About Spinocerebellar Ataxia Type 8

Spinocerebellar Ataxia 8, also known as spinocerebellar ataxia type 8, is related to spinocerebellar ataxia, autosomal recessive 8 and mitochondrial dna depletion syndrome 7, and has symptoms including muscle spasticity, tremor and abnormal pyramidal signs. An important gene associated with Spinocerebellar Ataxia 8 is ATXN8OS (ATXN8 Opposite Strand LncRNA). Affiliated tissues include spinal cord, eye and cerebellum, and related phenotypes are hyperreflexia and nystagmus

Major Symptoms of Spinocerebellar Ataxia Type 8

Spinocerebellar ataxia type 8 is a rare genetic disorder that primarily affects children. It is characterized by a progressive loss of balance, coordination, and fine motor skills, as well as an improvement in cognitive function. The symptoms often become apparent in the first few years of life and progress rapidly, leading to a significant impact on the affected child's quality of life. Some of the major symptoms of Spinocerebellar ataxia type 8 include progressive muscle weakness, rigidity, and decreased dexterity, as well as changes in the child's speech and gait.

Suitable Lifestyle for People with Spinocerebellar Ataxia Type 8

Suitable lifestyle options for people with Spinocerebellar ataxia type 8 include the following:

1. Stay physically active: This disease affects the body's coordination and balance, so patients should try to stay physically active, such as walking, jogging, and cycling. etc. to help maintain body function.

2. Avoid excessive fatigue: Patients with Spinocerebellar ataxia type 8 are prone to fatigue, so they need to pay attention to avoid excessive fatigue, such as avoiding standing or sitting for long periods of time.

3. Maintain a balanced diet: This disease may cause malnutrition in patients, so patients should maintain a balanced diet and eat more vegetables, fruits, whole grains and protein-rich foods.

4. Avoid infection: This disease may cause patients to develop infections, such as respiratory tract infections or oral infections, so they need to pay attention to personal hygiene, wash hands frequently, and avoid contact with sources of infection.

5. Follow the doctor's advice: Patients need to receive regular examination and treatment from the doctor, and follow the doctor's advice for treatment and care.

6. Get physical therapy: Physical therapy can help patients relieve muscle spasms and pain, so consider physical therapy.

7. Stay social: This disease can cause patients to feel lonely and lost, so stay social and stay in touch with family or friends.

Other Diseases

Spinocerebellar Ataxia Type 28 Spinocerebellar Ataxia Type 2 Spinocerebellar Ataxia Type 16 Spinocerebellar Ataxia Type 42 Spinocerebellar Ataxia Type 27 Spinocerebellar Ataxia Type 20 Spinocerebellar Ataxia Type 15 Spinocerebellar Ataxia Type 40 Spinocerebellar Ataxia Type 7 Spinocerebellar Ataxia Type 23

Related Products