NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test
Introduction to the Test
The NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic mutations associated with Prader-Willi syndrome. This condition is characterized by a range of symptoms including hypotonia, obesity, and cognitive impairment. Understanding the genetic basis of this syndrome is crucial for effective management and treatment.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to detect mutations in the NDN gene, which is implicated in the development of Prader-Willi syndrome. By analyzing the DNA, healthcare providers can confirm or rule out the diagnosis, providing critical information for patient care.
Who Should Consider This Test
Individuals who may benefit from the NDN Gene Prader-Willi Syndrome test include:
- Patients exhibiting symptoms of Prader-Willi syndrome such as severe obesity, developmental delays, or behavioral problems.
- Family members of individuals diagnosed with Prader-Willi syndrome, especially if there is a history of similar symptoms.
- Individuals with a family history of neurological disorders.
Benefits of Taking the Test
Taking the NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of Prader-Willi syndrome.
- Informed family planning and management strategies.
- Access to tailored treatment options based on genetic findings.
- Peace of mind for patients and their families.
Understanding Your Results
Once the test is completed, results will be interpreted by a qualified genetic counselor or neurologist. They will explain the findings and discuss the implications for you and your family, including potential health risks and management options.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
Don’t wait any longer to gain insights into your genetic health. To book the NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test, call us at +2348077798758 or reach out via WhatsApp. Our team is ready to assist you with any questions you may have and guide you through the testing process.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient and Genetic Counseling session to draw a pedigree chart of family members affected with NDN Gene Prader-Willi syndrome
