DelveInsight’s Sickle Cell Disease Market Insights report provides a thorough understanding of current treatment practices, emerging Sickle Cell Disease market share of the individual therapies, current and forecasted Sickle Cell Disease Market size from 2019 to 2032 segmented into 7MM (the USA, EU5 (the UK, Italy, Spain, France, and Germany), and Japan).
Sickle Cell Disease Overview
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality of hemoglobin called sickle hemoglobin (HbS) which encodes hemoglobin subunit β. HbS is inherited in an autosomal recessive way and can occur due to homozygosity for HbS (HbSS). HbS is functional and soluble when oxygenated, but upon deoxygenation it polymerizes, leading to the generation of deformed red blood cells known as sickled cells and dense erythrocytes.
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Some of the key highlights of the Sickle Cell Disease Market Report
Sickle Cell Disease Symptoms
Sickle Cell Disease Treatment
Sickle cell disease (SCD) is an umbrella term that defines a group of inherited diseases (including sickle cell anaemia (SCA), HbSC and HbSβ-thalassaemia,) characterized by mutations in the gene encoding the haemoglobin subunit β (HBB). The treatment starts with the recognition of pain in the sickle cell disease patients. Recurrent episodes of acute, severe pain are the hallmark of SCD. The pain is highly variable both within and among patients, and is the result of complex and poorly understood interactions between biological and psychosocial factors.
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Sickle Cell Disease Key Players
Sickle Cell Disease Drugs
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