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Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report

BACKGROUND: Hereditary spherocytosis (HS) is a common type of hemolytic anemia caused by a red cell membrane disorder. HS type 1 (HS1) is mostly caused by mutations in ankyrin (ANK1). Newborns with HS1 usually only exhibit anemia and mild jaundice. We herein report a case of HS1 and discuss its clin...

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Detalles Bibliográficos
Autores principales:	Wang, Jun-Fang, Ma, Li, Gong, Xiao-Hui, Cai, Cheng, Sun, Jing-Jing
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/PMC8283574/ https://www.ncbi.nlm.nih.gov/pubmed/34307574 http://dx.doi.org/10.12998/wjcc.v9.i19.5245

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