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Updated: Jul 9, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Jk(a) (Kidd-A) Variant in a Sickle Cell Disease Patient
Mohammad Barouqa1, Xuebao Zhang2, Ryan Walde2
1Transfusion Medicine, University of South Alabama College of Medicine, Mobile, USA.
Abstract:
Sickle cell disease (SCD) is a chronic and prevalent hemoglobin disorder with various manifestations and complications depending on the organs involved. Red cell transfusion either simple or exchange is crucial due to its prophylactic and therapeutic roles. We present a case showing serologic discrepancy between the red cells phenotype and the developed alloantibodies to emphasize the crucial role of molecular testing in SCD patients requiring chronic blood transfusion.
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