CACNA1A
Spinocerebellar Ataxia Type 6 Expansion Analysis
Spinocerebellar Ataxia Type 6 Expansion Analysis
The Spinocerebellar Ataxia Type 6 Expansion Analysis is used to identify expanded CAG repeat size in the gene associated with spinocerebellar ataxia, CACNA1A. This test can also identify disease-causing variants within a family to facilitate carrier screening.
Spinocerebellar ataxia type 6
Clinical Information
Spinocerebellar ataxia type 6 is a slowly progressive form of cerebellar ataxia with initial features that include lack of coordination and balance and dysarthria. Over time, vision problems including nystagmus and double vision, dysphagia, and tremors will develop. Average age of onset is in the 40s, and the rate of progression is typically slow with a normal lifespan.
SCA6 is inherited in an autosomal dominant pattern, and it is caused by a CAG trinucleotide repeat expansion in the CACNA1A gene. Repeat ranges are as follows: Normal (≤ 18), Intermediate (19), Pathogenic (≥ 20).
Technical Information
Specimen Requirements
Transport Instructions
Connect With Our Experts
Call 1-800-473-9411 to speak with our team of laboratory genetic counselors for questions or additional information.
Robin Fletcher, MS, CGC
Falecia Thomas, MS, CGC
Alex Finley, MS, CGC
