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  2. Myoclonus - Wikipedia

    en.wikipedia.org/wiki/Myoclonus

    Cortical reflex myoclonus is thought to be a type of epilepsy that originates in the cerebral cortex – the outer layer, or "gray matter", of the brain, responsible for much of the information processing that takes place in the brain. In this type of myoclonus, jerks usually involve only a few muscles in one part of the body, but jerks ...

  3. Myoclonic dystonia - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_dystonia

    Myoclonus is usually classified physiologically to optimize treatment. Myoclonus is a precursor effect to myoclonus dystonia and most commonly begins in childhood or adolescence. [4] [5] Myoclonus is classified as cortical, subcortical, peripheral or spinal. Cortical myoclonus is the most common of these four and affects the upper limbs and face.

  4. 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).

  5. Hyperkinesia - Wikipedia

    en.wikipedia.org/wiki/Hyperkinesia

    In the myoclonus EMG, there are typically brief, and sometimes rhythmic, bursts or pauses in the recording pattern. When the bursts last for 50 milliseconds or less they are indicative of cortical myoclonus, but when they last up to 200 milliseconds, they are indicative of spinal or brainstem myoclonus.

  6. Corticobasal syndrome - Wikipedia

    en.wikipedia.org/wiki/Corticobasal_syndrome

    limb myoclonus; plus two of: orobuccal or limb apraxia, cortical sensory deficit; alien limb phenomena (more than simple levitation) [8] The diagnosis is excluded if there is evidence of: Lewy body disease; multiple system atrophy; Alzheimer's disease; amyotrophic lateral sclerosis; semantic or logopenic variant primary progressive aphasia

  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. 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. Intermittent photic stimulation - Wikipedia

    en.wikipedia.org/wiki/Intermittent_photic...

    Photic stimulation may also be used to elicit myoclonus, especially cortical reflex myoclonus when present in photo-sensitive forms. IPS may be used to stimulate the visual system for patients with amblyopia. This system uses a visual stimulus that is usually red in color with a frequency of about 4 Hz to stimulate the neural pathway between ...