Načítá se...
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...
Uloženo v:
| Vydáno v: | Clin Case Rep |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2021
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8218318/ https://ncbi.nlm.nih.gov/pubmed/34188920 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.4226 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|