Protect Your Newborn from Fatal SPTB Gene Anemia
As expectant parents, the health of your newborn is your greatest concern. SPTB Gene Anemia is a serious genetic condition that can cause life-threatening hemolytic anemia in infants, often with devastating consequences. But there is hope – early detection through our advanced NGS genetic testing can identify this condition before symptoms appear, giving your baby the best possible start in life.
Understanding SPTB Gene Anemia Testing
SPTB Gene Anemia is a genetic disorder that affects red blood cells in newborns, causing them to break down prematurely (hemolysis). This can lead to severe anemia, jaundice, and in fatal cases, life-threatening complications. Our Next Generation Sequencing (NGS) technology examines the SPTB gene to identify mutations that could put your baby at risk.
The test is completely safe and requires only a small blood sample or extracted DNA. Our expert team, including specialist hematologists and genetic counsellors, ensures you receive comprehensive support throughout the testing process.
Who Should Consider This Life-Saving Test?
- Couples with a family history of neonatal anemia or unexplained infant deaths
- Parents who have lost a previous child to hemolytic anemia
- Families with known genetic blood disorders
- Expectant parents seeking comprehensive prenatal screening
- Couples planning pregnancy who want genetic carrier screening
If you’ve experienced the heartbreak of losing a child to unexplained anemia or have concerns about your family’s genetic health history, this test provides the answers you need.
Why Early Detection Matters for Your Family’s Health
Identifying SPTB Gene Anemia early can be life-saving. With proper medical management, many complications can be prevented or effectively treated. Benefits include:
- Peace of mind knowing your baby’s genetic health status
- Early intervention strategies if the condition is detected
- Informed family planning decisions for future pregnancies
- Reduced anxiety during pregnancy and after birth
- Access to specialist care and treatment options
Understanding Your Results with Confidence
We understand that waiting for genetic test results can be stressful. That’s why we provide:
- Clear, easy-to-understand reports with detailed explanations
- Genetic counselling sessions to help you understand the implications
- Family pedigree analysis to identify inheritance patterns
- Direct access to hematology specialists for result interpretation
- Personalised recommendations for next steps and management
Our team is here to support you every step of the way, ensuring you feel confident and informed about your results.
Affordable, Life-Saving Genetic Testing
| Test Option | Regular Price | Special Price | Turnaround Time |
|---|---|---|---|
| SPTB Gene Anemia NGS Test | ZAR 6,700 | 3-4 Weeks |
Consider this investment in your baby’s health: early detection can prevent costly hospitalisations and lifelong complications, making this test invaluable for your family’s wellbeing.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Specialist hematologists and certified genetic counsellors
- Advanced Technology: 99.9% accuracy with Next Generation Sequencing
- Complete Support: From testing to results interpretation and counselling
- Proven Track Record: Thousands of successful genetic tests performed
Take Action for Your Baby’s Health Today
Don’t wait until it’s too late. Early detection of SPTB Gene Anemia can save your baby’s life and prevent the heartbreak of neonatal complications.
Limited time special pricing available. Protect your family’s future with confidence and peace of mind.
Test Sample Requirements
We accept: Blood sample, Extracted DNA, or One drop of Blood on FTA Card
Preparation Required: Please bring clinical history and be prepared for a genetic counselling session to create a family pedigree chart.
