 2008, 21(5): 287-290. (in Chinese) DOI: 10.3969/j.issn.1007-8134.2008.05.011 孙艳玲, 赵景民, 辛绍杰, 等. 几种主要的先天性胆红素代谢障碍性肝病的临床及病理研究[J]. 传染病信息, 2008, 21(5): 287-290. DOI: 10.3969/j.issn.1007-8134.2008.05.011
[10]	CEBECAUEROVA D, JIRASEK T, BUDISOVA L, et al. Dual hereditary jaundice: Simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome[J]. Gastroenterology, 2005, 129(1): 315-320. DOI: 10.1053/j.gastro.2004.10.009
[11]	GAN Y, ZHANG HF, ZHU SS, et al. Clinical features of Dubin-Johnson syndrome[J]. Chin Gen Pract, 2011, 14(18): 2089-2090. (in Chinese) DOI: 10.3969/j.issn.1007-9572.2011.18.034 甘雨, 张鸿飞, 朱世殊, 等. Dubin-Johnson综合征临床特点分析[J]. 中国全科医学, 2011, 14(18): 2089-2090. DOI: 10.3969/j.issn.1007-9572.2011.18.034
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Clinical features of Dubin-Johnson syndrome: An analysis of 10 cases

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