نتایج جستجو برای: minor β
تعداد نتایج: 258041 فیلتر نتایج به سال:
Background & objective: β-Thalassemia minor is an asymptomatic hereditary disease. The first study on the relation of renal tubular dysfunction and β-thalassemia minor was performed in 2002 but those studies seem inadequate.The main goal of this study is through evaluation of renal tubular function in 100 patients with thalassemia minor. Materials & Methods: 100 patients with β- thalassemia...
introduction: the current study evaluated the value of red blood cell (rbc) indices and the corresponding cut- off points for β-thalassemia control programs in iran. materials and methods: 1,150 individuals (575 couples) with low rbc indices and normal hemoglobin a2 who had been referred to the genetic centre of isfahan, were tested during pre-marital screening analyses, in the 2 year period, 2...
background: objective: to determine pregnancy outcome of women with β-thalassemia minor. materials and methods: in this retrospective, case-control study in two universities affiliated hospitals in shiraz, all pregnancies occurred between 2006 and 2008 were included. patients were divided in two groups regarding the presence of β-thalassemia minor. patients in case and control groups were m...
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...
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...
Increased HbA2 is a characteristic finding in minor beta thalassemia. Minor β-thalassemia is a heterozygote form of β-thalassemia that carries thalassemia genes but does not cause thalassemia disease. Diagnosis of carriers is done by CBC, RBC Index, and HbA2 test. Very few cases of people with minorthalassemia have a normal HbA2. According to the results of this pilot study it seams that percen...
hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency in certain area particularly mediterranean and middle eastern countries. hemoglobinopathies include structural variants of hemoglobin (hb s, hb c, hbe,…) and thalassaemias which are inherited defects in the globin chains synthesis. the present study was conducted to determine the prevalence of h...
Background: Until now, no study has been reported investigating the association between β-thalassemia minor and Helicobacter pylori (H. pylori) infection. This study was designed to compare H. pylori infection rate between β-thalassemia minor patients and healthy controls. Methods: A number of 100 β-thalassemia minor patients (50 males, 50 females) and 100 gender-matched healthy...
OBJECTIVE Anti-apoptotic proteins such as Bcl-2 and Bcl-xL may play a role in the survival of erythroid progenitor cells. Information about these proteins in patients with β-thalassemia minor is limited. We aimed to determine the levels of serum Bcl-2 in patients with β-thalassemia minor. MATERIALS AND METHODS Ninety-seven patients (60 females and 37 males with mean age of 29±21 years) with β...
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