Sale!

MCCC2 Gene 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency NGS Genetic DNA Test

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

-28%

Living with unexplained metabolic symptoms can be worrying, especially when they affect your daily life. Our MCCC2 Gene Deficiency NGS Genetic DNA Test provides the answers you need for just ZAR 6,700. This advanced test detects 3-methylcrotonyl-CoA carboxylase 2 deficiency, a rare metabolic disorder that can cause serious health complications if left undiagnosed. Using cutting-edge Next Generation Sequencing technology, we deliver 99.9% accurate results within 3-4 weeks. Our comprehensive approach includes genetic counselling to help you understand your family’s health history and create a personalised care plan. Whether you’re in Johannesburg, Cape Town, or Durban, our nationwide service brings expert genetic testing to your doorstep. Take control of your metabolic health today with confidence and clarity.

📞 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

MCCC2 Gene Deficiency Test ZAR 6
MCCC2 Gene 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Find Clarity About Metabolic Health Concerns

When your body isn’t functioning as it should, and you’re experiencing unexplained symptoms, it can feel overwhelming and isolating. You deserve answers about your metabolic health, especially when it comes to rare conditions like 3-methylcrotonyl-CoA carboxylase 2 deficiency. Our MCCC2 Gene Deficiency Test provides the clarity and peace of mind you need to move forward with confidence in your health journey.

Understanding the MCCC2 Gene Deficiency Test

This specialised genetic test examines your MCCC2 gene using advanced Next Generation Sequencing (NGS) technology to identify mutations that cause 3-methylcrotonyl-CoA carboxylase 2 deficiency. This is a rare metabolic disorder where your body struggles to break down certain proteins properly, potentially leading to serious health complications if undiagnosed. Our test provides definitive answers with 99.9% accuracy, giving you the information needed for proper management and treatment.

Who Should Consider This Test?

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

  • Unexplained vomiting, lethargy, or poor feeding in infants
  • Developmental delays or muscle weakness
  • Metabolic acidosis episodes after illness or fasting
  • Family history of metabolic disorders or sudden infant death
  • Unexplained hypoglycaemia or abnormal organic acid levels
  • Previous abnormal newborn screening results

Early detection through genetic testing can prevent serious complications and guide appropriate dietary and medical management.

Why Early Detection Matters for Your Health

Getting tested for MCCC2 gene deficiency offers profound benefits for your long-term wellbeing:

  • Prevent Serious Complications: Early diagnosis allows for proactive management to prevent metabolic crises
  • Personalised Treatment Plans: Results guide specific dietary modifications and medical interventions
  • Family Planning Insights: Understand inheritance patterns for future family planning decisions
  • Peace of Mind: Eliminate uncertainty and anxiety about unexplained symptoms
  • Comprehensive Care Coordination: Connect with metabolic specialists for ongoing management

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. Our process is designed to provide clarity and support every step of the way:

  • Clear, Understandable Reports: Results are presented in easy-to-understand language with expert interpretation
  • Genetic Counselling Support: Included counselling sessions help you comprehend what your results mean for your health
  • Actionable Recommendations: Receive specific guidance on next steps and management options
  • Ongoing Support: Access to our team for any questions or concerns after receiving results
  • Family Guidance: Understand implications for other family members and recommended screening

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
MCCC2 Gene Deficiency NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Includes Genetic Counselling Comprehensive session included
Turnaround Time 3-4 Weeks
Sample Collection Blood, Extracted DNA, or Blood on FTA Card

Consider the long-term value: Early detection can prevent costly hospitalisations and provide lifelong health management guidance.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Expert Medical Team: Board-certified geneticists and metabolic specialists
  • Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
  • Comprehensive Support: From testing to results interpretation and ongoing care coordination
  • Proven Track Record: Thousands of successful genetic tests performed
  • Patient-Centred Approach: We prioritise your comfort, understanding, and wellbeing

Take the First Step Toward Metabolic Health Clarity

Don’t let uncertainty about metabolic symptoms control your life. Our MCCC2 Gene Deficiency Test provides the answers you need with the support you deserve.

Limited Time Offer: Book within the next 7 days to secure the special price of ZAR 6,700 and receive priority scheduling for your genetic counselling session.

“The clarity from our MCCC2 test gave us the direction we needed for our daughter’s care. The genetic counselling was invaluable.” – Recent Patient, Cape Town