What are the symptoms of motor neuron disease?

Because diseases of motor neurons are a collection of related health conditions, the symptoms of motor neuron diseases are similar regardless of the condition the patient has. Motor neuron disease has five forms, some more serious and life -threatening that others. All conditions affect the body's ability to perform voluntary movement. Symptoms over time generally worsen despite palliative care. Initial symptoms cannot predict a short and long -term prognosis of the patient.

Motor neuron diseases have five forms: ALS (amyotrophic lateral sclerosis), PLS (primary lateral sclerosis), PMA (progressive muscle atrophy), pity pseudo -skirt and progressive bulb bull. Symptoms of motor neuron diseases are generally associated with ALS, also known as Lou Gehrig's disease in the United States. Initial degeneration of neurons can begin in any part of the body; Loss of coordination and weakness usually occurs anywhere where symptoms begin. Symptoms with a speedLe wandered into the rest of the body in the moods of St St Making complete immobility. Ninety percent of patients die within six years of diagnosis.

In many respects, PLS is a less serious form of ALS. Like ALS, it generally occurs when an individual is an middle -aged. Although the initial symptoms are almost identical to the symptoms of ALS, PLS does not affect backbone neurons. Thus, the disease proceeds very slowly and most patients will not die. In some cases, however, PLS can develop into ALS. Several drugs showed a promise to relax muscle spasms associated with PLS.

Symptoms of motor neurons in PMA are similar to symptoms of ALS and PLS. The most common symptom is muscle atrophy. Whether atrophy is limited to one limb or spread through the body depends on the patient's specific physiology. Because atrophy is common to all forms of motoring diseases, lack of muscle convulsions and emotionalThe changes allow the presence of ALS and PMS to exclude the presence of ALS and PMS. The five -year PMA survival rate is between the als and Pls.

Visible symptoms of motor neuron diseases for pity pereudobulbar are limited to patient speech and ability to swallow. In the patient's mind, wild and sudden moods may also occur. These palsy can have a number of causes from ALS to cancer. The prognosis depends on the root cause.

Finally, the symptoms of motor neurons disease may indicate the presence of progressive Bulbar polio. Since 2011, there is no consensus in the medical community as to whether progressive polio is a separate condition or ALS. Like pseudo -skirt Palsy, the condition quickly threatens the ability of the patient to speak and swallow. There is no treatment and death generally occurs within one to three years.