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LIPT1 Gene Leigh Syndrome NGS Genetic DNA Test

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

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The LIPT1 Gene Leigh Syndrome NGS Genetic DNA Test provides crucial insights into rare metabolic disorders affecting energy production in cells. For ZAR 6,700, this advanced test uses Next Generation Sequencing technology to detect mutations in the LIPT1 gene, which can cause pyruvate and alpha-ketoglutarate dehydrogenase deficiencies. Early detection through this reliable test can help guide treatment decisions and provide families with much-needed answers. Our nationwide coverage across South Africa ensures accessibility for patients in Johannesburg, Cape Town, Durban, and Pretoria. With results in 3-4 weeks and comprehensive genetic counselling included, you can trust Oracle Genomics for accurate, confidential testing that brings clarity to complex neurological conditions.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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LIPT1 Gene Leigh Syndrome DNA Test | ZAR 6
LIPT1 Gene Leigh Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding LIPT1 Gene Leigh Syndrome: Your Path to Answers and Peace of Mind

When your child or loved one shows unexplained neurological symptoms, the uncertainty can be overwhelming. The LIPT1 Gene Leigh Syndrome NGS Genetic DNA Test offers clarity and direction for families facing complex metabolic disorders. At Oracle Genomics, we understand the emotional journey you’re on, and we’re here to provide the accurate, reliable genetic testing you need to make informed healthcare decisions.

What This Test Detects

The LIPT1 gene plays a critical role in energy production within your cells. When mutations occur in this gene, it can lead to deficiencies in pyruvate and alpha-ketoglutarate dehydrogenase – essential enzymes that help convert food into energy. This test uses advanced Next Generation Sequencing (NGS) technology to identify these genetic variations with exceptional accuracy, giving you and your healthcare team the information needed to develop an appropriate care plan.

Who Should Consider This Test

This test is particularly important for individuals experiencing:

  • Unexplained developmental delays or regression in infants and children
  • Neurological symptoms including seizures, muscle weakness, or coordination difficulties
  • Family history of Leigh syndrome or similar metabolic disorders
  • Abnormal metabolic test results suggesting energy production issues
  • Progressive neurological deterioration without clear cause

If you’ve been searching for answers about unexplained neurological symptoms in your family, this test could provide the clarity you need.

Why Early Detection Matters for Your Health

Identifying LIPT1 gene mutations early can significantly impact treatment outcomes and quality of life. Benefits include:

  • Targeted Treatment Planning: Knowing the specific genetic cause allows for personalised treatment approaches
  • Family Planning Guidance: Understanding inheritance patterns helps with future family decisions
  • Reduced Diagnostic Uncertainty: End the cycle of inconclusive tests and unanswered questions
  • Improved Symptom Management: Better understanding leads to more effective symptom control
  • Peace of Mind: Finally having answers can reduce anxiety and provide direction

Understanding Your Test Results

We know waiting for genetic test results can be stressful. Our comprehensive approach includes:

  • Clear, Understandable Reports: Results presented in plain language with medical interpretation
  • Genetic Counselling Session: Included with your test to help understand results and implications
  • Family Pedigree Analysis: Mapping family history to understand inheritance patterns
  • Clinical Correlation: Connecting genetic findings with clinical symptoms
  • Ongoing Support: Access to our team for questions about your results

Your results will be ready within 3-4 weeks, and we’ll guide you through every step of understanding what they mean for your health.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
LIPT1 Gene Leigh Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive NGS genetic analysis, genetic counselling session, family pedigree analysis, detailed results report, and ongoing clinical support.

Why Trust Oracle Genomics

  • Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Advanced NGS Technology: Using the latest genetic sequencing methods for maximum accuracy
  • Expert Medical Team: Working with qualified neurologists and genetic specialists
  • Confidential & Secure: Your genetic information is protected with strict privacy protocols
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Proven Track Record: Trusted by healthcare providers across South Africa

Take the First Step Toward Answers Today

Don’t let uncertainty about neurological symptoms continue to cause worry and stress. Early detection through genetic testing can provide the answers you need to move forward with confidence.

Limited Time Special: Save ZAR 2,650 on this essential genetic test – book now while this special pricing is available.

Convenient Nationwide Access: Whether you’re in Johannesburg, Cape Town, Durban, or Pretoria, we make genetic testing accessible across South Africa.

Ready to Get Started?

  • Online Booking: Schedule your test quickly and easily through our secure portal
  • Phone Consultation: Speak with our genetic specialists to discuss your specific situation
  • Healthcare Provider Referral: Ask your doctor about referring you for testing

Take action today – your journey to answers and peace of mind starts with one simple decision. Contact Oracle Genomics now to schedule your LIPT1 Gene Leigh Syndrome NGS Genetic DNA Test.