STT3A Gene Congenital Disorder of Glycosylation Type Iw NGS Genetic DNA Test
Introduction to the STT3A Gene Test
The STT3A Gene Congenital Disorder of Glycosylation Type Iw NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to detect genetic mutations associated with congenital disorders of glycosylation (CDG). These disorders impact the body’s ability to properly glycosylate proteins, which is vital for numerous biological processes. Early detection through this test can significantly influence treatment options and patient outcomes.
What Does the Test Measure?
This test specifically measures mutations in the STT3A gene, which is crucial for the glycosylation process. By utilizing Next-Generation Sequencing (NGS) technology, the test provides a comprehensive analysis of the gene, ensuring accurate detection of potential abnormalities.
Who Should Consider This Test?
This test is highly recommended for individuals who:
- Have a family history of congenital disorders of glycosylation.
- Exhibit symptoms such as developmental delays, neurological issues, or unexplained metabolic problems.
- Are seeking genetic counseling to understand their risks and the implications for their family.
Benefits of Taking the Test
Understanding your genetic makeup through the STT3A Gene test offers numerous benefits:
- Early diagnosis of potential metabolic disorders.
- Informed decision-making regarding treatment options.
- Guidance for family planning and risk assessment for future generations.
- Access to specialized care and resources tailored to your genetic needs.
Understanding Your Results
Results from the STT3A Gene test will be provided in a clear and comprehensive report. It is essential to review these results with a healthcare professional or genetic counselor who can help interpret the findings and discuss potential next steps.
Test Pricing Information
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| STT3A Gene Congenital Disorder of Glycosylation Type Iw NGS Genetic DNA Test | 400000 | 560000 |
Booking Your Test
Ready to take the next step in understanding your genetic health? Book your STT3A Gene Congenital Disorder of Glycosylation Type Iw NGS Genetic DNA Test today! For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: A clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with congenital disorder of glycosylation, type Iw.
Don’t wait until it’s too late! Understanding your genetic risks can lead to better health outcomes. Contact us today!
