Document Detail

The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand.
MedLine Citation:
PMID:  15034236     Owner:  NLM     Status:  MEDLINE    
We defined the molecular basis and correlated the hematological phenotypes with the globin genotypes in 52 patients with Hb H disease and 29 patients with AEBart's disease of northeast Thailand. Among the former group, the most prevalent molecular defect was found to be the interaction of alpha-thalassemia 1 (SEA type) with the Hb Constant Spring (Hb CS; 35 of 52 patients), followed by the deletion of three alpha-globin genes with the SEA type alpha-thalassemia 1 and the 3.7- or 4.2-kb deletion of alpha-thalassemia 2 (14 of 52 patients) and the interaction of the SEA alpha-thalassemia 1 with the Hb Paksé which was found in the remaining 3 patients. Among the 29 patients of the latter group, in 18 disease was caused by interactions of Hb E heterozygotes with the SEA alpha-thalassemia 1 and Hb CS. Interaction of Hb E heterozygotes with a deletional form of Hb H disease was detected in 7 patients and the Hb Paksé AEBart's disease was found in another 3 patients. A remaining patient with an unusually severe form of AEBart's disease with a lower Hb E level and observable Hb H was associated with a hitherto undescribed condition, the interaction of Hb E heterozygote with alpha-thalassemia 1 and an alpha2 codon 30 (GAG) deletion. Hematological characterization of the patients demonstrated that although disease in most of them was associated with thalassemia intermedia phenotypes, it was apparent that association with the nondeletional form of alpha-thalassemia 2 produced a more severe phenotype than that of the deletional one. Therefore, alpha-globin gene analysis of Hb H and AEBart's disease patients would be useful for predicting the clinical outcome and improving genetic counseling.
Supap Boonsa; Kanokwan Sanchaisuriya; Goonnapa Fucharoen; Surapon Wiangnon; Arunee Jetsrisuparb; Supan Fucharoen
Related Documents :
7677966 - A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-gl...
20670166 - Thrombin activatable fibrinolysis inhibitor (tafi): relationship to hemostatic alterati...
20087956 - Prolidase activity and oxidative status in patients with thalassemia major.
19010166 - Application of the mccluskey index to predict blood product requirements during liver t...
15877086 - Central corneal thickness and its relationship to the patient's origin.
22766916 - Echocardiographic parameters as cardiovascular event predictors in hemodialysis patients.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Acta haematologica     Volume:  111     ISSN:  0001-5792     ISO Abbreviation:  Acta Haematol.     Publication Date:  2004  
Date Detail:
Created Date:  2004-03-22     Completed Date:  2004-04-30     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  0141053     Medline TA:  Acta Haematol     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  149-54     Citation Subset:  IM    
Copyright Information:
Copyright 2004 S. Karger AG, Basel
Department of Clinical Chemistry, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Child, Preschool
DNA Mutational Analysis
Hematologic Tests
Molecular Epidemiology
Sequence Deletion
Thailand / epidemiology
Thalassemia / epidemiology,  genetics*
alpha-Thalassemia / epidemiology,  genetics*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Improvement of cardiac function in thalassemia major treated with L-carnitine.
Next Document:  Prefibrotic chronic idiopathic myelofibrosis--a diagnostic enigma?