Spinocerebellar ataxia➣How long can you live with spinocerebellar ataxia

This article will tell you about spinocerebellar ataxia and how long you can live with spinocerebellar ataxia. , I hope it will be helpful to everyone, don't forget to bookmark this site. List of contents of this article: 1. Is spinocerebellar ataxia cerebellar atrophy? 2. What is spinocerebellar ataxia? 3. What causes cerebellar ataxia? 4. How to treat spinocerebellar ataxia? Is spinocerebellar ataxia a cerebellar atrophy? Spinocerebellar ataxia is a genetic disease characterized by degeneration and dysregulation of the cerebellum and spinal cord, leading to symptoms such as decreased muscle coordination and ataxia. Spinocerebellar ataxia and cerebellar atrophy have similar symptoms, but they are different diseases. Spinocerebellar ataxia is considered a large system degenerative disease in neurology, and cerebellar atrophy is actually included in the group of diseases called spinocerebellar ataxia. Spinocerebellar ataxia belongs to autosomal dominant and recessive inheritance, and there are about 30 subtypes, which are represented by letters S, C, and A respectively. Cerebellar ataxia, also known as spinocerebellar atrophy, is a disease in which the patient's muscle tension or loss and voluntary movement are disordered due to various causes of cerebellar damage. Cerebellar ataxia is a syndrome characterized by abnormal cerebellar function due to various causes. Cerebellar ataxia is one of the symptoms of cerebellar atrophy, and cerebellar atrophy is a progressive disease. At this time, reasonable drugs should be selected to improve ataxia, smoking and alcohol should be quit during the period of taking, and good eating habits should be developed. Combined, moderate exercise. I can't control myself. Third, everyone should pay attention to observation and understanding in daily life. There are many differences between cerebellar ataxia and spinocerebellar atrophy. Cerebellar ataxia and spinocerebellar atrophy cannot be regarded as the same disease, and the treatment methods of the two diseases are also different. What is spinocerebellar ataxia? Spinocerebellar ataxia (SCA) is a group of hereditary diseases characterized by chronic progressive ataxia. Spinocerebellar ataxia has been found There are dozens of causative genes, most of which are autosomal dominant, but also autosomal recessive and X-linked. Spinocerebellar ataxia is a genetic disorder characterized by degeneration and dysregulation of the cerebellum and spinal cord, leading to symptoms such as decreased muscle coordination and ataxia. Spinocerebellar ataxia and cerebellar atrophy have similar symptoms, but they are different diseases. Spinocerebellar ataxia mainly refers to Friedreich's ataxia, which is a degenerative disease of the spinal cord and cerebellum. Friedreich's ataxia is an autosomal recessive genetic disease, the main clinical manifestations are ataxia, arched foot, optic atrophy, scoliosis, cardiomyopathy and so on. Spinocerebellar ataxia is a major type of hereditary ataxia disease and is an autosomal dominant genetic disease. Spinal ataxia, also known as spinocerebellar ataxia, is the most important type of hereditary ataxia, most of which are autosomal dominant, and a few are autosomal recessive. of subtypes. What causes cerebellar ataxia? 1. The causes of cerebellar ataxia are as follows: First, infectious factors. Infectious diseases may cause cerebellar ataxia, such as scarlet fever, diphtheria, etc. Clinically, viral infections, bacterial infections, mycoplasma infections, and tuberculin infections are more common, such as viral encephalitis, bacterial encephalitis, etc. 2. Main etiology and poisoning factors, including drug poisoning, CO, alcohol poisoning, etc. A large number of vitamin deficiencies, especially vitamin B and vitamin E are indispensable elements for ataxia patients. 3. The main causes of cerebellar ataxia are genetic and secondary causes. Secondary causes mainly include idiopathic cerebellar ataxia and acquired ataxia, such as alcohol poisoning, vitamin deficiency, metabolic diseases, multiple sclerosis, etc. 4. There are many reasons for cerebellar ataxia. If the patient has an acute onset, it is necessary to consider whether it is vascular disease, poisoning, or abnormal metabolism. There are many causes of vascular disease, which may be heart disease, blood disease, abnormal blood coagulation mechanism, and vasculitis. How to treat spinocerebellar ataxia? Levodopa drug treatment can relieve rigidity and other Parkinson-like symptoms, and chlorphenamine can also be given to relieve spasticity. Amantadine can improve ataxia and poisonous lentils Alkaline or citicoline can promote the synthesis of acetylcholine and so on. Ataxia is a neurological disorder characterized by impaired coordination, abnormal muscle tone, and tremors. At present, the treatment of ataxia is mainly for the treatment of symptoms, including two aspects of drug therapy and physical therapy. Drug therapy with levodopa, which relieves rigidity and other parkinsonian symptoms, can also be given chlorphenamine, which reduces spasticity, amantadine, which improves ataxia, and physostigmine or citicoline, which boosts acetylcholine synthesis etc. Amantadine can improve ataxia, and nitrazepam is the first choice for ataxia with myoclonus; neurotrophic drugs such as ATP, coenzyme A, inosine, and vitamin B group can be tried; (2) Surgical treatment: thalamus lesion is feasible (3) Rehabilitation training, physical therapy and walking aids may be beneficial. So far, there is no specific treatment for spinocerebellar ataxia. The principle of treatment is mainly symptomatic treatment and rehabilitation treatment to restore the patient's living ability. The main drugs are levodopa, chlorphenamine butyric acid, amantadine, clonazepam and other treatments. . This concludes the introduction about spinocerebellar ataxia and how long you can live with spinocerebellar ataxia. Did you find the information you need? If you want to know more about this, remember to bookmark and follow this site.