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85 Possible Causes for Postlingual Deafness

  • Deafness

    […] tract-based statistical analysis of diffusion tensor anisotropy in eight and ten adults with prelingual and postlingual deafness, respectively.[ncbi.nlm.nih.gov] The child with postlingual unilateral deafness rapidly integrated the normal acoustic hearing with the electrical signal from the cochlear implant and showed binaural benefits[ncbi.nlm.nih.gov] […] single-sided deafness (SSD).[ncbi.nlm.nih.gov]

  • Congenital Deafness

    As an example of a deafness phenotype, in DFNA10 results in a postlingual, initially progressive, and resulting, without the influence of presbycusis, in largely stable, flat[dizziness-and-balance.com] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org] Mohr-Tranebjaerg syndrome (DFN-1) Mohr-Tranebjaerg syndrome (DFN-1) is an X-linked recessive syndromic hearing loss characterized by postlingual sensorineural deafness in[dizziness-and-balance.com]

  • Autosomal Recessive Deafness 44

    Children with SNHL may be categorised into having either prelingual or postlingual deafness.[nzma.org.nz] deaf families and detecting mutation of the deafness genes Chin J Otorhinolaryngol 2002; Vol37, No.5, 348-351 Fialho et al 2003 A novel M163L mutation in GJB2 gene associated[davinci.crg.es] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org]

  • Autosomal Recessive Deafness 1B

    For the autosomal dominant forms of deafness, mutations in the COCH gene result in progressive postlingual deafness associated with severe attacks of vertigo and subjective[orpha.net] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org] Onset of deafness / hearing loss can be prelingual (hearing loss is present before speech develops), or postlingual (hearing loss occurs after the development of normal speech[bredagenetics.com]

  • Autosomal Dominant Deafness 11

    deaf families and detecting mutation of the deafness genes Chin J Otorhinolaryngol 2002; Vol37, No.5, 348-351 Fialho et al 2003 A novel M163L mutation in GJB2 gene associated[davinci.crg.es] […] sensorineural deafness maps to chromosome 14q12-13.[karger.com] As an example of a deafness phenotype, in DFNA10 results in a postlingual, initially progressive, and resulting, without the influence of presbycusis, in largely stable, flat[dizziness-and-balance.com]

  • Autosomal Recessive Deafness 42

    deaf families and detecting mutation of the deafness genes Chin J Otorhinolaryngol 2002; Vol37, No.5, 348-351 Fialho et al 2003 A novel M163L mutation in GJB2 gene associated[davinci.crg.es] As an example of a deafness phenotype, in DFNA10 results in a postlingual, initially progressive, and resulting, without the influence of presbycusis, in largely stable, flat[dizziness-and-balance.com] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org]

  • Sudden Hearing Loss

    We report an unusual family with four 35delG homozygous members, in which the parents were deaf-mute whilst both children had a postlingual progressive hearing loss.[ncbi.nlm.nih.gov] Recent studies have described progression of hearing loss in a proportion of cases with GJB2 deafness.[ncbi.nlm.nih.gov]

  • Autosomal Dominant Deafness 9

    deaf families and detecting mutation of the deafness genes Chin J Otorhinolaryngol 2002; Vol37, No.5, 348-351 Fialho et al 2003 A novel M163L mutation in GJB2 gene associated[davinci.crg.es] As an example of a deafness phenotype, in DFNA10 results in a postlingual, initially progressive, and resulting, without the influence of presbycusis, in largely stable, flat[dizziness-and-balance.com] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org]

  • Autosomal Dominant Deafness 28

    […] that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has material basis in mutation in the GRHL2 gene on chromosome 8q22.[malacards.org] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org] […] progressive, postlingual and is often observed clinically as the presence of unilateral or mild bilateral deafness 17.[ayubmed.edu.pk]

  • Autosomal Dominant Deafness 64

    deaf families and detecting mutation of the deafness genes Chin J Otorhinolaryngol 2002; Vol37, No.5, 348-351 Fialho et al 2003 A novel M163L mutation in GJB2 gene associated[davinci.crg.es] Genetics [ edit ] Nonsyndromic deafness can have different patterns of inheritance.[en.wikipedia.org] X-LINKED GENES DFN1 Xq22 Deafness dystonia protein ( DDP ) Mitochondrial import protein Postlingual but rapidly progressive in early childhood.[academic.oup.com]

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