Understanding Zellweger Syndrome and the PEX19 Gene Test
When you’re concerned about rare genetic conditions affecting your family’s health, the uncertainty can be overwhelming. Zellweger syndrome is a serious neurological disorder that affects infants, and understanding your genetic risk can provide the clarity you need to make informed decisions. Our PEX19 Gene NGS Genetic DNA Test offers the definitive answers you’re seeking, using the most advanced genetic technology available.
What Does This Test Detect?
This comprehensive test specifically examines the PEX19 gene for mutations that cause Zellweger syndrome spectrum disorders. Using next-generation sequencing (NGS) technology, we analyse your DNA with exceptional precision to identify any abnormalities in this critical gene. The PEX19 gene plays a vital role in peroxisome biogenesis – essential cellular structures that process toxic substances and produce important compounds. When this gene malfunctions, it can lead to the severe symptoms associated with Zellweger syndrome.
Who Should Consider This Test?
This test is particularly important if you or your family members have experienced:
- Family history of Zellweger syndrome or related peroxisomal disorders
- Unexplained infant neurological symptoms
- Plans for pregnancy with known genetic risk factors
- Previous children affected by developmental delays or metabolic issues
- Concerns about carrier status for rare genetic conditions
Why Early Detection Matters for Your Family’s Health
Early genetic testing provides invaluable benefits that extend beyond immediate diagnosis:
- Peace of Mind: Eliminate uncertainty and reduce the anxiety of not knowing
- Informed Family Planning: Make confident decisions about future pregnancies
- Early Intervention: Access appropriate medical care and support services sooner
- Genetic Counselling: Understand inheritance patterns and risks for other family members
- Medical Preparedness: Work with healthcare providers to develop proactive care plans
Understanding Your Test Results
We know that waiting for genetic test results can be stressful. That’s why we provide clear, comprehensive reports with expert interpretation. Our genetic counsellors will walk you through your results, explaining what they mean for you and your family in straightforward language. Whether your results show a mutation or provide reassuring clarity, you’ll have the professional support needed to understand the implications and next steps.
Comprehensive Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| PEX19 Gene Zellweger Syndrome NGS Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Considering the potential impact on your family’s health and future planning, this test represents exceptional value. The peace of mind and medical insights gained can be priceless when making important health decisions.
Why Trust Oracle Genomics?
At Oracle Genomics, we combine medical excellence with genuine patient care:
- Nationwide Coverage: Accessible testing centres across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
- Expert Genetic Counselling: Comprehensive pre-test counselling to ensure you’re fully informed
- Advanced NGS Technology: State-of-the-art genetic analysis for maximum accuracy
- Rapid Turnaround: Results typically within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Neurology Specialists: Tests reviewed by qualified neurologists
Take the First Step Toward Clarity
Don’t let uncertainty about genetic risks overshadow your family’s future. Our PEX19 Gene test provides the answers you need with the compassion and professionalism you deserve. With convenient locations across South Africa and comprehensive support throughout the process, taking this important step for your family’s health has never been easier.
Book your genetic counselling session today and take control of your family’s genetic health journey. Call us now or visit our website to schedule your appointment.
