Hb D/Talassemia beta associada à anemia crônica

Detalhes bibliográficos
Autor(a) principal: Naoum,Paulo C.
Data de Publicação: 2002
Outros Autores: Moraes,Magaly S., Radispiel,Janaína, Cavalheri,Priscila P., Valeri,Fábio F.
Tipo de documento: Artigo
Idioma: por
Título da fonte: Revista brasileira de hematologia e hemoterapia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000100010
Resumo: We describe a case of Hb D/Beta thalassemia associated with chronic anemia. Hematological analyses performed in a patient with chronic anemia demonstrating microcytosis and hypochromic in his erythrocytes. Specific laboratory diagnosis performed by alkaline and acid electrophoresis, and fetal determination by alkali resistance, indicated it to be Hb D associated with beta thalassemia. Analyses carried out on his family (father, mother and brother) confirmed the suspected diagnosis. Hb D/Beta thalassemia is a very rare interaction in the Brazilian population, and its determination required specific laboratorial techniques and hematological analyses.
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spelling Hb D/Talassemia beta associada à anemia crônicaWe describe a case of Hb D/Beta thalassemia associated with chronic anemia. Hematological analyses performed in a patient with chronic anemia demonstrating microcytosis and hypochromic in his erythrocytes. Specific laboratory diagnosis performed by alkaline and acid electrophoresis, and fetal determination by alkali resistance, indicated it to be Hb D associated with beta thalassemia. Analyses carried out on his family (father, mother and brother) confirmed the suspected diagnosis. Hb D/Beta thalassemia is a very rare interaction in the Brazilian population, and its determination required specific laboratorial techniques and hematological analyses.Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular2002-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000100010Revista Brasileira de Hematologia e Hemoterapia v.24 n.1 2002reponame:Revista brasileira de hematologia e hemoterapia (Online)instname:Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)instacron:ABHHTC10.1590/S1516-84842002000100010info:eu-repo/semantics/openAccessNaoum,Paulo C.Moraes,Magaly S.Radispiel,JanaínaCavalheri,Priscila P.Valeri,Fábio F.por2002-08-16T00:00:00Zoai:scielo:S1516-84842002000100010Revistahttp://www.rbhh.org/pt/archivo/https://old.scielo.br/oai/scielo-oai.phpsbhh@terra.com.br||secretaria@rbhh.org1806-08701516-8484opendoar:2002-08-16T00:00Revista brasileira de hematologia e hemoterapia (Online) - Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)false
dc.title.none.fl_str_mv Hb D/Talassemia beta associada à anemia crônica
title Hb D/Talassemia beta associada à anemia crônica
spellingShingle Hb D/Talassemia beta associada à anemia crônica
Naoum,Paulo C.
title_short Hb D/Talassemia beta associada à anemia crônica
title_full Hb D/Talassemia beta associada à anemia crônica
title_fullStr Hb D/Talassemia beta associada à anemia crônica
title_full_unstemmed Hb D/Talassemia beta associada à anemia crônica
title_sort Hb D/Talassemia beta associada à anemia crônica
author Naoum,Paulo C.
author_facet Naoum,Paulo C.
Moraes,Magaly S.
Radispiel,Janaína
Cavalheri,Priscila P.
Valeri,Fábio F.
author_role author
author2 Moraes,Magaly S.
Radispiel,Janaína
Cavalheri,Priscila P.
Valeri,Fábio F.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Naoum,Paulo C.
Moraes,Magaly S.
Radispiel,Janaína
Cavalheri,Priscila P.
Valeri,Fábio F.
description We describe a case of Hb D/Beta thalassemia associated with chronic anemia. Hematological analyses performed in a patient with chronic anemia demonstrating microcytosis and hypochromic in his erythrocytes. Specific laboratory diagnosis performed by alkaline and acid electrophoresis, and fetal determination by alkali resistance, indicated it to be Hb D associated with beta thalassemia. Analyses carried out on his family (father, mother and brother) confirmed the suspected diagnosis. Hb D/Beta thalassemia is a very rare interaction in the Brazilian population, and its determination required specific laboratorial techniques and hematological analyses.
publishDate 2002
dc.date.none.fl_str_mv 2002-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000100010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000100010
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dc.relation.none.fl_str_mv 10.1590/S1516-84842002000100010
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
publisher.none.fl_str_mv Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
dc.source.none.fl_str_mv Revista Brasileira de Hematologia e Hemoterapia v.24 n.1 2002
reponame:Revista brasileira de hematologia e hemoterapia (Online)
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reponame_str Revista brasileira de hematologia e hemoterapia (Online)
collection Revista brasileira de hematologia e hemoterapia (Online)
repository.name.fl_str_mv Revista brasileira de hematologia e hemoterapia (Online) - Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
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