Understanding DCLRE1C Gene Testing for Severe Combined Immunodeficiency
When you’re concerned about immune system disorders or have a family history of Severe Combined Immunodeficiency (SCID), finding clear answers becomes essential for your family’s health journey. Our DCLRE1C gene test offers the clarity and confidence you need through advanced genetic analysis specifically designed to detect Athabascan-type SCID mutations.
What This Test Detects
The DCLRE1C gene test uses cutting-edge Next-Generation Sequencing (NGS) technology to identify specific mutations in the DCLRE1C gene that cause Severe Combined Immunodeficiency Athabascan type. This condition affects the immune system’s ability to fight infections, making early detection crucial for proper management and treatment planning.
Unlike standard immune tests, our genetic analysis provides definitive information about the underlying cause of immune deficiencies, helping healthcare providers develop targeted treatment strategies.
Who Should Consider This Test
This test is particularly important for:
- Infants or children with recurrent, severe infections
- Individuals with family history of SCID or immune disorders
- Parents planning pregnancy with known family immune conditions
- Patients with unexplained immune system deficiencies
- Those with Athabascan heritage or known genetic risk factors
If you’ve noticed frequent illnesses, poor response to vaccines, or have concerns about inherited immune conditions, this test provides the answers you need.
Why Early Detection Matters for Your Health
Identifying DCLRE1C gene mutations early can significantly impact treatment outcomes and quality of life. Benefits include:
- Early Intervention: Allows for prompt treatment before serious complications develop
- Family Planning Guidance: Provides crucial information for future family decisions
- Targeted Treatment: Helps doctors create personalized care plans
- Peace of Mind: Reduces uncertainty about inherited conditions
- Prevention Strategies: Enables proactive health management
Understanding Your Test Results
We understand that waiting for genetic test results can be anxiety-provoking. Our process includes comprehensive genetic counselling to help you understand what your results mean for your health and family.
Your results will clearly indicate whether DCLRE1C gene mutations are present, and our genetic counsellors will explain the implications in straightforward language. We provide ongoing support to help you make informed decisions about next steps.
Transparent Pricing & Value
| Service | Regular Price | Special Price |
|---|---|---|
| DCLRE1C Gene Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
Results delivered within 3-4 weeks | Sample: Blood or DNA extraction
Why Trust Oracle Genomics
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Expert Guidance: Comprehensive genetic counselling included
- Proven Accuracy: Reliable results you can trust for important health decisions
- Patient-Focused Care: Empathetic support throughout your testing journey
Take Control of Your Immune Health Today
Don’t let uncertainty about immune disorders affect your family’s future. Early detection through DCLRE1C gene testing can provide the answers and peace of mind you deserve.
Book your genetic counselling session now and take the first step toward understanding your genetic health.
Available at our nationwide locations including Johannesburg, Cape Town, Durban, and Pretoria. Special pricing of ZAR 6,700 includes comprehensive genetic counselling and family pedigree analysis.
Limited time special pricing – secure your appointment today
