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A drastic reduction in the total red blood cells or RBC count or hemoglobin is known as anemia. It can be defined as the inability to carry optimum amount of oxygen by the blood. Sickle-cell diseases (SCD) are types of blood disorders which are usually inherited genetically. One of the common types of SCDs is the sickle-cell anemia or SCA. It essentially gives rise to an irregularity in hemoglobin, the protein that carries oxygen in the blood. Hemoglobin is found typically in the red blood cells of the body. As a result a sickle-like shaped cell is formed under certain conditions. Tribulations in sickle cell disease usually start to take shape at a very early age (within the first year of birth). This might lead to various health problems including pain attacks also known as the sickle-cell crisis, swelling in the limbs, microbial infections, and in certain cases, stroke. Chronic pain may develop with age. Sickle-cell diseases arise when an individual inherits abnormal copies of hemoglobin gene from each parent.
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Sickle Cell Anemia Therapeutics Market Global Market Analysis, Insights, Trends, and Opportunity Inference, 2014-2024 © Coherent market Insights. All Rights Reserved
REPORT DESCRIPTION A drastic reduction in the total red blood cells or RBC count or hemoglobin is known as anemia. It can be defined as the inability to carry optimum amount of oxygen by the blood. Sickle-cell diseases (SCD) are types of blood disorders which are usually inherited genetically. One of the common types of SCDs is the sickle-cell anemia or SCA. It essentially gives rise to an irregularity in hemoglobin, the protein that carries oxygen in the blood. Hemoglobin is found typically in the red blood cells of the body. As a result a sickle-like shaped cell is formed under certain conditions. Tribulations in sickle cell disease usually start to take shape at a very early age (within the first year of birth). This might lead to various health problems including pain attacks also known as the sickle-cell crisis, swelling in the limbs, microbial infections, and in certain cases, stroke. Chronic pain may develop with age. Sickle-cell diseases arise when an individual inherits abnormal copies of hemoglobin gene from each parent. According to Center for Disease Control and Prevention, as of 2016, around 100,000 people in the U.S. are affected by sickle cell diseases or SCDs. Sickle cell diseases are very common among black or African Americans. Around 1 in 13 babies belonging to the race are born with sickle cell diseases. Growing prevalence of the disease will give rise to an increased demand for sickle cell disease prevention and cure, thereby augmenting the growth of the overall sickle cell anemia therapeutics market. Sickle Cell Anemia Therapeutics Market: Overview
Request report sample for more professional and technical insights: https://www.coherentmarketinsights.com/insight/request-sample/161 REPORT DESCRIPTION Sickle Cell Anemia Therapeutics Market Segment: • On the basis of type of medication, the global market is classified into: • Antibiotics • Pain-relieving medications • Hydroxyurea • Others • On the basis of end user, the global market is classified into: • Government • Hospitals • Private Clinics • Others
REPORT DESCRIPTION • Major players involved in the sickle cell anemia therapeutics market include: • Bristol-Myers Squibb • GlycoMimetics • Pfizer • AntheraPharmaceuticals Inc. • GlycoMimetics, Inc. • Eli Lilly • Mast Therapeutics Sickle Cell Anemia Therapeutics Market: Key Players Ask For TOC: https://www.coherentmarketinsights.com/ongoing-insight/toc/161
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