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FASTKD2 Gene Mitochondrial Complex IV Deficiency NGS Genetic DNA Test

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

-28%

If you or your child are experiencing unexplained neurological symptoms, muscle weakness, or developmental delays, our FASTKD2 Gene Mitochondrial Complex IV Deficiency Test provides the answers you need. This comprehensive NGS genetic DNA test specifically identifies mutations in the FASTKD2 gene that cause mitochondrial respiratory chain complex IV deficiency – a serious condition affecting energy production in cells. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive precise genetic analysis using advanced next-generation sequencing technology. Our test includes professional genetic counselling to help you understand your family’s risk and create a clear health management plan. With results available within 3-4 weeks and nationwide coverage across South Africa, including Johannesburg, Cape Town, and Durban, we make accurate genetic testing accessible and trustworthy for every family concerned about mitochondrial disorders.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

FASTKD2 Gene Test | ZAR 6
FASTKD2 Gene Mitochondrial Complex IV Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Unexplained Neurological Symptoms with FASTKD2 Gene Testing

When your child struggles with developmental delays, muscle weakness, or unexplained neurological symptoms, the uncertainty can be overwhelming. You deserve clear answers and a path forward. Our FASTKD2 Gene Mitochondrial Complex IV Deficiency Test provides the precise genetic diagnosis needed to understand these complex conditions and create an effective treatment plan.

Understanding the FASTKD2 Gene Test

This advanced genetic test examines your DNA for mutations in the FASTKD2 gene, which plays a crucial role in mitochondrial function. Mitochondria are the energy powerhouses of your cells, and when complex IV (part of the respiratory chain) doesn’t work properly, it can lead to serious neurological and muscular problems. Using Next-Generation Sequencing (NGS) technology, we provide the most accurate analysis available, giving you and your healthcare team the information needed for proper diagnosis and management.

Who Should Consider This Test?

This test is essential if you or your child experience:

  • Unexplained muscle weakness or fatigue
  • Developmental delays in childhood
  • Neurological symptoms without clear cause
  • Family history of mitochondrial disorders
  • Progressive neurological deterioration
  • Exercise intolerance or poor stamina

Many South African families have found answers through this testing, helping them move from uncertainty to actionable health plans.

Why Early Detection Matters for Your Health

Identifying FASTKD2 gene mutations early provides significant benefits:

  • Accurate Diagnosis: Move beyond symptom management to understanding the root cause
  • Personalised Treatment: Develop targeted interventions based on your specific genetic profile
  • Family Planning Guidance: Understand inheritance patterns for future family decisions
  • Peace of Mind: Replace uncertainty with clear understanding and control
  • Prevent Complications: Early intervention can help manage symptoms and improve quality of life

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. That’s why we include comprehensive genetic counselling with every test. Our specialists will:

  • Explain your results in clear, understandable language
  • Discuss what the findings mean for your health and your family
  • Help create a pedigree chart to understand family inheritance patterns
  • Connect you with appropriate specialists for ongoing care
  • Provide emotional support throughout the process

Your results will be available within 3-4 weeks, and we ensure you have full support every step of the way.

Affordable, Accessible Genetic Testing

Service Regular Price Special Price
FASTKD2 Gene Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session INCLUDED
Family Pedigree Analysis INCLUDED
Results Interpretation INCLUDED

Consider this investment in your health: early diagnosis can prevent years of unnecessary medical visits and provide targeted treatment that improves quality of life.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Specialised neurological genetic testing with neurologist oversight
  • Advanced Technology: Next-Generation Sequencing for highest accuracy
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Complete Support: From testing through results interpretation and follow-up care
  • South African Focus: Understanding local healthcare needs and accessibility challenges

Take Control of Your Health Journey Today

Don’t let uncertainty about neurological symptoms control your life. With our FASTKD2 gene test, you can get the answers needed to move forward with confidence. Our special pricing of ZAR 6,700 makes this advanced genetic testing accessible to South African families who need answers.

Limited Time Offer: Save ZAR 2,650 off regular pricing while appointments are available

Convenient Testing: Simple sample collection with multiple options to suit your needs

Comprehensive Support: Genetic counselling included to ensure you understand your results

Ready to Begin? Choose Your Booking Method:

  • Online Booking: Secure your test appointment instantly
  • Telephone Consultation: Speak with our genetic specialists first
  • Clinic Visit: Visit one of our nationwide locations
  • Home Collection: Mobile phlebotomy services available in major cities

Your journey to answers starts with one simple decision. Book your FASTKD2 gene test today and take the first step toward understanding your health with confidence and clarity.