Perfil de beta talassemia heterozigota obtido a partir de análise data mining em banco de dados


Autoria(s): Domingos, Ana L. B.; Granzotto, Lucas A.; Belini Junior, Edis; Oliveira, Thiago Y. K.; Domingos, Ana C. B.; Bonini-Domingos, Claudia R.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/02/2010

Resumo

Variations in the phenotypic expression of heterozygous beta thalassemia reflect the formation of different populations. To better understand the profile of heterozygous beta-thalassemia of the Brazilian population, we aimed at establishing parameters to direct the diagnosis of carriers and calculate the frequency from information stored in an electronic database. Using a Data Mining tool, we evaluated information on 10,960 blood samples deposited in a relational database. Over the years, improved diagnostic technology has facilitated the elucidation of suspected beta thalassemia heterozygote cases with an average frequency of 3.5% of referred cases. We also found that the Brazilian beta thalassemia trait has classic increases of Hb A2 and Hb F (60%), mainly caused by mutations in beta zero thalassemia, especially in the southeast of the country.

Formato

78-79

Identificador

http://dx.doi.org/10.1590/S1516-84842010000100018

Revista Brasileira de Hematologia e Hemoterapia. Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, v. 32, n. 1, p. 78-79, 2010.

1516-8484

http://hdl.handle.net/11449/21434

10.1590/S1516-84842010000100018

S1516-84842010000100018

S1516-84842010000100018.pdf

Idioma(s)

por

Publicador

Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea

Relação

Revista Brasileira de Hematologia e Hemoterapia

Direitos

openAccess

Palavras-Chave #Data mining #beta thalassemia trait #Bioinformatics #Genetic diversity
Tipo

info:eu-repo/semantics/article