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Genet. mol. biol ; 28(3): 394-396, July-Sept. 2005. ilus, tab
Artículo en Inglés | LILACS | ID: lil-416317

RESUMEN

We report the coexistence of Hb Camperdown [beta104 (G6) Arg -> Ser] and beta°-thalassemia [beta39 (Gln -> stop codon)] in a nine-month-old Brazilian boy. He had a relatively more severe hypochromic and microcytic anemia in comparison to his mother's beta-thalassemia trait. His Hb Camperdown heterozygous father was clinically and hematologically normal. To our knowledge, this is the first description of an association of beta°-thalassemia with Hb Camperdown.


Asunto(s)
Humanos , Masculino , Femenino , Niño , Adolescente , Adulto , Persona de Mediana Edad , Hemoglobinas , Talasemia beta/genética , Brasil , Reacción en Cadena de la Polimerasa , Polimorfismo Genético
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