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NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about neurological symptoms or family history of Leigh syndrome? Our NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test provides the clarity you need for just ZAR 6,700. This advanced genetic test uses cutting-edge NGS technology to detect mutations in the NDUFA10 gene, which can cause this serious mitochondrial disorder. Early detection through our accurate testing can help guide treatment decisions and provide peace of mind for families across South Africa. Our comprehensive approach includes genetic counselling to understand your family history, ensuring you receive personalised care and support. With results delivered within 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, Durban and Pretoria, we make advanced genetic testing accessible and trustworthy for every South African family.

📞 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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NDUFA10 Leigh Syndrome DNA Test | ZAR 6
NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity for Neurological Health Concerns with NDUFA10 Leigh Syndrome Testing

When you’re worried about unexplained neurological symptoms or have a family history of Leigh syndrome, the uncertainty can be overwhelming. Our NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test provides the answers you need to move forward with confidence. For just ZAR 6,700 (regularly ZAR 9,350), you can access cutting-edge genetic testing that brings clarity to complex neurological conditions.

Understanding the NDUFA10 Leigh Syndrome Test

The NDUFA10 gene plays a crucial role in mitochondrial function, and mutations in this gene can lead to Leigh syndrome – a serious neurological disorder that typically appears in infancy or early childhood. Our Next-Generation Sequencing (NGS) technology examines your DNA with exceptional precision, identifying even the smallest genetic variations that could indicate this condition.

This isn’t just another test – it’s a comprehensive diagnostic journey that includes genetic counselling to map your family history, ensuring we understand your unique situation completely.

Who Should Consider This Test?

If you or your child experience any of these symptoms, this test could provide crucial answers:

  • Unexplained developmental delays or regression
  • Muscle weakness or movement difficulties
  • Breathing problems or feeding difficulties in infants
  • Seizures or episodes of lactic acidosis
  • Family history of mitochondrial disorders
  • Unexplained neurological symptoms in multiple family members

Many South African families have found peace of mind through early detection, allowing for better management of symptoms and informed family planning decisions.

Why Early Detection Matters for Your Family’s Health

Getting answers early can transform your approach to neurological health:

  • Guided Treatment: Accurate diagnosis helps healthcare providers develop targeted treatment plans
  • Family Planning: Understand inheritance patterns for informed reproductive decisions
  • Peace of Mind: Replace uncertainty with clear understanding of your genetic health
  • Proactive Management: Early intervention can help manage symptoms more effectively
  • Reduced Healthcare Costs: Avoid unnecessary tests and treatments through accurate diagnosis

Understanding Your Results with Compassion

We know waiting for genetic test results can be anxiety-provoking. That’s why we provide:

  • Clear Explanations: Results are explained in understandable language
  • Genetic Counselling Support: Professional guidance to help you understand implications
  • Next Steps Guidance: Clear recommendations for follow-up care
  • Family Support Resources: Connections to support networks and specialists

Your results will be available within 3-4 weeks, and our team will be there to support you every step of the way.

Affordable, Accessible Genetic Testing for South Africans

Test Option Regular Price Special Price Savings
NDUFA10 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 One drop Blood on FTA Card
  • Preparation: Clinical history and genetic counselling session required
  • Method: Next-Generation Sequencing (NGS) Technology

Why Trust Oracle Genomics?

We’re committed to making advanced genetic testing accessible to all South Africans:

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Specialised neurological genetics testing supervised by experts
  • Accuracy Guarantee: State-of-the-art NGS technology ensures reliable results
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Track Record: Trusted by healthcare providers and families nationwide

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about neurological health hold you back. Early detection through our NDUFA10 Leigh Syndrome test can provide the answers you need to make informed health decisions.

Book your test now and save ZAR 2,650 off the regular price!



Limited time special pricing available. Contact us today to secure your discounted rate and take control of your genetic health journey.