What are motor disorders? Survey of 14 common motor disorder
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Motor disorders are clinical syndromes that are associated with increasing or decreasing voluntary and involuntary movements, without weakness or spasm (muscle cramps) ...
Excessive motor disorders refer to deconous or non -motion, repetitive and involuntary movements, which are beyond normal movements ...
Hypokinetic disorders refer to Akinis (non -motion), hypochinosis (reduced range of motion), bramadium (reduced speed) and motor muscle stiffness. View ..
1 .... Atacial Motor Disorder
Ataxia is a winning analysis disorder that affects the brain, brain or spinal cord.
Dissey is a nerve disorder in the muscles characterized by involuntary muscle spasms.
Universal dishes cause the whole body to be involved ... Central containers only one part of the body, mainly neck (spasm or torticollis ), eyelids (called Blephaspasm ) meige ) and hand (clogging pronfer
Depending on the body involved, Dissey can be very disabling.. Targeting small areas of talmotomy (tlamotomy), palidus (pealidotomy) or other deep brain areas .... recently, deep brain irritation ( DBS) has been successful ... Other surgeries include a nerve movements in the neurotic roots in the neck and in the stream streng> Strong Strong> antry (strate> strat> strat> strat (Strong> strat> strat> strat> strate> strate> stry in nervous roots (Strong) and Motor vibration is an uncontrolled type of tremor that usually contains one or two hands or arm and exacerbation during basic movements. Or lifestyle changes can lead to symptoms.
Injecting Botox helps to cut nerve and muscle and reduce tremor .... In tlatum surgery, the tallam (an area in the depth of the brain receiving sensory messages) disappears. And then attaches to a neural stimulus ( neurostimulator ) beneath the clamp bone ... slow ... Huntington Disease is a progressive disease and a winning analysis in a series of specific neurons located in the brain ... The onset of the disease is usually between 35 and 50, which lasts 10 to 25 years ... It is estimated that Huntington is involved in every 10,000 people in the United States ... A specific type of Huntington is created at a young age (20 and younger) that makes up 16 % of the total. Symptoms include tremors, involuntary trunk and face, and rapid analysis of mental abilities and mental problems. There is no.. Therefore, treatment is focused on reducing symptoms, preventing complications, and helping patients and family members to adapt to everyday problems.
Doctors may prescribe antidepressant, antidepressant, sedative, mood stabilizer or Botox injection. These drugs are prescribed with the least effective dose because they all have side effects ... Huntington's complete progress will usually be more likely to be done in 10 to 30 years ...
Multiple Atrophy is a neurological disease (neuron winning analysis) that disrupts motion, blood pressure and other body actions. 3 .... Movement ( Essential Seismic)
4 ...
5 .... Motion Disorder MSA or Multiple System Atrophy
All three of these diseases are now known as MSA. Symptoms of this disease include muscle stiffness, slow movement, imbalance, insistence, dramatically reducing blood pressure in the topical that lead to dizziness, lightweight, weakness or blood pressure.
may be used to control the symptoms of the disease ... Orthustatic can be controlled with hypertension.
6 .... Motor Disorder Myoclonus
Myoclucles spasm is intermittent or intermittently one or more muscles. This disease is divided into several main groups and several subgroups .... The most common type of myoclasmia is from an area of the brain called the sensory cortex ...
involuntary movements in myoconus are usually regular rhythm and may be limited to a single muscle or a muscle group (focal) or several different muscle groups (multiple focus).
This muscle cramps may occur without cause or as a result of many diseases..
Some myoclonus -related diseases including celiac, Angleman syndrome, disease, after
Mioconus usually affects multiple (published) muscles and may occur due to a decrease in brain oxygen levels (hypoxia) or a metabolism disorder such as kidney failure or liver.
Spinal myoconus can be caused by focal spinal cord injury such as multimedia cache, sirinjomilia (spinal cord or Siringamilia) , trauma, ischemic myelopathic or infections such as herpes-sore, lemongrass and HIV ...
In this disease, involuntary movements are more diverse than myoconus of the brain and subcutaneous cortex.
The most common peripheral myoclonus is an attractive spasm (semi -pin) that can occur for no cause or due to pink nerve compression ... In this case, involuntary movements continue to fall asleep and can last only a few days to several months. ( Baveiia Nigra) Created responsible for moving ...
Disability or disruption to the activity of these nerve cells results in the loss of the production power of an important chemical called dopamine.
Parkinson's disease leads to many symptoms, including tremors, muscle stiffness, gradual disappearance of involuntary movements, which often lead to reduced mental skills and increased reaction time, changes in sound or reduces facial states, gradually loss of movements that cause depression or dementia ...
Many patients with Parkinson's treatment decrease with signs.. Some common used drugs are:
Dopamine precursors, dopamine agonists and anticholinergic ...
Surgery is performed when the drugs are proven. (PSP: Extraordinary nuclear paralysis)
PSP is a rare brain disorder that leads to permanent and dangerous neurological problems ...
People with PSP experience the gradual loss of specific nerve cells, swallowing, speech and eye movement .... These people often cause behavioral and cognitive changes that in turn cause mental outburst and reduce intellectual abilities ...
PSP mainly affects people between 40 and 60 years of age and usually progresses completely over 6 to 10 years. The disease is sometimes confused because of the similarity of symptoms to Parkinson's. Although the PSP cause is unknown, researchers know that in people with the disease, the protein ' It has genetics ... Unfortunately there is no effective drug for PSP treatment, but research is ongoing ... Medications that may be somewhat useful include levodopa, amtadine and Amityllen ...
9 .... Rate Syndrome
RETA Syndrome is a progressive neurological disorder that results in deactivation of symptoms such as reducing muscle strength, recurrent hand movements, irregular breathing, decreased emotional expression, delay in brain growth and head growth, walking abnormalities and seizures.
Reducing muscle strength is usually the first symptom of the disease. According to the International International Rate Syndrome Foundation, about 1 out of every 10,000 to 23,000 women with makeup syndrome are diagnosed, but the prevalence is probably higher because many patients are not identified.
Rate syndrome is caused by mutation in gene MECP2 in X chromosome. Children with this syndrome have normal growth until the age of 6 to 18 months old but their symptoms appear ...
The
rate syndrome severely deactivates its victims. So that these people need the help of others in all aspects of their daily lives..
Rate syndrome progresses to four main modes, each with its specific symptoms and therapeutic needs ...
Medications are used to control irregular breathing and motor disorders. Waterproofing drugs are used to control seizures.
to help patients with this syndrome to adapt to everyday challenges and maintain quality of life, training, professional therapies and their support services ... although it is very imminent, but patients are usually up to 50 years ... Secondary
Secondary Parkinsonism is a disorder with symptoms similar to Parkinson's disease, with factors such as side effects of drugs, various neurological diseases and brain diseases or brain injuries ...
such as Parkinson's disease, in secondary parkinsonism, symptoms such as tremors, muscle deficiency, lack Frequency and swallowing ...
Unlike Parkinson's disease, with precise control of the drugs, especially restricting the use of certain types of anti -medium drugs, the risk of secondary parkinism can be minimized.
Hepertonia is an increase in muscle contractions that lead to muscle stiffness or hardness and disruption to movement, speech and walking.
Hypertony is usually caused by damage to parts of the brain or spinal cord that control voluntarily movement. Use clonazepam. The treatment may also be prescribed by specific muscle exercises to help reduce the severity of symptoms.
Dissex Delay is a muscle disorder caused by prolonged exposure in some types of anti -Median or neuroleptic drugs.
TD with repetitive, involuntary and purposeless movements such as gym , lip collision, eyelid closure or quick movements and arms ...
TD can be mild and in many cases can be reversible ... Percentage of patients with severe or unknown TDs compared to patients who receive chronic anti -TDs ... Young people.
13 .... Torture Syndrome ( Tourt Syndrome)
Torta Syndrome is an inherited neural disorder characterized by involuntary movements and production of uncontrollable sounds called Tick (TICS) .
This disorder often shows at the age of 6 to 15, but may occur earlier (2 years) or after (20 years) ...
Incidentally, involuntary movements, especially on the face and then arms, legs and trunk are the first signs of this syndrome. These mites are repeated and fast ...
Audio mites usually occur with motion, but later they may replace one or more motor mites ... swallowing, straightening the throat, screaming and screaming are the features of the audio mites. Since all of these drugs are associated with potential side effects, they should be prescribed with the least effective dose ...
14 .... Wilson's disease
Wilson patient is a genetic disorder that results in excessive copper accumulation in the liver or brain..
Although copper accumulation begins at birth, symptoms can appear at the age of 6 to 40, but in most cases they appear in late puberty. Wilson's disease affects about 30,000 people worldwide. Receive defective genes ...
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