Protecting Your Newborn’s Future: CPT2 Gene Testing for Peace of Mind
As expectant parents or those with a newborn, the thought of rare genetic conditions can be overwhelming. We understand the mix of joy and concern that comes with welcoming a new life. Our CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency test is designed to provide the answers and reassurance you need during this precious time.
Understanding the CPT2 Gene Test
This advanced genetic test examines the CPT2 gene, which plays a crucial role in your body’s energy production from fats. When this gene doesn’t function properly, it can lead to Carnitine Palmitoyltransferase 2 Deficiency – a serious metabolic condition that can affect newborns. Our Next Generation Sequencing (NGS) technology provides the most accurate analysis available, giving you reliable information to make informed healthcare decisions.
Who Should Consider This Test?
This test is particularly important for:
- Families with a history of unexplained infant deaths or metabolic disorders
- Parents who have previously lost a child to sudden infant death
- Couples planning pregnancy with known family history of metabolic conditions
- Newborns showing symptoms of metabolic distress or feeding difficulties
- Families seeking peace of mind about their newborn’s genetic health
Why Early Detection Matters for Your Family
Early identification of CPT2 deficiency can be life-changing. With proper diagnosis:
- Your healthcare team can implement appropriate dietary management
- You can avoid metabolic crises through careful monitoring
- Your child receives targeted care from birth
- You gain peace of mind knowing you’ve taken proactive steps
- Future family planning decisions become more informed
Understanding Your Results with Confidence
We know waiting for genetic test results can be stressful. Our comprehensive genetic counselling ensures you understand your results completely. Our specialists will explain what the findings mean for your family’s health and guide you through next steps. Whether the results are reassuring or indicate the need for specific care, you’ll have the support and information needed to make the best decisions for your child.
Transparent Pricing – Investing in Your Family’s Health
| Service | Regular Price | Special Price |
|---|---|---|
| CPT2 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
Considering the potential to prevent serious health complications, this test represents excellent value for your family’s wellbeing.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Working with qualified general physicians and genetic specialists
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Comprehensive Support: Genetic counselling included with every test
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Peace of Mind
Don’t let uncertainty about your newborn’s health create unnecessary stress. Our simple testing process requires just a blood sample or DNA extraction, with results available in 3-4 weeks. The included genetic counselling session helps create a family health history that could benefit generations to come.
Early detection can make all the difference. Secure your family’s health future with confidence through Oracle Genomics.
