期刊文献+

X连锁隐性遗传聋哑(deaf-mute)家系的遗传学特征分析 被引量:8

Genetic Analysis in a Chinese Deaf-Mute Family with X linked Recessive Inheritance
下载PDF
导出
摘要 在进行中国人群的遗传性耳聋发病情况的调查中,发现了一个5代隔代遗传的聋哑家系(L021家系)。研究中调查家系成员64人,对其中的31人进行了系统的听力学检查,发现聋哑男性8位,听力表型为全聋及极重度聋,获得家系成员的血样31人份。家系图谱分析显示该家系为X连锁隐性遗传性耳聋家系,为先天性聋哑疾病分子病理机制的研究提供了模板。 In studying genetic factors in hearing loss among Chinese hearing-impaired population, a Chinese family with deaf-mute that had been reversion inherited through five generations was found (named pedigree L021). X linked recessive inheritance was hypothesized to be the transmission in this family. A total of 64 members in this family were investigated. Of these, audiometric evaluation was performed on 31 members, including 8 males with deaf-mute. Most affected individuals showed deafness or profound sensorineural hearing loss. Blood samples were obtained from 31 consented individuals in this family. Pedigree analysis indicates a X-linked recessive inheritance pattern in pedigree L021. The pedigree described herein provides an excellent model for further study on the molecular mechanism of congenital deaf-mute.
机构地区 北京复兴路
出处 《遗传》 CAS CSCD 北大核心 2004年第5期579-583,共5页 Hereditas(Beijing)
基金 国家自然基金面上项目(No.A30170530及No.A30370782)联合资助~~
关键词 聋哑 遗传性耳聋 X连锁 基因定位 Deaf-mute Hereditary Hearing Loss X linked Gene Mapping
  • 相关文献

参考文献14

  • 1Resendes B L, Williamson R E, Morton C C. At the speed of sound: gene discovery in the auditory system.Am J Hum Genet,2001, 69(5): 923-935.
  • 2Steel K P, Kros C J. A genetic approach to understanding auditory function.Nat Genet, 2001, 27(2): 143-149.
  • 3Morton C C. Genetics, genomics and gene discovery in the auditory system.Hum Mol Genet, 2002, 11: 1229-1240.
  • 4de Kok Y J, van der Maarel S M, Bitner-Glindzicz M, Huber I,Monaco A P, Malcolm S, Pembrey M E, Ropers H H, Cremers F P. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.Science,1995,267(5198): 685~688.
  • 5Jin H, M M,Tranebjaerg L, Kendall E, Fontan G, Jackson J, Subramony S H, Arena F, Lubs H, Smith S, Stevenson R, Schwartz C, Vetrie D., A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness
  • 6Koehler C M, Leuenberger D, Merchant S, Renold A, Junne T, Schatz G. Human deafness dystonia syndrome is a mitochondrial disease.Proc Natl Acad Sci USA,1999, 96(5): 2141-2146.
  • 7WANG Qiu-Ju, YANG Wei-Yan, HAN Dong-Yi, SHEN Yan. Establishment the system of the collecting,characterizing of the genetic resource for hereditary hearingimpairment.Chin J Otology,2003,3: 65-69.王秋菊,杨伟炎,韩东一, 沈
  • 8International Classification of Impairments, D, and Handicaps World Health Organization Geneva, 1980.
  • 9Dow G S, Poynter C I. The Dar family.Eugen News,1930,128-130.
  • 10Fraser G R. Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness.Ann Hum Genet,1965, 171-196.

共引文献1

同被引文献75

引证文献8

二级引证文献100

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