NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test
Introduction
The NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze genetic material. This test is pivotal for identifying mutations in the NDUFS3 gene, which is linked to Leigh Syndrome, a severe neurological disorder. Understanding your genetic predisposition can help in making informed health decisions and guide treatment options for affected individuals.
What the Test Measures
This test specifically measures the presence of pathogenic mutations in the NDUFS3 gene. By analyzing the DNA, it detects genetic variations that may contribute to the development of Leigh Syndrome, allowing for early diagnosis and management.
Who Should Consider This Test?
Individuals who exhibit symptoms of Leigh Syndrome or have a family history of the condition should consider this test. Symptoms may include progressive loss of mental and movement abilities, seizures, and respiratory distress. Risk factors include having relatives diagnosed with Leigh Syndrome or other neurological disorders.
Benefits of Taking the Test
- Early diagnosis of Leigh Syndrome, enabling timely intervention.
- Informed family planning for affected families.
- Access to tailored treatment options based on genetic findings.
- Peace of mind through understanding genetic health risks.
Understanding Your Results
Results from the NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test will provide insights into the genetic status of the individual tested. A genetic counselor will assist in interpreting these results and guide further actions based on the findings.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| NDUFS3 Gene Leigh Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the NDUFS3 Gene Leigh Syndrome 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 required, along with a genetic counseling session to draw a pedigree chart of family members affected with NDUFS3 Gene Leigh Syndrome.
Consult with a neurologist or a genetics specialist for further insights into your genetic health and the implications of test results.
