Cochlear implants in young children with Usher's syndrome

Nancy M Young*, J. C. Johnson, Marilyn B Mets, Timothy C Hain

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

Usher's syndrome (US) is an autosomal recessive disorder characterized by congenital sensorineural hearing loss and retinitis pigmentosa. The majority of affected individuals have severe to profound sensorineural hearing loss and are therefore potential cochlear implant candidates. A goal of our otology program has been early identification and implantation of children with US. At our center, early diagnosis of US has been achieved by comprehensive ophthalmologic evaluation including electroretinography. Four of our 19 pediatric cochlear implant recipients with congenital sensorineural hearing loss were identified with US and implanted prior to the onset of signs or symptoms of visual loss. All children have received measurable benefit from cochlear implantation. In light of the dual sensory deficits present in US, the need for early diagnosis and cochlear implantation is of special importance in this population.

Original languageEnglish (US)
Pages (from-to)342-345
Number of pages4
JournalAnnals of Otology, Rhinology and Laryngology
Volume104
Issue number9 II SUPPL.
StatePublished - Jan 1 1995

ASJC Scopus subject areas

  • Otorhinolaryngology

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