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TGFB2 Gene Loeys-Dietz Syndrome Type 4 NGS Genetic DNA Test

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

-28%

Facing concerns about Loeys-Dietz syndrome type 4? Our TGFB2 genetic test provides definitive answers with 99.9% accuracy using advanced NGS technology. For only ZAR 6,700 (regularly ZAR 9,350), you’ll receive comprehensive genetic counselling and a detailed family pedigree analysis. This test detects mutations in the TGFB2 gene that cause connective tissue disorders affecting the heart, blood vessels, and skeletal system. Early detection through our nationwide testing centres in Johannesburg, Cape Town, Durban, and Pretoria can help prevent serious complications and guide appropriate medical management. Our compassionate team ensures you understand every step, from sample collection to result interpretation. Take control of your genetic health with confidence and peace of mind.

📞 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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TGFB2 Loeys-Dietz Test ZAR 6
TGFB2 Gene Loeys-Dietz Syndrome Type 4 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Genetic Health: TGFB2 Loeys-Dietz Syndrome Testing

When you’re concerned about inherited connective tissue disorders affecting your heart, blood vessels, or skeletal system, finding clear answers becomes essential for your peace of mind and long-term health planning. Our TGFB2 Gene Loeys-Dietz Syndrome Type 4 NGS Genetic DNA Test provides the definitive clarity you need to make informed decisions about your healthcare journey.

What This Test Reveals About Your Health

The TGFB2 gene plays a crucial role in regulating connective tissue development throughout your body. When mutations occur in this gene, they can lead to Loeys-Dietz syndrome type 4 – a condition that affects the strength and integrity of your blood vessels, heart valves, and skeletal structure. Our advanced Next-Generation Sequencing (NGS) technology examines your TGFB2 gene with exceptional precision, identifying even the smallest genetic variations that could impact your health.

This isn’t just a test; it’s a comprehensive health assessment that considers your complete medical history and family background through professional genetic counselling sessions.

Who Should Consider This Genetic Test?

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

  • Unexplained aortic aneurysms or arterial tortuosity
  • Connective tissue abnormalities affecting joints or skin
  • Family history of sudden cardiac events at young ages
  • Craniofacial features associated with connective tissue disorders
  • Multiple miscarriages or pregnancy complications
  • Developmental delays with skeletal abnormalities

If you’re planning a family and have concerns about genetic inheritance, this test provides crucial information for making informed reproductive decisions.

Why Early Detection Matters for Your Future

Knowing your genetic status empowers you to take proactive steps toward managing your health. Early detection of TGFB2 mutations allows for:

  • Regular monitoring of cardiovascular health to prevent emergencies
  • Personalised treatment plans tailored to your genetic profile
  • Informed family planning decisions with genetic counselling support
  • Preventive measures to reduce complication risks
  • Peace of mind through definitive answers about your genetic health

Many patients find that understanding their genetic makeup reduces anxiety and helps them feel more in control of their health journey.

Understanding Your Test Results

Our comprehensive reporting makes your results easy to understand. You’ll receive:

  • Clear explanation of any TGFB2 gene mutations detected
  • Detailed analysis of what these findings mean for your health
  • Personalised recommendations for monitoring and management
  • Access to genetic counselling for result interpretation
  • Guidance on sharing results with your healthcare providers

Remember: A positive result doesn’t mean certain health problems will develop – it means you can take proactive steps to monitor and manage your health effectively.

Transparent Pricing & Exceptional Value

Service Regular Price Special Price Savings
TGFB2 Loeys-Dietz Syndrome Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Includes genetic counselling session and comprehensive family pedigree analysis

Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card

Why South Africans Trust Oracle Genomics

We understand that genetic testing involves sensitive personal health information. That’s why we’ve built our reputation on:

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Tests supervised by qualified general physicians
  • Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
  • Patient Privacy: Strict confidentiality protocols for all genetic information
  • Comprehensive Support: Genetic counselling included with every test

Thousands of South African families have trusted us with their genetic health journey – join them in taking control of your health future.

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about your genetic health create unnecessary anxiety. Our compassionate team is ready to guide you through every step of the testing process with professionalism and care.

Limited Time Special: Book your TGFB2 Loeys-Dietz Syndrome test at ZAR 6,700 – saving you ZAR 2,650 off the regular price. This special pricing won’t last forever.



Same-day appointments available at our Johannesburg, Cape Town, Durban, and Pretoria locations. Your genetic health journey starts with one simple decision.