MAGEL2 Gene Schaaf-Yang Syndrome NGS Genetic DNA Test
Introduction
The MAGEL2 Gene Schaaf-Yang Syndrome NGS Genetic DNA Test is a specialized genetic test that utilizes Next-Generation Sequencing (NGS) technology to analyze the MAGEL2 gene. This test is vital for diagnosing Schaaf-Yang syndrome, a rare genetic disorder characterized by developmental delays, intellectual disability, and distinctive physical features. Understanding the genetic underpinnings of this condition is crucial for effective management and support.
What the Test Measures
This genetic test detects mutations in the MAGEL2 gene, which are known to cause Schaaf-Yang syndrome. By identifying these mutations, healthcare providers can offer tailored treatment plans and genetic counseling for affected individuals and their families.
Who Should Consider This Test?
This test is recommended for individuals exhibiting symptoms such as:
- Developmental delays
- Intellectual disability
- Distinctive facial features
- Behavioral issues
Additionally, family members of individuals diagnosed with Schaaf-Yang syndrome may also benefit from this test to understand their own genetic risks.
Benefits of Taking the Test
- Accurate diagnosis of Schaaf-Yang syndrome
- Informed decision-making regarding treatment and management
- Access to genetic counseling and support resources
- Understanding potential risks for family members
Understanding Your Results
After the test, results will be provided to you in a clear and comprehensive format. It is important to discuss these results with a healthcare professional, who can help interpret the findings and provide guidance on next steps.
Test Information and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| MAGEL2 Gene Schaaf-Yang Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the MAGEL2 Gene Schaaf-Yang Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Ensuring proper pre-test instructions, including a clinical history and a genetic counseling session, is essential for the accuracy of your results.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Specialty: Pediatrics
Department: Genetics
Method: NGS Technology
Disease Type: Dysmorphology
