An overview of hereditary hearing loss

  • Bayazit Y
  • Yilmaz M
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Understanding the genetic basis of hearing loss is important because almost 50% of profound hearing loss are caused by genetic factors and more than 120 independent genes have been identified. In this review, after a brief explanation of some genetic terms (allele, heterozygosis, homozygosis, polymorphism, genotype and phenotype), classification of genetic hearing loss (syndromic versus nonsyndromic, and recessive dominant, X-linked and mitochondrial) was performed. Some of the most common syndromes (Usher, Pendred, Jervell and Lange-Nielsen, Waardenburg, branchio-oto-renal, Stickler, Treacher Collins and Alport syndromes, biotinidase deficiency and Norrie disease) causing genetic hearing loss were also explained briefly. The genes involved in hearing loss and genetic heterogeneity were presented.

Author-supplied keywords

  • Hereditary hearing loss
  • Mitochondrial hearing loss
  • Nonsyndromic hearing loss
  • Syndromic hearing loss
  • X-linked hearing loss

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  • Yildirim A. Bayazit

  • Metin Yilmaz

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