Literature DB >> 12621249

Homozygous hemoglobin Tak causes symptomatic secondary polycythemia in a Thai boy.

Voravarn S Tanphaichitr1, Vip Viprakasit, Gavivann Veerakul, Kleebsabai Sanpakit, Panutsaya Tientadakul.   

Abstract

Secondary polycythemia caused by high-oxygen-affinity hemoglobin is rare in children. Most patients with this condition have asymptomatic erythrocytosis. In this article the authors describe a young boy from Thailand with plethora, hypoxemia, and aggravated respiratory distress following a chest infection. Hematological and molecular studies revealed that the boy is homozygous for Hb Tak, an extended beta-globin variant with high oxygen affinity. This report of a patient who is homozygous for high-oxygen-affinity hemoglobin highlights the clinical significance of this hemoglobin disorder, which has been previously reported in several unrelated families from Southeast Asia.

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Year:  2003        PMID: 12621249     DOI: 10.1097/00043426-200303000-00016

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  3 in total

1.  Clinical and hematological characteristics of uncommon beta-globin variants in Thailand.

Authors:  Noppacharn Uaprasert; Ponlapat Rojnuckarin; Rung Settapiboon; Supaporn Amornsiriwat; Pranee Sutcharitchan
Journal:  Int J Hematol       Date:  2009-05-14       Impact factor: 2.490

Review 2.  Control of human beta-globin mRNA stability and its impact on beta-thalassemia phenotype.

Authors:  Isabel Peixeiro; Ana Luísa Silva; Luísa Romão
Journal:  Haematologica       Date:  2011-02-28       Impact factor: 9.941

3.  Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA2 Levels on Capillary Electrophoresis.

Authors:  Sitthichai Panyasai; Supachai Sakkhachornphop; Sakorn Pornprasert
Journal:  Indian J Hematol Blood Transfus       Date:  2017-04-04       Impact factor: 0.900

  3 in total

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