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  2. Myoclonic dystonia - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_dystonia

    Myoclonic dystonia or Myoclonus dystonia syndrome is a rare movement disorder that induces spontaneous muscle contraction causing abnormal posture. The prevalence of myoclonus dystonia has not been reported, however, this disorder falls under the umbrella of movement disorders which affect thousands worldwide. [ 1 ]

  3. Functional neurologic disorder - Wikipedia

    en.wikipedia.org/wiki/Functional_neurologic_disorder

    Movement disorders including tremors, dystonia (spasms), myoclonus (jerky movements) Visual symptoms including loss of vision or double vision; Speech symptoms including dysphonia (whispering speech), slurred or stuttering speech; Sensory disturbance including hemisensory syndrome (altered sensation down one side of the body)

  4. Myoclonus - Wikipedia

    en.wikipedia.org/wiki/Myoclonus

    Progressive myoclonus epilepsy (PME) is a group of diseases characterized by myoclonus, epileptic seizures, tonic–clonic seizures, and other serious symptoms such as trouble walking or speaking. These rare disorders often get worse over time and can be fatal.

  5. Dystonia - Wikipedia

    en.wikipedia.org/wiki/Dystonia

    Dystonia is often intensified or exacerbated by physical activity, and symptoms may progress into adjacent muscles. [4] The disorder may be hereditary or caused by other factors such as birth-related or other physical trauma, infection, poisoning (e.g., lead poisoning) or reaction to pharmaceutical drugs, particularly neuroleptics, [3] or stress.

  6. Ramsay Hunt syndrome type 1 - Wikipedia

    en.wikipedia.org/wiki/Ramsay_Hunt_syndrome_type_1

    Ramsay Hunt syndrome type 1 is a rare, degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment [1] It has also been alternatively called dyssynergia cerebellaris myoclonica , [ 2 ] [ 3 ] dyssynergia cerebellaris progressiva , [ 4 ] dentatorubral ...

  7. Sarcoglycanopathy - Wikipedia

    en.wikipedia.org/wiki/Sarcoglycanopathy

    The sarcoglycanopathies are a collection of diseases resulting from mutations in any of the five sarcoglycan genes: α, β, γ, δ or ε. The five sarcoglycanopathies are: α-sarcoglycanopathy, LGMD2D; β-sarcoglycanopathy, LGMD2E; γ-sarcoglycanopathy, LGMD2C; δ-sarcoglycanopathy, LGMD2F and ε-sarcoglycanopathy, myoclonic dystonia.

  8. Hyperkinesia - Wikipedia

    en.wikipedia.org/wiki/Hyperkinesia

    Juvenile-onset DRPLA presents with ataxia and symptoms consistent with progressive myoclonus epilepsy [16] (myoclonus, multiple seizure types and dementia). Other symptoms that have been described include cervical dystonia, [17] corneal endothelial degeneration [18] autism, and surgery-resistant obstructive sleep apnea. [19]

  9. Polyneuropathy in dogs and cats - Wikipedia

    en.wikipedia.org/wiki/Polyneuropathy_in_dogs_and...

    Botulism is very rare in dogs and usually follows feeding on carrion. [5] Symptoms include weakness, difficulty eating, acute facial nerve paralysis, and megaesophagus. Compared to other species, dogs and cats are relatively resistant to botulism. [6] Dancing Doberman disease primarily affects the gastrocnemius muscle in Dobermans.