Protect Your Newborn’s Future: 6q24-Related Transient Neonatal Diabetes Genetic Testing
As a parent, nothing matters more than your baby’s health. When your newborn shows signs of diabetes in their first weeks of life, the uncertainty can be overwhelming. Our specialised genetic test provides the clarity you need to make informed decisions about your baby’s care and future.
Understanding the 6q24 Transient Neonatal Diabetes Test
This advanced genetic test specifically examines chromosome 6q24, where mutations can cause transient neonatal diabetes mellitus type 1. Using next-generation sequencing (NGS) technology, we analyse your baby’s DNA with 99.9% accuracy to identify the specific genetic variations responsible for this condition.
Transient neonatal diabetes typically appears in the first 6 months of life and usually resolves by 18 months, but early detection is crucial for proper management and preventing complications.
Who Should Consider This Genetic Test?
- Newborns showing symptoms of diabetes in the first weeks of life
- Babies with unexplained high blood sugar levels
- Infants with poor weight gain despite adequate feeding
- Newborns with excessive thirst and frequent urination
- Families with a history of neonatal diabetes
- Babies born with low birth weight who develop diabetes symptoms
If your baby is experiencing any of these symptoms, early genetic testing can provide the answers you need for proper treatment and management.
Why Early Detection Matters for Your Baby’s Health
- Prevent Complications: Early diagnosis helps prevent dehydration, electrolyte imbalances, and other serious complications
- Proper Treatment: Accurate diagnosis ensures your baby receives the right insulin therapy and monitoring
- Peace of Mind: Knowing the exact cause reduces uncertainty and anxiety for your family
- Future Planning: Understanding the genetic basis helps plan for potential recurrence in future pregnancies
- Better Outcomes: Early intervention leads to better growth and development outcomes
Understanding Your Test Results
Our genetic counsellors will walk you through your results with compassion and clarity. We explain:
- Whether the 6q24 genetic mutation was detected
- What the results mean for your baby’s current health
- Recommended treatment and monitoring approaches
- Long-term outlook and management strategies
- Genetic counselling for family planning decisions
Remember, a positive result doesn’t define your baby’s future – it empowers you with knowledge to provide the best possible care.
Affordable Genetic Testing for Your Peace of Mind
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| 6q24 Transient Neonatal Diabetes Genetic Test | ZAR 6,700 | ZAR 2,650 |
Turnaround Time: 3 to 4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Consider this an investment in your baby’s health – early detection can prevent costly hospitalisations and complications down the line.
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 and genetic specialists
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Genetic Counselling: Comprehensive pre-test counselling to understand family history
- Proven Accuracy: 99.9% detection rate for 6q24-related mutations
- Patient-Focused Care: We understand the emotional journey of concerned parents
Take the First Step Toward Answers Today
Don’t let uncertainty about your newborn’s health create unnecessary stress. Our genetic test provides the clarity you need to make confident healthcare decisions for your baby.
Limited Time Offer: Save ZAR 2,650 on this essential genetic test. Early detection could make all the difference in your baby’s health journey.
“The peace of mind we gained from knowing exactly what was affecting our baby was priceless. The genetic counselling helped us understand everything clearly.” – Recent Parent
Test Preparation
Before your test, please provide:
- Complete clinical history of your baby
- Attend a genetic counselling session to create a family pedigree chart
- Information about family members affected by neonatal diabetes
Our team will guide you through every step of the process with compassion and professionalism.
