Understanding Prader-Willi Syndrome Genetic Testing
If you’re worried about your child’s development or have concerns about Prader-Willi syndrome in your family, you’re not alone. Many South African parents face these uncertainties, and getting clear answers can bring immense relief. Our Prader-Willi Syndrome Genetic DNA Test provides the definitive information you need to make informed healthcare decisions for your family.
What This Test Detects
This advanced genetic test specifically examines chromosome 15q11 for abnormalities that cause Prader-Willi syndrome. Using Next Generation Sequencing (NGS) technology, we can identify genetic changes that affect appetite regulation, growth, and development. Understanding these genetic factors helps create targeted management plans that can significantly improve quality of life.
Who Should Consider This Test
This test is particularly important for families noticing:
- Infants with poor muscle tone (hypotonia) and feeding difficulties
- Children showing excessive hunger and rapid weight gain
- Developmental delays in motor skills and speech
- Behavioural challenges including temper outbursts
- Family history of Prader-Willi syndrome or related conditions
Why Early Detection Matters
Early diagnosis of Prader-Willi syndrome allows for:
- Timely intervention with growth hormone therapy
- Proper nutritional management from an early age
- Access to specialised educational support
- Family planning and genetic counselling
- Improved long-term health outcomes
Understanding Your Results
Our genetic counselling session ensures you fully understand your test results. We provide clear explanations about what the findings mean for your child’s health and development. Positive results open doors to specialised care and support services, while negative results provide peace of mind and eliminate uncertainty.
Pricing and Value
| Test Option | Price | Savings |
|---|---|---|
| Regular Price | ZAR 9,350 | – |
| Special Price | ZAR 6,700 | ZAR 2,650 |
This investment in your family’s health provides lifelong benefits through early intervention and proper management.
Nationwide Accessibility
We serve patients across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and nationwide. Our sample collection is simple – requiring only blood or a small blood spot on an FTA card.
Take Action Today
Don’t let uncertainty about Prader-Willi syndrome affect your family’s peace of mind. Early detection through genetic testing can make a significant difference in managing this condition effectively. Our team of genetic specialists and neurologists are here to support you every step of the way.
Book your genetic counselling session and testing today to get the answers your family deserves. Results are typically available within 3-4 weeks, giving you the clarity needed to plan for your child’s future.
