Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/198603
Type: Artigo de periódico
Title: Hb H Disease Resulting From The Association Of An α-thalassemia Allele [-(α)] With An Unstable α-globin Variant [hb Icaria]: First Report On The Occurrence In Brazil.
Author: Kimura, Elza M
Oliveira, Denise M
Fertrin, Kleber
Pinheiro, Valéria R
Jorge, Susan E D C
Costa, Fernando F
de Fátima Sonati, Maria
Abstract: Hb H Disease is caused by the loss or inactivation of three of the four functional α-globin genes. Patients present chronic hemolytic anemia and splenomegaly. In some cases, occasional blood transfusions are required. Deletions are the main cause of this type of thalassemia ( α-thalassemia). We describe here an unusual case of Hb H disease caused by the combination of a common α(0) deletion [-( α) (20.5) ] with a rare point mutation (c.427T > A), thus resulting in an elongated and unstable α-globin variant, Hb Icaria, (X142K), with 31 additional amino-acid residues. Very high levels of Hb H and Hb Bart's were detected in the patient's red blood cells (14.7 and 19.0%, respectively). This is the first description of this infrequent association in the Brazilian population.
Subject: Hb H Disease
Hb Icaria
Alpha-thalassemia
Hereditary Hemoglobinopathies
Rights: aberto
Identifier DOI: 10.1590/S1415-47572009005000071
Address: http://www.ncbi.nlm.nih.gov/pubmed/21637442
Date Issue: 2009
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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