Ads
related to: myoclonus vs dyskinesia signs and symptoms- TD Treatment Options
Learn How A Treatment May Help TD.
Get Tips For Your Next Appointment.
- Download Resources
How Can You Help Manage Symptoms?
Download A Patient Brochure.
- Important Dosing Info
Read The Dosing Regimen For
A TD Treatment Option.
- Doctor Discussion Guide
Download The TD Doctor Discussion
Guide For Your Next Appointment.
- TD Treatment Options
Search results
Results from the WOW.Com Content Network
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.
Myoclonic dystonia or Myoclonus dystonia syndrome is a rare movement disorder that induces spontaneous muscle contraction causing abnormal posture. The prevalence of myoclonus dystonia has not been reported, however, this disorder falls under the umbrella of movement disorders which affect thousands worldwide. [1]
Late-onset dyskinesia, also known as tardive dyskinesia, occurs after long-term treatment with an antipsychotic drug such as haloperidol (Haldol) or amoxapine (Asendin). The symptoms include tremors and writhing movements of the body and limbs, and abnormal movements in the face, mouth, and tongue – including involuntary lip smacking, repetitive pouting of the lips, and tongue protrusions.
Hyperkinetic movement disorders refer to dyskinesia, or excessive, often repetitive, involuntary movements that intrude upon the normal flow of motor activity. Hypokinetic movement disorders fall into one of four subcategories: akinesia (lack of movement), hypokinesia (reduced amplitude of movements), bradykinesia (slow movement), and rigidity ...
Symptoms vary according to the kind of dystonia involved. In most cases, dystonia tends to lead to abnormal posturing, in particular on movement. Many individuals with the condition have continuous pain, cramping, and relentless muscle spasms due to involuntary muscle movements. Other motor symptoms are possible including lip smacking. [16]
There are three different subtypes of PD that include paroxysmal kinesigenic dyskinesia (PKD), paroxysmal nonkinesigenic dyskinesia (PNKD), and paroxysmal exercise-induced dystonia (PED). Other neurological diseases have similar symptoms to PD, such as epilepsy and Parkinson's. The different subtypes make accurate and quick diagnosis of PD ...
Often the symptoms of tardive dyskinesia are not apparent until the individual comes off of the antipsychotic drugs; however, when tardive dyskinesia worsens, the signs become visible. [24] Other dopamine antagonists and antiemetics can cause tardive dyskinesia, such as metoclopramide and promethazine, used to treat gastrointestinal disorders.
Juvenile-onset DRPLA presents with ataxia and symptoms consistent with progressive myoclonus epilepsy [16] (myoclonus, multiple seizure types and dementia). Other symptoms that have been described include cervical dystonia, [17] corneal endothelial degeneration [18] autism, and surgery-resistant obstructive sleep apnea. [19]
Ads
related to: myoclonus vs dyskinesia signs and symptoms