Sale!

DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test

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

-28%

The DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test provides crucial early detection for severe combined immunodeficiency disorders. For just ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next Generation Sequencing technology to identify mutations in the DCLRE1C gene that cause Omenn syndrome – a life-threatening immune condition. Our comprehensive testing process includes genetic counselling to understand your family history and create a detailed pedigree chart. With results available within 3-4 weeks, this test offers peace of mind and enables early intervention strategies. Oracle Genomics provides nationwide coverage across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria, ensuring accessible, professional healthcare for all families concerned about inherited immune disorders.

📞 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

DCLRE1C Gene Omenn Syndrome DNA Test | ZAR 6
DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

DCLRE1C Gene Omenn Syndrome DNA Test: Early Detection for Immune Health

If you’re concerned about inherited immune disorders in your family, the DCLRE1C Gene Omenn Syndrome test provides the clarity and peace of mind you deserve. This advanced genetic test helps identify mutations that can cause severe combined immunodeficiency, allowing for early intervention and better health outcomes for you and your loved ones.

Understanding Your DCLRE1C Gene Test

The DCLRE1C gene plays a critical role in your immune system’s development and function. When mutations occur in this gene, it can lead to Omenn syndrome – a severe form of combined immunodeficiency that affects the body’s ability to fight infections. Our Next Generation Sequencing (NGS) technology provides the most accurate analysis available, examining every aspect of this important gene to give you definitive answers about your genetic health.

This isn’t just another test – it’s a comprehensive health assessment that includes professional genetic counselling to understand your family’s unique medical history and create a detailed pedigree chart showing how this condition may have affected multiple generations.

Who Should Consider This Important Test?

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

  • Recurrent, severe infections from early childhood
  • Failure to thrive or poor growth in infants
  • Chronic skin rashes or eczema-like conditions
  • Family history of immune disorders or early infant deaths
  • Unexplained autoimmune conditions
  • Previous children with immune system problems

If you’re planning a family and have concerns about inherited conditions, this test provides valuable information for making informed reproductive decisions.

Why Early Detection Matters for Your Family’s Health

Getting tested for DCLRE1C gene mutations offers significant benefits:

  • Early Intervention: Identify at-risk infants before symptoms develop
  • Treatment Planning: Work with specialists to create targeted treatment strategies
  • Family Planning: Make informed decisions about having children
  • Peace of Mind: Eliminate uncertainty about genetic risks
  • Prevent Complications: Reduce the risk of life-threatening infections

Early detection can literally save lives by enabling prompt medical intervention and specialized care.

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide clear, comprehensive reports with expert interpretation. Your results will clearly indicate:

  • Whether DCLRE1C gene mutations were detected
  • The specific type of mutation found (if any)
  • What the results mean for your health
  • Recommended next steps and specialist referrals
  • Genetic counselling follow-up options

Our genetic counsellors are available to help you understand your results and discuss what they mean for your family’s health future.

Affordable, Accessible Genetic Testing

Service Regular Price Special Price Savings
DCLRE1C Gene Omenn Syndrome Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Test Details:

  • Turnaround Time: 3-4 weeks
  • Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
  • Method: Next Generation Sequencing (NGS) Technology
  • Specialty: Dermatologist recommended

Considering the potential healthcare costs of undiagnosed immune disorders, this test represents excellent value for your family’s health investment.

Why Trust Oracle Genomics?

Oracle Genomics is committed to providing world-class genetic testing services across South Africa:

  • Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
  • Medical Expertise: Tests supervised by qualified dermatologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Patient-Centred Care: Comprehensive genetic counselling included
  • Proven Reliability: Trusted by healthcare professionals nationwide

Take Control of Your Genetic Health Today

Don’t let uncertainty about genetic risks affect your family’s future. Early detection through the DCLRE1C Gene Omenn Syndrome test can provide the answers you need to make informed health decisions.

Book your test now and take advantage of our special pricing of ZAR 6,700. Our team is ready to guide you through the testing process and provide the professional support you deserve.

Multiple Booking Options Available:

  • Online booking through our secure portal
  • Telephone consultations with genetic counsellors
  • In-person appointments at our nationwide centres
  • Referrals from your healthcare provider

Limited time special pricing – secure your family’s health future today!