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SHOC2 Gene Noonan Syndrome-Like NGS Genetic DNA Test

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

-28%

The SHOC2 Gene Noonan Syndrome-Like NGS Genetic DNA Test provides crucial insights into genetic conditions affecting growth and development. For just ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next-Generation Sequencing technology to detect mutations in the SHOC2 gene, which can cause Noonan syndrome-like symptoms. Our comprehensive approach includes professional genetic counselling to help you understand your family’s health patterns. Early detection through this test can guide appropriate medical management and treatment planning. Available nationwide across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria, with results delivered within 3-4 weeks. Trust Oracle Genomics for accurate, reliable genetic testing that puts your family’s health 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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SHOC2 Noonan Syndrome DNA Test | ZAR 6
SHOC2 Gene Noonan Syndrome-Like NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding SHOC2 Gene Noonan Syndrome: Your Family’s Health Journey Starts Here

When you notice developmental delays or unusual physical features in your child, the uncertainty can be overwhelming. The SHOC2 Gene Noonan Syndrome-Like NGS Genetic DNA Test provides the clarity you need to understand your child’s health journey. At Oracle Genomics, we understand the emotional weight of genetic testing and provide compassionate, professional care every step of the way.

What Does This Test Detect?

The SHOC2 gene plays a crucial role in regulating cell growth and development. Mutations in this gene can lead to Noonan syndrome-like conditions, affecting multiple body systems. Our advanced Next-Generation Sequencing (NGS) technology examines the SHOC2 gene with exceptional accuracy, identifying even subtle genetic variations that might be missed by conventional testing methods.

This comprehensive analysis helps determine whether specific genetic changes are responsible for developmental concerns, providing essential information for your child’s healthcare team.

Who Should Consider This Test?

This test is particularly important for children and individuals showing:

  • Unusual facial features (wide-set eyes, low-set ears)
  • Growth delays or short stature
  • Heart abnormalities or murmurs
  • Developmental delays in motor skills or speech
  • Learning difficulties or intellectual challenges
  • Family history of similar symptoms
  • Unexplained bleeding tendencies or blood disorders

If your child exhibits any of these symptoms, early genetic testing can provide answers and guide appropriate medical care.

Why Early Detection Matters for Your Child’s Health

Understanding the genetic basis of your child’s condition offers multiple benefits:

  • Personalized Treatment Plans: Results guide healthcare providers in creating targeted treatment strategies
  • Family Planning Insights: Understand inheritance patterns for future family planning
  • Reduced Diagnostic Uncertainty: End the cycle of multiple doctor visits and inconclusive tests
  • Early Intervention Opportunities: Access appropriate therapies and support services sooner
  • Peace of Mind: Replace uncertainty with clear understanding and actionable information

Understanding Your Results: Clear Guidance Every Step

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

  • Professional Genetic Counselling: Before testing, our genetic counsellors help create a detailed family history pedigree
  • Clear Result Interpretation: Results are explained in understandable language with clinical significance
  • Follow-up Support: Guidance on next steps and connecting with appropriate specialists
  • Family Implications: Discussion about what results mean for other family members

Your results will clearly indicate whether a SHOC2 gene mutation was detected and what this means for your child’s health management.

Transparent Pricing & Exceptional Value

Service Regular Price Special Price Savings
SHOC2 Gene Noonan Syndrome-Like NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included:

  • Comprehensive NGS genetic analysis
  • Professional genetic counselling session
  • Family pedigree chart development
  • Detailed result interpretation
  • 3-4 week turnaround time
  • Multiple sample options (blood, extracted DNA, or blood spot card)

Why Trust Oracle Genomics?

Nationwide Accessibility: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria

Medical Expertise: Specialized in pediatric genetics with experienced genetic counsellors

Advanced Technology: State-of-the-art NGS technology for unparalleled accuracy

Patient-Centred Care: Empathetic approach focused on your family’s wellbeing

Proven Reliability: Trusted by healthcare professionals nationwide

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s health continue. Early detection through genetic testing can make a significant difference in their development and quality of life.

Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic test

Convenient Booking: Multiple sample collection options available

Quick Results: Receive answers within 3-4 weeks

Book Your Test Today:

  • Online Booking: Secure your appointment through our website
  • Phone Consultation: Speak with our genetic counselling team
  • Clinic Visit: Visit one of our nationwide locations
  • Home Collection: Convenient sample collection options available

Your child’s health journey deserves clarity and confidence. Contact Oracle Genomics today to schedule your SHOC2 genetic test and take control of your family’s health future.