Find Answers for Rare Genetic Disorders with PEX1 Gene Testing
When your child shows unexplained developmental delays, vision problems, or neurological symptoms, the uncertainty can be overwhelming. Our PEX1 Gene Peroxisome Biogenesis Disorder Type 1B test provides the clarity and answers your family deserves. Using cutting-edge NGS technology, we deliver accurate results that can guide treatment decisions and provide peace of mind.
Understanding the PEX1 Gene Test
The PEX1 gene plays a critical role in creating peroxisomes – essential cellular structures that break down toxic substances and produce important compounds. When this gene has mutations, it can lead to peroxisome biogenesis disorders that affect multiple body systems. Our advanced Next-Generation Sequencing (NGS) technology examines your DNA to identify these mutations with exceptional accuracy, providing definitive answers about this rare genetic condition.
Who Should Consider This Test?
This test is particularly important for families experiencing:
- Unexplained developmental delays in infants or children
- Vision problems including cataracts or retinal issues
- Hearing loss or neurological symptoms
- Liver dysfunction or feeding difficulties
- Family history of peroxisome biogenesis disorders
- Multiple affected siblings with similar symptoms
Early detection through genetic testing can help guide appropriate medical care and provide valuable information for family planning decisions.
Why Early Detection Matters for Your Family’s Health
Getting tested for PEX1 gene mutations offers significant benefits:
- Definitive Diagnosis: End the uncertainty and get clear answers about your child’s condition
- Treatment Guidance: Help healthcare providers develop targeted treatment plans
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and support services sooner
- Peace of Mind: Reduce anxiety by knowing exactly what you’re dealing with
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results. We provide:
- Clear explanation of positive or negative findings
- Guidance on what the results mean for your family’s health
- Information about inheritance patterns and recurrence risks
- Referrals to appropriate specialists and support services
- Ongoing support for managing the condition
Remember: A positive result provides valuable information for managing health, while a negative result can bring significant relief and peace of mind.
Affordable Genetic Testing with Clear Pricing
| Service | Regular Price | Special Price |
|---|---|---|
| PEX1 Gene Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Considering the potential lifetime costs of undiagnosed genetic conditions, this test represents excellent value for your family’s health investment.
Why Trust Oracle Genomics?
- Nationwide Coverage: Convenient testing centres across Johannesburg, Cape Town, Durban, and Pretoria
- Expert Genetic Counselling: Comprehensive pre-test and post-test counselling included
- Advanced Technology: State-of-the-art NGS technology for maximum accuracy
- Quick Turnaround: Results typically available within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Neurology Specialists: Tests supervised by experienced neurologists
Take the First Step Toward Clarity Today
Don’t let uncertainty about rare genetic disorders continue to worry your family. Our compassionate team is ready to help you get the answers you need.
Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic test. Book your appointment today and take control of your family’s genetic health journey.
