RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test
Introduction to the Test
The RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Warburg Micro Syndrome, a rare neurological disorder. This test employs Next Generation Sequencing (NGS) technology to provide accurate and comprehensive genetic analysis, which is crucial for understanding the underlying causes of the condition.
What the Test Measures
This genetic test specifically measures mutations in the RAB3GAP1 gene, which are known to contribute to the development of Warburg Micro Syndrome. By analyzing the DNA, the test can detect abnormalities that may lead to neurological symptoms and other related health issues.
Who Should Consider This Test?
This test is recommended for individuals presenting neurological symptoms or those with a family history of Warburg Micro Syndrome. Symptoms may include developmental delays, intellectual disability, and various neurological impairments. If you have risk factors or concerns regarding your genetic predisposition, this test can provide valuable insights.
Benefits of Taking the Test
- Early detection of genetic disorders, facilitating timely intervention.
- Informed decision-making regarding treatment options and family planning.
- Access to genetic counseling for better understanding and management of the condition.
- Peace of mind through knowledge of genetic health risks.
Understanding Your Results
After the test is completed, your results will be interpreted by qualified genetic counselors or medical professionals. They will guide you through the findings, helping you understand the implications of your results and the next steps for management or treatment.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. It is essential to provide a clinical history and consider a genetic counseling session to draw a pedigree chart of family members affected by the syndrome before proceeding with the test.
