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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 6
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Short Communication

First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok

Fan JiangPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China; ;Department of Obstetrics and Gynecology, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaView further author information
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Jian-Ying ZhouPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China; ;Department of Obstetrics and Gynecology, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaView further author information
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Jin-Mei YanPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China; ;Department of Obstetrics and Gynecology, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaView further author information
,
Yue-Cheng LuPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China; ;Department of Obstetrics and Gynecology, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaView further author information
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China; ;Department of Obstetrics and Gynecology, Guangzhou Women and Children Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaCorrespondence[email protected] [email protected]
View further author information
Pages 425-427 | Received 26 Oct 2016, Accepted 30 Nov 2016, Published online: 31 Mar 2017

References

  • Giardine B, Borg J, Viennas E, et al. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucl Acids Res. 2014;42:(Database issue):D1063–D1069 (http://globin.cse.psu.edu).
  • Fucharoen G, Srivorakun H, Singsanan S, et al. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system. Int J Lab Hematol. 2011;33(4):424–433.
  • Szuberski J, Oliveira JL, Hoyer JD. A comprehensive analysis of hemoglobin variants by high performance liquid chromatography (HPLC). Int J Lab Hematol. 2012;34(6):594–604.
  • Leung KF, Ma ES, Chan AY, et al. Clinical phenotype of haemoglobin Q-H disease. J Clin Pathol. 2004;57(1):81–82.
  • Iuchi I, Shimasaki S, Hidaka K, et al. Hemoglobin J Bangkok (β56[D7]Gly→Asp): a hemoglobin variant discovered by the hemoglobinopathy survey in Takamatsu district. Hemoglobin. 1981;5(2):199–204.
  • Singha K, Fucharoen G, Fucharoen S. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects. Acta Haematol. 2014;131(2):71–75.
  • Panyasai S, Pornprasert S. Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand. Clin Lab. 2014;60(7):1099–1103.
  • Lou JW, Wang T, Liu YH, et al. Prevalence and molecular characterization of structural hemoglobin variants in the Dongguan region of Guangdong Province, Southern China. Hemoglobin. 2014;38(4):282–286.

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