Find Clarity for Your Child’s Health Journey
When you notice unusual symptoms in your child’s development, the uncertainty can be overwhelming. The Mucopolysaccharidosis (MPS) Type 1 Hurler Quantitative Blood Test provides the definitive answers South African parents need to move forward with confidence and peace of mind.
Understanding MPS Type 1 Testing
MPS Type 1, also known as Hurler syndrome, is a rare genetic condition where the body lacks an essential enzyme needed to break down complex sugars. Without this enzyme, these substances build up in cells and cause progressive damage to multiple organs and systems. Our quantitative blood test measures the specific enzyme activity levels, providing clear diagnostic information that can guide treatment decisions and family planning.
Is This Test Right for Your Child?
This test is essential for children showing concerning symptoms such as:
- Coarse facial features that become more noticeable over time
- Developmental delays or regression in milestones
- Joint stiffness and limited mobility
- Recurrent respiratory infections and breathing difficulties
- Cloudy corneas affecting vision
- Enlarged liver and spleen
- Heart valve problems detected during check-ups
If your child exhibits these symptoms or has a family history of MPS disorders, this test provides critical diagnostic clarity.
Why Early Detection Matters for Your Family
Getting an accurate diagnosis through our MPS Type 1 test offers life-changing benefits:
- Early Intervention: Begin appropriate treatments before significant organ damage occurs
- Treatment Planning: Access enzyme replacement therapy and other specialized care
- Family Planning: Make informed decisions about future pregnancies
- Peace of Mind: Replace uncertainty with a clear path forward
- Improved Outcomes: Early diagnosis significantly improves quality of life and long-term prognosis
Understanding Your Results with Compassion
Our experienced pediatric genetic specialists provide clear, compassionate interpretation of your results:
- Normal Results: Normal enzyme activity levels provide reassurance and rule out MPS Type 1
- Abnormal Results: Low enzyme activity indicates MPS Type 1, and we immediately connect you with specialist care
- Comprehensive Support: Every result includes detailed explanations and next-step guidance
- Genetic Counseling: Access to expert counseling to understand implications for your family
We understand this can be an emotional time, and our team provides the support and guidance you need every step of the way.
Affordable, Life-Changing Testing
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| MPS Type 1 Quantitative Blood Test | ZAR 2,200 | ZAR 1,000 |
This represents exceptional value compared to the potential long-term healthcare costs of undiagnosed MPS Type 1.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Pediatric Specialists: Our team includes experienced geneticists and pediatric specialists
- Rapid Results: Sample processing daily by 4 PM with results in just 4 days
- Advanced Methodology: State-of-the-art enzyme assay technology for maximum accuracy
- Compassionate Care: We understand the emotional journey and provide supportive, understanding service
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s health create unnecessary stress. Early detection through our MPS Type 1 test can make a significant difference in treatment outcomes and quality of life.
Limited Time Offer: This special pricing of ZAR 2,200 won’t last forever. Secure your child’s health assessment today and gain the peace of mind your family deserves.
Test Specifications
- Sample Required: 10 mL (7.5 mL minimum) whole blood from 3 Lavender Top (EDTA) tubes OR Green Top (Sodium Heparin) tubes
- Shipping: Ship refrigerated. DO NOT FREEZE
- Preparation: Please provide brief clinical history
- Turnaround Time: Sample processed daily by 4 PM; Report available in 4 days
- Methodology: Enzyme assay
- Specialty: Pediatric Genetics
