Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report

Gilbert syndrome (GS) is a hereditary unconjugated hyperbilirubinemia that results from mutations in the bilirubin uridine diphosphate-glucuronosyltransferase (UGT1A1) gene. To the best of our knowledge, there are currently no reports that focus on patients with systemic lupus erythematosus (SLE) co...

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Detalles Bibliográficos
Autores principales: Ye, Naifang, Zhou, Zhuochao, Gong, Huiyun, Teng, Jialing, Han, Yue, Yang, Chengde, Ye, Junna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507055/
https://www.ncbi.nlm.nih.gov/pubmed/32973940
http://dx.doi.org/10.3892/etm.2020.9219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507055/
https://www.ncbi.nlm.nih.gov/pubmed/32973940
http://dx.doi.org/10.3892/etm.2020.9219

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