Understanding Your Infant’s Health: GPD1 Gene Hypertriglyceridemia Testing
As a parent, nothing matters more than your baby’s health. When routine blood tests reveal elevated triglyceride levels in your infant, it’s natural to feel concerned and uncertain. Transient infantile hypertriglyceridemia caused by GPD1 gene mutations is a temporary but serious condition that requires accurate diagnosis and proper management. Our specialised genetic test provides the clarity you need to make informed decisions about your child’s healthcare journey.
What This Test Detects
This advanced Next-Generation Sequencing (NGS) test specifically examines the GPD1 gene for mutations that cause temporary triglyceride elevation in infants. The GPD1 gene plays a crucial role in lipid metabolism, and when mutations occur, it can lead to dangerously high triglyceride levels during infancy that typically resolve as the child grows. Our test identifies these genetic variations with exceptional precision, giving you definitive answers about your baby’s condition.
Who Should Consider This Test
This test is essential for infants showing:
- Unexplained elevated triglyceride levels in blood tests
- Family history of lipid disorders or early heart conditions
- Poor weight gain or feeding difficulties
- Recurrent abdominal pain or digestive issues
- Developmental concerns potentially linked to metabolic issues
Why Early Detection Matters for Your Baby’s Future
Identifying GPD1 gene mutations early provides numerous health benefits:
- Prevent Complications: Early intervention can prevent pancreatitis and other serious complications
- Proper Management: Guides appropriate dietary and medical management strategies
- Family Planning: Provides valuable information for future family planning decisions
- Peace of Mind: Reduces uncertainty and anxiety about your child’s health trajectory
- Developmental Support: Ensures your baby receives the right support during critical growth periods
Understanding Your Results
Our comprehensive results package includes:
- Clear, easy-to-understand report explaining the genetic findings
- Detailed interpretation by our genetic specialists
- Personalised recommendations for management and follow-up care
- Access to genetic counselling to discuss results and implications
- Guidance for your paediatrician on appropriate treatment approaches
Transparent Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| GPD1 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling | Included | |
| Results Interpretation | Included | |
| Follow-up Support | Included | |
Considering the potential healthcare costs of undiagnosed or mismanaged hypertriglyceridemia, this test represents exceptional value for your family’s long-term health and peace of mind.
Nationwide Trust and Accessibility
Oracle Genomics brings professional genetic testing to families across South Africa. With collection facilities in Johannesburg, Cape Town, Durban, Pretoria, and major centres nationwide, we make advanced genetic care accessible to every South African family. Our team of genetic specialists and paediatric consultants ensures you receive the highest standard of care and support throughout your testing journey.
Take Action for Your Baby’s Health Today
Don’t let uncertainty about your infant’s triglyceride levels cause unnecessary worry. Early detection through genetic testing provides the answers you need to ensure your baby receives the right care at the right time. Our special pricing of ZAR 6,700 makes this crucial testing more accessible than ever.
Book your genetic counselling session today and take the first step toward understanding your baby’s genetic health. Call us now or complete our online booking form to schedule your appointment at a location convenient for you.
Turnaround time: 3-4 weeks | Sample: Blood, Extracted DNA, or Blood on FTA Card
