Find Peace of Mind with GM2 Gangliosidosis Testing
When concerns about Tay-Sachs or Sandhoff disease weigh on your mind, having clear answers becomes essential for your family’s future. We understand the emotional journey you’re facing, and we’re here to provide the accurate, reliable testing you need to make informed decisions about your health.
Understanding Your GM2 Gangliosidosis Test
This specialised blood test measures the enzyme activity levels that help identify Tay-Sachs and Sandhoff disease – serious genetic conditions that affect the nervous system. Using advanced enzyme assay technology, our test provides precise quantitative results that give you and your healthcare provider the information needed for proper diagnosis and management.
The test specifically detects deficiencies in hexosaminidase enzymes, which are crucial for breaking down certain fatty substances in nerve cells. When these enzymes don’t function properly, it can lead to the progressive neurological symptoms associated with GM2 gangliosidosis.
Who Should Consider This Test?
This test is particularly important for:
- Parents concerned about genetic conditions in their children
- Families with a history of Tay-Sachs or Sandhoff disease
- Individuals experiencing developmental delays or neurological symptoms
- Couples planning pregnancy who want genetic screening
- Healthcare providers needing diagnostic confirmation
If you’ve noticed symptoms like muscle weakness, loss of motor skills, vision problems, or developmental regression in your child, this test can provide the answers you need.
Why Early Detection Matters for Your Health
Getting tested early can make a significant difference in managing these conditions. Early detection allows for:
- Timely intervention and treatment planning
- Better understanding of disease progression
- Informed family planning decisions
- Access to appropriate support services
- Peace of mind through definitive answers
Knowing your status empowers you to take control of your health journey and make decisions that are right for your family.
Understanding Your Test Results
We know waiting for results can be stressful. That’s why we provide clear, easy-to-understand reports within just 4 days. Your results will show:
- Specific enzyme activity levels
- Clear interpretation of what the numbers mean
- Guidance on next steps if needed
- Recommendations for follow-up care
Our pediatric specialists are available to help you understand your results and provide the support you need throughout the process.
Affordable, Accessible Testing for South Africans
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| GM2 Gangliosidosis Quantitative Blood Test | ZAR 1,700 | ZAR 1,200 | ZAR 500 |
This special pricing makes comprehensive genetic testing accessible to families across South Africa.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
- Expert Pediatric Specialists: Our team understands the unique needs of genetic testing for children
- Rapid Results: Samples processed daily with results in just 4 days
- Accuracy Guaranteed: Advanced enzyme assay methodology ensures reliable results
- Professional Support: Guidance every step of the way
Test Information
Sample Requirements: 10 ml (7.5 mL minimum) whole blood from 3 Lavender Top (EDTA) / Green Top (Sodium heparin) tubes
Shipping: Ship refrigerated. DO NOT FREEZE
Important: Clinical details must accompany sample for accurate interpretation
Turnaround Time: Samples accepted daily by 4 pm; Reports available in 4 days
Take the First Step Toward Clarity
Don’t let uncertainty about genetic health conditions create unnecessary stress. Our GM2 Gangliosidosis test provides the answers you need to move forward with confidence.
Limited Time Offer: Secure your special ZAR 1,200 pricing while available. Early detection could make all the difference for your family’s health journey.
