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ATR Gene Seckel Syndrome Type 1 NGS Genetic DNA Test

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

-28%

Facing concerns about Seckel Syndrome in your family? Our ATR Gene Seckel Syndrome Type 1 NGS Genetic DNA Test provides definitive answers for South African families. For only ZAR 6,700, this advanced test uses Next Generation Sequencing technology to detect mutations in the ATR gene with exceptional accuracy. If you’re noticing developmental delays, growth concerns, or have a family history of Seckel Syndrome, this test offers crucial clarity. We understand the anxiety that comes with genetic uncertainty, which is why our comprehensive approach includes genetic counselling to help you understand your results. With nationwide coverage including Johannesburg, Cape Town, and Durban, and results in just 3-4 weeks, you can take confident steps toward understanding your family’s genetic health. Trust Oracle Genomics for reliable, compassionate genetic testing that puts your family’s wellbeing first.

📞 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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ATR Gene Seckel Syndrome DNA Test | ZAR 6
ATR Gene Seckel Syndrome Type 1 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Seckel Syndrome: Your Family’s Genetic Health Journey

When you’re concerned about your child’s growth and development, the uncertainty can feel overwhelming. Seckel Syndrome is a rare genetic condition that affects growth and development, and the ATR Gene Seckel Syndrome Type 1 NGS Genetic DNA Test provides the clarity South African families need to move forward with confidence. We understand the emotional weight of genetic testing, which is why we’ve created a compassionate, professional testing experience that prioritises your family’s wellbeing.

What This Test Reveals About Your Genetic Health

The ATR Gene Seckel Syndrome Type 1 test uses advanced Next Generation Sequencing (NGS) technology to examine the ATR gene for mutations associated with Seckel Syndrome. This isn’t just another genetic test – it’s a comprehensive analysis that provides definitive answers about whether specific genetic variations are present. The ATR gene plays a crucial role in DNA repair and cell division, and mutations can lead to the characteristic features of Seckel Syndrome, including growth delays and developmental concerns.

Who Should Consider This Genetic Test?

This test is particularly important for families who have noticed:

  • Significant growth delays in infancy or childhood
  • Microcephaly (small head size)
  • Distinctive facial features associated with Seckel Syndrome
  • Intellectual or developmental delays
  • Family history of Seckel Syndrome or similar conditions
  • Unexplained developmental concerns in multiple family members

If you’re planning a family and have concerns about genetic risks, this test can provide valuable information for your family planning decisions.

Why Early Detection Matters for Your Family’s Future

Getting clear answers about Seckel Syndrome provides more than just diagnosis – it offers direction. With definitive genetic information, you can:

  • Access appropriate medical care and interventions earlier
  • Connect with specialist healthcare providers who understand the condition
  • Make informed decisions about family planning
  • Reduce the anxiety of uncertainty with concrete information
  • Develop targeted support strategies for your child’s development
  • Participate in research and support communities with confidence

Understanding Your Results: Clear Guidance Every Step

We know that waiting for genetic test results can be stressful. That’s why our process includes comprehensive genetic counselling both before and after testing. Your results will be presented in clear, understandable language with:

  • Detailed explanation of any genetic variations found
  • Clear guidance on what the results mean for your family
  • Information about next steps and available resources
  • Support in understanding inheritance patterns and family implications
  • Connection to appropriate medical specialists if needed

Our genetic counsellors are available to answer your questions and provide the support you need throughout this journey.

Transparent Pricing for Peace of Mind

Service Regular Price Special Price
ATR Gene Seckel Syndrome Type 1 NGS Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session Included
Family Pedigree Analysis Included
Results Interpretation Included

This comprehensive package represents exceptional value compared to the potential costs of ongoing uncertainty and delayed interventions.

Why South African Families Trust Oracle Genomics

With testing centres across South Africa including Johannesburg, Cape Town, Durban, and Pretoria, we’re committed to making advanced genetic testing accessible to all South African families. Our NGS technology provides the highest level of accuracy available, and our team includes experienced genetic specialists who understand the unique needs of South African patients.

Every test is processed with the utmost care and precision, and our 3-4 week turnaround time means you get answers when you need them most. We accept multiple sample types including blood, extracted DNA, or a simple blood drop on an FTA card for your convenience.

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about Seckel Syndrome create unnecessary stress for your family. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you need. Early detection can make a significant difference in accessing appropriate care and support.

Book your test today and receive:

  • Comprehensive genetic counselling session
  • Family pedigree analysis
  • Definitive genetic results in 3-4 weeks
  • Clear results interpretation and guidance
  • Nationwide accessibility across South Africa

Contact Oracle Genomics now to schedule your ATR Gene Seckel Syndrome Type 1 NGS Genetic DNA Test and take control of your family’s genetic health journey.