POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B NGS Genetic DNA Test
Introduction
The POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B NGS Genetic DNA Test is a vital diagnostic tool that aids in the identification of genetic mutations associated with mitochondrial DNA depletion syndrome. This condition can lead to various debilitating neurological disorders, making early detection crucial for effective management and treatment.
What the Test Measures
This test specifically analyzes the POLG gene, which is responsible for mitochondrial DNA replication and maintenance. By utilizing Next Generation Sequencing (NGS) technology, the test can detect mutations that may lead to mitochondrial dysfunction.
Who Should Consider This Test
Individuals experiencing symptoms such as:
- Muscle weakness
- Neurological issues
- Seizures
- Developmental delays
Additionally, those with a family history of neurological disorders or mitochondrial diseases are encouraged to consider this test.
Benefits of Taking the Test
Taking the POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B NGS Genetic DNA Test offers several benefits, including:
- Early diagnosis of potential neurological disorders
- Informed decision-making regarding treatment options
- Genetic counseling for affected family members
Understanding Your Results
Results from this test provide crucial insights into genetic mutations. A healthcare professional will guide you through the interpretation of your results, helping you understand the implications for your health and any necessary follow-up actions.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Our team of experts is ready to assist you in your diagnostic journey.
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 clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B.
This test is conducted under the supervision of qualified neurologists in the genetics department, ensuring accuracy and reliability in results.
