| CANVAS | |
|---|---|
 | |
| Cerebellum and brainstem | |
| Specialty | Neurology |
| Symptoms | Difficulty walking. Poor coordination. Decreased sensation. Chronic cough. Dysphagia. |
| Usual onset | 40–60 years old |
| Duration | Long term |
| Causes | Genetic (inherited or new mutation) |
| Diagnostic method | Genetic testing |
| Treatment | Supportive care |
| Medication | Not available |
| Frequency | Unknown |
Cerebellar Ataxia with Neuropathy and Vestibular Areflexia Syndrome (CANVAS) is an autosomal recessive late-onset heredodegenerative multisystem neurological disease. The symptoms include poor balance and difficulty walking. Chronic cough and difficulty swallowing may also be present. Clinical findings include ataxia, sensory neuropathy, and absence of the vestibulo–ocular reflex. The syndrome was initially described in 2004. In 2019, the cause was identified as biallelic pentanucleotide expansion in the RFC1 gene.
Epidemiology
The prevalence of the disease is currently unknown, largely owing to its recent description and delineation from other forms of autosomal recessive cerebellar ataxia.
Prognosis and treatment
Specific treatment is lacking. A multidisciplinary approach to supportive care is recommended. The progression is typically slow, with 55% of patients needing mobility aids 10 years after onset, and 25% needing a wheelchair after 15 years.