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  2. Myoclonus - Wikipedia

    en.wikipedia.org/wiki/Myoclonus

    Treatment of myoclonus focuses on medications that may help reduce symptoms. Drugs used include sodium valproate, clonazepam, the anticonvulsant levetiracetam, and piracetam. [8] Dosages of clonazepam usually are increased gradually until the patient improves or side effects become harmful. Drowsiness and loss of coordination are common side ...

  3. Myoclonic dystonia - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_dystonia

    Many drugs used to treat myoclonus dystonia do not have a significant impact individually, but when combined, can work on different brain mechanisms to best alleviate symptoms. The method of treatment used depends on the severity of the symptoms presented in the individual, and whether the underlying cause of the syndrome is known.

  4. Juvenile myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Juvenile_myoclonic_epilepsy

    There are three principal seizure types which may occur in JME: myoclonus, generalized tonic–clonic seizures and absence seizures. Approximately one-third of patients have all three seizure types. [13] The majority of patients (58.2%) have frequent myoclonic jerks, [13] with some sources stating that all patients with JME have myoclonic ...

  5. Myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_epilepsy

    Familial adult myoclonus Epilepsy (FAME) This is a condition characterized by the repetition of non-coding sequences and has been identified using various abbreviations. Initially, it was associated with four primary gene locations: FAME1 (8q23.3–q24.1), FAME2 (2p11.1–q12.1), FAME3 (5p15.31–p15.1), and FAME4 (3q26.32–3q28).

  6. Piracetam - Wikipedia

    en.wikipedia.org/wiki/Piracetam

    Piracetam is a drug that has efficacy in cognitive disorders, vertigo, cortical myoclonus, dyslexia, and sickle cell anemia; sources differ on its usefulness for dementia. [3] [4] [5] Piracetam is sold as a medication in many European countries.

  7. Progressive myoclonus epilepsy - Wikipedia

    en.wikipedia.org/wiki/Progressive_myoclonus_epilepsy

    MEAK is a form of progressive myoclonus epilepsy that typically begins between the ages of 3 and 15 years (the average of onset is 10 years). The first symptoms may include ataxia and myoclonus (unsteadiness and difficulty coordinating movements), along with generalized tonic-clonic ("grand mal") seizures.

  8. Dystonia - Wikipedia

    en.wikipedia.org/wiki/Dystonia

    A variety of treatment strategies can be employed to address the unique needs of each individual. Potential treatment interventions include splinting, [ 32 ] therapeutic exercise, manual stretching , soft tissue and joint mobilization , postural training and bracing, [ 30 ] neuromuscular electrical stimulation , constraint-induced movement ...

  9. Unverricht–Lundborg disease - Wikipedia

    en.wikipedia.org/wiki/Unverricht–Lundborg_disease

    Antiepileptic drugs reduce the occurrence of seizures and myoclonus, which leads to a decrease in the damage caused in the brain due to seizures and the body due to falls resulting from the seizures. As a result, individuals with Unverricht–Lundborg disease are now much less likely to end up in a wheelchair, which eliminates the chance of ...