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NDUFAF6 Gene Leigh Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about neurological symptoms in your child? The NDUFAF6 Gene Leigh Syndrome NGS Genetic DNA Test provides the clarity you need. For only ZAR 6,700 (regularly ZAR 9,350), this advanced genetic test offers early detection of this rare mitochondrial disorder that affects the nervous system. Using cutting-edge Next Generation Sequencing technology, we deliver highly accurate results within 3-4 weeks. Our test is particularly crucial for families with a history of developmental delays, muscle weakness, or neurological symptoms in children. Early diagnosis can help guide treatment decisions and provide peace of mind. With genetic counselling included and nationwide coverage across South Africa, including Johannesburg, Cape Town, Durban and Pretoria, we make this essential testing accessible and trustworthy for every 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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NDUFAF6 Leigh Syndrome DNA Test | ZAR 6
NDUFAF6 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 Your Child’s Neurological Health

When your child shows unexplained neurological symptoms, the uncertainty can be overwhelming. The NDUFAF6 Gene Leigh Syndrome test provides the answers you need to move forward with confidence and understanding. This rare mitochondrial disorder affects the nervous system, and early detection through our advanced genetic testing can make a significant difference in managing your child’s health journey.

Understanding the NDUFAF6 Leigh Syndrome Test

Leigh syndrome is a severe neurological disorder that typically appears in infancy or early childhood, affecting the central nervous system. The NDUFAF6 gene plays a crucial role in mitochondrial function, and mutations in this gene can lead to progressive neurological deterioration. Our Next Generation Sequencing (NGS) technology examines this specific gene with exceptional accuracy, providing definitive answers about whether your child carries this genetic mutation.

This isn’t just a test – it’s a pathway to understanding. By identifying the specific genetic cause of neurological symptoms, families can make informed decisions about care, treatment, and future planning.

Who Should Consider This Test?

This test is particularly important if your child or family member shows:

  • Unexplained developmental delays or regression
  • Muscle weakness or poor muscle tone
  • Movement disorders or coordination problems
  • Vision or hearing problems
  • Breathing difficulties
  • Seizures or epilepsy
  • Family history of similar neurological conditions

If you’ve been searching for answers to these concerning symptoms, this test could provide the clarity you’ve been seeking.

Why Early Detection Matters for Your Family

Getting a definitive diagnosis through genetic testing offers multiple benefits:

  • Peace of Mind: End the uncertainty and know exactly what you’re dealing with
  • Targeted Treatment: Guide medical decisions and potential interventions
  • Family Planning: Understand inheritance patterns for future children
  • Support Access: Connect with appropriate medical specialists and support groups
  • Proactive Management: Monitor and manage symptoms more effectively

Early diagnosis can significantly impact the quality of life and management strategies for affected individuals.

Understanding Your Results – We’re Here to Help

Receiving genetic test results can feel overwhelming, which is why we include comprehensive genetic counselling with every test. Our certified genetic counsellors will:

  • Explain your results in clear, understandable language
  • Discuss what the findings mean for your child’s health
  • Guide you through next steps and available resources
  • Help you understand inheritance patterns and family implications
  • Connect you with appropriate medical specialists

You won’t face this journey alone – we provide the support and guidance you need every step of the way.

Transparent Pricing – Investing in Your Family’s Health

Service Regular Price Special Price Savings
NDUFAF6 Leigh Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included:

  • Comprehensive NGS genetic analysis
  • Genetic counselling session
  • Family pedigree chart creation
  • Detailed results interpretation
  • Ongoing support and guidance

Considering the cost of ongoing specialist visits and diagnostic uncertainty, this test represents excellent value for gaining definitive answers.

Why Trust Oracle Genomics?

We understand that genetic testing requires absolute confidence in accuracy and professionalism:

  • Nationwide Coverage: Accessible testing across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
  • Expert Team: Working with leading neurologists and genetic specialists
  • Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
  • Fast Turnaround: Results typically within 3-4 weeks
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Comprehensive Support: From initial consultation through results interpretation

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s neurological health continue. Every day without answers can mean delayed interventions and increased anxiety.

Book your test now and get:

  • Definitive answers about NDUFAF6 Leigh Syndrome
  • Professional genetic counselling included
  • Special pricing of ZAR 6,700 (save ZAR 2,650)
  • Nationwide accessibility
  • Peace of mind for your family’s future

Contact us today to schedule your genetic counselling session and begin the journey toward understanding your child’s health. Our compassionate team is ready to support you through this important process.

Call now or book online – your family’s health journey deserves clarity and confidence.