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作 者:刘宁毅[1]
机构地区:[1]钦州市第二人民医院检验科,广西钦州535000
出 处:《中国热带医学》2013年第5期567-568,607,共3页China Tropical Medicine
基 金:广西自然科学基金项目(No.2010GXNSFA013263)
摘 要:目的应用基因诊断技术探讨高危地中海贫血(地贫)儿童的常见基因谱的分布特征。方法用钦州地区168例高危地贫的儿童样本分别检测α-地贫及β-地贫基因型,而α-地贫分为3种α缺失型基因检测(--SEA/,-α3.7/-α4.2)和3种非缺失突变型α地贫(HbCS,HbQS,HbWS)。α缺失型基因检测应用单管多重PCR技术进行检测,非缺失突变型α地贫和β-地贫(检测中国人常见的17种位点)均采用反向斑点杂交法。结果在168例进行地贫基因检查的钦州地区高危地贫儿童中,检出α-地贫49例,占29.17%;其中缺失型α-地贫39例,占α-地贫79.59%,非缺失突变型α地贫10例,占α-地贫20.41%,检出β-地贫27例,占16.07%;其中双重杂合子5例,占2.98%;检出复合αβ-地贫12例,占7.14%;总检出率是55.36%。结论钦州地区是地贫高发区,应选择适当的检测方法对育龄人群进行大面积的地贫产前筛查,这对优生优育、干预地贫儿出生有着重要作用。Objective To analyze the genotypes of high-risk thalassemia(thalassemia) children.Methods Samples were collected from 168 children with high-risk thalassemia and the genotypes of α-thalassemia and β-thalassemia were detected.The α-thalassemia cases were detected for three alpha deletion genotypes(-SEA/-a 3.7/-a 4.2)and three non-deletion mutant α-thalassemia(HbCS HbQS HbWS).The alpha deletion genotype was detected with single-tube multiplex PCR technology,non-deletion mutant α-thalassemia and β-thalassemia(17 sites) in common Chinese people were detected with by using reverse dot blot hybridization.Results Totally 49 α-thalassemia cases were detected from 168 children at high risk of thalassemia,accounted for 29.17%;including 39 deletion α-thalassemia cases,accounting for 79.59% of the alpha-thalassemia cases,10 non-deletion mutant a-thalassemia cases,accounting for 20.41% of α-thalassemia.Twenty-seven deletion β-thalassemia cases were detected accounting for 16.07%;including double heterozygotes in 5 cases,accounting for 2.98%;detection composite αβ-groundpoor in 12 cases,accounting for 7.14%;the total detection rate was 55.36%.Conclusions The incidence of thalassemia in Qinzhou is high,and large-scale screening of thalassemia among population of child-bearing age is indicated for improvement of prenatal care and reduce the incidence of thalassemia ion Qinzhou.
分 类 号:R556.61[医药卫生—血液循环系统疾病]
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