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Results 1 - 9 of 9 for Myoclonic tremor
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  1. Action myoclonus–renal failure syndrome 
    ... the head, torso, legs, and tongue. Eventually, the tremors worsen to become myoclonic jerks, which can be triggered by voluntary movements ...
    https://medlineplus.gov/.../action-myoclonus-renal-failure-syndrome - Genetics
  2. CLN4 disease 
    ... disease often develop seizures and uncontrollable muscle jerks (myoclonic epilepsy), a decline in intellectual function (dementia), problems with coordination and balance (ataxia), tremors or other involuntary movements (motor tics), and speech ...
    https://medlineplus.gov/genetics/condition/cln4-disease - Genetics
  3. Progressive myoclonic epilepsy type 1 
    ... involuntary rhythmic shaking. This shaking is called intentional tremor because it worsens during intentional movements.People with progressive myoclonic epilepsy type 1 may live into adulthood. Life ...
    https://medlineplus.gov/.../progressive-myoclonic-epilepsy-type-1 - Genetics
  4. Spinal muscular atrophy with progressive myoclonic epilepsy 
    ... PME may also have episodes of rhythmic shaking (tremors), usually in the hands; these tremors are not thought to be related to epilepsy. ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
  5. ADCY5-related dyskinesia 
    ... dyskinesia typically appear as sudden (paroxysmal) jerks, twitches, tremors, muscle tensing (dystonia), or writhing (choreiform) movements, and ...
    https://medlineplus.gov/genetics/condition/adcy5-related-dyskinesia - Genetics
  6. Spinal muscular atrophy 
    ... or walk unaided. They often have involuntary trembling (tremors) in their fingers, a spine that curves side- ... individuals usually experience mild to moderate muscle weakness, tremors, and mild breathing problems. People with spinal muscular ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  7. Beta-propeller protein-associated neurodegeneration 
    ... Parkinsonism can include unusually slow movement (bradykinesia), rigidity, tremors, an inability to hold the body upright and ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  8. STXBP1 encephalopathy 
    ... such as difficulty coordinating movements (ataxia), involuntary trembling (tremors), and muscle stiffness (spasticity). In some cases, areas ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  9. Cerebral folate transport deficiency 
    ... and recurrent seizures (epilepsy). Movement problems such as tremors and difficulty coordinating movements (ataxia) can be severe, ... A, Cormand B, Artuch R. Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics