Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn

A term male newborn born to a mother who had hereditary spherocytosis presented with neonatal jaundice at 20 hours of life. Complete blood count showed hemoglobin 17.1 g/dL, MCV 104.2 fL, MCH 32.9 pg, and MCHC 31.6 g/dL. The patient had indirect hyperbilirubinemia requiring phototherapy. The maximum...

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Detalhes bibliográficos
Publicado no:Case Rep Hematol
Main Authors: Fanhchaksai, Kanda, Manowong, Suphara, Natesirinilkul, Rungrote, Sathitsamitphong, Lalita, Charoenkwan, Pimlak
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2019
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6530122/
https://ncbi.nlm.nih.gov/pubmed/31205791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/5925731
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