| Literature DB >> 28950779 |
Qiang Zhang1,2, Xin Fan2, Mingli Xu1, Yijia Zhang1, Huiling Xu1, Xiaojun Wen1, Wanjun Zhou1.
Abstract
Thalassemia is the most common monogenic disease, with the highest incidence in Guangxi Zhuang Autonomous Region, People's Republic of China (PRC). The blood test result was not consistent with α-globin gene testing in one of the patients during daily screening. It was confirmed that there were multiple mutations at the α2-globin gene polyadenylation (polyA) signal site: HBA2: c.*64(T>C), HBA2: c.*68(A>C), HBA2: c.*71(G>A), HBA2: c.*74(C>A), HBA2: c.*82(G>A), HBA2: c.*92(A>G) and HBA2: c.*98(T>C) and compound - -SEA/αα by sequencing of the HBA1 and HBA2 genes of the proband and core family members. After that, we found a further two cases of unrelated patients with this type of mutation. The mutation is not an accidental phenomenon, and likely to occur with a considerable incidence in Guangxi Zhuang Autonomous Region, PRC. We analyzed the hematological manifestations of this type of thalassemia and showed that it was a Hb H (β4) disease caused by rare mutations. We suggest that it is essential to pay attention to this mutation during future clinical diagnoses and genetic counseling of patients.Entities:
Keywords: Hb H disease; multiple mutations; polyadenylation (poly A) signal site; α-Thalassemia (α-thal)
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Year: 2017 PMID: 28950779 DOI: 10.1080/03630269.2017.1366917
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849