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1.
Braz. j. med. biol. res ; 43(9): 910-913, Sept. 2010. ilus, tab
Artículo en Inglés | LILACS | ID: lil-556859

RESUMEN

Mutations in Bruton's tyrosine kinase (BTK) gene are responsible for X-linked agammaglobulinemia (XLA), which is characterized by recurrent bacterial infections, profound hypogammaglobulinemia, and decreased numbers of mature B cells in peripheral blood. We evaluated 5 male Brazilian patients, ranging from 3 to 10 years of age, from unrelated families, whose diagnosis was based on recurrent infections, markedly reduced levels of IgM, IgG and IgA, and circulating B cell numbers <2 percent. BTK gene analysis was carried out using PCR-SSCP followed by sequencing. We detected three novel (Ala347fsX55, I355T, and Thr324fsX24) and two previously reported mutations (Q196X and E441X). Flow cytometry revealed a reduced expression of BTK protein in patients and a mosaic pattern of BTK expression was obtained from mothers, indicating that they were XLA carriers.


Asunto(s)
Niño , Preescolar , Humanos , Masculino , Agammaglobulinemia/genética , Enfermedades Genéticas Ligadas al Cromosoma X/genética , Mutación/genética , Proteínas Tirosina Quinasas/genética , Agammaglobulinemia/enzimología , Citometría de Flujo , Enfermedades Genéticas Ligadas al Cromosoma X/enzimología , Reacción en Cadena de la Polimerasa , Polimorfismo Conformacional Retorcido-Simple
2.
Braz J Med Biol Res ; 43(9): 910-3, 2010 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-20721470

RESUMEN

Mutations in Bruton's tyrosine kinase (BTK) gene are responsible for X-linked agammaglobulinemia (XLA), which is characterized by recurrent bacterial infections, profound hypogammaglobulinemia, and decreased numbers of mature B cells in peripheral blood. We evaluated 5 male Brazilian patients, ranging from 3 to 10 years of age, from unrelated families, whose diagnosis was based on recurrent infections, markedly reduced levels of IgM, IgG and IgA, and circulating B cell numbers <2%. BTK gene analysis was carried out using PCR-SSCP followed by sequencing. We detected three novel (Ala347fsX55, I355T, and Thr324fsX24) and two previously reported mutations (Q196X and E441X). Flow cytometry revealed a reduced expression of BTK protein in patients and a mosaic pattern of BTK expression was obtained from mothers, indicating that they were XLA carriers.


Asunto(s)
Agammaglobulinemia/genética , Enfermedades Genéticas Ligadas al Cromosoma X/genética , Mutación/genética , Proteínas Tirosina Quinasas/genética , Agammaglobulinemia Tirosina Quinasa , Agammaglobulinemia/enzimología , Niño , Preescolar , Citometría de Flujo , Enfermedades Genéticas Ligadas al Cromosoma X/enzimología , Humanos , Masculino , Reacción en Cadena de la Polimerasa , Polimorfismo Conformacional Retorcido-Simple
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