Protect Your Baby’s Future with CYP24A1 Hypercalcemia Genetic Testing
As a parent, nothing matters more than your child’s health and wellbeing. When your infant shows signs of excessive calcium levels or there’s a family history of metabolic disorders, the uncertainty can be overwhelming. Our CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test provides the answers you need with the accuracy and compassion you deserve.
Understanding the CYP24A1 Hypercalcemia Test
This specialised genetic test examines the CYP24A1 gene using Next-Generation Sequencing (NGS) technology to identify mutations that cause infantile hypercalcemia – a condition where babies have dangerously high calcium levels in their blood. The CYP24A1 gene normally helps regulate vitamin D metabolism, and when it doesn’t function properly, calcium can build up to toxic levels affecting your baby’s development and organ function.
Who Should Consider This Important Test?
This test is essential for infants and families experiencing:
- Unexplained high calcium levels in blood tests
- Failure to thrive or poor weight gain
- Excessive vomiting or feeding difficulties
- Dehydration despite adequate fluid intake
- Family history of calcium metabolism disorders
- Previous siblings with similar symptoms
- Developmental delays or neurological symptoms
If your baby shows any of these concerning signs, early genetic testing can provide life-changing answers.
Why Early Detection Matters for Your Child’s Health
Getting this test done early can:
- Prevent permanent kidney damage and kidney stones
- Avoid developmental delays and growth problems
- Enable targeted treatment and dietary management
- Provide peace of mind for your entire family
- Help plan for future pregnancies with genetic counselling
- Reduce hospitalisations and emergency visits
Early intervention based on accurate genetic information can significantly improve your child’s quality of life.
Understanding Your Test Results
Our comprehensive results package includes:
- Clear, easy-to-understand genetic findings
- Detailed explanation of what the results mean for your child
- Personalised recommendations for management and treatment
- Access to genetic counselling for family planning
- Ongoing support from our medical team
We believe knowledge empowers better healthcare decisions, and we’re here to guide you every step of the way.
Affordable Genetic Testing for South African Families
| Test Description | Regular Price | Special Price |
|---|---|---|
| CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test | ZAR 6,700 |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Preparation: Clinical history and genetic counselling session included
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified general physicians
- Advanced Technology: Latest NGS technology for maximum accuracy
- Genetic Counselling: Comprehensive family history assessment included
- Patient-Focused Care: Empathetic support throughout your testing journey
Take Action for Your Child’s Health Today
Don’t wait for symptoms to worsen. Early detection through genetic testing can make all the difference in your child’s development and long-term health. Our special price of ZAR 6,700 makes this life-changing test accessible to South African families.
Book your test now and get the answers you need:
- Call our dedicated genetic counselling team
- Visit one of our nationwide collection centres
- Schedule a consultation with your healthcare provider
Your child’s health is worth investing in. Contact us today to begin your genetic testing journey with confidence and care.
