Spinocerebellar ataxia what drugs to take

Spinocerebellar ataxia is a familial degenerative disease. For this degenerative disease, it is actually a relatively refractory disease in the entire neurology department. Drugs are rarely targeted, because there are too many types. There are more than 40 types of autosomal dominant spinocerebellar ataxia, each type of gene is different, and it is difficult to target drugs. At this stage, a new drug called tatirelin is marketed in Japan. However, after the domestic patient test, after buying it, it was found that the effect was not very good. Therefore, many patients had this disease, hoping to see if they could be treated with drugs, but the results were actually not very satisfactory. There are also drugs that can improve symptoms, but they cannot cure them. For example, taking drugs such as idebenone and butylphthalide can improve mitochondrial function. Eating coenzyme Q10, vitamin B family including B1, B12, vitamin E may nourish brain cells. In addition, such as tandospirone, buspirone, can improve ataxia symptoms.