Sura Thanyachai, Busabaratana Manisa, Youngcharoen Supak, Wisedpanichkij Raewadee, Viprakasit Vip, Trachoo Objoon
Division of Medical Genetics and Molecular Medicine, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Eur J Haematol. 2007 Sep;79(3):251-4. doi: 10.1111/j.1600-0609.2007.00907.x. Epub 2007 Jul 26.
Haemoglobin (Hb) Hope [beta136(H14)Gly-->Asp(GGT-->GAT)] is one of the unstable haemoglobin variants of the beta-globin chain, which is demonstrated in people of various ethnic backgrounds. Here we report a Thai female patient with clinical thalassaemia intermedia since childhood. This patient had experienced neither blood transfusion nor hospitalisation. Hb Bart's-H and a large amount of Hb Hope were identified by high-performance liquid chromatography (HPLC) assay and the diagnosis of homozygous Hb Hope was definitely achieved by direct sequencing of exon 3 of beta-globin gene. Furthermore, we could identify that her brother carried the mutation of homozygous Hb Hope without abnormal alpha globin chain involvement, and another family member had heterozygous Hb Hope in association with -alpha(3.7) mutation, and both of them were clinically silent.
血红蛋白(Hb)Hope [β136(H14)甘氨酸→天冬氨酸(GGT→GAT)] 是β珠蛋白链不稳定血红蛋白变异体之一,在不同种族背景的人群中均有发现。在此,我们报告一名自幼患有中间型临床地中海贫血的泰国女性患者。该患者既未接受过输血治疗,也未住院治疗。通过高效液相色谱(HPLC)分析鉴定出了Hb Bart's-H和大量的Hb Hope,通过对β珠蛋白基因第3外显子的直接测序明确诊断为纯合子Hb Hope。此外,我们发现她的哥哥携带纯合子Hb Hope突变且无异常α珠蛋白链受累,另一名家庭成员为杂合子Hb Hope合并-α(3.7)突变,他们两人在临床上均无明显症状。