Find Answers for Unexplained Neurological Symptoms with DLAT Gene Testing
When your child struggles with developmental delays, neurological symptoms, or metabolic issues without clear cause, the uncertainty can be overwhelming. Our DLAT Gene Pyruvate Dehydrogenase E2 Deficiency test provides the clarity you need to understand these complex health challenges and take proactive steps toward better management.
Understanding the DLAT Gene Test
This advanced genetic test examines your DLAT gene using Next-Generation Sequencing (NGS) technology to identify mutations that cause pyruvate dehydrogenase E2 deficiency. This rare metabolic disorder affects how your body converts food into energy, particularly impacting brain development and function. Our test provides definitive answers about whether this condition is causing the neurological symptoms you’re experiencing.
Who Should Consider This Test?
This test is particularly important if you or your child experience:
- Unexplained developmental delays in infancy or childhood
- Neurological symptoms like seizures, muscle weakness, or coordination problems
- Metabolic acidosis or lactic acidosis episodes
- Family history of similar neurological or metabolic conditions
- Diagnostic uncertainty despite multiple medical evaluations
Early identification can significantly improve quality of life through targeted interventions.
Why Early Detection Matters for Your Health
Getting tested provides life-changing benefits:
- Peace of Mind: End the diagnostic uncertainty and get definitive answers
- Personalised Treatment: Develop targeted management strategies based on your specific genetic profile
- Family Planning: Understand inheritance patterns for future family planning decisions
- Prevent Complications: Early intervention can prevent serious neurological damage
- Comprehensive Support: Our included genetic counselling helps you navigate next steps with confidence
Understanding Your Results
We know waiting for genetic test results can be stressful. Our team provides:
- Clear, easy-to-understand reports explaining your results in plain language
- Professional genetic counselling to help interpret findings and implications
- Personalised recommendations for next steps and management options
- Ongoing support and resources for your healthcare journey
- Connection to specialists who understand your specific condition
You’ll never face your results alone – we’re here to guide you every step of the way.
Affordable, Life-Changing Genetic Testing
| Service | Regular Price | Special Price | Value |
|---|---|---|---|
| DLAT Gene Test with Genetic Counselling | R6,700 | Save R2,650 | |
| Turnaround Time | 3-4 Weeks | ||
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | ||
Consider this investment in your health: early detection can prevent years of medical uncertainty and potentially save thousands in future healthcare costs.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified general physicians and genetic specialists
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Complete Support: Genetic counselling included to ensure you understand your results
- Proven Track Record: Trusted by healthcare professionals and patients nationwide
Take Control of Your Health Journey Today
Don’t let uncertainty about neurological symptoms continue to worry you. Our DLAT gene test provides the answers you need to move forward with confidence.
Limited Time Offer: Book within the next 7 days to secure your special pricing of R6,700. Early detection could change everything – take the first step toward clarity today.
