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  2. 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.

  3. 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.

  4. Myoclonus - Wikipedia

    en.wikipedia.org/wiki/Myoclonus

    Myoclonus is a brief, involuntary, irregular (lacking rhythm) twitching of a muscle, a joint, or a group of muscles, different from clonus, which is rhythmic or regular.

  5. List of neurological conditions and disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_neurological...

    Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome; Cerebral gigantism; Cerebral palsy; Cerebral vasculitis; Cerebrospinal fluid leak; Cervical spinal stenosis; Charcot–Marie–Tooth disease; Chiari malformation; Chorea; Chronic ...

  6. Familial encephalopathy with neuroserpin inclusion bodies

    en.wikipedia.org/wiki/Familial_encephalopathy...

    In severe cases, the condition causes seizures and episodes of sudden, involuntary muscle jerking or twitching (myoclonus) in addition to dementia. These signs can appear as early as a person's teens. Less severe cases are characterized by a progressive decline in intellectual functioning beginning in a person's forties or fifties. [citation ...

  7. 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).

  8. Megalencephalic leukoencephalopathy with subcortical cysts

    en.wikipedia.org/wiki/Megalencephalic...

    The presence of frontal and temporal subcortical cysts is the main factor when diagnosing a patient with this disease. [11] In the late stages of the disease, patients have been noted to develop impaired coordination, overresponsive reflexes, and even seizures.

  9. List of regions in the human brain - Wikipedia

    en.wikipedia.org/wiki/List_of_regions_in_the...

    Subcortical areas: Septal nuclei; Amygdala; Nucleus accumbens; Diencephalic structures: Hypothalamus; Mammillary bodies; Anterior nuclei of thalamus; Other areas that have been included in the limbic system include the: Stria medullaris; Central gray and dorsal and ventral nuclei of Gudden