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NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test

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

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Facing concerns about neurological symptoms in your child? The NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test provides definitive answers for families seeking clarity about this rare mitochondrial disorder. For only ZAR 6,700 (regularly ZAR 9,350), our advanced Next Generation Sequencing technology delivers highly accurate results that can guide treatment decisions and provide peace of mind. This comprehensive test specifically examines the NDUFS3 gene mutations responsible for Leigh syndrome, helping South African families understand inherited risks and make informed healthcare choices. With results available within 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, Durban and Pretoria, you can trust Oracle Genomics for professional, compassionate genetic testing services backed by neurological expertise.

📞 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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NDUFS3 Leigh Syndrome DNA Test | ZAR 6
NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding NDUFS3 Leigh Syndrome: Your Path to Clarity and Peace of Mind

When your child shows neurological symptoms or developmental delays, the uncertainty can be overwhelming. The NDUFS3 Gene Leigh Syndrome Genetic Test provides the definitive answers you need to understand this rare mitochondrial disorder and make informed decisions about your family’s health journey.

What This Test Reveals About Your Health

The NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test uses advanced Next Generation Sequencing technology to examine the NDUFS3 gene for mutations that cause Leigh syndrome. This comprehensive analysis helps identify inherited patterns and provides crucial information for managing this progressive neurological condition that primarily affects infants and young children.

Our test specifically targets the genetic variations responsible for mitochondrial complex I deficiency, giving you and your healthcare team the precise information needed to develop appropriate care strategies.

Is This Test Right for Your Family?

Consider the NDUFS3 Leigh Syndrome Genetic Test if your child experiences:

  • Developmental regression or loss of motor skills
  • Muscle weakness or poor muscle tone
  • Movement disorders or coordination difficulties
  • Breathing problems or respiratory issues
  • Feeding difficulties and failure to thrive
  • Family history of mitochondrial disorders
  • Unexplained neurological symptoms in early childhood

Early genetic testing can provide clarity when symptoms suggest possible Leigh syndrome, helping you avoid diagnostic uncertainty and delays in appropriate care.

Why Early Detection Matters for Your Child’s Future

Getting definitive answers through genetic testing provides multiple life-changing benefits:

  • Accurate Diagnosis: Move beyond symptom management to understanding the root cause of neurological concerns
  • Informed Treatment Planning: Work with neurologists to develop targeted care strategies
  • Family Planning Guidance: Understand inheritance patterns for future family decisions
  • Reduced Diagnostic Uncertainty: End the emotional toll of not knowing what’s affecting your child
  • Early Intervention Opportunities: Access appropriate therapies and support services sooner

Understanding Your Results with Compassionate Support

Receiving genetic test results can feel overwhelming, which is why we provide comprehensive support throughout the process. Your results will clearly indicate whether NDUFS3 gene mutations are present and what this means for your family’s health.

We include genetic counselling sessions to help you understand the implications of your results and connect you with appropriate neurological specialists across South Africa. Our team ensures you never feel alone in interpreting this important health information.

Transparent Pricing for Peace of Mind

Service Regular Price Special Price Savings
NDUFS3 Leigh Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Test Details:

  • Turnaround Time: 3-4 Weeks
  • Sample Type: Blood, Extracted DNA, or Blood on FTA Card
  • Includes Genetic Counselling Session
  • Specialist: Neurological Genetics

Considering the potential savings from avoiding unnecessary treatments and getting early intervention, this test represents excellent value for your family’s health investment.

Why South African Families Trust Oracle Genomics

With nationwide coverage including Johannesburg, Cape Town, Durban, and Pretoria, we bring expert genetic testing services to communities across South Africa. Our commitment to accuracy, patient empathy, and professional excellence ensures you receive the highest quality care.

We understand the emotional journey of genetic testing and provide compassionate support every step of the way, from initial consultation through result interpretation and specialist referrals.

Take the First Step Toward Clarity Today

Don’t let uncertainty about neurological symptoms continue to cause anxiety. The NDUFS3 Leigh Syndrome Genetic Test provides the answers you need to move forward with confidence.

Book your test now and receive:

  • Comprehensive NGS genetic analysis
  • Professional genetic counselling session
  • Clear, understandable results interpretation
  • Nationwide accessibility across South Africa
  • Special pricing of ZAR 6,700 (save ZAR 2,650)

Contact Oracle Genomics today to schedule your consultation and take control of your family’s genetic health journey.