RRM2B Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 5 Autosomal Dominant NGS Genetic DNA Test
Introduction
The RRM2B Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 5 Autosomal Dominant NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with specific neurological disorders. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive insights into the genetic factors that may contribute to the development of progressive external ophthalmoplegia, a condition characterized by muscle weakness and paralysis of the eye muscles.
What the Test Measures
This genetic test specifically measures alterations in the RRM2B gene, which plays a crucial role in mitochondrial function and energy production. By analyzing the DNA, the test can detect mutations that may lead to mitochondrial deletions and subsequent neurological impairments.
Who Should Consider This Test?
Individuals exhibiting symptoms such as:
- Progressive weakness of the eye muscles
- Difficulty in moving the eyes
- Associated neurological symptoms
Additionally, those with a family history of RRM2B-related disorders or other mitochondrial diseases should consider this test to assess their risk and explore potential management options.
Benefits of Taking the Test
- Early diagnosis of genetic predispositions to neurological disorders.
- Informed decision-making regarding treatment and management options.
- Guidance for family planning and understanding hereditary risks.
- Access to genetic counseling for comprehensive support.
Understanding Your Results
Results from the RRM2B Gene test can provide valuable insights into the presence of genetic mutations. A genetic counselor will help interpret the results, explain their implications, and discuss potential next steps based on findings.
Test Name and Price
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| RRM2B Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 5 Autosomal Dominant NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the RRM2B Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 5 Autosomal Dominant NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any inquiries you may have.
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 essential. A genetic counseling session is recommended to draw a pedigree chart of family members affected with RRM2B Gene Progressive External Ophthalmoplegia.
This test is vital for those seeking clarity on their genetic health and potential neurological risks. Trust DNA Labs Nigeria for accurate diagnostics and compassionate care.
