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ATXN2 Gene Spinocerebellar Ataxia Type 2 Autosomal Dominant NGS Genetic DNA Test

Original price was: R9,350.Current price is: R6,700.

-28%

Facing concerns about hereditary neurological conditions? Our ATXN2 Gene Spinocerebellar Ataxia Type 2 test provides definitive answers about your genetic risk for autosomal dominant neurological disorders. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive comprehensive testing using advanced NGS technology with 99.9% accuracy. This test is crucial for individuals with family history of movement disorders, balance problems, or coordination difficulties. Early detection allows for proactive health management and informed family planning decisions. Our nationwide service includes professional genetic counselling to help you understand your results and make empowered healthcare choices. Take control of your neurological health today with trusted, reliable genetic testing.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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ATXN2 Gene SCA2 Test | ZAR 6
ATXN2 Gene Spinocerebellar Ataxia Type 2 Autosomal Dominant NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Risk for Hereditary Neurological Conditions

If you’re worried about unexplained balance problems, coordination difficulties, or have a family history of neurological disorders, you’re not alone. Many South Africans face concerns about hereditary conditions that can affect movement and coordination. Our ATXN2 Gene Spinocerebellar Ataxia Type 2 test provides the clarity and peace of mind you deserve.

What This Test Detects

This advanced genetic test specifically identifies mutations in the ATXN2 gene that cause Spinocerebellar Ataxia Type 2 (SCA2), an autosomal dominant neurological condition. Using Next-Generation Sequencing (NGS) technology, we analyse your DNA with 99.9% accuracy to determine if you carry the genetic variations associated with this progressive movement disorder.

Who Should Consider This Test

This test is particularly important if you experience:

  • Unexplained balance problems or coordination difficulties
  • Family history of movement disorders or ataxia
  • Progressive speech difficulties or swallowing problems
  • Eye movement abnormalities or tremors
  • Planning for pregnancy with family neurological history

Why Early Detection Matters for Your Health

Early identification of SCA2 genetic risk provides significant benefits:

  • Proactive health management and monitoring
  • Informed family planning decisions
  • Access to appropriate neurological care
  • Peace of mind through definitive answers
  • Opportunity for early intervention strategies

Understanding Your Results

Your results will be clearly explained by our genetic counselling team. We provide:

  • Clear positive/negative interpretation
  • Personalised risk assessment
  • Family implications discussion
  • Next steps guidance
  • Ongoing support resources

Pricing and Value

Regular Price ZAR 9,350
Special Price ZAR 6,700
Turnaround Time 3-4 Weeks
Sample Type Blood or Extracted DNA

Nationwide Trust and Accessibility

Oracle Genomics serves patients across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and nationwide. Our neurological genetics specialists ensure you receive the highest standard of care and accurate results.

Take Control of Your Neurological Health Today

Don’t let uncertainty about hereditary conditions affect your peace of mind. Our comprehensive genetic testing provides the answers you need to make informed health decisions. Book your ATXN2 Gene SCA2 test now and take the first step toward understanding your genetic health with confidence.

Call us today or book online to schedule your genetic counselling session and testing.