Analysis of the Haematological Phenotype and Molecular Characteristics of Rare Abnormal Haemoglobin

• Published in: Molecular genetics & genomic medicine Vol. 12; no. 9; pp. e70012 - n/a
• Main Authors: Ge, Yanfen, Zheng, Guansheng, Xian, Luhua, Luo, Yanfei, Liu, Junru, Lin, Ting, Cui, Wenhao, Yang, Yujing, Shan, Huizhuang
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.09.2024; John Wiley and Sons Inc; Wiley
• Subjects: Adolescent; Adult; Anemia; Blood; Blood diseases; Blood tests; Capillary electrophoresis; Child; China; DNA sequencing; Electrophoresis; Epidemiology; Erythrocyte Indices; Female; Gene sequencing; Genes; Genotype & phenotype; haemoglobin; haemoglobinopathy; Hb Fukuyama; Hb Port Phillip; Hb Saint Etienne; Hematology; Hemoglobin; Hemoglobinopathies - blood; Hemoglobinopathies - diagnosis; Hemoglobinopathies - epidemiology; Hemoglobinopathies - genetics; Hemoglobins, Abnormal - genetics; Humans; Liquid chromatography; Male; Middle Aged; Mutation; Original; Patients; Peripheral blood; Phenotype; Phenotypes; Phenotypic variations; Physiology; Point mutation; Population studies; China; United States > US; Guangdong China; Japan; Hb Saint Etienne; haemoglobinopathy; haemoglobin; Hb Fukuyama; Hb Port Phillip
• ISSN: 2324-9269; 2324-9269
• DOI: 10.1002/mgg3.70012

ABSTRACT Background Haemoglobinopathy refers to a group of common monogenic inherited conditions associated with variations in the haemoglobin molecule; however, there is relatively limited reporting on abnormal haemoglobinopathy in the Chinese population, especially rare abnormal haemoglobin (Hb). The aim of this study was to explore the clinical characteristics of haemoglobinopathy to supplement data for the epidemiological investigation of Hb variants in Guangdong province of China. Methods Peripheral blood was collected from five patients (including a family) for Complete blood count, Hb electrophoresis, High‐performance liquid chromatography analysis and degenerative globin body testing. Hb variants were further analysed by PCR and DNA sequencing. Results The research subjects were diagnosed with different types of abnormal Hb. The blood routine of the Hb Fukuyama (HBB:c.232C>T) diagnosed individual showed microcytic hypochromic anaemia, with a lower Hb level (64 g/L), mean corpuscular volume (MCV) of 71.5 fL and mean corpuscular haemoglobin (MCH) of 21.5 pg. Individuals diagnosed with Hb Port Phillip (HBA2:c.275T>C) exhibit a MCH level that is slightly below average, at 26.4 pg. The Hb Saint Etienne (HBB:c.279C>G) diagnosed individual showed macrocytic hypochromic anaemia, and the proband had a low Hb level (116 g/L), MCV of 102.2 fL and MCH of 29.4 pg. Conclusion We confirmed the presence of Hb Fukuyama (HBB:c.232C>T) in China for the first time. Three rare patients with the Hb Saint Etienne (HBB:c.279C>G) phenotype and one patient with Hb Port Phillip (HBA2:c.275T>C) phenotype were included. Our research enriches the gene mutation map of haemoglobinopathy in Guangdong province and improves the detection system of haemoglobinopathy for population prevention and eugenics. The research subjects were diagnosed with different types of abnormal haemoglobin. We confirmed the presence of Hb Fukuyama in China for the first time. Three rare patients with the Hb Saint Etienne phenotype and one patient with Hb Port Phillip phenotype were included.