Teen Health - Diseases & Disorders, Teens - People with Special Needs
Log in to track your reading progress.
Overview
Contains information on the biological and medical aspects of this hereditary disease, the proper treatment of infants and young children who have the disease, living and growing up with sickle cell anemia, and the hoped-for cures now being developed.Editorials
School Library Journal
Gr 6 Up-An overview of a hereditary blood disorder that primarily affects people of African and Mediterranean descent. Beshore relates its history, and explains how the disease is passed from one generation to another. He discusses how to live with sickle cell anemia, as well as the new treatments and ongoing research. The text is matter-of-fact; the diagrams are clear and easy to understand. Black-and-white photographs augment the text.-Martha Gordon, formerly at South Salem Library, NYMary Romano Marks
Today some 2.5 million Americans, particularly those of African and Mediterranean ancestry, are affected by sickle-cell anemia, a hereditary blood disorder that causes their red blood cells to become sickle shaped. Chronicling the history of this ancient disease, Beshore relates its distribution, various forms, symptoms, and treatment. His informative overview describes how the disease is transmitted from parent to child, the importance of genetic testing, and the development of comprehensive screening and treatment centers throughout the U.S. He also follows two typical sickle-cell patients from childhood into adulthood, explaining how their lives have been affected. A valuable resource for general information and research. Readings and resources are appended.Book Details
Published
August 1, 1994
Publisher
Franklin Watts
Pages
94
Format
Binding
ISBN
9780531125106