Clinical and genetic definition of serum bilirubin levels for the diagnosis of Gilbert syndrome and hypobilirubinemia

BACKGROUND AND AIMS: Gilbert syndrome (GS) is genotypically predetermined by UGT1A1*28 homozygosity in Europeans and is phenotypically defined by hyperbilirubinemia using total bilirubin (TB) cutoff ≥1mg/dL (17 μmol/L). The prevalence of illnesses associated with GS and hypobilirubinemia has never b...

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Detalles Bibliográficos
Autores principales: Poynard, Thierry, Deckmyn, Olivier, Peta, Valentina, Sakka, Mehdi, Lebray, Pascal, Moussalli, Joseph, Pais, Raluca, Housset, Chantal, Ratziu, Vlad, Pasmant, Eric, Thabut, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519483/
https://www.ncbi.nlm.nih.gov/pubmed/37738404
http://dx.doi.org/10.1097/HC9.0000000000000245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519483/
https://www.ncbi.nlm.nih.gov/pubmed/37738404
http://dx.doi.org/10.1097/HC9.0000000000000245

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