Analysis of five Chinese individuals with rare thalassemia mutation HBB: c. 93-21G>A
10.3760/cma.j.cn511374-20240108-00015
- VernacularTitle:中国罕见型地中海贫血 HBB: c．93-21G>A突变5例
- Author:
Guangkuan ZENG
1
;
Yiyuan GE
;
Xiaomin MA
;
Xiaohua YU
;
Bairu LAI
;
Yuwei LIAO
;
Lili LIU
;
Yanbin CAO
;
Yanqing ZENG
;
Yuchan HUANG
;
Jianlian LIANG
;
Liye YANG
Author Information
1. 阳江市人民医院精准医学检测中心，阳江 529500
- Keywords:
Beta-thalassemia;
HBB: c. 93-21G>A;
DNA sequencing analysis
- From:
Chinese Journal of Medical Genetics
2024;41(10):1171-1175
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To explore the hematological phenotype and genotypic characteristics of five Chinese individuals with a rare thalassemia mutation HBB: c. 93-21G>A. Methods:A retrospective study was carried out on five individuals identified by the People′s Hospital of Yangjiang and Guangzhou Hybribio Co., Ltd. from May 2018 to September 2022. Routine blood test and hemoglobin electrophoresis were performed, and the genotypes of five subjects were determined by using PCR combined with reverse dot blotting (RDB), nested PCR, Gap-PCR and Sanger sequencing. This study was approved by Medical Ethics Cornmittee of the People′s Hospital of Yangjiang (Ethics No. 20240001).Results:Among the five individuals, hematological data of one was unavailable, and the remaining four had presented with microcytosis and hypochromia. The results of hemoglobin electrophoresis indicated that all of them had a HbA 2 level of ≥4.7%. Genetic analysis showed that one case had harbored compound heterozygous mutations of ααα anti3.7 triplet and HBB: c. 93-21G>A, one had compound heterozygous mutations of -α 3.7 and HBB: c. 93-21G>A, whilst the remaining three were heterozygous for the HBB: c. 93-21G>A mutation. Conclusion:The hematological phenotype of β-thalassemia carriers ( HBB: c. 93-21G>A) is similar to that of other β + thalassemia heterozygotes with mild β-thalassemia characteristics.
