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ATXN8OS Gene Spinocerebellar Ataxia Type 8 Autosomal Dominant NGS Genetic DNA Test

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

-28%

Facing concerns about neurological conditions or family history of movement disorders? Our ATXN8OS Gene Spinocerebellar Ataxia Type 8 test provides the clarity you need. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive genetic test uses advanced NGS technology to detect autosomal dominant inheritance patterns. We understand the anxiety that comes with potential genetic conditions, which is why we include professional genetic counselling to help you understand your family history and results. Early detection can make a significant difference in managing symptoms and planning for the future. Our test is designed with South African patients in mind, offering nationwide coverage and results you can trust within 3-4 weeks. Take control of your neurological health today with confidence and professional support.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

ATXN8OS Gene SCA8 Test | ZAR 6
ATXN8OS Gene Spinocerebellar Ataxia Type 8 Autosomal Dominant NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Your Neurological Health with ATXN8OS Gene Testing

When movement difficulties, coordination problems, or family history of neurological conditions create uncertainty in your life, having clear answers becomes essential. We understand the emotional weight of wondering about genetic conditions that could affect your mobility and quality of life. Our ATXN8OS Gene Spinocerebellar Ataxia Type 8 test provides the definitive answers you need to plan for your health future with confidence.

Understanding Your ATXN8OS Gene Test

This specialised genetic test examines the ATXN8OS gene for mutations that cause Spinocerebellar Ataxia Type 8, a progressive neurological condition that affects coordination and movement. Using Next-Generation Sequencing (NGS) technology, we provide the most accurate analysis available, giving you reliable results you can trust for making important health decisions.

The test follows an autosomal dominant inheritance pattern, meaning if one parent carries the gene mutation, there’s a 50% chance of passing it to each child. Understanding this pattern helps you make informed choices about family planning and early intervention.

Who Should Consider This Important Genetic Test?

This test is particularly important if you experience:

  • Progressive coordination difficulties or balance problems
  • Family history of movement disorders or ataxia
  • Speech difficulties that have developed over time
  • Eye movement abnormalities or vision coordination issues
  • Concerns about passing genetic conditions to children
  • Unexplained neurological symptoms affecting daily activities

Many South Africans with European ancestry may have increased risk factors, making early detection particularly valuable for our diverse population.

Why Early Detection Matters for Your Health Journey

Getting tested provides more than just answers – it gives you the power to take control of your health:

  • Peace of Mind: Eliminate uncertainty about your genetic status
  • Early Intervention: Begin appropriate management strategies sooner
  • Family Planning: Make informed decisions about having children
  • Treatment Planning: Work with neurologists to create personalised care plans
  • Psychological Relief: Reduce the stress of not knowing

Understanding Your Results with Professional Support

We know that receiving genetic test results can be emotionally challenging. That’s why every test includes comprehensive genetic counselling to help you understand what your results mean for you and your family. Our genetic counsellors will:

  • Explain your results in clear, understandable language
  • Discuss implications for family members
  • Help create a pedigree chart of affected relatives
  • Provide resources and next-step recommendations
  • Connect you with appropriate neurological specialists

You’ll never face your results alone – we’re here to support you every step of the way.

Transparent Pricing – Exceptional Value for Your Health

Service Regular Price Special Price Savings
ATXN8OS Gene Test with Genetic Counselling ZAR 9,350 ZAR 6,700 ZAR 2,650

Includes: Comprehensive genetic analysis, genetic counselling session, detailed results report, and professional interpretation

Why South Africans Trust Oracle Genomics

Nationwide Coverage

Convenient testing available throughout South Africa, including Johannesburg, Cape Town, Durban, and Pretoria

Expert Genetic Team

Our specialised neurologists and genetic counsellors provide professional guidance tailored to South African patients

Advanced Technology

Using NGS technology for the most accurate and reliable genetic analysis available

Quick Turnaround

Receive your comprehensive results within 3-4 weeks, allowing for timely health decisions

Simple Testing Process

We make genetic testing straightforward and comfortable:

  • Sample Options: Blood draw, extracted DNA, or simple finger-prick blood spot on FTA card
  • Preparation: Bring your clinical history and be ready to discuss family medical background
  • Genetic Counselling: Included session to create your family pedigree chart
  • Professional Support: Ongoing access to our neurological genetics team

Take the First Step Toward Neurological Health Clarity

Don’t let uncertainty about genetic conditions control your future. With our special pricing of ZAR 6,700 and comprehensive support services, there’s never been a better time to get the answers you deserve.

Limited time special pricing – secure your test while savings last!

Available at our centres in Johannesburg, Cape Town, Durban, Pretoria and nationwide locations.