Cochlear implantation in a case with Waardenurg syndrome

Cochlear Implants International

Volumn 5, Issue SUPPL. 1, 2004, Pages 212-214

  Moon, Sung Kyun ^a   Choi, Ho Seok ^a   Lee, Seung Joo ^a   Choung, Yun Hoon ^a   Park, Keehyun ^a  

^a Ajou University School of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

ARTICLE; AUDITORY THRESHOLD; CASE REPORT; COCHLEA PROSTHESIS; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; EAR SURGERY; FAMILY STUDY; GENE MUTATION; HEARING IMPAIRMENT; HOSPITAL DISCHARGE; HUMAN; IRIS DISEASE; KOREA; SEMICIRCULAR CANAL; SEQUENCE ANALYSIS; TEMPORAL BONE; VESTIBULAR TEST; WAARDENBURG SYNDROME;

EID: 9944265026     PISSN: 14670100     EISSN: None     Source Type: Journal    
DOI: 10.1002/cii.238     Document Type: Article

References (7)

1. Lalwani A, Baldwin C, Morell R, Friedman T, San Agustin T, Milunsky A et al. (1994) A locus for Waardenburg syndrome type II maps to chromosome 1p13.3-2.1. American Journal of Human Genetics 55(Suppl): A14.
2. Nakashima S, Sando I, Takahashi H, Hashida Y (1992) Temporal bone histopathologic findings of Waardenburg's syndrome: a case report. Laryngoscope 102(5): 563-567.
3. Oysu C, Oysu A, Aslan I, Tinaz M (2001) Temporal bone imaging findings in Waardenburg's syndrome. International Journal of Pediatric Otorhinotaryngology 58(3): 215-221.
4. Selicorni A, Guerneri S, Ratti A, Pizzuti A (2002) Cytogenetic mapping of a novel locus for type II Waardenburg syndrome. Human Genetics 110(1): 64-67.
5. Sugii A, Iwaki T, Doi K, Takahashi Y, Yamamoto K, Fuse Y et al. (2000) Cochlear implant in a young child with Waardenburg syndrome. Advances in Otorhinolaryngology 57:215-219.
6. Tassabehji M, Newton VE, Liu XZ, Brady A, Donnai D, Krajewska-Walasek M et al. (1995) The mutational spectrum in Waardenburg syndrome. Human Molecular Genetics 4(11): 2131-2137.
7. Waardenburg P (1951) A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair with congenital deafness. American Journal of Human Genetics 3: 195-253.