SNRPN Gene Prader-Willi Syndrome NGS Genetic DNA Test
Introduction
The SNRPN Gene Prader-Willi Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Prader-Willi syndrome (PWS). This condition is a complex genetic disorder characterized by various symptoms, including intellectual disability, obesity, and behavioral problems. Early diagnosis through this test can significantly improve management and treatment outcomes for affected individuals.
What the Test Measures
This test specifically detects mutations in the SNRPN gene, which play a crucial role in the development of Prader-Willi syndrome. By utilizing Next-Generation Sequencing (NGS) technology, the test provides a comprehensive analysis of the genetic material, ensuring accurate and reliable results.
Who Should Consider This Test?
Individuals who exhibit symptoms of Prader-Willi syndrome or have a family history of the condition should consider this test. Common symptoms include:
- Hypotonia (decreased muscle tone)
- Feeding difficulties in infancy
- Obesity in childhood
- Behavioral problems
- Intellectual disability
Additionally, individuals with a clinical history suggestive of PWS should consult their healthcare provider about this test.
Benefits of Taking the Test
- Early diagnosis allows for timely intervention and management of symptoms.
- Understanding genetic predispositions can aid in family planning.
- Access to tailored treatment strategies based on genetic findings.
- Informed decision-making regarding lifestyle and healthcare options.
Understanding Your Results
Results from the SNRPN Gene Prader-Willi Syndrome NGS Genetic DNA Test will be interpreted by qualified genetic counselors and medical professionals. They will explain the implications of the findings, including the likelihood of developing symptoms associated with Prader-Willi syndrome. It is essential to discuss results with a healthcare provider to understand the next steps and management options.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the SNRPN Gene Prader-Willi Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A genetic counseling session is recommended to draw a pedigree chart of family members affected with SNRPN Gene Prader-Willi syndrome.
Consult with a neurologist or genetic specialist for further information and to determine if this test is right for you.
