SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test
Introduction
The SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test is a specialized diagnostic test that plays a crucial role in identifying mutations in the ATXN3 gene. This gene is associated with spinocerebellar ataxia type 3 (SCA3), a progressive neurological disorder that affects coordination and balance. Understanding the genetic basis of this condition is essential for proper diagnosis and management.
What the Test Measures
This test specifically detects mutations in the ATXN3 gene, which are responsible for SCA3. By analyzing the genetic material in a blood sample, healthcare providers can determine if a patient carries the mutation, aiding in the diagnosis of this neurological disorder.
Who Should Consider This Test
Individuals who exhibit symptoms such as:
- Loss of coordination
- Difficulty with balance
- Uncontrolled movements
- Muscle stiffness or weakness
should consider this test. Additionally, those with a family history of SCA3 or related neurological disorders may also benefit from testing.
Benefits of Taking the Test
- Early diagnosis of SCA3 can lead to better management strategies.
- Understanding your genetic risk can inform family planning decisions.
- Access to appropriate support and resources for managing symptoms.
Understanding Your Results
Your test results will indicate whether or not mutations in the ATXN3 gene are present. A positive result may confirm the diagnosis of SCA3, while a negative result can provide reassurance. It is essential to discuss your results with a healthcare provider for appropriate interpretation and guidance.
Test Pricing
| Test Name | Discount Price (KSh) | Regular Price (KSh) |
|---|---|---|
| SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test | 8000 | 15000 |
Sample Collection and Instructions
For the SCA3 test, a sample of 4 mL (2 mL min.) whole blood is required, collected in a Lavender top (EDTA) tube. The sample should be shipped refrigerated and must not be frozen. A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for processing.
Branches and Booking
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu, making it convenient for you to access our services. To book the SCA3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test, please call or WhatsApp us at +254711564616.
Take charge of your neurological health today with our reliable and efficient testing services!
