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

ABSTRACT

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.


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Middle Aged , Hemoglobins , beta-Thalassemia/genetics , Brazil , Polymerase Chain Reaction , Polymorphism, Genetic
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