期刊文献+

孕早期绒毛产前诊断地中海贫血1072例分析 被引量:3

Analysis of Chorionic Villus Sampling Applied to Prenatal Diagnosis of 10 72 Cases of Thalassemia in First Trimester
下载PDF
导出
摘要 目的探讨地中海贫血高风险妊娠的产前诊断效果,为控制该类患儿的出生提供参考。方法孕10~15周孕妇1 072例,取绒毛样本进行α-和β-地中海贫血基因检测。结果在1 072例绒毛样本中,727例进行α-地贫基因分析,568例(78.13%)检出α-地贫;336例进行β-地贫基因分析,256例(76.19%)检出β-地贫;9例进行α-和β-地贫基因分析,均检出地贫基因。其中共检出Hb Bart's症142例和β-地贫纯合子或双重杂合子胎儿75例,均在产前诊断后1周内终止妊娠。结论采用绒毛进行地中海贫血产前诊断能有效地减少该类患儿的出生。 Objective To control the birth of children with thalassemia by applying prenatal diagnosis to high risk pregnancy. Methods Chorionic villi samplings were performed in 1 072 pregnancies of gestational age of 10 to 15 weeks for the gene detection of α- or β-thalassemia. Results Out of 1 072 chorionic villi samples,727 were given gene analysis of α-thalassemia,568( 78. 13%) were carriers with α-thalassemia; 336 were given gene analysis ofβ-thalassemia,256( 76. 19%) were carriers with β-thalassemia; 9 were given gene analysis of α- and β-thalassemia,all of which were carriers with thalassemia. There were 142 cases of Hb Bart's disease and 75 cases of homozygous or double heterozygous β-thalassemia,they all received termination of pregnancy within one week after prenatal diagnosis.Conclusion Chorionic villi sampling is a feasible and effective technique for prenatal diagnosis of thalassemia,which might effectively control the birth of children with thalassemia.
出处 《广西医学》 CAS 2014年第12期1709-1711,共3页 Guangxi Medical Journal
基金 广西医药卫生科研课题(重2012020 Z2014146)
关键词 地中海贫血 产前诊断 绒毛 基因检测 Thalassemia Prenatal diagnosis Chorionic villus Gene detection
  • 相关文献

参考文献5

二级参考文献24

  • 1朱军,周光萱,代礼,王艳萍,梁娟,缪蕾.1996~2000年全国围产期先天性心脏病发生率的分析[J].四川大学学报(医学版),2004,35(6):875-877. 被引量:63
  • 2廖灿,潘敏,李东至,钟燕芳,魏佳雪,易翠兴,李坚,钟惠珠.B超引导下的脐静脉穿刺术在产前诊断应用中的安全性研究[J].中华妇产科杂志,2004,39(12):813-815. 被引量:38
  • 3李影林.红细胞渗透脆性试验.中华医学检验全书(上),1996:232.
  • 4唐智宁 梁徐 等.检验ξ珠蛋白肽链诊断α地中海贫血[J].中华血液学杂志,1988,9:687-688.
  • 5中华人民共和国卫生部.全国妇幼卫生监测暨年报资料汇编(2009)[C].全国妇幼卫生监测办公室,2010:25-27.
  • 6Bonaiti C, Briard ML, Feingold J, et al. An epidemiological and genetic study of facial clefting in France. I Epidemiology and frequence in relatives[J]. J Med Genet, 1982,19 ( 1 ) : 8 - 15.
  • 7Xiong F, Sun M, Zhang X,et al. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China[J]. Clin Genet, 2010,78(2) : 139-148.
  • 8Liao C,Mo QH,Li J,et al. Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year pro- spective program in Guangzhou Maternal and Neonatal hospi- tal[J]. Prenat Diagn, 2005,25 (2) ; 163-171.
  • 9Zheng CG, Liu M, Du J, et al. Molecular spectrum of a- and β-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China[J]. Haematologica, 2011,35 (1) : 28-39.
  • 10Li DZ,Liao C,Li J,et al. Prenatal diagnosis of b-thalasse- mia in Southern China[J]. Eur J Obstet Gynecol Reprod Biol, 2006,128 (1) : 81-85.

共引文献93

同被引文献42

引证文献3

二级引证文献25

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部