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Updated: Aug 9, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
[Sickle cell disease – clinical manifestations and diagnostics]
Erik Wilhelm Vinnes1, Paul Kjetel Soldal Lillemoen1, Olav Klingenberg2
1Avdeling for medisinsk biokjemi og farmakologi, Haukeland universitetssjukehus.
Abstract:
Sickle cell disease is a group of diseases presenting with a set of characteristic acute and chronic manifestations. Sickle cell disease has traditionally been uncommon in the Northern European population; however, due to demographic changes, it is increasingly also something that Norwegian clinicians should be cognisant of. In this clinical review article we wish to present a brief introduction to sickle cell disease, with an emphasis on its aetiology, pathophysiology, clinical manifestation and how the diagnosis is established based on laboratory testing.
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