Protect Your Newborn’s Future with Early Cystic Fibrosis Detection
As a parent, the health of your newborn is your highest priority. We understand the mix of joy and concern that comes with welcoming a new baby into your family. Our Cystic Fibrosis Newborn Screen Test provides the peace of mind you deserve, detecting this genetic condition early when intervention is most effective.
Understanding the Cystic Fibrosis Newborn Screen
Cystic fibrosis is a genetic condition that affects breathing and digestion, but early detection through our simple heel prick test can make all the difference. The test measures specific markers in your baby’s blood that indicate whether further testing for cystic fibrosis is needed. It’s a quick, minimally invasive procedure that provides invaluable information about your child’s health.
Our advanced fluoroimmunoassay method ensures the highest accuracy, giving you results you can trust for your most precious family member.
Every Newborn Deserves This Essential Screening
While cystic fibrosis can affect any baby, early screening is particularly important for:
- All newborns – Early detection before symptoms appear
- Babies with family history – When parents or siblings have cystic fibrosis
- Infants showing early signs – Such as salty-tasting skin or breathing difficulties
- Parents seeking peace of mind – Knowing you’ve taken every precaution for your baby’s health
Don’t wait for symptoms to appear – early screening can prevent serious complications and improve your child’s quality of life.
Why Early Detection Matters for Your Baby’s Health
Early diagnosis of cystic fibrosis through newborn screening provides life-changing benefits:
- Immediate treatment – Begin specialised care before lung damage occurs
- Better growth and development – Early nutritional support improves outcomes
- Reduced hospitalisations – Prevent serious infections and complications
- Improved life expectancy – Early intervention significantly extends and improves quality of life
- Family planning guidance – Understand genetic risks for future children
For just ZAR 250, you’re investing in your child’s lifelong health and wellbeing.
Understanding Your Results – Clear Guidance Every Step
We know waiting for test results can be stressful. That’s why we provide:
- Next-day reporting – Quick results to ease your mind
- Clear, understandable explanations – No confusing medical jargon
- Follow-up guidance – What to do if further testing is needed
- Professional support – Access to paediatric specialists if required
Most babies receive normal results, providing immediate peace of mind. For the few who need further testing, early detection means early treatment and better outcomes.
Affordable Protection for Your Newborn’s Health
| Test | Regular Price | Special Price | Value |
|---|---|---|---|
| Cystic Fibrosis Newborn Screen | ZAR 250 | Early detection that could save thousands in future healthcare costs |
Turnaround: Sample Monday through Friday by 9am; Report Next day
Why South African Parents Trust Oracle Genomics
- Nationwide Coverage – Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Paediatric Specialists – Working with leading child health professionals
- State-of-the-Art Technology – Advanced fluoroimmunoassay for maximum accuracy
- Quick Turnaround – Next-day results to ease parental anxiety
- Simple Process – Just 1 drop of heel prick blood on filter paper
Don’t Wait – Protect Your Baby’s Health Today
Early detection of cystic fibrosis can change your child’s life. For just ZAR 250, you can have the peace of mind that comes from knowing you’ve taken this essential step for your newborn’s health.
Limited availability – Book today to secure your newborn’s screening
Remember: Clinical details and drug history must accompany sample. Ship refrigerated or frozen.
