What Are The Potential Signs Of Spinocerebellar Ataxia?

Spinocerebellar ataxia seems to be a genetic disease with many subtypes. However, the most common appears to be SCA3. The disease may be passed from parent to child. Individuals with the gene mutations that cause it may sometimes be asymptomatic. Of course, the warning signs may appear at any point. They seem to be able to worsen at any point as well. Symptoms may affect an individual's movement, vision, and learning, among other functions.