beta-thalassemia (-thal)
Serum Antioxidant Levels in Children with Beta-Thalassemia Major
... Cu is present largely in the form of organic complexes, many of which are metalloproteins acting as enzymes. In our study serum Cu level was found to be significantly increased in patients when compared with controls ...
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Frequency of Celiac Disease in Children with Beta Thalassemia major
... with thalassemia never be considered as celiac disease ...in thalassemia major and celiac disease and recognition and treatment of celiac disease may improve survival of thalassemia ...with ...
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Serum Dickkopf-1 and Correlation with Bone Mineral Density in Patients with Beta Thalassemia Major in North-Eastern of Iran
... Beta-thalassemia syndromes are a family of inherited disorders associated with decreased or absent globin chains production; it leads to hemoglobin reduction in red blood cells and anemia [1]. Osteoporosis ...
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INTELLIGENCE AND BEHAVIORAL PATTERNS IN PATIENTS WITH COOLEY'S ANEMIA (HOMOZYGOUS BETA-THALASSEMIA); A STUDY BASED ON 138 CONSECUTIVE CASES
... COOLEY'S ANEMIA (HOMOZYGOUS BETA-THALASSEMIA); A STUDY INTELLIGENCE AND BEHAVIORAL PATTERNS IN PATIENTS WITH. Services[r] ...
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Cardiac abnormalities in patients with beta thalassemia
... in beta-thalassemia major patients with normal left ventricular systolic function are similar to those seen in conditions with an increased preload, probably because of chronic ...dependent ...
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Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study
... 88 beta-thalassemia alleles from eight homozygous or compound heterozygous beta-thalassemia patients, 57 beta-thalassemia/HbE patients, and 15 heterozygous beta- ...
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Characterization of molecular hemoglobin c and beta thalassemia
... ABSTRACT. The hemoglobinopathies are a group of hereditary alterations prevalent in many parts of the world, but significantly affect the Brazilian population for its abundant miscegenation. These alterations in ...
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COVID-19: Beta-Thalassemia Subjects Immunised?
... We conducted a multi-group descriptive observational transversal study in order to define a hypothetical relationship between beta thalassemia and SARS-CoV-2 immunization. The source and targeted ...
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Co-existing iron deficiency/overload in beta-thalassemia trait
... Beta-thalassemia syndrome (BTS) is a group of hereditary blood disorders characterised by genetic mutations in β- globin chain genes resulting in reduced or absent β- globin chain synthesis. The imbalanced ...
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In Patients with Minor Beta-Thalassemia, Cognitive Performance Is Related to Length of Education, But not to Minor Beta-Thalassemia or Hemoglobin Levels
... minor beta-thalassemia would have higher hemoglobin levels than healthy controls, and this was ...minor beta-thalassemia could be clearly distinguished from healthy controls at a biological ...
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Iron overload in beta thalassemia major patients
... with beta thalassemia major suffer from chronic anemia due to hemolysis and ineffective ...in thalassemia patients, cause further accumulation of ...with beta thalassemia major ...
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Study on Clinical Profile of Beta Thalassemia Major Children
... This is to certify that this dissertation titled “STUDY ON CLINICAL PROFILE OF BETA THALASSEMIA MAJOR CHILDREN” submitted by DR.M.S.NISHA to the Tamilnadu DR. M.G.R medical university, Chennai in partial ...
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Genotype–phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis
... heterozygous beta-thalassemia patients were in thalassemia ...three beta-thalassemia/HbE patients were classified in 58 thalassemia major and 4 thalassemia intermedia ...
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Sickle Cell Beta Thalassemia: A Rare Entity
... cell beta thalassemia syndromes and hemoglobinopathies in which HbS is in association with abnormal hemoglobin like sickle cell hemoglobin C disease (hemoglobin SC ...
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Cytogenetic mutation in a family with sickle-cell beta-thalassemia in North Sumatera, Medan, Indonesia: A preliminary study
... In Hb S / β + -Thalassemia, the variable amount of Hb A dilutes Hb S and effectively inhibits the age of cell damage due to polymerization. Hb A levels vary from <5% to 45%. The level of hemolysis and higher Hb ...
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Heterozygous Beta Thalassemia in Parents of Children with Beta Thalassemia Major
... heterozygous beta thalassemia were detected in survey of 100 families of the known beta thalassemia major ...heterozygous beta thalassemia were pathans and 16 ...
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Assessment Hepatomegaly and liver Enzymesin 100 Patients with beta Thalassemia Major in Mashhad, Iran
... This work is a descriptive cross- sectional study. The study was carried out retrospectively. Medical records of all patients aged between 2- 18 years were used from 400 records of major beta thalassemia ...
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Globin synthesis in fractionated Normoblasts of beta thalassemia heterozygotes
... total beta chain production is higher in the early cells than in the later cells or that alpha chain production in the early cells is reduced to the level of beta chain ...the beta A/beta S ...
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Heterogeneity of DNA deletion in gamma delta beta thalassemia
... thalassemia. The deletion removes the linked epsilon, gamma-, and delta-globin structural genes and terminates within the coding portion of the beta-globin gene. Since the extent of DNA deletion in this ...
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Economic burden of beta thalassemia/Hb E and beta thalassemia major in Thai children
... newborn thalassemia (thal): b -thal/Hb E, homozygous b -thal, and Hb H disease constitute 30%, 6%, and 64%, ...of thalassemia is presented elsewhere ...
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