Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai.
Department of Pediatrics, Center of Excellence for Medical Genomics, Medical Genomics Cluster, Faculty of Medicine, Chulalongkorn University.
J Pediatr Hematol Oncol. 2021 Jul 1;43(5):e723-e726. doi: 10.1097/MPH.0000000000001937.
Hemoglobin (Hb) H/Constant Spring disease is a common nondeletional Hb H disease, typically causing a more severe phenotype than the deletional Hb H disease counterpart. Hb Tak, resulting from a dinucleotide insertion (+AC) at codon 146 of beta-globin gene, has an increased oxygen affinity and usually presents with polycythemia. We studied a case of a 4-year-old Thai boy with a severe, early-onset anemia. To our knowledge, he is the first reported patient with Hb H/Constant Spring disease and heterozygous Hb Tak. Trio-whole-exome sequencing does not identify other genetic variants that may contribute to the severity of anemia. The observation suggests that coinherited Hb H/Constant Spring and heterozygous Hb Tak lead to severe hemolytic anemia.
血红蛋白 H/Constant Spring 病是一种常见的非缺失型血红蛋白 H 病,通常比缺失型血红蛋白 H 病具有更严重的表型。由β-珠蛋白基因 146 密码子的二核苷酸插入(+AC)引起的 Hb Tak 增加了氧亲和力,通常表现为红细胞增多症。我们研究了一例 4 岁泰国男孩的严重早发性贫血。据我们所知,他是首例报道的血红蛋白 H/Constant Spring 病和杂合子 Hb Tak 的患者。三人体外全基因组测序未发现其他可能导致贫血严重程度的遗传变异。观察结果表明,共遗传的血红蛋白 H/Constant Spring 和杂合子 Hb Tak 导致严重的溶血性贫血。