نتایج جستجو برای: prevention of thalassemia
تعداد نتایج: 21183850 فیلتر نتایج به سال:
Introduction: One of the most common types of anemia is Iron deficiency anemia that its main differential diagnosis is β-thalassemia minor. The rapid and accurate screening of β-thalassemia minor has particular importance for pre-marriage medical counseling and the prevention of the birth of neonates with β-thalassemia major and differentiating it from iron deficiency anemia to avoid unnecessar...
Thalassemia is one of the most common genetic disorders in Egypt. With the total population of 70 million, there are approximately 600,000 affected individuals and more than 20 million thalassemia carriers. Thalassemia is therefore one of the major health problems in Egypt. B-Thalassemias are priority genetic diseases for prevention programs. Rapid genotype characterization is fundamental in th...
BACKGROUND Thalassemic disorders are the most prevalent monogenic hereditary diseases around the world caused by decreased and altered synthesis or agenesis in one or more globin chains. Families who have a child with thalassemia major face a myriad of significant problems. Hormozgan province ranks second with thalassemic patients in Iran. Therefore, current research is aimed to analyze the rep...
Background: Patients with thalassemia major require frequent blood transfusions. Blood transfusion can lead to the adverse reactions. Reporting and evaluating the transfusion reactions are among the goals of implementing the hemovigilance system to improve blood recipients’ safety. This study aimed to compare the transfusion reactions in the thalassemia patients before and after implementation ...
OBJECTIVE To devise a strategy for prevention of beta thalassemia in newborns through reliable screening of indexed families. METHODS The cross-sectional study was conducted over six months in 2011 and comprised blood samples collected from subjects belonging to different ethnic groups from families of beta thalassemia major children registered with the Abbottonian Medical Association Blood C...
Background and purpose: More than 3% of the world population are infected with Hepatitis Ç virus (HÇV) and 50-80% of these patients progress to chronic disease. Âpproximately 50% of chronically infected patients do not respond to treatment. The purpose of this study was to determine the risk factors for hepatitis Ç virus among high-risk populations (Ïntravenous drug addicts and patients with ...
Sclrostin is a biomarker interrupted in bone resorption process by binding to LRP5 and/or LRP6 family, and prevent Wingless-type signaling (Wnt) which important both development the maintain of mass. Sixty (60) patients with thalassemia major were enrolled from period 2/5/2021 1/9/2021 summer assessment role sclrostin predisposing for osteoporosis β-thalassemia (β-TM). Patients ages (2-40 year)...
OBJECTIVE Thalassemia is one of the most common genetic disorders worldwide. Cap +1 mutation which causes 'silent beta thalassemia' is present around all ethnic groups of Pakistan. This study was designed to detect the frequency of Cap+1 mutation in Pakistani Population. METHODS Molecular genetic for Cap+1 beta thalassemic mutation was done by extracting DNA from whole blood by using Genomic ...
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