GJB1 Gene CMTX1 NGS Genetic DNA Test
Introduction
The GJB1 Gene CMTX1 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the GJB1 gene, which are associated with Charcot-Marie-Tooth Disease Type 1X (CMTX1). This test employs Next-Generation Sequencing (NGS) technology to provide accurate results, making it essential for individuals with a family history of neurological disorders.
What the Test Measures
This genetic test specifically detects mutations in the GJB1 gene that can lead to CMTX1, a hereditary condition that affects the peripheral nerves, resulting in muscle weakness and sensory loss.
Who Should Consider This Test
Individuals who may benefit from the GJB1 Gene CMTX1 NGS Genetic DNA Test include:
- Those with a family history of CMTX1 or related neurological disorders.
- Patients exhibiting symptoms such as muscle weakness, numbness, or difficulty walking.
- Individuals undergoing genetic counseling for hereditary conditions.
Benefits of Taking the Test
Taking the GJB1 Gene CMTX1 NGS Genetic DNA Test offers several advantages:
- Early diagnosis and management of CMTX1.
- Informed family planning and genetic counseling.
- Access to targeted therapies and support resources.
Understanding Your Results
Results from the GJB1 Gene CMTX1 NGS Genetic DNA Test will be provided in a detailed report. A genetic counselor will assist in interpreting the results and discussing the implications for you and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GJB1 Gene CMTX1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To book the GJB1 Gene CMTX1 NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with any inquiries and help you through the booking 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 the patient undergoing the test and a genetic counseling session to draw a pedigree chart of family members affected by GJB1 Gene CMTX1.
This test is conducted by specialists in the field of genetics and neurology, ensuring the highest level of care and expertise.
