Understanding MPI Gene Glycosylation Disorder Type 1B
When you’re concerned about inherited health conditions affecting your family, the uncertainty can be overwhelming. Our MPI Gene Glycosylation Disorder Type 1B NGS Genetic DNA Test provides the clarity you need to make informed health decisions. This specialised test examines the MPI gene for mutations that disrupt normal glycosylation processes – essential cellular functions that impact multiple body systems.
What This Test Detects
Using advanced Next-Generation Sequencing (NGS) technology, we analyse your DNA to identify specific mutations in the MPI gene. These mutations cause Congenital Disorders of Glycosylation Type 1B (CDG1B), which affect how your body processes sugars and proteins. The test provides comprehensive coverage of the entire MPI gene, ensuring no potential mutation goes undetected.
Who Should Consider This Test
This test is particularly important if you or your child experience:
- Unexplained liver dysfunction or hepatomegaly
- Developmental delays or failure to thrive in infancy
- Recurrent bleeding or coagulation problems
- Gastrointestinal issues including vomiting and diarrhoea
- Family history of similar metabolic disorders
- Unexplained hypoglycaemia or protein-losing enteropathy
Why Early Detection Matters
Identifying MPI gene mutations early can significantly impact treatment outcomes and quality of life. With proper diagnosis:
- Targeted management strategies can be implemented
- Nutritional interventions like mannose supplementation may be recommended
- Regular monitoring can prevent complications
- Family planning decisions become more informed
- Peace of mind replaces uncertainty about your health future
Understanding Your Results
Our genetic counsellors provide clear, compassionate explanations of your results. We’ll help you understand what any detected mutations mean for your health and guide you through next steps. Negative results provide reassurance, while positive findings open doors to proper management and support.
Comprehensive Pricing & Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| MPI Gene Glycosylation Disorder Type 1B Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
This investment in your health provides lifelong value through early detection and proper management guidance.
Trust & Professional Excellence
Oracle Genomics brings you:
- Nationwide coverage across Johannesburg, Cape Town, Durban, and Pretoria
- Advanced NGS technology for maximum accuracy
- Expert genetic counselling included with your test
- 3-4 week turnaround for timely results
- Multiple sample options: blood, extracted DNA, or FTA card
- Professional medical oversight by general physicians
Take Control of Your Genetic Health Today
Don’t let uncertainty about inherited conditions affect your family’s wellbeing. Our MPI Gene Glycosylation Disorder Type 1B test provides the answers you need with the professional care you deserve. Early detection through accurate genetic testing can transform health outcomes and provide the peace of mind every family deserves.
Book your confidential genetic consultation today and take the first step toward understanding your genetic health. Our team is ready to support you through every step of this important health journey.
