Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-26T22:46:11.692Z Has data issue: false hasContentIssue false
  • English
  • Français

Cochlear implantation of a deaf blind patient with mitochondrial cytopathy

Published online by Cambridge University Press:  29 June 2007

Helen E. Cullington
Helen E. Cullington*
Affiliation:
Hearing and Balance Centre, Institute of Sound and Vibration Research, University of Southampton, Highfield, Southampton, UK.
*
Address for correspondence: Helen E. Cullington, Hearing and Balance Centre, Institute of Sound and Vibration Research, University of Southampton, Highfield, Southampton SO17 1BJ.
Get access Rights & Permissions [Opens in a new window]

Abstract

Genetic defects of the mitochondrial DNA often cause sensorineural hearing impairment, accompaniment by disorders of organs within the body. This case report describes cochlear implantation of a 33-year-old deaf blind female with mitochondrial cytopathy. The outcome was very successful, and vastly improved quality of life for this patient. Many cases of mitochondrial cytopathy cause progressive deafness; it is, therefore, likely that other patients with this unusual disorder will present for cochlear implant assessment.

Keywords

Cochlear implantMitochondriaCytopathy
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 113 , Issue 4 , April 1999 , pp. 353 - 354
Copyright
Copyright © JLO (1984) Limited 1999

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Gold, M., Rapin, I. (1994) Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss. International Journal of Pediatric Otorhinolaryngology 30: 91–104.CrossRefGoogle ScholarPubMed
Jacobs, H. T., Shah, Z. H., Migliosi, V., Lehtinen, S. K., Rovis, A., O'Dell, K. (1998) Nuclear candidate genes for ‘mitochondrial deafness’. In Developments in Genetic Hearing Impairment (Stephens, D., Read, A., Martini, A., eds.) Whurr, London, pp 104–115.Google Scholar
Schapira, A. H. (1993) Mitochondrial cytopathies. Current Opinions in Neurobiology 3(5): 760–767.CrossRefGoogle ScholarPubMed