SCA14 Spinocerebellar Ataxia PRKCG Gene Mutation Test
Introduction to the Test
The SCA14 Spinocerebellar Ataxia PRKCG Gene Mutation Test is a vital diagnostic tool used to identify mutations in the PRKCG gene, which is associated with the hereditary condition known as spinocerebellar ataxia. This neurological disorder affects coordination and balance, leading to significant challenges in daily activities. Early diagnosis through this test allows for better management and understanding of the condition, enabling patients and their families to make informed healthcare decisions.
What the Test Measures
This test specifically detects mutations in the PRKCG gene, which plays a crucial role in the functioning of the brain’s cerebellum. By analyzing a sample of whole blood, the test can reveal whether an individual carries genetic variations linked to SCA14, providing insight into their risk of developing this disorder.
Who Should Consider This Test?
The SCA14 Spinocerebellar Ataxia PRKCG Gene Mutation Test is recommended for individuals who exhibit symptoms of ataxia, such as:
- Unsteady gait or difficulty walking
- Coordination problems
- Speech difficulties
- Family history of spinocerebellar ataxia or related disorders
If you have risk factors or are experiencing symptoms, consulting with a neurologist about this test is crucial.
Benefits of Taking the Test
- Provides clarity on genetic predisposition to spinocerebellar ataxia.
- Facilitates early diagnosis and intervention strategies.
- Guides family planning and genetic counseling.
- Helps in the management of symptoms and overall quality of life.
Understanding Your Results
Results from the SCA14 Spinocerebellar Ataxia PRKCG Gene Mutation Test will indicate whether a mutation is present. A positive result means a higher risk of developing the disorder, while a negative result suggests no identified mutation. It’s essential to discuss your results with a healthcare provider for accurate interpretation and guidance on next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 150,000 NGN |
| Regular Price | 300,000 NGN |
Booking the Test
To schedule your SCA14 Spinocerebellar Ataxia PRKCG Gene Mutation Test, please contact us at DNA Labs Nigeria. You can reach us via phone or WhatsApp at +2348077798758. Our team is ready to assist you with the booking process and provide any additional information you may need.
Test Details
Turnaround Time: 10-12 days
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.
Method: PCR, Sequencing
Department: Molecular Diagnostics
Specialty: Neurologist
Disease Type: Neurologic Disorder – Ataxia
