期刊文献+

眼-耳-脊柱序列征的遗传学研究现状

The genetic etiology research progress of oculo-auriculo-vertebral spectrum
原文传递
导出
摘要 眼-耳-脊柱序列征(oculo-auriculo-vertebral spectrum,OAVS)是临床常见的出生缺陷,主要累及眼、耳、上下颌及脊柱等.目前,OAVS的遗传基础已被公认,但致病基因尚未明确.从染色体分析、基因组拷贝数检测、致病基因鉴定和小鼠模型对OAVS的可能病因进行综述,并对OAVS的研究策略进行了分析和展望. Oculo-auriculo-vertebral spectrum (OAVS)is one of common birth defects,which involves primarily optical,aural,maxillomandibular and spinal abnormal development.To date,the hereditary basis of OAVS has been generally accepted,but the responsible gene remains unclear.This article reviewed the possible etiology of OAVS in chromosome analysis,genome copy number detection,gene identification and mouse model,and analyzed the strategy for OAVS research.
作者 黄雪霜 潘博 王乐 Huang Xueshuang;Pan Bo;Wang Le(Biomedical Research Center,Hunan University of Medicine,Huaihua 418000,China)
出处 《中华整形外科杂志》 CAS CSCD 北大核心 2018年第9期769-773,共5页 Chinese Journal of Plastic Surgery
基金 湖南省科技厅基金项目(2015JC3070) 湖南省教育厅基金项目(168186) 中国医学科学院医学与健康科技创新工程项目(2016-12M-1-002)
关键词 染色体 异常 拷贝数目变异 基因 Chromosome,abnormality Copy number variation Gene
  • 相关文献

参考文献1

二级参考文献12

  • 1沈岩.致病基因的定位候选克隆[J].生命科学,1999,11:205-208.
  • 2Moore KL,Persaud TV.Before we are born:Essentials of embryology and birth defects[M].Philadelphia Saunders,1993:118.
  • 3Townes PL,White MR.Inherited partial trisomy 8q (22 leads to qter)[J].Am J Dis Child,1978,132(10):498-501.
  • 4Hathout EH,Elmendorf E,Bartley J.Hemifacial microsomia and abnormal chromosome 22[J].Am J Med Genet,1998,76(1):71-73.
  • 5Herman GE,Greenberg F,Ledbetter DH.Multiple congenital abnormalities/mental retardation (mca/mr) syndrome with Goldenhar complex due to a terminal del (22q)[J].Am J Med Genet,1988,29(4):909-915.
  • 6Kobrynski L,Chitayat D,Zahed L,et al.Trisomy 22 and facioauriculovertebral (goldenhar) sequence[J].Am J Med Genet,1993,46(1):68-71.
  • 7Garavelli L,Virdis R,Donadio A,et al.Oculo-auriculo-vertebral spectrum in Klinefelter syndrome[J].Genet Couns,1999,10 (3):321-324.
  • 8Hodes ME,Gleiser S,DeRosa GP,et al.Trisomy 7 mosaicism and manifestations of Goldenhar syndrome with unilateral radial hypoplasia[J].J Craniofac Genet Dev Biol,1981,1 (1):49-55.
  • 9Wilson GN,Barr M.Trisomy 9 mosaicism:another etiology for the manifestations of Goldenhar syndrome[J].J Craniofac Genet Dev Biol,1983,3(4):313-316.
  • 10Ryan CA,Finer NN,Ives E.Discordance of signs in monozygotic twins concordant for the goldenhar anomaly[J].Am J Med Genet,1988,29(4):755-761.

共引文献11

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