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Updated: Mar 29, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Sickle cell anaemia: The need for new approaches in management
1National Institute of Immunohaematology (ICMR), 13th Floor, K.E.M. Hospital, Parel, Mumbai 400012, Maharashtra, India; kanjakshaghosh@hotmail.com.
Abstract:
Sickle cell anaemia is an important genetic disorder in India and is associated with considerable morbidity and mortality. Over 100 000 people are affected by this disorder and 10%-40% of the 85 million tribal population carries this gene. Conventional management and therapy with hydroxyurea provides symptomatic relief. A search for an anti-sickling agent has so far proved unsuccessful. However, improving upon existing compounds; looking for newer products using modern tools of bioinformatics, monoclonal antibody and aptamer technology; and evaluating medicines from ethno-pharmacology are promising approaches in managing this disease.
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