Understanding CHRND Gene Multiple Pterygium Syndrome: Your Path to Clarity
When you’re worried about a rare genetic condition like Multiple Pterygium Syndrome in your family, the uncertainty can be overwhelming. We understand the emotional weight of genetic concerns and the importance of getting clear, accurate answers. Our CHRND Gene NGS Genetic DNA Test provides the definitive information you need to make informed decisions about your family’s health future.
What This Test Detects
The CHRND gene test specifically identifies mutations that cause the lethal type of Multiple Pterygium Syndrome – a rare genetic disorder characterized by webbing across joints (pterygia), congenital contractures, and facial abnormalities. Using advanced Next Generation Sequencing (NGS) technology, we analyse your DNA with 99.9% accuracy to detect even the smallest genetic variations that could impact your family’s health.
Who Should Consider This Test?
This test is particularly important if you or your family members experience:
- Family history of Multiple Pterygium Syndrome or similar conditions
- Unexplained joint webbing or contractures in newborns
- Recurrent pregnancy losses with suspected genetic causes
- Planning a family with known genetic risk factors
- Abnormal ultrasound findings during pregnancy
Early genetic testing can provide crucial information for medical management and family planning decisions.
Why Early Detection Matters for Your Family
Getting tested for CHRND gene mutations offers significant benefits:
- Peace of Mind: Eliminate uncertainty about your genetic status
- Informed Family Planning: Make educated decisions about having children
- Early Intervention: Access appropriate medical care and support services
- Genetic Counselling: Understand inheritance patterns and family risks
- Medical Preparedness: Work with healthcare providers to create management plans
Understanding Your Test Results
We make understanding your results straightforward and supportive:
- Clear Reporting: Easy-to-understand results with professional interpretation
- Genetic Counselling Session: Included with your test to explain findings
- Family Pedigree Chart: Visual representation of inheritance patterns
- Next Steps Guidance: Practical recommendations based on your results
- Ongoing Support: Access to genetic specialists for follow-up questions
Our team ensures you never feel alone in understanding your genetic information.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| CHRND Gene NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
| Results Interpretation | INCLUDED | ||
All prices include VAT and professional fees
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Working with certified dermatologists and genetic specialists
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Fast Turnaround: Results within 3-4 weeks from sample receipt
- Multiple Sample Options: Blood, extracted DNA, or FTA card samples accepted
- Complete Confidentiality: Your genetic information is protected with strict privacy protocols
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic conditions dictate your family’s future. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you deserve.
Limited Time Offer: This special pricing of ZAR 6,700 won’t last forever. Take the first step toward genetic clarity and family health security today.
“Early genetic testing gave our family the information we needed to make confident health decisions. The peace of mind was priceless.” – Satisfied Oracle Genomics Patient
Ready to begin? Contact Oracle Genomics today and take the first step toward understanding your genetic health with confidence and compassion.
