Ataxia panel is used to identify genetic variants associated with ataxia, a group of rare inherited disorders that affect coordination and balance. This panel tests for genetic variants in genes that are important for the function of the cerebellum, a part of the brain that is involved in motor coordination and balance.
This panel is designed for individuals with a family history of ataxia or for those who have symptoms of the condition, such as gait abnormalities, tremors, and difficulty with fine motor tasks. Early diagnosis through genetic testing can help inform treatment and management decisions, including physical and occupational therapy, assistive devices, and monitoring for complications. It can also inform family planning decisions and provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 8 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
Questo prodotto è destinato esclusivamente ai clienti che hanno già acquistato un test MyGenome