Sickle Cell Anemia, From Basic Science to Clinical Practice

Although sickle cell anemia was the very first molecular disease to be identified, its complex and fascinating pathophysiology is still not completely understood. A single mutation in the beta-globin gene incurs various molecular and cellular systems that contribute to the myriad of symptoms associated with the illness. Our knowledge regarding sickle cell illness systems, while still not finish, has expanded substantially over the last decades. Sickle Cell Anemia: From Basic Science to Scientific Practice intends to supply an update on our current understanding of the illness’s pathophysiology and utilize this details as a basis to discuss its manifestations in youth and adulthood. Current therapies and prospects for the development of new methods for the management of the disease are also covered.

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