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  2. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy

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

    Usually, people with this disorder have ataxia, mild–moderate sensorineural hearing loss, narcolepsy, and cataplexy. These symptoms start happening when an affected person is about 30 years old. [6] [7] A bit later in life, people with ADCADN start showing a decline in executive function known as dementia.

  3. Familial Danish dementia - Wikipedia

    en.wikipedia.org/wiki/Familial_Danish_dementia

    Familial Danish dementia is an extremely rare, neurodegenerative disease characterized by progressive cataracts, loss of hearing, cerebellar ataxia, paranoid psychosis, and dementia. Neuropathological hallmarks include extensive atrophy of all areas of the brain, chronic diffuse encephalopathy , and the presence of exceedingly thin and nearly ...

  4. Autosomal dominant cerebellar ataxia - Wikipedia

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

    Autosomal dominant cerebellar ataxia (ADCA) is a form of spinocerebellar ataxia inherited in an autosomal dominant manner. ADCA is a genetically inherited condition that causes deterioration of the nervous system leading to disorder and a decrease or loss of function to regions of the body.

  5. Spinocerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia

    Many patients with hereditary or idiopathic forms of ataxia have other symptoms in addition to ataxia. Medications or other therapies might be appropriate for some of these symptoms, which could include tremor, stiffness, depression, spasticity, and sleep disorders, among others. Both onset of initial symptoms and duration of disease are variable.

  6. Hearing loss - Wikipedia

    en.wikipedia.org/wiki/Hearing_loss

    The association between age-related hearing loss and Alzheimer's disease was found to be nonsignificant, and this finding supports the hypothesis that hearing loss is associated with dementia independent of Alzheimer pathology. [32] There are several hypotheses about the underlying causal mechanism for age-related hearing loss and cognitive ...

  7. Nonsyndromic deafness - Wikipedia

    en.wikipedia.org/wiki/Nonsyndromic_deafness

    Many genes related to deafness are involved in the development and function of the inner ear. Gene mutations interfere with critical steps in processing sound, resulting in hearing loss. Different mutations in the same gene can cause different types of hearing loss, and some genes are associated with both syndromic and nonsyndromic deafness.

  8. Gerstmann–Sträussler–Scheinker syndrome - Wikipedia

    en.wikipedia.org/wiki/Gerstmann–Sträussler...

    Symptoms start with slowly developing dysarthria (difficulty speaking) and cerebellar truncal ataxia (unsteadiness) and then the progressive dementia becomes more evident. In the early stages of GSS, people with the condition may also exhibit clumsiness and experience difficulty walking.

  9. Causes of hearing loss - Wikipedia

    en.wikipedia.org/wiki/Causes_of_hearing_loss

    Strokes – Depending on what blood vessels are affected by the stroke, one of the symptoms can be deafness; Superior semicircular canal dehiscence, a gap in the bone cover above the inner ear, can lead to low-frequency conductive hearing loss, autophony, and vertigo. Syndromic hearing loss can be either conductive or sensorineural. It occurs ...

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