SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test
Introduction
The SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test is a vital diagnostic tool for assessing genetic mutations associated with spinocerebellar ataxia type 8 (SCA8). This test is particularly significant as it aids in the identification of individuals at risk for developing this neurological disorder, allowing for early medical intervention and management strategies.
What the Test Measures
This test specifically measures the presence of mutations in two key components: ATXN8OS CTG Repeat and ATXN8 CAG Repeat. These mutations are linked to the development of SCA8, a condition characterized by progressive loss of coordination and balance.
Who Should Consider This Test
Individuals who exhibit symptoms such as:
- Unexplained balance issues
- Difficulty coordinating movements
- Family history of ataxia or other neurological disorders
- Neurological symptoms that are unexplained by other conditions
should consider undergoing this test. Additionally, those with risk factors for genetic disorders may benefit from testing.
Benefits of Taking the Test
- Early detection of genetic mutations associated with SCA8.
- Informed decision-making regarding treatment and management.
- Access to genetic counseling and support resources.
- Peace of mind for patients and families regarding their health status.
Understanding Your Results
Results from the SCA8 test will indicate whether the ATXN8OS and ATXN8 gene mutations are present. A positive result may suggest a higher risk for developing SCA8, while a negative result may provide reassurance. It is essential to discuss results with a healthcare provider to understand their implications fully.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test | 15,000 KSh | 30,000 KSh |
Sample Collection and Instructions
The sample type required for this test is 4 mL (2 mL min.) whole blood collected in a 1 Lavender top (EDTA) tube. It is crucial to ship the sample refrigerated and not to freeze it. Additionally, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for processing.
Branches and Booking
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. To book the SCA8 Spinocerebellar Ataxia ATXN8OS ATXN8 Gene Mutation Test, please call or WhatsApp us at +254711564616.
Take charge of your health today by booking your test!
