Understanding Criggler Najjar Syndrome: Your Path to Genetic Clarity
When persistent jaundice or unexplained liver concerns affect your family, the uncertainty can be overwhelming. At Oracle Genomics, we understand the emotional weight of genetic health questions. Our Criggler Najjar Syndrome genetic testing provides the definitive answers South African families need to make informed health decisions with confidence and peace of mind.
What Does This Test Detect?
Criggler Najjar Syndrome is a rare genetic disorder that affects the liver’s ability to process bilirubin, leading to persistent jaundice and potential neurological complications if untreated. Our advanced Sanger Sequencing technology precisely identifies the specific genetic mutations in the UGT1A1 gene responsible for this condition. This isn’t just a test – it’s a comprehensive genetic investigation that provides the clarity needed for proper medical management and family planning.
Who Should Consider This Genetic Screening?
This test is particularly important if you or your family members experience:
- Persistent jaundice that doesn’t resolve in newborns
- Family history of unexplained liver disorders
- Elevated bilirubin levels without clear cause
- Planning for pregnancy with known genetic risks
- Neurological symptoms potentially related to bilirubin toxicity
Early genetic identification can prevent serious complications and guide appropriate treatment strategies.
Why Early Detection Matters for Your Family’s Health
Genetic knowledge is power when it comes to rare disorders. By identifying Criggler Najjar Syndrome early, you gain:
- Prevention of serious complications through timely treatment
- Informed family planning decisions with genetic counselling
- Personalized treatment approaches based on your specific genetic profile
- Peace of mind through definitive diagnosis
- Reduced anxiety about unexplained symptoms
Understanding Your Genetic Results
We know waiting for genetic results can be stressful. That’s why we provide comprehensive, easy-to-understand reports accompanied by expert genetic counselling. Your results will clearly indicate whether the UGT1A1 gene mutations associated with Criggler Najjar Syndrome are present, along with detailed explanations of what this means for your health and family planning. Our genetic specialists are available to discuss your results and next steps, ensuring you never feel alone in this journey.
Transparent Pricing – Your Health Investment
| Test Option | Regular Price | Special Price | Value |
|---|---|---|---|
| Criggler Najjar Syndrome Genetic Test | ZAR 9,000 | Save ZAR 3,000 |
Consider this: Early detection can prevent hospitalizations and long-term complications that could cost significantly more than this one-time genetic investment.
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Conducted by qualified genetic specialists and gynecologists
- Accuracy Guaranteed: Advanced Sanger Sequencing technology ensures 99.9% accuracy
- Quick Turnaround: Results delivered within 7-8 days
- Simple Process: Just 2ml blood sample required
- Doctor’s Prescription: Professional medical oversight for your safety
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about genetic health conditions create unnecessary anxiety. With our special pricing of ZAR 9,000, there’s never been a better time to gain the genetic insights your family deserves.
Important: Early detection of genetic conditions can significantly improve treatment outcomes. Don’t delay – take control of your genetic health journey today.
Join thousands of South African families who have found answers and peace of mind through Oracle Genomics genetic testing. Your health journey matters to us.
