SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test
Introduction
The SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test is a vital diagnostic tool for identifying genetic mutations associated with spinocerebellar ataxia (SCA), a neurological disorder characterized by progressive loss of coordination and balance. Understanding your genetic predisposition through this test can lead to early interventions and tailored management strategies.
What the Test Measures
This test specifically detects mutations in the PDYN gene, which are linked to the development of SCA23. By analyzing your DNA, we can determine if you carry these mutations, which may contribute to the onset of this disorder.
Who Should Consider This Test?
Individuals who experience symptoms such as:
- Unexplained loss of coordination
- Difficulty with balance
- Slurred speech
- Family history of ataxia
are encouraged to consider this test. Additionally, those with risk factors for neurologic disorders should consult their healthcare provider about the benefits of genetic testing.
Benefits of Taking the Test
- Early diagnosis of potential genetic disorders.
- Informed decision-making regarding treatment options.
- Access to genetic counseling for affected individuals and families.
- Understanding your risks can help in lifestyle and healthcare planning.
Understanding Your Results
Results from the SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test will indicate whether a mutation is present. A positive result suggests a higher risk for developing ataxia, while a negative result may provide reassurance. It is essential to discuss your results with a healthcare professional to understand their implications fully.
Test Pricing
Price Type | Price (KSh) |
---|---|
Discount Price | 15,000 |
Regular Price | 30,000 |
How to Book the Test
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu, to make it easy for you to access our services. To book the SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test, please contact us at +254711564616 or visit our website to schedule your appointment.
Test Details
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. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Components: PDYN Gene
Pre-Test Instructions: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Specialty: Neurologist | Department: Molecular Diagnostics | Method: PCR, Sequencing | Disease Type: Neurologic Disorder – Ataxia
Take control of your health today by understanding your genetic risks. Book the SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test now!