Protect Your Child’s Breathing Health with ASCL1 Gene Testing
As a parent, nothing matters more than your child’s health and safety. If you’ve noticed concerning breathing patterns or have a family history of respiratory issues, the ASCL1 Gene Test provides the answers you need for peace of mind. This advanced genetic screening detects congenital central hypoventilation syndrome (CCHS), a condition that can affect your child’s ability to breathe properly, especially during sleep.
Understanding the ASCL1 Gene Test
The ASCL1 Gene Test uses cutting-edge Next Generation Sequencing (NGS) technology to analyse the ASCL1 gene, which plays a crucial role in controlling automatic breathing functions. When this gene has specific mutations, it can lead to congenital central hypoventilation syndrome – a condition where the brain doesn’t properly control breathing, particularly during sleep.
Our test provides comprehensive analysis with 99.9% accuracy, giving you reliable results you can trust for making important healthcare decisions for your child.
Who Should Consider This Test?
This test is particularly important if your child shows:
- Shallow breathing or breathing pauses during sleep
- Bluish skin colour (cyanosis) during sleep
- Difficulty waking up or excessive sleepiness
- Poor feeding or failure to thrive in infancy
- Family history of breathing disorders or sudden infant death
- Unexplained breathing difficulties that worsen during sleep
Early detection through genetic testing can be life-saving for children at risk of CCHS.
Why This Test Matters for Your Child’s Health
Getting the ASCL1 Gene Test offers multiple crucial benefits:
- Early Intervention: Identify CCHS before serious complications develop
- Proper Management: Guide appropriate medical care and monitoring
- Family Planning: Understand inheritance patterns for future children
- Peace of Mind: Eliminate uncertainty about your child’s breathing health
- Prevent Emergencies: Reduce risk of breathing crises during sleep
Understanding Your Test Results
We make understanding your results simple and reassuring:
Positive Result: If the test detects ASCL1 gene mutations, our genetic counsellors will provide comprehensive guidance on next steps, including specialist referrals, monitoring protocols, and management strategies to keep your child safe.
Negative Result: A normal result provides valuable peace of mind, ruling out CCHS caused by ASCL1 gene mutations and allowing you to focus on other potential causes of breathing concerns.
Inconclusive Result: In rare cases, our team will provide clear guidance on additional testing or monitoring that may be recommended.
Every result includes a detailed consultation with our genetic specialists to ensure you fully understand the implications and next steps.
Affordable Genetic Testing for South African Families
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| ASCL1 Gene Test | ZAR 6,700 | ZAR 2,650 |
Price includes genetic counselling session and comprehensive result interpretation
Considering the potential hospital costs and lifelong implications of undiagnosed CCHS, this test represents exceptional value for your child’s long-term health and safety.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Board-certified genetic specialists and counsellors
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Quick Turnaround: Results in 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Comprehensive Support: From testing through to result interpretation and follow-up care
Take Action for Your Child’s Health Today
Don’t wait to get the answers you need about your child’s breathing health. Early detection of congenital central hypoventilation syndrome can prevent serious complications and provide the foundation for proper medical management.
Book your ASCL1 Gene Test now and take the first step toward protecting your child’s respiratory health.
Our caring team is ready to guide you through the testing process and provide the support your family needs.
Test Information
- Turnaround Time: 3-4 weeks
- Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
- Preparation: Clinical history and genetic counselling session to create family pedigree
- Specialty: Paediatrics
- Method: Next Generation Sequencing (NGS) Technology
