Overview Of Spinocerebellar Ataxia Symptoms

Spinocerebellar ataxia is a genetic disease. The most common type is SCA3. The gene mutations that cause it are passed from parent to child. Thankfully, many individuals with these do not show symptoms, though they can appear at any point. Of course, the signs vary between types. In most cases, they affect physical movement, learning, and vision.

A spinocerebellar ataxia cure does not exist. However, patients have hope! There are many options for spinocerebellar ataxia treatment available to patients. Physical therapy for SCA is quite common. Many patients also use assistive devices for spinocerebellar ataxia!