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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. [citation needed] SNHL is usually permanent and can be mild, moderate, severe ...

  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. Cortical deafness - Wikipedia

    en.wikipedia.org/wiki/Cortical_deafness

    Cortical deafness is an auditory disorder where the patient is unable to hear sounds but has no apparent damage to the structures of the ear (see auditory system ). It has been argued to be as the combination of auditory verbal agnosia and auditory agnosia. Patients with cortical deafness cannot hear any sounds, that is, they are not aware of ...

  5. Waardenburg syndrome - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_syndrome

    Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye ), a white forelock or patches of light skin. These basic features constitute type 2 of the condition; in type 1, there ...

  6. Nonsyndromic deafness - Wikipedia

    en.wikipedia.org/wiki/Nonsyndromic_deafness

    Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Nonsyndromic deafness constitutes 75% of all hearing loss cases, and an estimated 100 genes are thought to be linked to this condition.

  7. Universal neonatal hearing screening - Wikipedia

    en.wikipedia.org/wiki/Universal_neonatal_hearing...

    A newborn infant undergoes a hearing screening. Universal neonatal hearing screening ( UNHS ), which is part of early hearing detection and intervention ( EHDI) programmes, refer to those services aimed at screening hearing of all newborns, regardless of the presence of a risk factor for hearing loss. UNHS is the first step in the EHDI program ...

  8. Autoimmune inner ear disease - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_inner_ear_disease

    Autoimmune inner ear disease. Autoimmune inner ear disease (AIED) was first defined by Dr. Brian McCabe in a landmark paper describing an autoimmune loss of hearing. [ 2] The disease results in progressive sensorineural hearing loss (SNHL) that acts bilaterally and asymmetrically, and sometimes affects an individual's vestibular system.

  9. Auditory agnosia - Wikipedia

    en.wikipedia.org/wiki/Auditory_agnosia

    Auditory agnosia is a form of agnosia that manifests itself primarily in the inability to recognize or differentiate between sounds. It is not a defect of the ear or "hearing", but rather a neurological inability of the brain to process sound meaning. While auditory agnosia impairs the understanding of sounds, other abilities such as reading ...

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