Sale!

DNM1L Gene Encephalopathy Genetic DNA Test

Original price was: R9,350.Current price is: R6,700.

-28%

Facing concerns about mitochondrial disorders or neurological symptoms in your family? Our DNM1L Gene Encephalopathy Genetic DNA Test provides crucial answers for ZAR 6,700 (regular ZAR 9,350). This comprehensive test uses advanced NGS technology to detect mutations in the DNM1L gene, which can cause severe neurological conditions affecting mitochondrial function. Early detection through genetic testing can guide treatment decisions and provide clarity for family planning. Our experienced neurologists and genetic counsellors ensure you receive accurate, reliable results within 3-4 weeks. We offer nationwide coverage across South Africa, including Johannesburg, Cape Town, and Durban, making advanced genetic testing accessible to all families. Take control of your family’s health journey with confidence and professional support.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

DNM1L Gene Encephalopathy Test ZAR 6
DNM1L Gene Encephalopathy Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Understanding DNM1L Gene Encephalopathy: Your Path to Clarity and Peace of Mind

When neurological symptoms appear in your family, the uncertainty can be overwhelming. You deserve clear answers and a path forward. Our DNM1L Gene Encephalopathy Genetic DNA Test provides the definitive information you need to understand inherited mitochondrial disorders and make informed healthcare decisions for your family’s future.

What This Test Detects

The DNM1L gene plays a crucial role in maintaining healthy mitochondrial function throughout your body. When mutations occur in this gene, it can lead to severe neurological conditions affecting brain development and function. Our advanced Next-Generation Sequencing (NGS) technology examines your DNA to identify these specific genetic variations, providing clear answers about potential inherited risks.

Think of mitochondria as the powerhouses of your cells – when they don’t function properly due to DNM1L mutations, it can impact energy production in critical organs, particularly the brain and nervous system.

Who Should Consider This Test

This test is particularly important if you or your family members experience:

  • Unexplained neurological symptoms in infancy or childhood
  • Developmental delays or regression in motor skills
  • Family history of mitochondrial disorders
  • Multiple affected family members with similar neurological conditions
  • Planning for pregnancy with known family genetic risks
  • Unexplained seizures or movement disorders

Many South African families find peace of mind through genetic testing, especially when facing complex neurological symptoms that traditional diagnostics haven’t fully explained.

Why Early Detection Matters for Your Family’s Health

Understanding your genetic profile provides more than just answers – it offers tangible benefits for your family’s wellbeing:

  • Informed Treatment Decisions: Guide healthcare providers toward appropriate interventions and management strategies
  • Family Planning Clarity: Make confident decisions about future pregnancies with complete genetic information
  • Early Intervention Opportunities: Access specialised care and support services sooner
  • Reduced Diagnostic Uncertainty: End the cycle of multiple tests and unclear results
  • Peace of Mind: Replace anxiety with knowledge and a clear path forward

Understanding Your Results with Professional Support

We understand that genetic test results can feel overwhelming. That’s why every test includes comprehensive genetic counselling to help you understand your results in context. Our experienced neurologists and genetic counsellors will:

  • Explain your results in clear, understandable language
  • Discuss what the findings mean for your health and family
  • Provide guidance on next steps and available resources
  • Help you develop a personalised healthcare plan
  • Connect you with appropriate specialists if needed

You’ll never face your results alone – our team provides ongoing support throughout your healthcare journey.

Transparent Pricing and Exceptional Value

Service Regular Price Special Price Turnaround Time
DNM1L Gene Encephalopathy Test ZAR 9,350 ZAR 6,700 3-4 Weeks

What’s Included: Comprehensive genetic analysis, detailed results report, genetic counselling session, family pedigree chart development, and ongoing support from our neurological specialists.

Sample Collection: Simple blood draw, extracted DNA, or convenient blood spot on FTA card – we make testing accessible regardless of your location.

Why South African Families Trust Oracle Genomics

Nationwide Coverage

Available across South Africa including Johannesburg, Cape Town, Durban, Pretoria and surrounding areas. We bring advanced genetic testing to your community.

Expert Neurological Team

Our specialists have extensive experience in mitochondrial disorders and genetic neurology, ensuring accurate interpretation and personalised care.

Advanced NGS Technology

We use cutting-edge Next-Generation Sequencing for the most accurate and comprehensive genetic analysis available.

Complete Genetic Counselling

Every test includes professional genetic counselling to ensure you fully understand your results and their implications.

Take the First Step Toward Clarity Today

Don’t let uncertainty about genetic risks control your family’s future. With results in just 3-4 weeks and comprehensive support every step of the way, you can gain the clarity you need to make informed healthcare decisions.

Limited Time Offer: Save ZAR 2,650 on your DNM1L Gene Encephalopathy Test. Book your appointment today to secure this special pricing.

Ready to Learn More? Call us at 0861 UBUNTU (828688) or visit our clinics in Johannesburg, Cape Town, or Durban for a confidential consultation.