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PDYN Gene Spinocerebellar Ataxia Type 23 Autosomal Dominant NGS Genetic DNA Test

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

-28%

Facing concerns about hereditary neurological conditions? Our PDYN Gene Spinocerebellar Ataxia Type 23 test provides definitive answers about your genetic risk. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive NGS genetic test offers life-changing clarity for South African families. We understand the anxiety that comes with neurological symptoms and family history of movement disorders. Our test delivers 99.9% accuracy using advanced next-generation sequencing technology, giving you reliable results within 3-4 weeks. Every test includes professional genetic counselling to help you understand your results and make informed health decisions. Take control of your neurological health journey with confidence and peace of mind.

📞 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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PDYN SCA23 Genetic Test | ZAR 6
PDYN Gene Spinocerebellar Ataxia Type 23 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 movement difficulties, balance problems, or family history of neurological disorders create uncertainty, getting definitive answers becomes essential for your peace of mind. Our PDYN Gene Spinocerebellar Ataxia Type 23 test provides the clarity South African families need to understand their genetic health and plan for the future with confidence.

Understanding Your PDYN Gene Test

This specialised genetic test examines the PDYN gene for mutations that cause Spinocerebellar Ataxia Type 23, a hereditary neurological condition that affects coordination and movement. Using advanced Next-Generation Sequencing (NGS) technology, we provide comprehensive analysis with exceptional accuracy, giving you reliable information about your genetic risk profile.

The test is particularly important because spinocerebellar ataxias can be inherited in an autosomal dominant pattern, meaning if one parent carries the gene mutation, there’s a 50% chance of passing it to each child. Early detection through genetic testing allows for proactive health management and informed family planning decisions.

Who Should Consider This Genetic Test?

This test is recommended if you experience:

  • Progressive balance and coordination difficulties
  • Family history of movement disorders or ataxia
  • Unexplained speech changes or swallowing problems
  • Concerns about passing neurological conditions to children
  • Early symptoms of cerebellar dysfunction
  • Known PDYN gene mutations in your family

Many South Africans with these symptoms spend years seeking answers. Our test provides definitive genetic information that can end diagnostic uncertainty and guide appropriate medical care.

Why Early Detection Matters for Your Health

Getting tested for PDYN gene mutations offers significant benefits:

  • Peace of Mind: End the uncertainty about your genetic risk
  • Proactive Planning: Make informed decisions about family planning and future healthcare
  • Early Intervention: Access appropriate neurological care and management strategies
  • Family Awareness: Help relatives understand their potential risk and testing options
  • Treatment Guidance: Work with neurologists to develop personalised care plans

Early genetic testing can transform anxiety into actionable health information, empowering you to take control of your neurological wellbeing.

Understanding Your Test Results

We make understanding your genetic results straightforward and reassuring:

  • Positive Result: Indicates a PDYN gene mutation is present. Our genetic counsellors will explain what this means for your health and connect you with neurological specialists for ongoing care.
  • Negative Result: No PDYN gene mutation detected. This provides significant relief and clarity about your genetic risk profile.
  • Uncertain Variant: Rarely, we may identify genetic changes of uncertain significance. Our team provides comprehensive guidance on monitoring and next steps.

Every test includes a genetic counselling session to ensure you fully understand your results and their implications for you and your family.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
PDYN Gene SCA23 Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included: Comprehensive NGS genetic analysis, genetic counselling session, detailed results report, and professional interpretation by neurological genetics specialists.

Considering the lifelong impact of genetic information and potential healthcare savings from early detection, this test represents exceptional value for South African families.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: 99.9% accuracy using cutting-edge NGS methodology
  • Rapid Turnaround: Results within 3-4 weeks from sample collection
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Complete Preparation: Includes clinical history assessment and pedigree chart development

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about hereditary neurological conditions control your future. Our PDYN gene test provides the answers you need to make informed health decisions with confidence.

Limited Time Special: Book now to secure your ZAR 6,700 pricing (save ZAR 2,650)



Thousands of South African families have found clarity through our genetic testing services. Join them in taking control of your neurological health journey today.