Expressivity of hearing loss in cases with Usher syndrome type IIA

André M. Sadeghi, Edward S. Cohn, William J. Kimberling, Glenn Halvarsson, Claes Möller

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Objective: The purpose of this study was to compare the genotype/phenotype relationship between siblings with identical USH2A pathologic mutations and the consequent audiologic phenotypes, in particular degree of hearing loss (HL). Decade audiograms were also compared among two groups of affected subjects with different mutations of USH2A. Design: DNA samples from patients with Usher syndrome type II were analysed. The audiological features of patients and affected siblings with USH2A mutations were also examined to identify genotype-phenotype correlations. Study sample: Genetic and audiometric examinations were performed in 18 subjects from nine families with Usher syndrome type IIA. Results: Three different USH2A mutations were identified in the affected subjects. Both similarities and differences of the auditory phenotype were seen in families with several affected siblings. A variable degree of hearing loss, ranging from mild to profound, was observed among affected subjects. No significant differences in hearing thresholds were found the group of affected subjects with different pathological mutations. Conclusions: Our results indicate that mutations in the USH2A gene and the resulting phenotype are probably modulated by other variables, such as modifying genes, epigenetics or environmental factors which may be of importance for better understanding the etiology of Usher syndrome.

Original languageEnglish (US)
Pages (from-to)832-837
Number of pages6
JournalInternational Journal of Audiology
Volume52
Issue number12
DOIs
StatePublished - Dec 1 2013

Fingerprint

Hearing Loss
Mutation
Usher Syndromes
Phenotype
Siblings
etiology
Genetic Association Studies
environmental factors
Epigenomics
Group
Hearing
Genes
Type 2A Usher syndrome
Hearing Impairment
Expressivity
Syndrome
Genotype
examination
DNA

Keywords

  • Genotype-phenotype correlation
  • Hereditary hearing loss
  • Retinitis pigmentosa
  • USH2A
  • Usherin

ASJC Scopus subject areas

  • Language and Linguistics
  • Linguistics and Language
  • Speech and Hearing

Cite this

Sadeghi, A. M., Cohn, E. S., Kimberling, W. J., Halvarsson, G., & Möller, C. (2013). Expressivity of hearing loss in cases with Usher syndrome type IIA. International Journal of Audiology, 52(12), 832-837. https://doi.org/10.3109/14992027.2013.839885

Expressivity of hearing loss in cases with Usher syndrome type IIA. / Sadeghi, André M.; Cohn, Edward S.; Kimberling, William J.; Halvarsson, Glenn; Möller, Claes.

In: International Journal of Audiology, Vol. 52, No. 12, 01.12.2013, p. 832-837.

Research output: Contribution to journalArticle

Sadeghi, AM, Cohn, ES, Kimberling, WJ, Halvarsson, G & Möller, C 2013, 'Expressivity of hearing loss in cases with Usher syndrome type IIA', International Journal of Audiology, vol. 52, no. 12, pp. 832-837. https://doi.org/10.3109/14992027.2013.839885
Sadeghi, André M. ; Cohn, Edward S. ; Kimberling, William J. ; Halvarsson, Glenn ; Möller, Claes. / Expressivity of hearing loss in cases with Usher syndrome type IIA. In: International Journal of Audiology. 2013 ; Vol. 52, No. 12. pp. 832-837.
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