Why Choose UT Southwestern for Ataxia Care?
Ataxia is a sign of dysfunction in the cerebellum – the part of the brain that controls balance and muscle coordination. It’s not a single disease but a symptom of various conditions affecting the brain and nervous system.
Our experts are fellowship-trained in movement disorders and have expertise in neurogenetics to identify and treat patients’ specific form of ataxia. We’re also active in research studies to identify novel genetic causes of ataxia and offer clinical studies to better understand and treat the disease.
Because of the complexity of ataxia, our team evaluates the most appropriate options for each patient to treat symptoms.
- In some cases, we treat the underlying causes of the disorder to improve the condition or prevent it from getting worse.
- Some ataxias, such as those caused by autoimmune disorders, can be treated with immunosuppression to improve or stabilize symptoms.
- Some ataxias are due to inherited conditions, and treatments for some genetic forms of ataxia are now available.
- Some types might be related to something as simple as a vitamin deficiency and can be treated by taking a daily supplement.