Detection of Coinherited Hb H-Constant Spring/Paksé Disease and Hb E by Capillary Electrophoresis and High Performance Liquid Chromatography

REFERENCES

• Fucharoen S, Winichagoon P, Thonglairuam V. β-Thalassemia associated with α-thalassemia in Thailand. Hemoglobin. 1988;12(5–6):581–592.
   PubMed Web of Science ®Google Scholar
• Tanphaichitr VS, Mahasandana C, Suvatte V, Yodthong S, Pung-Amritt P, Seeloem J. Prevalence of Hemoglobin E, α-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok. Southeast Asian J Trop Med Public Health. 1995;26(Suppl 1):271–274.
   PubMedGoogle Scholar
• Fucharoen G, Fucharoen S, Wanhakit C, Srithong W. Molecular basis of α0-thalassemia in northeast of Thailand. Southeast Asian J Trop Med Public Health 1995;26(Suppl 1):249–251.
   PubMedGoogle Scholar
• Winichagoon P, Higgs DR, Goodbourn SE, Clegg JB, Weatherall DJ, Wasi P. The molecular basis of α-thalassaemia in Thailand. EMBO J. 1984;3(8):1813–1818.
   PubMed Web of Science ®Google Scholar
• Fucharoen S, Winichagoon P. Hemoglobinopathies in Southeast Asia. Hemoglobin. 1987;11(1):65–88.
   PubMed Web of Science ®Google Scholar
• Laig M, Pape M, Hundrieser J, . The distribution of the Hb Constant Spring gene in Southeast Asian populations. Hum Genet. 1990;84(2):188–190.
   PubMed Web of Science ®Google Scholar
• Pichanun D, Munkongdee T, Klamchuen S, . Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand. Hemoglobin. 2010;34(6):582–586.
   PubMed Web of Science ®Google Scholar
• Boonsa S, Sanchaisuriya K, Fucharoen G, Wiangnon S, Jetsrisuparb A, Fucharoen S. The diverse molecular basis and hematological features of Hb H and AEBar’s diseases in Northeast Thailand. Acta Haematol. 2004;111(3):149–154.
   PubMed Web of Science ®Google Scholar
• Jetsrisuparb A, Sanchaisuriya K, Fucharoen G, . Development of severe anemia during fever episodes in patients with Hemoglobin E trait and Hemoglobin H disease combinations. J Pediatr Hematol Oncol. 2006;28(4):249–253.
   PubMed Web of Science ®Google Scholar
• Sanchaisuriya K, Fucharoen G, Fucharoen S. Hb Paksé [(α2) codon 142 (TAA→TAT or Term→Tyr) in Thai patients with EABart’s disease and Hb H disease. Hemoglobin. 2002;26(3):227–235.
   PubMed Web of Science ®Google Scholar
• Waye JS, Eng B, Patterson M, Chui DH, Olivieri NF. Identification of a novel termination codon mutation (TAA→TAT, Ter→Tyr) in the α2 globin gene of a Laotian girl with Hemoglobin H disease. Blood. 1994;83(11):3418–3420.
   PubMed Web of Science ®Google Scholar
• Ne W, Harano K, Harano T, . Hb Constant Spring [α142, Term→Gln (TAA>CAA in α2)] in the α-thalassemia of anemic patients in Myanmar. Hemoglobin. 2008;32(5):454–461.
   PubMed Web of Science ®Google Scholar
• Singsanan S, Fucharoen G, Savongsy O, Sanchaisuriya K, Fucharoen S. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations. Ann Hematol. 2007;86(9):665–669.
   PubMed Web of Science ®Google Scholar
• Hunt DM, Higgs DR, Winichagoon P, Clegg JB, Weatherall DJ. Haemoglobin Constant Spring has an unstable α chain messenger RNA. Br J Haematol. 1982;51(3):405–413.
   PubMed Web of Science ®Google Scholar
• Waneesorn J, Panyasai S, Kongthai K, Singboottra P, Pornprasert S. Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb Constant Spring [Hb CS; α142, Term→Gln (TAA>CAA in α2)]. Hemoglobin. 2011;35(4):338–345.
   PubMed Web of Science ®Google Scholar
• Pornprasert S, Phusua A, Suanta S, Saetung R, Sanguansermsri T. Detection of α-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis. Eur J Haematol. 2008;80(6):510–514.
   PubMed Web of Science ®Google Scholar
• Pornprasert S, Wiengkum T, Srithep S, Chainoi I, Singboottra P, Wongwiwatthananukit S. Detection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting analysis. Korean J Lab Med. 2011;31(3):138–142.
   PubMed Web of Science ®Google Scholar
• Fucharoen S, Sanchaisuriya K, Fucharoen G, Panyasai S, Devenish R, Luy L. Interaction of Hemoglobin E and several forms of α-thalassemia in Cambodian families. Haematologica. 2003;88(10):1092–1098.
   PubMed Web of Science ®Google Scholar
• Pornprasert S, Treesuwan K. Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in northern Thailand. Hemoglobin. 2012;36(5):491–496.
   PubMed Web of Science ®Google Scholar
• Yin XL, Wu ZK, Zhou XY, . Co-inherited β-thalassemia trait and Hb H disease: clinical characteristics and interference in diagnosis of thalassemia by high-performance liquid chromatography. Int J Lab Hematol. 2012;34(4):427–431.
   PubMed Web of Science ®Google Scholar
• Fucharoen S, Winichagoon P, Pootrakul P, Piankijagum A, Wasi P. Differences between two types of Hb H disease, α-thalassemia 1/α-thalassemia 2 and α-thalassemia 1/Hb Constant Spring. Birth Defects Orig Artic Ser. 1987;23(5A):309–315.
   PubMedGoogle Scholar
• Tangvarasittichai O, Jeenapongsa R, Sitthiworanan C, Sanguansermsri T. Laboratory investigations of Hb Constant Spring. Clin Lab Haematol. 2005;27(1):47–49.
   PubMedGoogle Scholar
• Pornprasert S, Panyasai S, Waneesorn J, Kongthai K, Singboottra P. Quantification of Hemoglobin Constant Spring in heterozygote and homozygote by a capillary electrophoresis method. Int J Lab Hematol. 2012;34(2):143–147.
   PubMed Web of Science ®Google Scholar
• Schrier SL, Bunyaratvej A, Khuhapinant A, . The unusual pathobiology of Hemoglobin Constant Spring red blood cells. Blood. 1997;89(5):1762–1769.
   PubMed Web of Science ®Google Scholar
• Wajcman H, Traeger-Synodinos J, Papassotiriou I, . Unstable and thalassemic α chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia. Hemoglobin. 2008;32(4):327–349.
   PubMed Web of Science ®Google Scholar
• Giordano PC, Harteveld CL, Michiels JJ, . Atypical Hb H disease in a Surinamese patient resulting from a combination of the – –SEA and –α 3.7 deletions with Hb C heterozygosity. Br J Haematol. 1997;96(4):801–805.
   PubMed Web of Science ®Google Scholar
• Harteveld CL, Oosterhuis WP, Schoenmakers CH, . α-Thalassaemia masked by β gene defects and a new polyadenylation site mutation on the α2-globin gene. Eur J Haematol. 2010;84(4):354–8.
   PubMed Web of Science ®Google Scholar