期刊文献+

SLC26A4相关非综合征性感音神经性耳聋人工耳蜗植入后的疗效评估 被引量:7

原文传递
导出
摘要 在过去的10余年中,人工耳蜗植入(CI)在非综合征性感音神经性耳聋(NSSNHL)儿童的听觉康复中取得了巨大的成功,自引入我国后,逐渐得到推广和认可,至今已经在各地医疗机构大规模开展.在此发展过程中,针对先天性耳聋的病因研究也不断深入,尤其是日渐普及的聋病基因筛查和鉴定为许多先天性聋儿找到了聋病发生的根源.根据流行病学的调查结果所示,中国聋儿的主要遗传性基因是GJB2、SLC26A4和mtDNA 12srRNA突变,在接受人工耳蜗植入的患儿中也有类似的特征.
出处 《中华医学杂志》 CAS CSCD 北大核心 2015年第22期1784-1786,共3页 National Medical Journal of China
  • 相关文献

参考文献8

  • 1Van Camp G,Willems PJ,Smith RJ.Nonsyndromic hearing impairment:unparalleled heterogeneity[J].Am J Hum Genet,1997,60(4):758-764.
  • 2Abe S,Usami S,Hoover DM,et al.Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31,the region containing the Pendred gene[J].Am J Med Genet,1999,82(4):322-328.
  • 3Jerger J,Jenkins H,Fifer R,et al.Stapedius reflex to electrical stimulation in a patient with a cochlear implant[J].Ann Otol Rhinol Laryngol,1986,95(2 Pt 1):151-157.
  • 4Fahy CP,Carney AS,Nikolopoulos TP,et al.Cochlear implantation in children with large vestibular aqueduct syndrome and a review of the syndrome[J].Int J Pediatr Otorhinolaryngol,2001,59(3):207-215.
  • 5王翠翠,戴朴,韩东一.微创人工耳蜗植入术后残余听力保留的效果观察[J].中华耳科学杂志,2013,11(3):375-379. 被引量:20
  • 6Gratacap M,Thierry B,Rouillon I,et al.Pediatric Cochlear Implantation in Residual Hearing Candidates[J].Ann Otol Rhinol Laryngol,2015.pii:0003489414566121.[Epub ahead of print].
  • 7Yan YJ,Li Y,Yang T,et al.The effect of GJB2 and SLC26A4 gene mutations on rehabilitativeoutcomes in pediatric cochlear implant patients[J].Eur Arch Otorhinolaryngol,2013,270(11):2865-2870.
  • 8颜玉君,李蕴,杨涛,黄琦,吴皓.GJB2及SLC26A4基因突变患儿耳蜗植入效果分析[J].中华耳科学杂志,2011,9(2):163-167. 被引量:9

二级参考文献37

  • 1Morton CC, Nance WE. Newborn hearing screening -- a silent revolution. N Engl J Med, 2006, 354(20): 2151-2164.
  • 2Morton NE. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci, 1991, 630: 16-31.
  • 3Grundfast KM, Siparsky N,Chuong D. Genetics and molecular biology of deafness. Update. Otolaryngol Clin North Am, 2000, 33(6): 1367-1394.
  • 4Everett LA, Glaser B, Beck JC, et al. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet, 1997, 17(4): 411-422.
  • 5Tong MC, Leung EK, Au A, et al. Age and outcome of cochlear implantation for patients with bilateral congenital deafness in a Cantonese-speaking population. Ear Hear, 2007, 28 (2 Suppl.): 56S-58S.
  • 6Connor CM, Zwolan TA. Examining multiple sources of influence on the reading comprehension skills of children who use cochlear implants. J Speech Lang Hear Res, 2004, 47(3) : 509-526.
  • 7Lin FR, Ceh K, Bervinchak D, et al. Development of a communicative performance scale for pediatric cochlear implantation. Ear Hear, 2007, 28(5): 703-712.
  • 8Rajput K, Brown T, Bamiou DE. Aetiology of hearing loss and other related factors versus language outcome after cochlear implantation in children. Int J Pediatr Otorhinolaryngol, 2003, 67(5): 497-504.
  • 9Robbins AM, Renshaw JJ, Berry SW. Evaluating meaningful auditory integration in profoundly hearing impaired children. Am J Otol,1991, 12 Suppl: 144-150.
  • 10Nikolopoulos TP, Archbold SM, Gregory S. Young deaf children with heating aids or cochlear implants: early assessment package for monitoring progress. Int J Pediatr Otorhinolaryngol, 2005, 69 (2): 175-186.

共引文献27

同被引文献61

引证文献7

二级引证文献13

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