SCA2 Spinocerebellar Ataxia ATXN2 Gene Mutation Test
Introduction
The SCA2 Spinocerebellar Ataxia ATXN2 Gene Mutation Test is a vital diagnostic tool for individuals at risk of hereditary ataxia, a condition characterized by progressive loss of coordination and balance. This test analyzes the ATXN2 gene for mutations that may lead to this debilitating neurologic disorder. Understanding your genetic predisposition can empower you to make informed health decisions.
What the Test Measures
This test specifically measures mutations in the ATXN2 gene, which are associated with Spinocerebellar Ataxia type 2 (SCA2). By identifying these mutations, healthcare providers can assess the likelihood of developing ataxia and tailor management plans accordingly.
Who Should Consider This Test?
Individuals who may benefit from the SCA2 test include:
- Those with a family history of ataxia or other neurologic disorders.
- Patients exhibiting symptoms such as unsteady gait, difficulty with fine motor skills, or coordination issues.
- Individuals seeking clarity regarding their genetic risk factors.
Benefits of Taking the Test
Taking the SCA2 Spinocerebellar Ataxia ATXN2 Gene Mutation Test offers several advantages:
- Early detection and diagnosis of potential neurologic disorders.
- Informed decision-making regarding lifestyle and healthcare management.
- Access to genetic counseling and support resources.
- Peace of mind for individuals with a family history of the condition.
Understanding Your Results
Results from the SCA2 test will indicate whether a mutation in the ATXN2 gene is present. A positive result suggests a higher risk of developing SCA2, while a negative result may provide reassurance. It is important to discuss your results with a healthcare provider for a comprehensive understanding and to explore potential next steps.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SCA2 Spinocerebellar Ataxia ATXN2 Gene Mutation Test | 98,500 NGN | 125,000 NGN |
Booking the Test
To schedule your SCA2 Spinocerebellar Ataxia ATXN2 Gene Mutation Test, please contact us at +2348077798758. Ensure you have the duly filled Genomics Clinical Information Requisition Form (Form 20) ready, as it is mandatory for processing your test.
Test Parameters
- Turnaround Time: Sample Tuesday by 11 am; Report Saturday
- Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
- Method: PCR, Fragment analysis
- Specialty: Neurologist
- Department: Molecular Diagnostics
- Disease Type: Neurologic Disorder – Ataxia
