Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports

BACKGROUND: Both Gilbert's syndrome (GS) and hereditary spherocytosis (HS) are common genetic disorders. However, comorbidity of GS with HS has always been considered a rare phenomenon, and it can impede accurate diagnoses in the presence of isolated unconjugated hyperbilirubinemia. CASE SUMMAR...

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Detalles Bibliográficos
Autores principales: Kang, Ling-Ling, Liu, Ze-Lin, Zhang, Hou-De
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262690/
https://www.ncbi.nlm.nih.gov/pubmed/32518793
http://dx.doi.org/10.12998/wjcc.v8.i10.2001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262690/
https://www.ncbi.nlm.nih.gov/pubmed/32518793
http://dx.doi.org/10.12998/wjcc.v8.i10.2001

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