Understanding MCEE Gene Methylmalonyl-CoA Epimerase Deficiency
When you’re worried about your child’s health or have a family history of metabolic disorders, the uncertainty can be overwhelming. Our MCEE gene test provides the clarity and peace of mind you deserve. This advanced genetic screening helps identify methylmalonyl-CoA epimerase deficiency early, allowing for proactive medical management that can significantly improve health outcomes.
What This Test Detects
The MCEE gene test examines your DNA for mutations in the methylmalonyl-CoA epimerase gene. This enzyme plays a crucial role in breaking down certain proteins and fats in your body. When this gene doesn’t function properly, it can lead to serious metabolic complications that often appear in infancy or early childhood. Our test uses next-generation sequencing (NGS) technology, the gold standard in genetic testing, to provide comprehensive and accurate results.
Who Should Consider This Test?
This test is particularly important if you or your child experience:
- Unexplained vomiting, lethargy, or poor feeding in infants
- Developmental delays or failure to thrive
- Metabolic acidosis or other abnormal lab results
- Family history of methylmalonyl-CoA epimerase deficiency
- Previous child with unexplained metabolic disorders
- Planning pregnancy with known family risk factors
Many South African families find relief in getting definitive answers rather than living with uncertainty about their child’s health.
Why Early Detection Matters for Your Family
Identifying MCEE gene mutations early can transform your child’s health journey:
- Prevent Metabolic Crises: Early intervention can prevent life-threatening metabolic emergencies
- Guide Treatment: Results help doctors create targeted dietary and medical plans
- Family Planning: Understand risks for future pregnancies
- Peace of Mind: Replace uncertainty with clear medical guidance
- Developmental Support: Early intervention supports normal development
Understanding Your Results
Our genetic counselling team will walk you through your results with compassion and clarity. We explain what the findings mean for your health and provide:
- Clear interpretation of genetic variants
- Personalised medical recommendations
- Family risk assessment
- Referrals to metabolic specialists if needed
- Ongoing support for your healthcare journey
Remember, a positive result doesn’t mean certain illness – it means we can take proactive steps to protect your health.
Transparent Pricing & Value
| Regular Price | ZAR 9,350 |
| Special Price | ZAR 6,700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card |
Consider this an investment in your family’s health that could prevent costly emergency hospitalisations and long-term complications.
Why Trust Oracle Genomics?
- Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Working with general physicians and metabolic specialists
- Advanced Technology: Using NGS technology for maximum accuracy
- Genetic Counselling: Comprehensive pre- and post-test counselling included
- Proven Track Record: Trusted by South African families for accurate genetic testing
Take Control of Your Family’s Health Today
Don’t let uncertainty about metabolic disorders affect your peace of mind. Early detection through our MCEE gene test can provide the answers you need to protect your child’s health and development.
Limited Time Offer: Save ZAR 2,650 on your genetic testing
Convenient Testing: Multiple sample options available nationwide
Expert Support: Genetic counselling included with every test
Your family’s health is our priority. Trust Oracle Genomics for accurate, compassionate genetic testing that puts you first.
