SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test
Introduction to the SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test
The SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test is a vital diagnostic tool that helps identify mutations in the ATXN3 gene, which can lead to the development of spinocerebellar ataxia type 3 (SCA3), a hereditary neurodegenerative disorder. Understanding your genetic makeup is crucial for determining your risk factors and managing potential symptoms effectively.
What the Test Measures
This test specifically detects mutations in the ATXN3 gene, which plays a significant role in the development of SCA3. By analyzing your DNA, we can identify any abnormalities that may indicate a predisposition to this neurologic disorder.
Who Should Consider This Test?
This test is recommended for individuals who:
- Have a family history of spinocerebellar ataxia or related disorders.
- Exhibit symptoms such as balance issues, coordination problems, or unexplained neurological symptoms.
- Are at risk due to genetic factors and want to understand their potential health implications.
Benefits of Taking the Test
Taking the SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test provides several benefits:
- Early identification of genetic predisposition to SCA3, allowing for proactive health management.
- Informed decision-making regarding lifestyle and health interventions.
- Access to genetic counseling and support for affected individuals and their families.
Understanding Your Results
Once the test is completed, you will receive a comprehensive report detailing the findings. It is essential to discuss your results with a qualified healthcare professional, such as a neurologist, who can help interpret the data and guide you on the next steps.
Test Pricing
Discount Price | Regular Price |
---|---|
80,000 NGN | 150,000 NGN |
Booking Information
To book the SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and any inquiries you may have.
Test Details
- Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
- Test Components: ATXN3 Gene
- Method: PCR, Fragment analysis
- Department: Molecular Diagnostics
- Specialty: Neurologist
- Turnaround Time: Sample Tue by 11 am; Report Sat
- Pre-Test Instructions: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.