Find Answers for Unexplained Magnesium Deficiency
If you’ve been struggling with persistent fatigue, muscle weakness, or heart palpitations that doctors can’t explain, you’re not alone. Many South Africans live with undiagnosed genetic conditions affecting magnesium levels. Our FXYD2 Gene Hypomagnesemia Type 2 test provides the clarity you deserve, helping you understand your body’s unique needs and preventing serious health complications down the line.
Understanding Your FXYD2 Gene Test
This specialised genetic test examines your FXYD2 gene using Next Generation Sequencing (NGS) technology – the gold standard in genetic analysis. The FXYD2 gene plays a crucial role in how your kidneys manage magnesium levels. When this gene has mutations, it can lead to hypomagnesemia type 2, a condition where your body struggles to retain adequate magnesium despite normal dietary intake.
Think of it as finding the root cause rather than just treating symptoms. While blood tests show low magnesium levels, our genetic test reveals why this is happening at the most fundamental level.
Who Should Consider This Test?
This test is particularly important if you experience:
- Unexplained muscle weakness or cramps
- Persistent fatigue that doesn’t improve with rest
- Heart palpitations or irregular heart rhythms
- Neurological symptoms like tremors or seizures
- Family history of magnesium deficiency disorders
- Children with developmental delays or growth concerns
- Resistance to standard magnesium supplementation
Many patients tell us they’ve visited multiple doctors without finding answers. This test provides the missing piece to your health puzzle.
Why Early Detection Matters for Your Health
Getting tested isn’t just about diagnosis – it’s about prevention and proper management. Early detection of FXYD2 gene mutations can:
- Prevent serious complications like cardiac arrhythmias
- Guide targeted treatment strategies that actually work
- Provide peace of mind for family planning decisions
- Help manage symptoms more effectively
- Reduce unnecessary medical tests and treatments
- Give you control over your health journey
One of our Johannesburg patients shared: “After years of unexplained symptoms, this test finally gave me answers and a clear path forward.”
Understanding Your Results – We’re Here to Help
We understand that genetic testing can feel overwhelming. That’s why every test includes comprehensive genetic counselling to help you understand your results in clear, simple terms. Our caring specialists will:
- Explain what your results mean for your health
- Discuss management options and lifestyle adjustments
- Help you understand family implications
- Provide ongoing support and resources
- Connect you with appropriate healthcare providers
Your results come with a detailed report that your doctor can use to create a personalised treatment plan.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| FXYD2 Gene Hypomagnesemia Type 2 NGS Test | ZAR 6,700 | ZAR 2,650 | |
| Genetic Counselling Session | Included at no extra cost | ||
| Family Pedigree Analysis | Included at no extra cost | ||
| Results Interpretation | Included at no extra cost | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
We’ve helped thousands of South Africans across Johannesburg, Cape Town, Durban, and Pretoria take control of their genetic health. Our commitment includes:
- Nationwide Coverage: Accessible testing across South Africa
- Medical Expertise: Working with general physicians and specialists
- 99.9% Accuracy: Using certified NGS technology
- Patient-Centred Care: We listen and understand your concerns
- Confidential Service: Your privacy is our priority
- Ongoing Support: We’re here throughout your health journey
Take the First Step Toward Clarity
Don’t let unexplained symptoms control your life. Early detection through genetic testing can provide the answers you need to manage your health effectively. Our caring team is ready to guide you through this important journey.
Important: Early detection can prevent serious complications. Don’t wait until symptoms worsen – take control of your health today.
