About Spinocerebellar Ataxia Type 21

Spinocerebellar Ataxia 21, also known as spinocerebellar ataxia type 21, is related to spinocerebellar ataxia, autosomal recessive 21 and hereditary ataxia, and has symptoms including cerebellar ataxia, tremor and cogwheel rigidity. An important gene associated with Spinocerebellar Ataxia 21 is TMEM240 (Transmembrane Protein 240). Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are abnormality of extrapyramidal motor function and gait ataxia

Major Symptoms of Spinocerebellar Ataxia Type 21

Spinocerebellar ataxia type 21 is a neurodegenerative disorder that primarily affects the cerebellum, leading to symptoms such as unsteadiness, balance difficulties, and difficulty with gait and coordination. The disease can also cause changes in speech and language, leading to difficulties with articulation and comprehension. In addition, it may affect the brain's ability to regulate muscle tone, leading to muscle weakness and floppiness. The symptoms of Spinocerebellar ataxia type 21 can vary from person to person, but these are some of the most common ones.

Suitable Lifestyle for People with Spinocerebellar Ataxia Type 21

Suitable lifestyle options for people with Spinocerebellar ataxia type 21 include the following:

1. Stay physically active: This disease affects the coordination and balance of the body, so patients should try to stay physically active to help maintain body functions.

2. Avoid excessive fatigue: Spinocerebellar ataxia type 21 is a hereditary disease. Patients may already have certain physical discomforts, so excessive fatigue should be avoided to avoid aggravating symptoms.

3. Eat a reasonable diet: Patients should follow the doctor's recommendations and pay attention to a balanced and diverse diet to ensure adequate nutrition.

4. Maintain a good mental state: This disease may have an impact on the patient's emotional and mental health, so one should try to maintain a good mental state to reduce symptoms.

5. Follow the doctor's treatment recommendations: Patients should follow the doctor's treatment recommendations and take medications on time to help control disease progression.

6. Get regular physical check-ups: People suffering from this disease should get regular physical check-ups to ensure that their physical condition receives timely attention and treatment.

Other Diseases

Spinocerebellar Ataxia Type 13 Spinocerebellar Ataxia Type 40 Spinocerebellar Ataxia Type 5 Spinocerebellar Ataxia Type 23 Spinocerebellar Ataxia Type 10 Spinocerebellar Ataxia Type 12 Spinocerebellar Ataxia Type 38 Spinocerebellar Ataxia Type 3 Spinocerebellar Ataxia Type 17 Spinocerebellar Ataxia Type 8

Related Products