Charlevoix-Saguenay spastic ataxia

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy.

Also known as: ARSACS, Charlevoix-Saguenay spastic ataxia, SPAX6, autosomal recessive spastic ataxia type 6, autosomal recessive spastic ataxia of Charlevoix-Saguenay, sacs, spastic ataxia 6, autosomal recessive, spastic ataxia Charlevoix-Saguenay type

19 clinical trials for this condition and its sub-types, 1 tagged with Charlevoix-Saguenay spastic ataxia itself.