1Waardenburg PJ.Anewsyndrome combining developmenal anomaliesof the eyelids,eyebrows and nose root with pigmentary defects of irisand head hair with congenital deafness[J].AmJ Hum Genet,1951,3:195.

2Klein D.Historical background and evidence for dominant inheritance of the Klein Waardenburg syndrome(type III)[J].AmJ Med Genet,1983,14:231.

3Shah KN,Dalal SJ,Desai MP,et al.White forelock,pigmentary disor-der of irides,andlong segment Hirschsprung disease:possible variant of Waardenburg syndrome[J].J Pediatric,1981,99:432.

4Veres G,Karpati S,Karaszi V,et al.Waardenburg syndrome[J].Orv Hetil.2004,145:1523.

5Ishikiriyama S,Tonoki H,Shibuya Y,et al.Waardenburg syndrome type I ina child with de noveinversion(2)(q35q37.3)[J].AmJ MedGenet,1989,33:505.

6Tsukamoto K,Tohma T,Ohta T,et al.Cloning and characterization of the inversion breakpoint at chromosome2q35in a patient with Waar-denburg syndrometype I[J].Hum Mol Genet,1992,1:315.

7Fujimoto A,Reddy KS,Spinks R.Interstitial deletion of chromosome4,del(4)(q12q21.1),in a mentallyretared boy with a piebaldt rait,due to maternal insertion,ins(8;4)[J].AmJ Med Genet,1998,75:78.

8杨淑芝,杨伟炎,袁慧军.Waardenburg综合征研究现状[J].临床耳鼻咽喉科杂志,2005,19:910.

9Farrer LA,Grundfast KM,Amos J,et al.Waardenburg syndrome(WS)type I is caused by defects at multiple loci,one of whichis near ALPP onchromosome:first report of the WS consortium[J].Am J Hum Genet,1992,50:902.

10Steel KP,Barkway C.Another rolefor melanocyte:theirimportancefor normal stria vascularis development in the mammalian inner ear[J].Development,1989,7:453.

11Liu XZ,Newton VE,Read AP.Waardenburgsyndrometype II:phe-notypic finding and diagnostic criteria[J].AmJ Med Genet,1995,55:95.

12陈连军,方栩,方丽.Waardenburg综合征1例[J].临床皮肤科杂志,2002,29:366.

13Newton VE.Clinical features of the Waardenburgsyndromes[J].Adv Otorhinolaryngol,2002,61:201.

14Jutras B,Russell LJ,Hurteau AM,et al.Auditory neuropathyinsib-lings with Waardenburg’s syndrome[J].Int J Pediatr Otorhinolaryn-gol,2003,67:1133.

15Madden C,Halsted MJ,Hopkin RJ,et al.Temporal bone abnormali-ties associated with hearinglossin Waardenburgsyndrome[J].Laryn-goscope,2003,113:2035.

16Black FO,Pesznecker SC,Allen K,Avestibular phenotype for Waar-denburg syndrome[J].Otol Neurotol,2001,22:188.

17王秋菊,侯军华,张立.Waardenburg综合征的遗传学分析[J].听力学及言语疾病杂志,2003,11:1.

18Migirov L,Henkin Y,Hildesheimer M,et al.Cochlear implantation in Waardenburg’s syndrome[J].Acta Otolaryngol,2005,125:713.

19Loundon N,Rouillon I,Munier N,et al.Cochlear implantation in children withinternal ear malformations[J].Otol Neurotol,2005,26:668.

20Daneshi A,Hassanzadeh S,Farhadi M.Cochlear implantation in children with Waardenburg syndrome[J].J Laryngol Otol,2005,119:719.

21韩东一,武文明,郗昕,等.先天性内耳畸形的人工耳蜗植入[J].中华耳鼻咽喉科杂志,2004,2:85.