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

BACKGROUND: Dubin-Johnson syndrome (DJS) is a benign autosomal recessive liver disease involving mutations of the ABCC2 gene. It is characterized by chronic or intermittent conjugated hyperbilirubinemia, with chronic idiopathic jaundice as the main clinical manifestation. Genetic alterations of the...

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Detalles Bibliográficos
Autores principales: Wu, Huan, Zhao, Xue-Ke, Zhu, Juan-Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852649/
https://www.ncbi.nlm.nih.gov/pubmed/33585635
http://dx.doi.org/10.12998/wjcc.v9.i4.878

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852649/
https://www.ncbi.nlm.nih.gov/pubmed/33585635
http://dx.doi.org/10.12998/wjcc.v9.i4.878

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