Spinocerebellar ataxia

Spinocerebellar ataxia (SCA) is a group of hereditary ataxias that are characterized by progressive problems with movement. SCA symptoms can vary depending on the specific type and severity of the condition, but they generally involve progressive issues with movement and coordination.

Our research in SCA is focused on establishing the clinical validity of using wearable sensors for objective assessment of disease symptoms in different types of CMT disease.