PubMed · 2000 · 46 citations · 21 references
MedicineAudiologyOphthalmologyCochlear ImplantsOtologyPediatric OtolaryngologyCochlear ImplantationHearing ImpairmentHearing LossNeuro-otologic ExaminationPediatric Cochlear ImplantationPediatric Cochlear ImplantsCochlear Implantation In ChildrenCochlear Implants In ChildrenEarly Cochlear ImplantationEarly DiagnosisNeuro-ophthalmologic ExaminationOphthalmologic FindingsOphthalmologic ManifestationsUsher Syndrome
PURPOSE: To screen severe to profound, preverbal hearing-impaired children for Usher syndrome by ophthalmologic examinations, including electroretinographic testing. These patients are especially good candidates for early cochlear implants, which will improve listening and spoken language skills. METHODS: Consecutive patients over 2 years of age, given a diagnosis of severe to profound, preverbal hearing loss, were screened for Usher syndrome by a complete ophthalmologic examination including an electroretinogram. RESULTS: Five of 48 patients screened (10.4%) were diagnosed with Usher syndrome and received cochlear implants. CONCLUSION: All children with severe to profound, preverbal sensorineural hearing loss should be screened for Usher syndrome by ophthalmologic examination including electroretinogram.
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A Clinical Sign of Canal Paresis
G. Michael Halmagyi, Ian S. Curthoys · Archives of Neurology · 1988 · 1.3K citations
Localization of two genes for usher syndrome type I to chromosome 11
Richard J. Smith, E.C. Lee, William J. Kimberling et al. · Genomics · 1992 · 221 citations
Localization of Usher syndrome type II to chromosome 1q
William J. Kimberling, Michael D. Weston, Claes Möller et al. · Genomics · 1990 · 217 citations