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Updated: Oct 5, 2025
07:24
A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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[Sickle cell disease, a genetic haemoglobin disease]
1Centre de la drépanocytose, hôpital Tenon, 4 rue de La Chine, 75020 Paris, France.
Revue De L'Infirmiere
|January 29, 2022
Abstract:
Sickle cell disease is the number one genetic disease in France in terms of the number of children diagnosed each year in the neonatal period. Throughout their lives, people with sickle cell disease are likely to develop acute complications that require urgent treatment. Chronic complications are more common amongst adults than in children.
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