地中海贫血
血红蛋白电泳
血红蛋白
医学
胎儿血红蛋白
贫血
胃肠病学
内科学
遗传学
分子生物学
生物
怀孕
胎儿
作者
Jicheng Wang,Cuize Yao,Yanlin Huang,Ling Liu,Tenglong Yuan,Dan-Qing Qin
标识
DOI:10.19746/j.cnki.issn.1009-2137.2021.04.035
摘要
OBJECTIVE To analyze the hematological characteristics of Chinese Gγ+(Aγδβ)0-thalassemia,SEA-HPFH and Taiwan type β-thalassemia. METHODS Hemoglobin electrophoresis and blood routine test were used to analyze the hematological indexes of all peripheral blood samples,PCR-Flow fluorescent hybridization and Gap-PCR were used to detect the globin gene mutations and the data were analyzed statistically. RESULTS The 3 types of deletion β- Thalassemia patients were showed as hypochromic small cell anemia. The MCH and MCV values of Taiwan type β-thalassemia patients were the lowest. The results of hemoglobin electrophoresis showed that the increasing of HbF was found in all of the 3 types. Except for the decreasing of Hb A2 in Chinese Gγ+(Aγδβ)0-thalassemia,the levels of Hb A2 in the other two deletion β-thalassemia patients were significantly increased. Except for Hb, there were significant differences in MCV, MCH, Hb A2 and HbF between Chinese Gγ+(Aγδβ)0-thalassemia and SEA-HPFH(P<0.001). CONCLUSION Through analyze the hematological characteristics, it can be provide that the guidance for the differential diagnosis and genetic consultation of the three commonest deletion β-thalassemia in Chinese.
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