期刊文献+

一例嵌合型13q倒位重复胎儿的遗传学分析

Genetic analysis of a fetus with mosaicism of 13q inversion duplication
原文传递
导出
摘要 目的分析1例产前诊断的嵌合型13q倒位重复的形成机制,探讨其基因型与表型的对应关系。方法分别于孕23周和孕32周抽取胎儿羊水和脐带血样,联合应用G显带染色体核型分析、单核苷酸多态性微阵列和荧光原位杂交技术对其进行检测,并复习相关文献。结果胎儿的核型最终被确定为47,XY,+inv dup(13)(q14.3q34)/46,XY。孕妇于40周生育一男婴,除鼻梁处有一红斑(血管瘤)外,暂未发现其他异常。结论嵌合型13q倒位重复病例应充分考虑其新着丝粒的位置和嵌合比例,为遗传咨询和风险评估提供参考。 Objective To report on a case of mosaicism 13q inversion duplication,analyze its mechanism,and discuss the correlation between its genotype and phenotype.Methods Amniotic fluid and umbilical cord blood were collected at 23 and 32 weeks of gestation,respectively.Combined with G-banding chromosome karyotyping analysis,single nucleotide polymorphism array(SNP-array)and fluorescence in situ hybridization(FISH)were used to confirm the result.Results The karyotype of the fetus was determined as 47,XY,+inv dup(13)(q14.3q34)/46,XY.After careful counseling,the couple decided to continue with the pregnancy,and had given birth to a boy at 40 weeks’gestation.Except for a red plaque(hemangioma)on the nose bridge,no obvious abnormality(intelligence to be evaluated)was discovered.Conclusion To provide reference for clinical genetic counseling and risk assessment,the location and proportion of new centromere formation should be fully considered in the case of mosaicism 13q inversion duplication.
作者 罗婷婷 车铭 程德华 张丽芳 张涛 曾艳 Luo Tingting;Che Ming;Chen Dehua;Zhang Lifang;Zhang Tao;Zen Yan(Shaoxing Maternal and Child Health Care Hospital,Shaoxing,Zhejiang 312000,China;Institute of Reproduction and Stem Cell Engineering,Central South University,Changsha,Hunan 410078,China)
出处 《中华医学遗传学杂志》 CAS CSCD 2022年第1期76-80,共5页 Chinese Journal of Medical Genetics
基金 浙江省医药卫生科技计划(2020KY986)。
关键词 13q倒位重复 新着丝粒 嵌合 13q inversion duplication New centromere Mosaicism
  • 相关文献

参考文献1

二级参考文献9

  • 1Ballif BC, Rorem EA, Sundin K, et al. Detection of low-level mosalcism by array CGH in routine dlagnostie speclmens[J]. Am J Med Genet A,2006,140(24) :2757-2767. 被引量:1
  • 2Hoang S, Ahn J, Mann K, et al. Detection o{ mosaicism {or genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform[J]. Eur J Med Genet, 2011,54(2):121-129. 被引量:1
  • 3Forabosco A, Percesepe A, Santucci S. Incidence of non-age- dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses[J]. Eur J Hum Genet, 2009,17(7) :897- 903. 被引量:1
  • 4Shehab MI, Mazen I, Bint S. Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGH[J]. Am J Med Genet A, 2011,155(10) :2496-2500. 被引量:1
  • 5de Azevedo Moreira LM, Freitas LM, Gusmko FA, et al. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl[J]. Birth Defects Res A Clin Mol TeratOl, 2003,67 (12) 985-988. 被引量:1
  • 6Chen CP, Wang LK, Chern SR, et al. Mosaic tetrasomy 9p at amnioeentesis prenatal diagnosis, molecular cytogenetic characterization, and literature review [J]. Taiwan J OhstetGynecol,2014 ,53(1) :79-85. 被引量:1
  • 7Chen CP, Chang TY, Chern SR,et al. Prenatal diagnosis of low- level mosaic tetrasomy 9p by amniocentesis[J]. Prenat Diagn, 2007,27(4) :383-385. 被引量:1
  • 8McAul[ffe F, Winsor EJ, Chitayat D. Tetrasomy 9p Mosaicism Associated with a Normal Phenotype[J]. Fetal Diagn Ther,2005, 20(3) :219-222. 被引量:1
  • 9Repnikova EA, Astbury C, Reshmi SC, et al. Meroarray comparative genomic hybridization and cytogenetic characterization of tissue-specific mosaicism in three patients[J]. Am J Med Genet A, 2012 ,158(8) :1924-1933. 被引量:1

共引文献2

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