PMP22 Gene Dejerine-Sottas Disease NGS Genetic DNA Test
Introduction
The PMP22 Gene Dejerine-Sottas Disease NGS Genetic DNA Test is a cutting-edge diagnostic tool used to detect genetic mutations associated with Dejerine-Sottas disease, a hereditary neuropathy. This test is crucial for patients experiencing symptoms of neurological disorders, as it provides definitive insights into their genetic makeup and potential health risks.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to analyze the PMP22 gene, which is responsible for producing a protein essential for the normal functioning of peripheral nerves. By identifying mutations in this gene, the test can confirm or rule out the diagnosis of Dejerine-Sottas disease.
Who Should Consider This Test
Individuals who exhibit symptoms such as muscle weakness, sensory loss, or difficulty walking should consider this test. Additionally, those with a family history of Dejerine-Sottas disease or other hereditary neuropathies are strongly encouraged to undergo testing.
Benefits of Taking the Test
- Provides a definitive diagnosis for patients with unexplained neurological symptoms.
- Facilitates appropriate management and treatment options based on genetic findings.
- Offers valuable information for family planning and genetic counseling.
- Helps in understanding the prognosis and potential progression of the disease.
Understanding Your Results
After the test, results will be interpreted by a qualified geneticist or neurologist who will explain the findings in detail. Understanding these results is vital for making informed decisions regarding treatment and lifestyle adjustments.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| PMP22 Gene Dejerine-Sottas Disease NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Book Your Test Today
Don’t wait to take control of your health. To schedule your PMP22 Gene Dejerine-Sottas Disease NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with any questions and guide you through the booking process.
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 PMP22 Gene Dejerine-Sottas disease.
Specialty: Neurology | Department: Genetics | Method: NGS Technology | Disease Type: Neurological Disorders
