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AFG3L2 Gene Spinocerebellar Ataxia Type 28 Autosomal Dominant NGS Genetic DNA Test

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

-28%

Facing concerns about hereditary neurological conditions? Our AFG3L2 gene test provides definitive answers about spinocerebellar ataxia type 28, an autosomal dominant condition that can affect multiple generations. For just ZAR 6,700 (special price from ZAR 9,350), you gain access to cutting-edge NGS technology that delivers 99.9% accuracy in detecting this hereditary condition. Many South African families live with uncertainty about their genetic health – our test offers clarity and peace of mind. Early detection through genetic testing can help you make informed health decisions and potentially slow disease progression. With nationwide coverage including Johannesburg, Cape Town, Durban, and Pretoria, professional genetic counselling is included to help you understand your family’s health patterns. Take control of your neurological health today with our trusted, comprehensive genetic analysis.

📞 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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AFG3L2 Gene Test ZAR 6
AFG3L2 Gene Spinocerebellar Ataxia Type 28 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 Hereditary Neurological Conditions

When neurological symptoms run in your family, the uncertainty can be overwhelming. Our AFG3L2 gene test provides the answers you need about spinocerebellar ataxia type 28 – a condition that can affect coordination, balance, and movement across generations. Many South African families have lived with unanswered questions about their genetic health for years. Today, you can take the first step toward understanding your family’s neurological patterns and making informed health decisions.

Understanding Your AFG3L2 Gene Test

This specialised genetic test examines the AFG3L2 gene using Next Generation Sequencing (NGS) technology to identify mutations associated with spinocerebellar ataxia type 28. This is an autosomal dominant condition, meaning if one parent carries the gene mutation, there’s a 50% chance their children could inherit it. Our test provides 99.9% accuracy in detecting these genetic variations, giving you reliable information about your neurological health inheritance patterns.

Who Should Consider This Genetic Test?

This test is particularly important if you or your family members experience:

  • Progressive coordination difficulties and balance problems
  • Family history of similar neurological symptoms across generations
  • Unsteady gait or difficulty with fine motor skills
  • Speech changes or swallowing difficulties
  • Eye movement abnormalities
  • Concerns about passing neurological conditions to children

If multiple family members show similar symptoms, genetic testing can provide crucial insights into your family’s health patterns.

Why Early Genetic Detection Matters for Your Health

Understanding your genetic status empowers you to:

  • Make informed family planning decisions
  • Access appropriate neurological care and monitoring
  • Participate in clinical trials and emerging treatments
  • Reduce anxiety through definitive answers
  • Create personalised health management plans
  • Connect with support communities and resources

Early detection through genetic testing can significantly impact your quality of life and healthcare journey.

Understanding Your Test Results

We know waiting for genetic results can be anxiety-provoking. Our comprehensive approach includes:

  • Clear, understandable reports written in plain language
  • Professional genetic counselling session to explain your results
  • Family pedigree analysis to understand inheritance patterns
  • Personalised recommendations based on your specific results
  • Ongoing support and connection to neurological specialists

Whether your results are positive or negative, you’ll receive the guidance and support needed to make the best decisions for your health.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
AFG3L2 Gene Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive genetic analysis, professional genetic counselling, family pedigree chart creation, detailed results interpretation, and ongoing support access.

Consider the long-term value: Early detection can lead to better health outcomes and potentially reduce future healthcare costs.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Specialised neurological genetic testing with neurologist oversight
  • Cutting-Edge Technology: NGS technology ensuring 99.9% accuracy
  • Comprehensive Support: Genetic counselling and family history analysis included
  • Proven Track Record: Trusted by South African families for genetic health insights
  • Clear Communication: Results explained in understandable terms with ongoing support

Take Control of Your Neurological Health Today

Don’t let uncertainty about hereditary conditions control your family’s future. With results in just 3-4 weeks and nationwide accessibility, there’s no reason to delay getting the answers you deserve.

Book Your Test Now

Secure your special pricing of ZAR 6,700 while available. Limited appointments for comprehensive genetic counselling.

Speak With Our Team

Have questions? Our genetic specialists are available to discuss your concerns and guide you through the process.

Limited Time Special Pricing

Save ZAR 2,650 on your genetic testing. This special offer won’t last – secure your family’s health clarity today.

Ready to begin? Simply provide a blood sample and your clinical history. We’ll handle the genetic counselling session and create your family pedigree chart to ensure comprehensive analysis.