Spinocerebellar Ataxia
Also known as: Hereditary Ataxia
Description
Spinocerebellar Ataxia is the most common hereditary form of Ataxia. Its onset occurs during middle to late childhood. The major pathological changes are found in the posterior columns of the Spinal Cord.
These Substances Alleviate Spinocerebellar Ataxia
Quinones
Spinocerebellar Ataxia patients have been found to have abnormally low levels of Coenzyme Q10 and supplemental Coenzyme Q10 may reduce Muscle Weakness and may increase walking ability in Spinocerebellar Ataxia patients. [1]
You have read 54% of this topic
Keep reading Spinocerebellar Ataxia
- Spinocerebellar Ataxia may Cause these Ailments (Symptoms)
- Musculoskeletal System
- Nervous System
- Type of Spinocerebellar Ataxia
- Every cited reference behind this topic
- All 5,000+ interlinked topics, search and notes
No credit card needed to start a trial. Already a member? Log in