期刊文献+

孕中晚期终止妊娠原因分析 被引量:3

Termination reason of pregnancy in second and third trimester
原文传递
导出
摘要 目的研究本产前诊断中心就诊患者终止妊娠情况及原因分析。方法回顾性分析2004年至2015年底12年间到本产前诊断中心就诊却引产的病人716例,对其就诊原因,引产原因等情况进行分析。结果在716例引产病人中,因产前筛查高风险就诊346例,因高龄等原因在本院直接行产前诊断370例,查明染色体异常的有191例(26.68%),染色体正常223例(31.14%),未行染色体核型检查的302例(42.18%)。21三体、18三体、性染色体异常是终止妊娠最常见的染色体原因;染色体正常胎儿却终止妊娠的原因主要为在孕中期或孕晚期出现胎儿畸形;其次为孕妇原因。未行染色体检查而终止妊娠的主要原因为胎儿畸形或死胎。结论目前的染色体检查只能发现1/4的引产病人病因,不良妊娠病因的查明有待于更多遗传学检测方法的应用。 Objective:To investigate the rate and reasons of pregnancy termination in one prenatal diagnosis center during recent 12 years. Methods:The database of 716 cases of pregnancy termination from 2004 to 2015 were reviewed,to investigate the reasons for prenatal diagnosis,and the causes for termination. Results:Among 716 cases of pregnancy termination,346 cases were patients with high risk in prenatal screening,and 370 cases were patients with advanced maternal age and other abnormal indexes. 190(26.53%)cases had chromosome abnormality,223 cases(31.14%)had normal chromosome kayotypes,303(42.31%)cases didn′t carry on chromosome analysis. Trisomy 21,trisomy 18 and sex chromosome abnormalities were the most common types of chromosome abnormalities for termination of pregnancy. Congenital-malformations fetus and the healthy problem of the pregnancy women were the important reasons to termination in fetus with normal chromosome kayotypes. For the fetus who didn′t carry on chromosome analysis,the main reasons for termination were congenital malformations and stillbirth. Conclusion:Only about 1/4(26.53%)of cases of pregnancy termination were found due to chromosome abnormarlities, more advanced genetic tests need to adapted in the clinic to find the genetic causes of termination of pregnancy.
出处 《中国优生与遗传杂志》 2018年第2期74-76,共3页 Chinese Journal of Birth Health & Heredity
关键词 终止妊娠 染色体 产前筛查 产前诊断 Termination of pregnancy Chromosome Prenatal screening Prenatal diagnosis
  • 相关文献

参考文献2

二级参考文献25

  • 1殷春霞,张伯锋,郭瑞军.胎儿骨骼发育异常的超声检查[J].中华超声影像学杂志,2004,13(9):710-712. 被引量:5
  • 2黄林环,方群.常见胎儿骨骼发育异常的产前诊断[J].中华妇产科杂志,2006,41(11):779-782. 被引量:14
  • 3高雪峰,杨丽萍,李丹,邵敏杰.Y染色体倒位的细胞遗传学和分子生物学研究[J].中国优生与遗传杂志,2006,14(12):44-45. 被引量:14
  • 4Liao C,Li DZ.Pregnancy outcome following prenatal diagnosis of sex chromosome abnormalities in China's Mainland.Prenat Diagn,2008,28:443-444.
  • 5Mezei G,Papp C,Tóth-Pál E,et al.Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy.Obstet Gyneco1,2004,104:94-101.
  • 6Linden MG,Bender BG,Robinson A.Intrauterine diagnosis of sex chromosome aneuploidy.Obstet Gynecol,1996,87:468-475.
  • 7Koeberl DD,McGillivray B,Sybert VP.Prenatal diagnosis of 45,X/46,XX mosaicism and 45,X:implications for postnatal outcome,Am J Hum G enet,1995,57:661-666.
  • 8Meschede D,Louwen F,Nippert I,et al.Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies.Am J Med Genet,1998,80:330-334.
  • 9Shaw SW,Chueh HY,Chang SD,et al.Perental decisions regarding prenatally detected fetal sex chromosomal abnormality and the impact of genetic counselling:an analysis of 57 cases in Taiwan.Aust N Z J Obstet Gynaecol,2008,48:155-159.
  • 10Warman ML, Cormier-Daire V, Hall C, et al. Nosology and classification of genetic skeletal disorders: 2010 revision[J]. AmJMedGenetA, 2011, 155A(5):943 -968.

共引文献13

同被引文献30

引证文献3

二级引证文献10

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