POLG Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1 Autosomal Dominant NGS Genetic DNA Test
Introduction
The POLG Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1 Autosomal Dominant NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze genetic variations in the POLG gene. This test is crucial for individuals experiencing symptoms of progressive external ophthalmoplegia and related neurological disorders. Understanding your genetic predisposition can provide valuable insights into your health and guide future medical decisions.
What the Test Measures
This test specifically measures mutations in the POLG gene, which are associated with mitochondrial dysfunction, leading to various neurological disorders. By identifying these mutations, healthcare providers can better understand the underlying causes of symptoms and tailor treatment plans accordingly.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Progressive weakness of the eye muscles
- Difficulties with eye movement
- Family history of mitochondrial disorders
Additionally, those with risk factors such as a known family history of POLG-related disorders or unexplained neurological symptoms should consider this test.
Benefits of Taking the Test
- Early diagnosis of potential genetic disorders.
- Informed family planning and risk assessment.
- Guidance for personalized treatment options.
- Access to genetic counseling for affected family members.
Understanding Your Results
Results from the POLG Gene test will indicate whether any mutations are present in the POLG gene. A positive result may suggest a higher risk for developing associated neurological disorders, while a negative result may provide reassurance. It is essential to discuss results with a healthcare provider to understand their implications fully.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Book the Test
To schedule your POLG Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1 Autosomal Dominant NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to book online. Our team is here to assist you with any questions and ensure you receive the best care possible.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test is either blood or extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history and genetic counseling session are recommended to discuss family history and draw a pedigree chart of affected family members.
