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34 Possible Causes for Bilateral Prelingual Sensorineural Hearing Loss

  • Mitochondrial Non-Syndromic Sensorineural Deafness

    Clinical Presentation In general, sensorineural hearing loss with no other associated findings GJB2 (Connexin 26) or GJB6 (Connexin 30) variants – hearing loss is bilateral[arupconsult.com] , bilateral, sensorineural, syndromic or non-syndromic hearing loss of any degree for six mitochondrial variants previously associated with deafness.[content.iospress.com] The prevalence of bilateral sensorineural hearing loss is 1 in 500 newborns and 3.5 per 1000 adolescents.[egl-eurofins.com]

  • KID Syndrome

    RESULTS: Four subjects had prelingual, bilateral, profound sensorineural hearing loss, whereas the fifth subject had significant residual hearing that exhibited no progression[ncbi.nlm.nih.gov]

  • Autosomal Recessive Deafness 23

    Clinical Presentation In general, sensorineural hearing loss with no other associated findings GJB2 (Connexin 26) or GJB6 (Connexin 30) variants – hearing loss is bilateral[arupconsult.com] The prevalence of bilateral sensorineural hearing loss is 1 in 500 newborns and 3.5 per 1000 adolescents.[egl-eurofins.com] Familial cases with sensorineural hearing loss had 35delG mutation, thereby demonstrating a strong positive family history of hearing loss different to other findings [ 19[karger.com]

  • Autosomal Recessive Deafness 46

    Clinical Presentation In general, sensorineural hearing loss with no other associated findings GJB2 (Connexin 26) or GJB6 (Connexin 30) variants – hearing loss is bilateral[arupconsult.com] The prevalence of bilateral sensorineural hearing loss is 1 in 500 newborns and 3.5 per 1000 adolescents.[egl-eurofins.com] […] and stable with prelingual onset Mitochondrial variants often cause sensorineural hearing loss that varies in severity and onset m.7445 A G variant Palmar keratoderma Progressive[arupconsult.com]

  • Autosomal Recessive Deafness 88

    Clinical Presentation In general, sensorineural hearing loss with no other associated findings GJB2 (Connexin 26) or GJB6 (Connexin 30) variants – hearing loss is bilateral[arupconsult.com] The prevalence of bilateral sensorineural hearing loss is 1 in 500 newborns and 3.5 per 1000 adolescents.[egl-eurofins.com] […] and stable with prelingual onset Mitochondrial variants often cause sensorineural hearing loss that varies in severity and onset m.7445 A G variant Palmar keratoderma Progressive[arupconsult.com]

  • Autosomal Recessive Deafness 84

    DFNB84 is clinically characterized by progressive, bilateral sensorineural hearing loss, with prelingual onset.[cags.org.ae] Familial cases with sensorineural hearing loss had 35delG mutation, thereby demonstrating a strong positive family history of hearing loss different to other findings [ 19[karger.com] However, our findings regarding prelingual, bilateral, symmetrical and severe to profound hearing loss with a wide variability in the extent of the loss are similar to other[karger.com]

  • Autosomal Dominant Deafness 56

    Clinical Presentation In general, sensorineural hearing loss with no other associated findings GJB2 (Connexin 26) or GJB6 (Connexin 30) variants – hearing loss is bilateral[arupconsult.com] Familial cases with sensorineural hearing loss had 35delG mutation, thereby demonstrating a strong positive family history of hearing loss different to other findings [ 19[karger.com] […] and stable with prelingual onset Mitochondrial variants often cause sensorineural hearing loss that varies in severity and onset m.7445 A G variant Palmar keratoderma Progressive[arupconsult.com]

  • Usher Syndrome Type 1J

    ., prelingual) profound bilateral sensorineural hearing loss No significant vestibular responses Retinitis pigmentosa (RP) Normal general health and intellect; otherwise normal[centogene.com]

  • Autosomal Recessive Deafness 84B

    DFNB84 is clinically characterized by progressive, bilateral sensorineural hearing loss, with prelingual onset.[cags.org.ae] Familial cases with sensorineural hearing loss had 35delG mutation, thereby demonstrating a strong positive family history of hearing loss different to other findings [ 19[karger.com] However, our findings regarding prelingual, bilateral, symmetrical and severe to profound hearing loss with a wide variability in the extent of the loss are similar to other[karger.com]

  • Digitorenocerebral Syndrome

    , profound, prelingual sensorineural hearing loss and 3) progressive optic neuropathy.[mendelian.co] […] muscle weakness and atrophy (first appearing and more prominent in the lower extremities than the upper) which usually manifests with foot drop and gait disturbance, 2) bilateral[mendelian.co]

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