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Books > Medicine > Clinical & internal medicine > Haematology

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Focus on Sickle Cell Research (Paperback) Loot Price: R2,580
Discovery Miles 25 800
You Save: R1,408 (35%)
Focus on Sickle Cell Research (Paperback): Ralph L. Plasmar

Focus on Sickle Cell Research (Paperback)

Ralph L. Plasmar

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List price R3,988 Loot Price R2,580 Discovery Miles 25 800 | Repayment Terms: R242 pm x 12* You Save R1,408 (35%)

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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.

General

Imprint: Nova Biomedical Books
Country of origin: United States
Release date: October 2004
Editors: Ralph L. Plasmar
Dimensions: 180 x 260 x 20mm (L x W x T)
Format: Paperback
Pages: 249
ISBN-13: 978-1-59033-920-6
Categories: Books > Medicine > Clinical & internal medicine > Haematology
LSN: 1-59033-920-7
Barcode: 9781590339206

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