نتایج جستجو برای: major thalassemia
تعداد نتایج: 636036 فیلتر نتایج به سال:
Background and Objective: β-Thalassemia major is a chronic genetic disease which is determined with symptoms and signs of a chronic severe anemia. Children with β-Thalassemia major have several risk factors for cognitive problems. The purpose of this study was to compare the cognitive function in β-thalassemia major children and healthy counterparts. Methods: This cross-sectio...
Background: b-thalassemia major is a common hereditary blood disease that can affect patients’ oral health and quality of life. The present study aims to determine the relationship between health of deciduous teeth and the Oral Health-Related Quality of Life (OHRQoL) in children diagnosed with β-thalassemia major compared with healthy children. Materials and Methods This cross-sectional study w...
Thalassemia is a hereditary disease caused by abnormalities in red blood cells which the individual has gene disorder that causes reduced production of hemoglobin cells. People with Thalassemia, especially type Major, need routine therapy and medication. These medication activities sometimes cause various problems obstacles lives people thalassemia both physically psychologically. Individuals a...
Background: Transfusion is the mainstay treatment of patients with thalassemia major and occasionally in thalassemia intermediate. Alloimmunization is an unwanted side effect of blood transfusion. The present study intended to determine the frequency of alloimmunization in patients with β- thalassemia major and thalassemia intermediate in Southwest Iran. Patients and Methods: This was a cross-...
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