Corticobasal ganglia degeneration is generally incurable. Corticobasal ganglion degeneration is a gradually worsening disease and a chronic progressive neuropathy, the main manifestations of which are asymmetric episodes of ankylosing tonic syndrome, loss of use, dystonia and postural abnormalities, and it is more commonly seen in people between the ages of 40 and 70. Corticobasal ganglia degeneration starts with irregular motor abnormalities, such as dystonia, etc. As the disease progresses, ataxia, ophthalmoplegia and other symptoms will appear, and as the disease progresses, cognitive impairment and language disorders will occur. Drug treatment does not have much effect, and the symptoms can be relieved by physical methods and surgery, but it does not solve the problem fundamentally and cannot be cured. Most patients die 4-6 years after the onset of the disease. Diagnosed with corticobasal ganglia degeneration, it should be treated as early as possible to control the condition and relieve the symptoms, and it is recommended to take more rest and avoid falls.