Find Answers for Unexplained Developmental Concerns
When your child shows developmental delays or neurological symptoms without clear cause, the uncertainty can be overwhelming. Our DPM1 Gene Glycosylation Disorder Type 1E test provides the clarity you need to understand these complex health challenges. Using cutting-edge NGS technology, we deliver accurate genetic insights that can transform your family’s healthcare journey.
Understanding Your DPM1 Gene Test
Glycosylation Disorder Type 1E is a rare genetic condition caused by mutations in the DPM1 gene. This gene plays a crucial role in creating essential proteins that help your body function properly. When this process is disrupted, it can lead to developmental delays, neurological issues, and other health concerns. Our test examines your DNA using Next Generation Sequencing (NGS) technology – the most advanced method available – to identify any mutations in the DPM1 gene with exceptional accuracy.
Who Should Consider This Test?
This test is particularly important if your child or family member experiences:
- Unexplained developmental delays in infancy or childhood
- Neurological symptoms like seizures or muscle weakness
- Failure to thrive or growth concerns
- Family history of similar symptoms
- Multiple unexplained health issues without clear diagnosis
Early testing can provide answers that help guide appropriate medical care and support.
Why Early Detection Matters for Your Family
Getting a definitive diagnosis through genetic testing offers multiple benefits:
- Peace of Mind: End the diagnostic odyssey and uncertainty
- Personalised Care: Guide treatment decisions based on specific genetic findings
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and support services sooner
- Reduced Healthcare Costs: Avoid unnecessary tests and treatments
Understanding Your Results with Confidence
We understand that waiting for genetic test results can be anxiety-provoking. That’s why we include professional genetic counselling with every test. Our specialists will:
- Explain your results in clear, understandable language
- Create a detailed family pedigree chart to understand inheritance patterns
- Discuss what the results mean for your family’s health
- Provide guidance on next steps and available resources
- Connect you with appropriate medical specialists if needed
Your results will be available within 3-4 weeks, and we’ll support you every step of the way.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| DPM1 Gene Glycosylation Disorder Type 1E NGS Test | ZAR 6,700 | |
| Includes genetic counselling and family pedigree analysis | ||
This comprehensive package represents excellent value compared to the potential costs of ongoing undiagnosed medical care.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Advanced Technology: Using NGS – the gold standard in genetic testing
- Professional Expertise: Working with qualified genetic counsellors and medical professionals
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Proven Accuracy: Reliable results you can trust for important healthcare decisions
Take the First Step Toward Answers Today
Don’t let uncertainty about your family’s health continue. Our DPM1 gene test provides the clarity you need to make informed decisions about care and treatment.
Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic testing package. Book today to secure your special pricing.
Simple Testing Process
We offer flexible sample collection options to suit your needs:
- Blood draw at one of our nationwide partner clinics
- Extracted DNA from previous testing
- Convenient blood spot on FTA card (just one drop needed)
Our team will guide you through the simple preparation process, which includes providing clinical history and attending a genetic counselling session.
