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MT-ND5 Gene Leigh Syndrome Mitochondrial Complex I Deficiency NGS Genetic DNA Test

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

-28%

Facing concerns about mitochondrial disorders or unexplained neurological symptoms? Our MT-ND5 Gene Leigh Syndrome NGS Genetic DNA Test provides definitive answers for ZAR 6,700 (regularly ZAR 9,350). This comprehensive test uses advanced Next-Generation Sequencing technology to detect mutations in the MT-ND5 gene, which causes mitochondrial complex I deficiency leading to Leigh syndrome. Early detection through genetic testing can help guide treatment decisions, provide family planning insights, and prevent disease progression. Our test includes professional genetic counselling to help you understand your results and their implications for your family’s health. With nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban, we make accurate 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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MT-ND5 Leigh Syndrome DNA Test | ZAR 6
MT-ND5 Gene Leigh Syndrome Mitochondrial Complex I Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity for Unexplained Neurological Symptoms

When your child or family member experiences mysterious neurological symptoms, developmental delays, or muscle weakness, the uncertainty can be overwhelming. Our MT-ND5 Gene Leigh Syndrome NGS Genetic DNA Test provides the answers you need to move forward with confidence and clarity.

Understanding Your MT-ND5 Genetic Test

This advanced genetic test specifically examines the MT-ND5 gene, which plays a crucial role in your body’s energy production system. When this gene contains mutations, it can lead to mitochondrial complex I deficiency – a condition that affects how your cells generate energy, particularly in high-energy organs like the brain and muscles.

Using cutting-edge Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional accuracy to identify even the smallest genetic variations that could be causing Leigh syndrome symptoms.

Who Should Consider This Genetic Test?

This test is particularly important if you or your child experiences:

  • Unexplained developmental regression or delays
  • Progressive neurological symptoms that worsen over time
  • Muscle weakness, poor muscle tone, or movement disorders
  • Vision or hearing problems without clear cause
  • Family history of mitochondrial disorders or Leigh syndrome
  • Unexplained seizures or epilepsy-like symptoms
  • Breathing difficulties or feeding problems in infants

If you’ve been searching for answers without success, this targeted genetic test could provide the breakthrough you need.

Why Early Detection Matters for Your Health

Getting a definitive diagnosis through genetic testing offers life-changing benefits:

  • Personalised Treatment Planning: Knowing the specific genetic cause allows doctors to create targeted treatment strategies
  • Family Planning Insights: Understand inheritance patterns and make informed decisions about future pregnancies
  • Prevent Disease Progression: Early intervention can help manage symptoms and slow disease advancement
  • Peace of Mind: End the diagnostic odyssey and uncertainty about what’s causing symptoms
  • Access to Specialised Care: Connect with neurologists and mitochondrial disorder specialists

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process:

  • Clear, Understandable Reports: Your results come with easy-to-understand explanations
  • Professional Genetic Counselling: Included with your test to help interpret results and discuss implications
  • Family Pedigree Analysis: We create a detailed family history chart to understand inheritance patterns
  • 3-4 Week Turnaround: Most results are available within this timeframe
  • Ongoing Support: Our team remains available to answer questions after you receive results

Transparent Pricing & Exceptional Value

Service Regular Price Special Price Savings
MT-ND5 Gene Leigh Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session INCLUDED at no extra cost
Family Pedigree Analysis INCLUDED at no extra cost
Result Interpretation Support INCLUDED at no extra cost

Considering the potential to prevent years of unnecessary medical investigations and provide targeted treatment, this test represents exceptional value for South African families.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Specialised neurological genetic testing with neurologist oversight
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Comprehensive Support: From initial consultation through to result interpretation
  • South African Focus: Understanding local healthcare needs and family dynamics

Take the First Step Toward Answers Today

Don’t let uncertainty about neurological symptoms continue to cause stress and worry. Early genetic testing can provide the clarity needed to make informed health decisions and access appropriate care.



Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic test package. Book before this special pricing ends to secure your family’s health future.

“Getting the genetic diagnosis finally gave us answers after years of uncertainty. The genetic counselling helped our entire family understand what it meant for our future.” – Satisfied Oracle Genomics Patient