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Thalassemia

by Lambert M. Surhone - Sold by Dodax EU
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Lambert M. Surhone Thalassemia
Lambert M. Surhone - Thalassemia

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Description

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Thalassaemia is an inherited autosomal recessive blood disease. In thalassemia, the genetic defect results in reduced rate of synthesis of one of the globin chains that make up hemoglobin. Reduced synthesis of one of the globin chains can cause the formation of abnormal hemoglobin molecules, thus causing anemia, the characteristic presenting symptom of the thalassemias. Thalassemia is a quantitative problem of too few globins synthesized, whereas sickle-cell anemia (a hemoglobinopathy) is a qualitative problem of synthesis of an incorrectly functioning globin. Thalassemias usually result in underproduction of normal globin proteins, often through mutations in regulatory genes. Hemoglobinopathies imply structural abnormalities in the globin proteins themselves.

Contributors

Editor Lambert M. Surhone

Editor Miriam T. Timpledon

Editor Susan F. Marseken

Product Details

DUIN 35UGKJBC2NH

GTIN 9786130969547

Pages 128

Product type Paperback

Dimension 8.66 x 5.91 x 0.28  inches

Product Weight 6.60 ounces

$46.79
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