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HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test

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

-28%

As a parent, watching your newborn struggle with cyanosis (bluish skin) can be terrifying. Our HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test provides the answers you need for your baby’s health. For just ZAR 6,700 (regularly ZAR 9,350), this advanced genetic test uses Next Generation Sequencing technology to detect mutations in the HBG2 gene that cause temporary cyanosis in newborns. Early detection means proper management and peace of mind. Our nationwide coverage ensures access in Johannesburg, Cape Town, Durban, and Pretoria. With results in 3-4 weeks and comprehensive genetic counselling included, you’ll have the clarity needed to protect your baby’s health journey.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

HBG2 Gene Cyanosis Test | ZAR 6
HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Protect Your Newborn from Cyanosis with Advanced Genetic Testing

As a parent, seeing your newborn baby with bluish skin (cyanosis) can be one of the most frightening experiences. That temporary blue discolouration isn’t just concerning – it could indicate an underlying genetic condition affecting your baby’s haemoglobin production. Our HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test provides the clarity and peace of mind every parent deserves.

Understanding the HBG2 Gene Cyanosis Test

This specialised genetic test examines the HBG2 gene, which plays a crucial role in producing gamma-globin chains in fetal haemoglobin. When mutations occur in this gene, it can cause transient neonatal cyanosis – temporary blue skin discolouration in newborns that typically resolves but may indicate underlying health concerns.

Using cutting-edge Next Generation Sequencing (NGS) technology, we analyse your baby’s DNA with exceptional accuracy to identify any HBG2 gene mutations. This isn’t just a test; it’s your first step toward understanding and managing your newborn’s health condition.

Is This Test Right for Your Baby?

Consider this test if your newborn shows:

  • Bluish skin discolouration (cyanosis) that appears temporary
  • Unexplained breathing difficulties in the first weeks of life
  • Family history of haemoglobin disorders or genetic conditions
  • Previous siblings with similar transient cyanosis episodes
  • Concerns about inherited genetic conditions affecting blood oxygen

Early detection through genetic testing can prevent unnecessary worry and ensure proper medical management.

Why Early Detection Matters for Your Baby’s Health

Getting this test provides crucial benefits:

  • Peace of Mind: Know exactly what’s causing your baby’s symptoms
  • Proper Management: Work with healthcare providers on the right care plan
  • Family Planning: Understand genetic risks for future pregnancies
  • Early Intervention: Address potential complications before they develop
  • Reduced Anxiety: Replace uncertainty with clear, actionable information

Understanding Your Test Results

We make understanding your results straightforward and reassuring:

  • Clear Explanations: Our genetic counsellors explain findings in simple terms
  • Actionable Guidance: Receive specific recommendations for next steps
  • Family Implications: Understand what results mean for your family’s health
  • Medical Referrals: Get connected with appropriate specialists if needed
  • Ongoing Support: Access follow-up consultations for additional questions

Remember: Knowledge is power when it comes to your baby’s health.

Affordable Genetic Testing for Peace of Mind

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 Timely results for prompt action
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient collection options
Genetic Counselling Included Professional guidance and support

Consider this investment in your baby’s health: early detection can prevent costly emergency care and provide priceless peace of mind.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Specialised haematologists and genetic counsellors
  • Advanced Technology: Next Generation Sequencing for maximum accuracy
  • Patient-Focused Care: Empathetic support throughout your testing journey
  • Proven Reliability: Trusted by healthcare providers nationwide

Take Action for Your Baby’s Health Today

Don’t let uncertainty about your newborn’s health create unnecessary stress. Early detection through genetic testing provides the answers you need to ensure your baby receives the right care.

Book your genetic counselling session now to:

  • Discuss your baby’s symptoms and family history
  • Create a comprehensive pedigree chart
  • Understand the testing process and what to expect
  • Get your questions answered by genetic experts

Your baby’s health journey starts with clarity. Contact Oracle Genomics today to schedule your appointment and take the first step toward peace of mind.

Limited time special pricing: Save ZAR 2,650 on your HBG2 Gene Cyanosis Test

Test Preparation Requirements

To ensure accurate results, please bring:

  • Complete clinical history of the patient
  • Information about family members affected by similar conditions
  • Be prepared for a genetic counselling session to create a family pedigree chart

Our team will guide you through every step of the process with compassion and professionalism.