Hb D/Talassemia beta associada à anemia crônica
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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Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
2002
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oai:scielo:S1516-848420020001000102002-08-16Hb D/Talassemia beta associada à anemia crônicaNaoum,Paulo C.Moraes,Magaly S.Radispiel,JanaínaCavalheri,Priscila P.Valeri,Fábio F.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.info:eu-repo/semantics/openAccessAssociação Brasileira de Hematologia e Hemoterapia e Terapia CelularRevista Brasileira de Hematologia e Hemoterapia v.24 n.1 20022002-03-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000100010pt10.1590/S1516-84842002000100010 |
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Brasil |
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BR |
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revista |
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America del Sur |
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Portuguese |
| format |
Digital |
| author |
Naoum,Paulo C. Moraes,Magaly S. Radispiel,Janaína Cavalheri,Priscila P. Valeri,Fábio F. |
| spellingShingle |
Naoum,Paulo C. Moraes,Magaly S. Radispiel,Janaína Cavalheri,Priscila P. Valeri,Fábio F. Hb D/Talassemia beta associada à anemia crônica |
| author_facet |
Naoum,Paulo C. Moraes,Magaly S. Radispiel,Janaína Cavalheri,Priscila P. Valeri,Fábio F. |
| author_sort |
Naoum,Paulo C. |
| title |
Hb D/Talassemia beta associada à anemia crônica |
| 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 |
| 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. |
| publisher |
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular |
| publishDate |
2002 |
| url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000100010 |
| work_keys_str_mv |
AT naoumpauloc hbdtalassemiabetaassociadaaanemiacronica AT moraesmagalys hbdtalassemiabetaassociadaaanemiacronica AT radispieljanaina hbdtalassemiabetaassociadaaanemiacronica AT cavalheripriscilap hbdtalassemiabetaassociadaaanemiacronica AT valerifabiof hbdtalassemiabetaassociadaaanemiacronica |
| _version_ |
1756423373639909376 |