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Sickle Cell Simply Explained

List Price: $17.95
SKU:
9781491897768
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  • Product Details

    Author:
    John Koramoa
    Format:
    Paperback
    Pages:
    192
    Publisher:
    Authorhouse (June 20, 2014)
    ISBN-13:
    9781491897768
    Weight:
    7.68oz
    Dimensions:
    5" x 8"
    File:
    BTPS-Lakeside_03172026-20260317.xml
    Folder:
    BTPS
    As low as:
    $13.82
    Publisher Identifier:
    P-BTPS
    Discount Code:
    A
    List Price:
    $17.95
    Language:
    English
    Audience:
    General/trade
    ISBN-10:
    1491897767
    Country of Origin:
    United States
    Pub Discount:
    65
    Imprint:
    Authorhouse
  • Overview

    Sickle cell disease is the most common genetic disease world-wide. For a person to suffer the disease, he or she has to inherit the faulty gene from each parent. It affects millions of people in the world. It is a chronic illness of serious proportions. Medical, psychological and socioeconomic consequences place a great burden on sufferers and their Carers. In the past sufferers of sickle cell anaemia survived for a few years only.When only one sickle cell gene is inherited by a person with normal haemoglobin, the condition is referred to as the carrier state or the trait. Individuals with the trait have no medical problems under normal conditions of life. This is how the gene has been able to survive and be passed on from generation to generation. The trait can thus have serious implications for marriage and childbearing. It is therefore, imperative for people intending to have children to know about it in order to help prevent the disease. Sickle cell disease which was once thought to be restricted to only a few areas, especially among Black people, is now known to be world-wide. It has been described as a world—health problem.This book provides information in an easily readable format for everybody to understand sickle cell and its related conditions. There is the need for greater awareness and knowledge of the disease and the trait to avoid confusion, misunderstanding and myths, which hamper their proper management and prevention. At present there is no readily available cure for sickle cell disease. However, with proper management of the many ill-effects of the disease, sufferers can be assisted to live comfortable lives and for many years. Life-style measures are paramount and are referred to in some detail in the book. It is a great resource.