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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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Therapeutic strategies in Sickle Cell Anemia: The past present and future

Queenie Fernandes1

  • 1University of Greenwich, United Kingdom.

Life Sciences
|April 25, 2017
PubMed

Sickle Cell Anemia (SCA) was one of the first hemoglobinopathies to be discovered. It is distinguished by the mutation-induced expression of a sickle cell variant of hemoglobin (HbS) that triggers erythrocytes to take a characteristic sickled conformation. The complex physiopathology of the disease and its associated clinical complications has initiated multi-disciplinary research within its field. This review attempts to lay emphasis on the evolution, current standpoint and future scope of therapeutic strategies in SCA.

Keywords:
HemoglobinopathiesSickle Cell AnemiaSickle Cell ResearchSickle Cell Therapeutics

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