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Focus on Sickle Cell Research (Paperback)
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Focus on Sickle Cell Research (Paperback)
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Sickle cell anaemia is an inherited blood disorder, characterised
primarily by chronic anaemia and periodic episodes of pain and
occurring in approximately 1 in every 400 African-American infants
born in the United States each year. Individuals of Mediterranean,
Arabian, Caribbean, South and Central American, and East Indian
ancestry can also be affected. The underlying problem involves
haemoglobin, a component of the red cells in the blood. The
haemoglobin molecules in each red blood cell carry oxygen from the
lungs to the body organs and tissues and bring back carbon dioxide
to the lungs. In sickle cell anaemia, the haemoglobin is defective.
After the haemoglobin molecules give up their oxygen, some of them
may cluster together and form long, rod-like structures. These
structures cause the red blood cells to become stiff and to assume
a sickle shape. Unlike normal red cells, which are usually smooth
and donut-shaped, the sickled red cells cannot squeeze through
small blood vessels. Instead, they stack up and cause blockages
that deprive the organs and tissue of oxygen-carrying blood. This
process produces the periodic episodes of pain and ultimately can
damage the tissues and vital organs and lead to other serious
medical problems. Unlike normal red blood cells, which last about
120 days in the bloodstream, sickled red cells die after only about
10 to 20 days. Because they cannot be replaced fast enough, the
blood is chronically short of red blood cells, a condition called
anaemia. Sickle cell anaemia is caused by an error in the gene that
tells the body how to make haemoglobin. The defective gene tells
the body to make the abnormal haemoglobin that results in deformed
red blood cells. This book gathers the latest research in this
important field.
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