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CBS Gene Homocystinuria Genetic DNA Test

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

-28%

Facing concerns about inherited metabolic disorders? Our CBS Gene Homocystinuria DNA test provides definitive answers about cystathionine beta-synthase deficiency, a serious inherited condition that affects how your body processes proteins. For just ZAR 6,700 (regularly ZAR 9,350), this comprehensive Next-Generation Sequencing test delivers unparalleled accuracy in detecting genetic mutations that could impact your family’s health. Early detection through this test can prevent devastating complications like blood clots, vision problems, and developmental delays. Our experienced genetic counsellors guide you through the entire process, ensuring you understand your results and their implications. With nationwide coverage including Johannesburg, Cape Town, and Durban, accessing this life-changing genetic insight has never been easier or more affordable. Take control of your genetic health today with confidence in our medical expertise and commitment to your wellbeing.

📞 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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CBS Gene Homocystinuria DNA Test | ZAR 6
CBS Gene Homocystinuria Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Genetic Health: CBS Gene Homocystinuria DNA Testing

When you’re concerned about inherited health conditions affecting your family, the uncertainty can be overwhelming. Our CBS Gene Homocystinuria DNA test provides the clarity you need to make informed decisions about your health and your family’s future. This comprehensive genetic analysis specifically detects cystathionine beta-synthase deficiency, a serious metabolic disorder that, when identified early, can be effectively managed to prevent life-altering complications.

What This Test Reveals About Your Health

The CBS Gene Homocystinuria test uses advanced Next-Generation Sequencing (NGS) technology to examine your DNA for mutations in the CBS gene. This gene plays a crucial role in processing the amino acid homocysteine, and when it doesn’t function properly, it can lead to a buildup of harmful substances in your body. Our test provides definitive answers about whether you carry genetic variations that could affect your metabolic health or be passed to future generations.

Who Should Consider This Genetic Test?

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

  • Unexplained blood clotting disorders or thrombosis at a young age
  • Vision problems like lens dislocation or severe myopia
  • Developmental delays or intellectual disability in children
  • Marfan-like physical features (tall, thin build, long limbs)
  • Family history of homocystinuria or related metabolic disorders
  • Osteoporosis or bone abnormalities at a young age
  • Previous pregnancy losses or fertility concerns

If any of these situations sound familiar, this test could provide the answers you’ve been seeking.

Why Early Detection Matters for Your Health

Identifying CBS gene mutations early can transform health outcomes by:

  • Preventing serious complications like strokes, heart attacks, and blood clots
  • Enabling early intervention through dietary management and vitamin therapy
  • Providing family planning guidance for future pregnancies
  • Reducing anxiety through definitive genetic information
  • Creating personalised treatment plans based on your specific genetic profile

Knowledge truly is power when it comes to managing inherited metabolic conditions.

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. That’s why we provide comprehensive support throughout the process:

  • Clear, easy-to-understand reports explaining your genetic findings
  • Professional genetic counselling session included with your test
  • Personalised recommendations based on your results
  • Family pedigree analysis to understand inheritance patterns
  • Ongoing support from our medical team for any questions

Your results will be delivered within 3-4 weeks, and we’ll be with you every step of the way to ensure you feel confident and informed.

Affordable Genetic Testing for South African Families

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time savings of ZAR 2,650
Turnaround Time 3-4 Weeks Rapid results for timely decisions
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient collection options
Included Services Genetic Counselling & Family Pedigree Analysis Complete support package

Consider this: the cost of managing untreated homocystinuria complications can far exceed the investment in early detection. This test represents exceptional value for your long-term health.

Why Trust Oracle Genomics With Your Genetic Health?

  • Nationwide Coverage – Available throughout South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise – Our team includes specialised genetic counsellors and medical professionals
  • Advanced Technology – Using cutting-edge NGS technology for unparalleled accuracy
  • Patient-Focused Care – We prioritise your comfort, understanding, and peace of mind
  • Proven Track Record – Thousands of South Africans have trusted us with their genetic testing needs

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about inherited health conditions dictate your family’s future. With our special pricing of ZAR 6,700, there’s never been a better time to gain the genetic insights that could protect your health for generations to come.



Limited Time Offer: This special pricing of ZAR 6,700 (save ZAR 2,650) won’t last forever. Secure your family’s genetic health while this opportunity is available.

“The peace of mind we gained from understanding our genetic risks was priceless. The counselling helped us make informed decisions about our family’s future.” – Recent Patient