Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test
Introduction
The Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test is a vital diagnostic tool used to identify genetic mutations associated with Prader-Willi Syndrome (PWS), a complex genetic disorder characterized by various physical, mental, and behavioral challenges. Early detection of PWS is crucial for effective management and intervention, allowing families to access necessary support and resources.
What the Test Measures
This test specifically detects methylation changes in the genes associated with Prader-Willi Syndrome. By analyzing the DNA from a blood sample, the test can confirm the presence of genetic abnormalities that may lead to the syndrome, providing critical information for diagnosis.
Who Should Consider This Test
Individuals who may benefit from this test include:
- Newborns and children displaying symptoms of PWS, such as hypotonia, developmental delays, and obesity.
- Families with a history of genetic disorders or known cases of Prader-Willi Syndrome.
- Patients with unexplained developmental issues or behavioral problems.
Benefits of Taking the Test
Taking the Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test offers several benefits:
- Early diagnosis leading to timely medical intervention.
- Access to specialized care and support for affected individuals.
- Informed family planning and genetic counseling.
- Improved quality of life through early management of symptoms.
Understanding Your Results
Once the test is completed, results will be available within 12 working days. A healthcare professional will provide a detailed explanation of the findings, helping you understand the implications of the results and the next steps for management or further testing if necessary.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test | KSh 22,000 | KSh 36,000 |
Sample Collection and Instructions
The sample required for this test is 4 mL (2 mL min.) of whole blood collected in a Lavender top (EDTA) tube. It is crucial to ship the sample refrigerated and to avoid freezing. Additionally, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for processing the test.
Our Locations
DNA Labs Kenya has branches across all major cities, ensuring convenient access to our services. We also offer home sample collection services for your convenience.
Book Your Test Today!
Don’t wait any longer to secure the health and well-being of your loved ones. Book the Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test today! For inquiries or to schedule your appointment, call or WhatsApp us at +254711564616.
