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Post‐transfusion hyperhemolysis syndrome in a patient with beta thalassemia major

Hyperhemolysis syndrome (HS) is characterized by the occurrence of severe anemia with post‐transfusion hemoglobin and hematocrit levels being markedly lower than those present prior to transfusion. A high index of suspicion of HS in a multi‐transfused thalassemia patient allows prompt institution of...

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Detalles Bibliográficos
Autores principales:	Kasinathan, Ganesh, Sathar, Jameela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2021
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218318/ https://www.ncbi.nlm.nih.gov/pubmed/34188920 http://dx.doi.org/10.1002/ccr3.4226

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