Understanding Your Genetic Risk for Hypobetalipoproteinemia
If you’ve been struggling with unexplained low cholesterol levels, or have family members with similar health patterns, you’re not alone. Many South Africans live with undiagnosed genetic conditions that affect how their bodies process fats and cholesterol. Our APOB Gene Hypobetalipoproteinemia Type 1 test provides the clarity you need to understand your genetic makeup and take proactive steps toward better health management.
What This Test Reveals About Your Health
Hypobetalipoproteinemia Type 1 is a genetic condition that affects your body’s ability to produce apolipoprotein B, a crucial protein needed to transport cholesterol and fats through your bloodstream. Using advanced Next-Generation Sequencing (NGS) technology, this test examines your APOB gene for specific mutations that could be impacting your cholesterol metabolism. Think of it as reading your body’s genetic instruction manual to understand why you might have unusually low LDL cholesterol levels.
Who Should Consider This Genetic Test?
This test is particularly important if you experience:
- Persistently low LDL cholesterol levels without clear explanation
- Family history of similar cholesterol patterns across generations
- Digestive issues related to fat absorption
- Neurological symptoms that might be linked to vitamin deficiencies
- Concerns about passing genetic conditions to your children
- Unexplained liver function abnormalities
Many patients in Johannesburg, Cape Town, and Durban have found life-changing answers through this genetic insight.
Why Early Detection Matters for Your Health
Understanding your APOB gene status empowers you to:
- Prevent serious complications like fatty liver disease and neurological damage
- Create personalised nutrition plans that address your specific needs
- Make informed family planning decisions with genetic counselling support
- Monitor and manage potential vitamin deficiencies proactively
- Reduce anxiety about unexplained health symptoms
- Access appropriate medical care and monitoring strategies
Understanding Your Test Results
We know waiting for genetic results can be stressful. That’s why we provide comprehensive support throughout the process. Your results will clearly indicate whether specific APOB gene mutations were detected, and our genetic counselling team will help you understand what this means for your health. Whether the results show a genetic variation or provide reassuring clarity, you’ll receive personalised guidance on next steps for managing your health effectively.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| APOB Gene Hypobetalipoproteinemia Type 1 NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Included in your test: Genetic counselling session, family pedigree analysis, comprehensive results interpretation, and ongoing support.
Why Trust Oracle Genomics?
With collection centres across South Africa including major cities like Johannesburg, Cape Town, Durban, and Pretoria, we make genetic testing accessible and convenient. Our NGS technology provides 99.9% accuracy, and all testing is conducted in CAP-accredited laboratories. Every test includes professional genetic counselling to ensure you fully understand your results and their implications for your health journey.
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about your genetic health create unnecessary worry. Early detection of APOB gene mutations can significantly improve your quality of life and help prevent serious health complications. Book your test today and receive:
- Convenient sample collection (blood or simple FTA card)
- Professional genetic counselling included
- Results within 3-4 weeks
- Nationwide coverage across South Africa
- Ongoing support from our medical team
Call now to schedule your test or visit our website to book online. Take control of your genetic health today.
