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  2. Sensorineural hearing loss - Wikipedia

    en.wikipedia.org/wiki/Sensorineural_hearing_loss

    Sensorineural hearing loss (SNHL) is a type of hearing loss in which the root cause lies in the inner ear, sensory organ (cochlea and associated structures), or the vestibulocochlear nerve (cranial nerve VIII). SNHL accounts for about 90% of reported hearing loss.

  3. Ocular albinism late onset sensorineural deafness - Wikipedia

    en.wikipedia.org/wiki/Ocular_albinism_late_onset...

    Ocular albinism late onset sensorineural deafness (OASD) is a rare, X-linked recessive disease characterized by intense visual impairments, reduced retinal pigments, translucent pale-blue irises and moderately severe hearing loss from adolescence to middle-age. [1] It is a subtype of Ocular Albinism (OA) that is linked to Ocular albinism type I ...

  4. Diagnosis of hearing loss - Wikipedia

    en.wikipedia.org/wiki/Diagnosis_of_hearing_loss

    Mixed hearing loss is a combination of conductive and sensorineural hearing loss. Chronic ear infection (a fairly common diagnosis) can cause a defective ear drum or middle-ear ossicle damages, or both. In addition to the conductive loss, a sensory component may be present. Central auditory processing disorder

  5. Category:Syndromes with sensorineural hearing loss - Wikipedia

    en.wikipedia.org/wiki/Category:Syndromes_with...

    Pages in category "Syndromes with sensorineural hearing loss" The following 10 pages are in this category, out of 10 total. This list may not reflect recent changes .

  6. Sensorineural deafness - Wikipedia

    en.wikipedia.org/?title=Sensorineural_deafness&...

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  7. Jervell and Lange-Nielsen syndrome - Wikipedia

    en.wikipedia.org/wiki/Jervell_and_Lange-Nielsen...

    The sensorineural hearing loss in Jervell and Lange-Nielsen syndrome is present from birth and can be diagnosed using audiometry or physiological tests of hearing. [7] The cardiac features of JLNS can be diagnosed by measuring the QT interval corrected for heart rate (QTc) on a 12-lead electrocardiogram (ECG). The QTc is less than 450 ms in 95% ...

  8. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy

    en.wikipedia.org/wiki/Autosomal_dominant...

    This condition was first discovered in 1995 by Melberg et al. when they described 5 members of a 4-generation Swedish family where cerebellar ataxia and sensorineural deafness presented as an autosomal dominant trait, 4 of them had narcolepsy and 2 had diabetes mellitus. The oldest members had psychiatric symptoms, neurological anomalies, and ...

  9. Causes of hearing loss - Wikipedia

    en.wikipedia.org/wiki/Causes_of_hearing_loss

    The most common type of congenital hearing loss in developed countries is DFNB1, also known as connexin 26 deafness or GJB2-related deafness. The most common dominant syndromic forms of hearing loss include Stickler syndrome and Waardenburg syndrome. The most common recessive syndromic forms of hearing loss are Pendred syndrome and Usher syndrome.