Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated individuals from the southernmost Brazilian state of Rio Grande do Sul were screened for deletional forms of -thalassemia. One hundred and one individuals had microcytic anemia (MCV < 80 fL) and a normal hemoglobin pattern (Hb A2 < 3.5% and Hb F < 1%). The subjects were screened for - 3.7, - 4.2, - 20.5, —SEA and—MED deletions but only the - 3.7 allele was detected. The - 3.7 allele frequency in Brazilians of European and African ancestry was 0.02 and 0.12, respectively, whereas in individuals with microcytosis the frequency was 0.20. The prevalence of -thalassemia was significantly higher in individuals with microcytosis than in healthy indiv...
ABSTRACTIntroduction:Hemoglobin S (HbS) is one of the most common inherited hematological disorders ...
To compare the features of sickle-cell anemia in Brazil with those in other locales, we studied the ...
p. 292-298Hemoglobinopathies are hereditary disorders of the hemoglobin molecule with a high prevale...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions ...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do...
-Thalassemia, arising from a defect in -globin chain synthesis, is often caused by deletions involvi...
ABSTRACT. The ethnic composition of the Brazilian popula-tion favors high frequencies of the-α3.7 de...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions invol...
Alpha-thalassemia (α-thal) is one of the most common monogenic disorders in the world. Its clinical ...
IntroductionCases with microcytosis not responding adequately to iron supplementation are diagnostic...
Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), and the alph...
Hemoglobinopathies are the most common recessive diseases worldwide but their prevalence in Uruguay ...
ABSTRACTIntroduction:Hemoglobin S (HbS) is one of the most common inherited hematological disorders ...
To compare the features of sickle-cell anemia in Brazil with those in other locales, we studied the ...
p. 292-298Hemoglobinopathies are hereditary disorders of the hemoglobin molecule with a high prevale...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions ...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do...
-Thalassemia, arising from a defect in -globin chain synthesis, is often caused by deletions involvi...
ABSTRACT. The ethnic composition of the Brazilian popula-tion favors high frequencies of the-α3.7 de...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions invol...
Alpha-thalassemia (α-thal) is one of the most common monogenic disorders in the world. Its clinical ...
IntroductionCases with microcytosis not responding adequately to iron supplementation are diagnostic...
Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), and the alph...
Hemoglobinopathies are the most common recessive diseases worldwide but their prevalence in Uruguay ...
ABSTRACTIntroduction:Hemoglobin S (HbS) is one of the most common inherited hematological disorders ...
To compare the features of sickle-cell anemia in Brazil with those in other locales, we studied the ...
p. 292-298Hemoglobinopathies are hereditary disorders of the hemoglobin molecule with a high prevale...