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Language and speech perception outcomes in hearing-impaired children with and without connexin 26 mutations.

Abstract
This study addressed the question of whether a hearing loss caused by mutations in the connexin 26 gene had a significant effect on language and speech perception outcomes in children using cochlear implants or hearing aids. The families of children who had participated in two previous studies of language development were invited to participate in this genetic study. From the 52 children whose families agreed to participate, 15 children with connexin 26 mutations in both chromosomes were identified. After taking into account other factors which are known to affect language development and speech perception in children with impaired hearing, no significant differences were found between the 15 children where connexin 26 was known to be the cause of deafness and the other 37 children in the study.
AuthorsHans-Henrik M Dahl, Melissa Wake, Julia Sarant, Zeffie Poulakis, Kirby Siemering, Peter Blamey
JournalAudiology & neuro-otology (Audiol Neurootol) 2003 Sep-Oct Vol. 8 Issue 5 Pg. 263-8 ISSN: 1420-3030 [Print] Switzerland
PMID12904681 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2003 S. Karger AG, Basel
Chemical References
  • Connexins
  • Connexin 26
Topics
  • Child
  • Child, Preschool
  • Cochlear Implants
  • Connexin 26
  • Connexins (genetics)
  • Female
  • Hearing Aids
  • Hearing Loss (genetics, physiopathology)
  • Humans
  • Language Development
  • Language Tests
  • Male
  • Mutation
  • Polymerase Chain Reaction (methods)
  • Speech Perception

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