Abstract
Spinocerebellar ataxia 6 (SCA6) is a rather rare neurodegenerative disorder, one of autosomal dominant spinocerebelar ataxias. It is caused by expansion of unstable CAG triplet repeats in the gene responsible for the voltage-dependent calcium channel mapped to the chromosome 19.
The disease is characterized by progressive paleo- and neocerebellar symptomatology. The onset of the disease is typically in middle- and older-age.
The authors describe a case of 62-year-old women with sudden development of gait deterioration. This was fi rst diagnosed as a post-ischemic stroke state.
However, clinical symptoms progressed into gait ataxia. No analogical case was found in family history.
Genetic testing, performed after all other potential causes of the condition were excluded, indicated SCA6. Our case report emphasises the importance of considering rare conditions as part of diff erential diagnosis.
In this case, this protected the patient from further diagnostic testing as well as, importantly, enabled predictive testing in relatives in risk.