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Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. The most common type is known as sickle cell anemia. It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells.
Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous), but does not display the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele (is homozygous).
Miller said a national donor blood shortage could severely impact treatment for Americans with sickle cell disease, and in some cases it could be life-threatening. Shortages would mean that ...
Sickle cell-beta thalassemia is caused by inheritance of a sickle cell allele from one parent and a beta thalassemia allele from the other. Mutations. A sickle allele is always the same mutation of the beta-globin gene (glutamic acid to valine at amino acid six). In contrast, beta-thalassemia alleles can be created by many different mutations ...
In people with sickle cell disease, red blood cells, which are normally disk-shaped, take on a crescent or sickle shape. That shape can cause blood cells to clump together, blocking blood flow and ...
Having sickle cell disease also raises your risk for severe illness from COVID-19.” According to the CDC, sickle cell disease occurs among about 1 out of every 365 Black or...
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