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Sickle Cell Anemia: From Basic Science to Clinical Practice - by  Elena Ledger (Hardcover) - 1 of 1

Sickle Cell Anemia: From Basic Science to Clinical Practice - by Elena Ledger Hardcover

$136.99

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Highlights

  • A sickle cell disease is a group of blood disorders that a person inherits from parents.
  • Author(s): Elena Ledger
  • 205 Pages
  • Medical, Hematology

Description



About the Book



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.



Book Synopsis



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.
Dimensions (Overall): 11.0 Inches (H) x 8.5 Inches (W) x .5 Inches (D)
Weight: 1.69 Pounds
Suggested Age: 22 Years and Up
Number of Pages: 205
Genre: Medical
Sub-Genre: Hematology
Publisher: American Medical Publishers
Format: Hardcover
Author: Elena Ledger
Language: English
Street Date: March 8, 2022
TCIN: 1008944715
UPC: 9781639271856
Item Number (DPCI): 247-47-3881
Origin: Made in the USA or Imported
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Estimated ship dimensions: 0.5 inches length x 8.5 inches width x 11 inches height
Estimated ship weight: 1.69 pounds
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