| Literature DB >> 12621249 |
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.Entities:
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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