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  2. 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 ...

  3. Deaf animal - Wikipedia

    en.wikipedia.org/wiki/Deaf_animal

    Deafness in animals can occur as either unilateral (one ear affected) or bilateral (both ears affected). This occurrence of either type of deafness seems to be relatively the same in both mixed-breed animals and pure-breed animals. [5] Research has found a significant association between deafness in dogs and the pigment genes piebald and merle ...

  4. Mohr–Tranebjærg syndrome - Wikipedia

    en.wikipedia.org/wiki/Mohr–Tranebjærg_syndrome

    Mohr–Tranebjærg syndrome (MTS) is a rare X-linked recessive syndrome also known as deafness–dystonia syndrome and caused by mutation in the TIMM8A gene. It is characterized by clinical manifestations commencing with early childhood onset hearing loss, followed by adolescent onset progressive dystonia or ataxia, visual impairment from early adulthood onwards and dementia from the 4th ...

  5. Canine cognitive dysfunction - Wikipedia

    en.wikipedia.org/wiki/Canine_cognitive_dysfunction

    Canine cognitive dysfunction (CCD) is a disease prevalent in dogs that exhibit symptoms of dementia or Alzheimer's disease shown in humans. [1] CCD creates pathological changes in the brain that slow the mental functioning of dogs resulting in loss of memory, motor function, and learned behaviors from training early in life.

  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. Speech and language impairment - Wikipedia

    en.wikipedia.org/wiki/Speech_and_language_impairment

    The DSM-5 and the ICD-10 are both used to make specific diagnostic decisions. Speech and language disorders commonly include communication issues, but also extend into various areas such as oral-motor function—sucking, swallowing, drinking, or eating.

  8. Wendy Williams Is “Incapacitated” Amid Dementia Diagnosis ...

    www.aol.com/wendy-williams-incapacitated-amid...

    Wendy Williams was deemed “permanently incapacitated” due to frontotemporal dementia and primary progressive aphasia. The update follows a 2022 guardianship case initiated by Wells Fargo over ...

  9. Congenital sensorineural deafness in cats - Wikipedia

    en.wikipedia.org/wiki/Congenital_sensorineural...

    Deafness can occur in white cats with yellow, green or blue irises, although it is mostly likely in white cats with blue irises. [4] In white cats with one blue eye and one eye of a different color (odd-eyed cats), deafness is more likely to affect the ear on the blue-eyed side. [1] Approximately 50% of white cats have one or two blue eyes. [5]