To examine the switch from fetal to adult hemoglobin at the cellular level, erythroid progenitor cells from newborn infants and adults were cultured in methyl cellulose with erythropoietin. Individual erythroid colonies were labeled with [3H]leucine at various times, and globin synthesis patterns examined by gel electrophoresis and fluorography. The percent gamma- or beta-globin synthesis was d...

background: beta-thalassemia patients have a high prevalence for hepatitis c virus (hcv) infection. in developing countries, hcv antibody is reported to be high in this group of patients. this study aims to determine the distribution of hcv amongst beta-thalassemia patients in northern iran. materials and methods: this study was undertaken from october 2010 to june 2011 on 245 beta-thalassemia ...

background: major thalassemia is an autosomal recessive disease with complications, mortality and serious pathology. today, the life expectancy of patients with major thalassemia has increased along with therapeutic advances. therefore, they need lifelong care, and caring for them would incur many costs. being aware of the patients’ costs can be effective for controlling and managing the costs ...

background and aims: nowadays introduction of regular blood transfusion therapy has obviously improved the life expectancy of patients with thalassemia. however, these patients face with newer challenges which influence their quality of life (qol). in this study, the aim of this study was to measure qol among patients with β-thalassemia major (β-tm). methods: a cross-sectional study was done at...

BACKGROUND beta-thalassemia occurs from the imbalanced globin chain synthesis due to the absence or inadequate beta-globin chain production. The excessive unbound alpha-globin chains precipitate in erythroid precursors and mature red blood cells leading to ineffective erythropoiesis and hemolysis. DESIGN AND METHODS In vitro globin chain synthesis in reticulocytes from different types of thal...