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自身免疫性感音神经性聋患者候选基因--凝血因子C同源物突变筛查 被引量:2

A candidate gene screening of coagulation factor C homology in patients with autoimmune sensorineural hearing loss
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摘要 目的通过对22例自身免疫性感音神经性聋(autoimmune sensorineural hearing loss,ASNHL)患者进行凝血因子C同源物基因(coagulation factor C homology,COCH)全序列分析,探索自身免疫性感音神经性聋与COCH突变的相关性。方法应用聚合酶链反应(PCR)产物直接测序方法对22例自身免疫性感音神经性聋患者进行COCH全序列分析。结果在22例自身免疫性感音神经性聋病例中未发现COCH突变和多态。结论初步探索了ASNHL与COCH突变的相关性,未发现COCH突变和多态,还需进一步收集临床病例来证实。 Objective To investigate the potential relationship between the autoimmune sensorineural hearing loss (ASNHL) and coagulation factor C homology gene(COCH) mutation, a mutation screening of COCH was conducted among 22 cases with ASNHL. Methods PCR product sequencing was applied to 200 bp up-stream and down-stream of exons 2 to 12 of COCH gene among 22 cases with ASNHL. Results None of polymorphisms and mutations is found in these cases. Conclusion The relationship between the ASNHL and COCH mutation is preliminarily probed and no polymorphisms and mutations of COCH were detected. Clinical studies with large numbers of patients will help us to clarify this issue.
出处 《中华耳科学杂志》 CSCD 2008年第3期302-305,共4页 Chinese Journal of Otology
基金 国家自然科学基金面上项目(30371523) 国家自然科学基金海外青年学者合作基金(30528025)
关键词 自身免疫性感音神经性聋 凝血因子C同源物基因 候选基因 Autoimmune sensorineural hearing loss Coagulation factor C homology gene Candidate gene
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参考文献18

  • 1[1]McCabe BF.Autoimmune sensorineural hearing loss.Ann Otol Rhinol Laryngol,1979,88 (5 Pt 1):585-589.
  • 2[2]Robertson NG,Khetarpal U,Gutiérrez-Espeleta GA,et al.Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening.Genomics,1994,23(1):42-50.
  • 3[3]Robertson NG,Lu L Heller S,et al.Mutations in a novel cochlear gene cause DFNA9,human nonsyndromic deafness with vestibular dysfunction.Nature Genet,1998,20(3):299-303.
  • 4[4]Manolis EN,Yandavi N,Nadol JB Jr,et al.A gene for non-syndromic autosomal dominant progressive postlingtual sensorineural hearing loss maps to chromosome 14q112-13.Hum Mol Genet,1996,5(7):1047-1050.
  • 5[5]Robertson NG,Cremers CWRJ,Huygen PLM,et al.Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.Hum Mol Genet,2006,15(7):1071-1085.
  • 6[6]Boulassel MR,Deggouj N,Tomasi JP,et al.Inner ear autoantibodies and their targets in patients with autoimmune inner ear diseases.Acta Otolaryngol,2001,121 (1):28-34.
  • 7[7]Back MJ,Park HM,Johnson JM,et al.Increased frequencies of cochlin-specific T cells in patients with autoimmune sensorineural hearing Ioss.J Immunol,2006,177(6):4203--4210.
  • 8顾瑞,邹静,于黎明.自身免疫性感音神经性听力减退的测听结果[J].中华耳鼻咽喉科杂志,1995,30(1):20-23. 被引量:17
  • 9[9]Smith RJH,Van Camp G.Deafness and Hereditary Hearing Loss Overview[EB/OL].(2003-09-03)[2007-01-30]www.geneclinics.org/profiles/deafness-overview/details.html
  • 10孙勍,杨淑芝,康东洋,张昕,曹菊阳,刘新,戴朴,袁慧军,韩东一.中国人群迟发性耳聋家系及散发病例凝血因子C同源物基因突变分析[J].中华医学杂志,2007,87(44):3107-3110. 被引量:2

二级参考文献13

  • 1顾瑞,中华耳鼻咽喉科杂志,1992年,27卷,27页
  • 2Steel KP. New interventions in hearing impairment. BMJ, 2000, 320 : 622-625.
  • 3Van Camp G, Willems PJ, Smith RJ. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet, 1997.60 : 758-764.
  • 4Van Camp G, Smith RJ. Loci for nonsyndromic hearing impairment [ EB/OL], [ 2006-07-161. http://webhost, aa. ac. be/hhh/.
  • 5Van Camp G, Smith RJ. Recommendations for the description of genetic and audiological data for families with nonsyndromic hereditary hearing impairment [ EB/OL ]. [ 2003-09-23 ] http ://dnalab-www.uia. ac. be/hhh.
  • 6Fransen E, Verstreken M, Verhagen WI, et al. High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene. Hum Mol Genet, 1999, 8: 1425-1429.
  • 7de Kok YJM, Bom SJ, Brunt TM, et M. A pro51-to-ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects. Hum Mol Genet, 1999. 8: 361-366.
  • 8Robertson NG, Lu L Heller S, et al. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndronfic deafness with vestibular dysftmction. Nat Genet, 1998, 20:299-303.
  • 9Robertson NG, Lu L Heller S, et al. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndronfic deafness with vestibular dysftmction. Nat Genet, 1998, 20:299-303.
  • 10Usami S, Takahashi K, Yuge I, et al. Mutations in the COCH gene are a frequent cause of autosomM dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease. Ear J Hum Genet, 2003, 11 : 744-748.

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