About Spinocerebellar Ataxia Type 7

Spinocerebellar Ataxia 7, also known as spinocerebellar ataxia type 7, is related to spinocerebellar ataxia 1 and olivopontocerebellar atrophy, and has symptoms including muscle spasticity, abnormal pyramidal signs and abnormality of extrapyramidal motor function. An important gene associated with Spinocerebellar Ataxia 7 is ATXN7 (Ataxin 7), and among its related pathways/superpathways are Deubiquitination and Chromatin organization. The drugs Riluzole and Excitatory Amino Acid Antagonists have been mentioned in the context of this disorder. Affiliated tissues include eye, spinal cord and cerebellum, and related phenotypes are hyperreflexia and dysarthria

Major Symptoms of Spinocerebellar Ataxia Type 7

Spinocerebellar ataxia type 7 is a rare genetic disorder that primarily affects the cerebellum, resulting in symptoms such as unsteadiness, balance difficulties, and difficulty with gait and balance. The symptoms often become apparent in the late teenage years or early twenties and can significantly impact daily life. Additionally, patients may experience changes in their personality and social behavior, such as increased anxiety and decreased motivation. Treatment options are limited and typically focused on managing symptoms and improving quality of life.

Suitable Lifestyle for People with Spinocerebellar Ataxia Type 7

A suitable lifestyle for people with Spinocerebellar ataxia type 7 includes the following:

1. Stay physically active: This disease affects the body's coordination and ability to move, so staying physically active is very important to maintain body function and prevent other complications. .

2. Avoid mental stress: Patients with Spinocerebellar ataxia type 7 may experience mental stress, such as anxiety and depression, and these emotions can have a negative impact on the disease. Therefore, patients should try to reduce mental stress and find ways to relax that suit themselves.

3. Maintain a balanced diet: Patients need to consume sufficient nutrients to support body functions and maintain good health. It is recommended to maintain a balanced diet, including protein, vitamins and minerals.

4. Carry out proper training and exercise: This disease may affect muscle coordination, but proper training and exercise can help maintain muscle function and improve body coordination.

5. Receive medical care: Patients need to receive regular medical care, including rehabilitation training, medication, and regular examinations, to help control disease progression and prevent complications.

6. Stay socially connected: Patients need to stay connected to family, friends, and the community to provide emotional support and help maintain social connections. It is important to note that these recommendations apply to people with Spinocerebellar ataxia type 7, but specific lifestyle changes should be based on the patient's specific situation and the advice of their doctor.

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