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Classification/Types Of Multiple System Atrophy

Rigid Muscles – The muscle of the patient becomes unbending and the excess movement of the muscles causes pain and spasm .

Bradykinesia – The patient has a slow walking ability.2

Neuropsychiatric Features – Patients with MSA - P observers log Z’s disturbances . Other features include natural depression , apathy , Rapid eye apparent movement , anxiousness and sleep conduct upset .

Although the exact crusade of the development of MSA - P is not cognize the experimental condition is characterized by the presence of aggregate of α - synuclein in various parts of the brain , especially in oligodendroglia . This is combined with the mien of the striatonigral pathway neurodegeneration .

Multiple System Atrophy With Cerebellar Features(MSA - C)- This type of multiple system atrophy is also know as sporadic olivopontocerebellar atrophy . The symptoms are predominantly relate to cerebellar ataxia . The cause of this type is the aggregation of α - synuclein , peculiarly in the oligodendroglia in combining with olivopontocerebellar structures neurodegeneration . The patient role suffering from this type of MSA also shows some symptoms of MSA - P. Most of the symptom are related to a want of muscle coordination . The term is characterized by the presence of the following symptoms-

Multiple System Atrophy

The autonomic spooky system is part of the nervous system that is creditworthy for controlling the unvoluntary body process . Involuntary activity are those activities that are not in unmediated ascendence such as blood pressure , digestion , temperature regulation , etc . When there is neurodegeneration of autonomic nervous scheme , the controlling ability of the brainiac takes a toll and it is seeable in various physiological dysfunctions . This unnatural condition is termed as multiple system dystrophy . This condition is inveterate and reformist and importantly impairs the calibre of biography . The general symptom associate with the condition are perilously low line pressing on standing up , poor temperature regularisation , gut dysfunction causingconstipationandurinary incontinence . The secernment of saliva , weeping , and sweat reduces and the patient also know intimate disfunction and emotional distress .

Conclusion

Multiple organization atrophy is divided into two major eccentric on the basis of part of the mind affected and the come with symptom . The types of MSA are MSA - P , the Parkinson variant , and MSA - C , the Cerebellum stochastic variable . Symptoms of both the conditions may overlap but MSA - P has predominating Parkinson symptoms while MSA - C has the dominate symptom of cerebellar ataxia . In MSA - P , the neurodegeneration of the striatonigral footpath occurs while in MSA - C , neurodegeneration of olivopontocerebellar structures is seen .

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