When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Progressive myoclonus epilepsy - Wikipedia

    en.wikipedia.org/wiki/Progressive_myoclonus_epilepsy

    Symptoms often include action or stimuli induced myoclonus, seizures, neuropathy, cognitive decline, and spike and wave or no cerebral discharges. [4] The prognosis of those diagnosed with PME is poor. The person often becomes reliant on a wheelchair, enters a vegetative state due to myoclonus, and has a shortened life expectancy. [4] [3]

  3. 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 ...

  4. 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 ...

  5. Dravet syndrome - Wikipedia

    en.wikipedia.org/wiki/Dravet_syndrome

    Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic form of epilepsy, with prolonged seizures that are often triggered by hot temperatures or fever. [1] It is very difficult to treat with anticonvulsant medications.

  6. Myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_epilepsy

    If the abnormal brain wave activity is persistent and results from ongoing seizures, then a diagnosis of myoclonic epilepsy may be considered. [1] 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 ...

  7. Creutzfeldt–Jakob disease - Wikipedia

    en.wikipedia.org/wiki/Creutzfeldt–Jakob_disease

    As of 2025, there is no cure or effective treatment for CJD. [63] Some of the symptoms like twitching can be managed, but otherwise treatment is palliative care. [63] Psychiatric symptoms like anxiety and depression can be treated with sedatives and antidepressants. Myoclonic jerks can be handled with clonazepam or sodium valproate.

  8. Lance–Adams syndrome - Wikipedia

    en.wikipedia.org/wiki/Lance–Adams_syndrome

    It is a disease that presents Myoclonus as a sequela of hypoxic disorders in the brain due to asphyxiation and cardiopulmonary arrest. [ 2 ] [ 3 ] It is exacerbated by mental and physical anxiety such as intention, intentional movement, and tension.

  9. Myoclonic astatic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_astatic_epilepsy

    Status epilepticus with myoclonic, astatic, myoclonic-astatic, or absence seizures is another ominous sign, especially when prolonged or appearing early. Failure to suppress the EEG abnormalities (4- to 7-Hz rhythms and spike-wave discharges) during therapy and absence of occipital alpha-rhythm with therapy also suggest a poor prognosis (Doose ...