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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. Myoclonus - Wikipedia

    en.wikipedia.org/wiki/Myoclonus

    Earlier age of seizure onset is correlated with a higher risk of cognitive impairment. 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.

  4. Anti-Hu associated encephalitis - Wikipedia

    en.wikipedia.org/wiki/Anti-Hu_associated...

    Risk factors: Smoking, male gender: ... It can cause psychiatric symptoms such as depression, ... Opsoclonus-myoclonus syndrome (OMS) is a condition that develops in ...

  5. Tardive dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Tardive_dyskinesia

    Tardive myoclonus, a rare disorder, presents as brief jerks of muscles in the face, neck, trunk, and extremities. [ 13 ] "AIMS Examination": This test is used when psychotropic medications have been prescribed because people sometimes develop tardive dyskinesia due to prolonged use of antipsychotic medications.

  6. 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.

  7. Opsoclonus myoclonus syndrome - Wikipedia

    en.wikipedia.org/wiki/Opsoclonus_myoclonus_syndrome

    Opsoclonus myoclonus syndrome (OMS), also known as opsoclonus-myoclonus-ataxia (OMA), is a rare neurological disorder of unknown cause which appears to be the result of an autoimmune process involving the nervous system. It is an extremely rare condition, affecting as few as 1 in 10,000,000 people per year.

  8. A simple tool may be able to predict your risk for both ...

    www.aol.com/news/score-predicting-dementia-risk...

    A noninvasive tool for predicting dementia and stroke risk may also help assess someone’s risk of developing depression late in life, a new study has found. ... one of 12 factors that could help ...

  9. Unverricht–Lundborg disease - Wikipedia

    en.wikipedia.org/wiki/Unverricht–Lundborg_disease

    Unverricht–Lundborg disease was first known as one of two different diseases, depending on the location of the individual who had it: Baltic myoclonus or Mediterranean myoclonus. [7] The reason for the different names was partly regional but also because the prognosis of the disease was different for individuals with each due to the way that ...

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