SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test
Introduction
The SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test is a vital diagnostic tool used to identify mutations in the ATXN8OS and ATXN8 genes, which are associated with Spinocerebellar Ataxia type 8 (SCA8). This neurological disorder leads to progressive loss of coordination and balance, significantly impacting the quality of life.
What the Test Measures
This test detects specific genetic mutations, including:
- ATXN8OS CTG Repeat
- ATXN8 CAG Repeat
By analyzing these genetic markers, healthcare providers can assess an individual’s risk of developing this disorder.
Who Should Consider This Test
This test is recommended for individuals who:
- Exhibit symptoms such as unsteady gait, difficulty with fine motor skills, or slurred speech.
- Have a family history of Spinocerebellar Ataxia or related neurological disorders.
- Are experiencing unexplained neurological symptoms.
Benefits of Taking the Test
Understanding your genetic predisposition through the SCA8 test can provide numerous benefits:
- Early detection of potential neurological disorders.
- Informed decision-making regarding lifestyle and health management.
- Guidance for family planning and genetic counseling.
Understanding Your Results
Once the test is complete, your results will indicate whether any mutations were detected. It is essential to discuss these results with your healthcare provider, who can help interpret them in the context of your overall health and family history.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test | 150,000 NGN | 300,000 NGN |
How to Book the Test
To book the SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test, please contact us at +2348077798758. Our team is ready to assist you in scheduling your appointment and guiding you through the process.
Additional Information
Turnaround time for results is typically from sample collection on Tuesday by 11 am, with reports available by Saturday. The test requires a sample of 4 mL (2 mL minimum) of whole blood in a Lavender top (EDTA) tube, which should be shipped refrigerated and not frozen. A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory before testing.
For further inquiries or assistance, feel free to reach out to our dedicated staff. We are here to provide you with the best diagnostic services in Nigeria.
