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Int J Pediatr Otorhinolaryngol. 2010 Oct;74(10):1107-12. doi: 10.1016/j.ijporl.2010.06.010. Epub 2010 Jul 22.

Cochlear implantation in common forms of genetic deafness.

Author information

1
Department of Otolaryngology, University of Miami Ear Institute, Miami, FL 33136, United States.

Abstract

Genetic factors are among the main etiologies of severe to profound hearing loss and may play an important role in cochlear implantation (CI) outcomes. While genes for common forms of deafness have been cloned, efforts to correlate the functional outcome of CIs with a genetic form of deafness carried by the patient have been largely anecdotal to date. It has been suggested that the differences in auditory performance may be explained by differences in the number of surviving spiral ganglion cells, etiology of hearing loss, and other factors. Knowledge of the specific loci and mutations involved in patients who receive cochlear implants may elucidate other factors related to CI performance. In this review article, current knowledge of cochlear implants for hereditary hearing loss will be discussed with an emphasis on relevant clinical genotype-phenotype correlations.

PMID:
20655117
PMCID:
PMC2939287
DOI:
10.1016/j.ijporl.2010.06.010
[Indexed for MEDLINE]
Free PMC Article

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