Find Clarity for Prader-Willi Syndrome Concerns
When your child shows signs of developmental delays or feeding difficulties, the uncertainty can be overwhelming. Our NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test provides the definitive answers you need to move forward with confidence. Using cutting-edge Next-Generation Sequencing technology, we deliver accurate results that can guide your family’s healthcare decisions.
Understanding the NDN Gene Prader-Willi Test
This advanced genetic test specifically examines the NDN gene, which plays a crucial role in Prader-Willi syndrome – a complex genetic condition affecting appetite, growth, and cognitive development. Our NGS technology provides comprehensive analysis with exceptional accuracy, ensuring you receive reliable information about this rare genetic disorder.
Unlike basic genetic screening, our test offers detailed insights that can confirm or rule out Prader-Willi syndrome, helping you and your healthcare team develop the most appropriate care plan for your child’s unique needs.
Who Should Consider This Test?
This test is particularly important for infants and children showing:
- Poor feeding and failure to thrive in infancy
- Developmental delays and learning difficulties
- Hypotonia (poor muscle tone)
- Excessive appetite and weight gain in early childhood
- Behavioural challenges and emotional regulation difficulties
- Family history of Prader-Willi syndrome or related genetic conditions
If you’ve noticed these symptoms in your child, our test can provide the clarity needed to access appropriate support and interventions.
Why Early Detection Matters for Your Child’s Health
Early diagnosis of Prader-Willi syndrome through our accurate testing enables:
- Timely Interventions: Access to early therapies and support services
- Appropriate Medical Management: Tailored healthcare plans for optimal development
- Family Planning Guidance: Understanding inheritance patterns for future pregnancies
- Educational Support: Access to specialised learning programs and resources
- Peace of Mind: Clear answers that reduce uncertainty and anxiety
Early detection can significantly improve long-term outcomes and quality of life for children with Prader-Willi syndrome.
Understanding Your Test Results
We understand that waiting for genetic test results can be stressful. Our comprehensive reporting includes:
- Clear, easy-to-understand results with professional interpretation
- Follow-up genetic counselling to discuss findings and implications
- Guidance on next steps and available support resources
- Connection to specialist healthcare providers if needed
Our genetic counsellors are available to help you understand your results and navigate the healthcare system with confidence.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Turnaround Time |
|---|---|---|---|
| NDN Gene Prader-Willi NGS Test | ZAR 6,700 | 3-4 Weeks |
What’s Included: Comprehensive genetic analysis, genetic counselling session, pedigree chart creation, detailed results report, and professional interpretation.
This investment in your child’s health can save thousands in unnecessary medical investigations and provide direction for appropriate care.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Expert Genetic Counselling: Professional guidance throughout your testing journey
- Advanced NGS Technology: State-of-the-art genetic analysis for maximum accuracy
- Neurology Specialists: Tests supervised by qualified neurologists
- Multiple Sample Options: Blood, extracted DNA, or FTA card samples accepted
Take the First Step Toward Clarity
Don’t let uncertainty about your child’s development continue. Early detection through our reliable NDN Gene Prader-Willi testing can provide the answers you need to access appropriate support and interventions.
Limited Time Offer: Special pricing of ZAR 6,700 available for immediate bookings. Regular price ZAR 9,350.
