Literature DB >> 29032691

Conjugated hyperbilirubinemia after surgery. A diagnosis of Dubin-Johnson syndrome confirmed by genetic testing.

Maria Luisa Baranguán Castro1, Ruth García Romero1, María Dolores Miramar Gallart2.   

Abstract

Dubin-Johnson syndrome is a rare benign inherited disorder, caused by mutations in ABCC2 gen, and it is characterized by predominantly conjugated hyperbilirubinemia that can be increased by intercurrent infectious illnesses or surgical procedures. We report the case of a 10 year-old patient who showed, after a surgical procedure for peritonitis due to appendicitis, jaundice and predominantly conjugated hyperbilirubinemia, and he was diagnosed with Dubin-Johnson syndrome by genetic testing.

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Year:  2017        PMID: 29032691     DOI: 10.17235/reed.2017.4989/2017

Source DB:  PubMed          Journal:  Rev Esp Enferm Dig        ISSN: 1130-0108            Impact factor:   2.086


  2 in total

1.  Clinical characteristics and ABCC2 genotype in Dubin-Johnson syndrome: A case report and review of the literature.

Authors:  Huan Wu; Xue-Ke Zhao; Juan-Juan Zhu
Journal:  World J Clin Cases       Date:  2021-02-06       Impact factor: 1.337

2.  Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin-Johnson syndrome in a Chinese gril: A case report.

Authors:  Yuan Li; Yang Li; Yang Yang; Wen-Rui Yang; Jian-Ping Li; Guang-Xin Peng; Lin Song; Hui-Hui Fan; Lei Ye; You-Zhen Xiong; Zhi-Jie Wu; Kang Zhou; Xin Zhao; Li-Ping Jing; Feng-Kui Zhang; Li Zhang
Journal:  World J Clin Cases       Date:  2019-10-26       Impact factor: 1.337

  2 in total

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