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• W2045589980 abstract "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." @default.
• W2045589980 created "2016-06-24" @default.
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• W2045589980 date "2006-01-01" @default.
• W2045589980 modified "2023-10-15" @default.
• W2045589980 title "An Overview of Hereditary Hearing Loss" @default.
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• W2045589980 doi "https://doi.org/10.1159/000091090" @default.
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