Cargando…
“Gilbert’s-like” syndrome as part of a spectrum of persistent unconjugated hyperbilirubinemia in post-chronic hepatitis patients
Gilbert’s syndrome (GS) patients present with remittent unconjugated hyperbilirubinemia. In this study, we investigated the correlation between polymorphisms in the gene encoding UDP-glucuronosyltransferase, UGT1A1, and the development of unconjugated hyperbilirubinemia in clinical GS and post-hepat...
Autores principales: | Ye, Jin, Cui, Lianlian, Zhou, Yingqiao, Huang, Ying, Banafa, Omar, Hou, Xiaohua, Ding, Zhen, Lin, Rong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792633/ https://www.ncbi.nlm.nih.gov/pubmed/29386646 http://dx.doi.org/10.1038/s41598-018-19847-4 |
Ejemplares similares
-
Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia
por: Aiso, Mitsuhiko, et al.
Publicado: (2017) -
Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report
por: Ye, Naifang, et al.
Publicado: (2020) -
Gilbert or Crigler–Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity
por: Cozzi, Laura, et al.
Publicado: (2022) -
Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia
por: Kim, Jin Ju, et al.
Publicado: (2020) -
An Epileptic Patient with Recurrent Hyperbilirubinemia Caused by Gilbert Syndrome
por: Zhang, Yaoyao, et al.
Publicado: (2020)