Cox15 Gene Leigh Syndrome NGS Genetic DNA Test
Introduction
The Cox15 Gene Leigh Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that aids in the identification of genetic mutations linked to Leigh syndrome, a severe neurological disorder. This test leverages Next Generation Sequencing (NGS) technology to provide comprehensive insights into the genetic underpinnings of this condition, allowing for early diagnosis and management strategies.
What the Test Measures
This test specifically measures mutations in the Cox15 gene, which are known to contribute to the development of Leigh syndrome. By analyzing the genetic material, healthcare providers can determine if a patient has inherited mutations that may lead to neurological complications.
Who Should Consider This Test?
Individuals who exhibit symptoms of Leigh syndrome, such as developmental delays, neurological deficits, or unexplained metabolic issues, should consider this test. Additionally, families with a history of Leigh syndrome or other neurological disorders may benefit from understanding their genetic risks.
Benefits of Taking the Test
- Early identification of genetic risks associated with Leigh syndrome.
- Informed decision-making regarding treatment and management options.
- Access to genetic counseling for affected families.
- Contribution to ongoing research and understanding of neurological disorders.
Understanding Your Results
Test results will indicate whether mutations in the Cox15 gene are present. A genetic counselor will help interpret these results, providing guidance on the implications for the patient and their family. Understanding these results can lead to tailored management plans and support resources.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Cox15 Gene Leigh Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the Cox15 Gene Leigh Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your test and answering any questions 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 required, along with a genetic counseling session to draw a pedigree chart of family members affected with Cox15 Gene Leigh syndrome.
For more information about the Cox15 Gene Leigh Syndrome NGS Genetic DNA Test, please do not hesitate to reach out. Your health and peace of mind are our top priorities.
