Alpha Thalassemia and Haplotypes of Beta Globin in Sickle Cell Disease - Rodrigues, Daniela de Oliveira Werneck; Sudário, Lysla Cardoso; Ribeiro, Luiz Claudio
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Sickle cell disease (DF) is the most common hereditary monogenic disease in Brazil. The term DF includes sickle cell anemia (AF) and pathological conditions in which the hemoglobin S gene is associated with other hereditary hemoglobinopathies such as SC, S/beta0 and S/beta+ thalassemia (S/b), SD Punjab, among others. There is a description of 5 haplotypes of the globine chain cluster (¿S) linked to HbS: Asia, Senegal, Benin, Bantu (CAR) and Cameroon. The DF can also coexist with ¿-talassemias (¿-Tal). The most severe complication in the DF is stroke, which is responsible for 20% of mortality.…mehr

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Produktbeschreibung
Sickle cell disease (DF) is the most common hereditary monogenic disease in Brazil. The term DF includes sickle cell anemia (AF) and pathological conditions in which the hemoglobin S gene is associated with other hereditary hemoglobinopathies such as SC, S/beta0 and S/beta+ thalassemia (S/b), SD Punjab, among others. There is a description of 5 haplotypes of the globine chain cluster (¿S) linked to HbS: Asia, Senegal, Benin, Bantu (CAR) and Cameroon. The DF can also coexist with ¿-talassemias (¿-Tal). The most severe complication in the DF is stroke, which is responsible for 20% of mortality. The causes and factors that would increase the risk of strokes are not completely known. Several lines of evidence suggest that a genetic signature could influence the development of strokes.
Autorenporträt
Hematólogo de la Fundación Hemominas - Brasil . Doctorado en Salud Brasileña por la Universidade Federal de Juiz de Fora. Miembro de la Red Global de Anemia Falciforme. Investigador de los estudios multicéntricos internacionales REDS III y REDS IV sobre la seguridad de las transfusiones en la anemia falciforme.