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Three cases of Hb Q-H disease found in a Cantonese family

Chaohui Hu1, Ling Zhang, Jianghu Pan

  • 1Guangzhou Kingmed Center for Clinical Laboratory, Guangdong, Guangzhou 510330, P.R. China. huzh@kingmed.com.cn

Molecular Medicine Reports
|April 7, 2011
PubMed

Hemoglobin (Hb) Q-Thailand, also known as G-Taichung, Mahidol, Kurashiki-I and Asabara, is an α-globin chain variant that results from a point mutation (GAC→CAC; Asp→His) at codon 74 of the α1-globin gene on chromosome 16p with a leftward single α-globin gene deletion (-α(4.2)). Co-inheritance of Hb Q-Thailand with α-thalassemia (mainly --(SEA)) results in thalassemia intermedia, termed Hb Q-H disease. The aim of the present study was to identify Hb Q-H disease in a Cantonese family. The presence of the Hb variant was confirmed by cellulose acetate electrophoresis. DNA analysis, based on polymerase chain reaction and sequencing, was developed to identify the α(Q-Thailand) mutation and common α-thalassemia gene deletions. Three cases of Hb Q-H disease and two Hb Q-Thailand carriers were found in the family. The 3-day-old proband with Hb Q-H disease did not show anemia (Hb 144 g/l), having 25.47% Hb F(Q) (α(Q)₂γ₂) in the total Hb; the other two cases of Hb Q-H disease manifested mild-to-moderate anemia. None required regular transfusions.

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