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Sickle Cell Anemia: From Basic Science to Clinical Practice - Hardcover
$136.99
In stock
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by Elena Ledger (Editor)
A sickle cell disease is a group of blood disorders that a person inherits from parents. They usually occur when the person inherits two abnormal copies of the hemoglobin gene. Sickle cell anemia is the most common type of sickle cell disease. It causes an abnormality in hemoglobin, the oxygen-carrying protein found in red blood cells. The problems due to sickle cell anemia begin to appear around 5 to 6 months of age. It leads to problems such as sickle cell crisis, swelling in hands and feet, stroke and bacterial infections. The care of people suffering from sickle cell anemia includes infection prevention with vaccination and antibiotics, folic acid supplementation and pain medication. A bone marrow transplant is also used in certain cases. This book consists of contributions made by international experts. It contains some path-breaking studies in sickle cell anemia. It will serve as a valuable source of reference for graduate and post graduate students.
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Standard U.S. returns are accepted for eligible new, unopened items within 30 days of carrier delivery. Returns are by mail. Customers are responsible for standard return shipping, there is no restocking fee, and standard exchanges are not offered. Once an approved return is received and inspected, the refund is issued to the original payment method within 5 business days. Damaged, defective, or incorrect items are handled at no return-shipping cost to the customer.
Return eligibility is subject to the full policy. Opened, read, or unsealed books with broken seals or visible wear are final sale. Digital downloads, gift cards, and personalized products are non-refundable. Original shipping charges are not refunded for standard returns. Contact us within 7 days of delivery about damaged, defective, or incorrect items.
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