NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test
Introduction
The NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test is a crucial diagnostic tool for identifying genetic mutations associated with Leigh syndrome, a severe neurological disorder. This test employs Next Generation Sequencing (NGS) technology to provide a comprehensive analysis of the NDUFA10 gene, which plays a vital role in mitochondrial function. Understanding your genetic makeup can lead to better management and treatment options for affected individuals.
What the Test Measures
This genetic test specifically measures mutations in the NDUFA10 gene. These mutations can disrupt mitochondrial energy production, leading to various neurological symptoms and complications.
Who Should Consider This Test?
Individuals who exhibit symptoms such as developmental delays, loss of motor skills, or other neurological issues should consider this test. Additionally, those with a family history of Leigh syndrome or related mitochondrial disorders are encouraged to undergo testing.
Benefits of Taking the Test
- Early diagnosis of Leigh syndrome, allowing for timely intervention.
- Informed decision-making regarding treatment and management options.
- Providing clarity for families regarding genetic risks and inheritance patterns.
- Access to genetic counseling for personalized support and guidance.
Understanding Your Results
Results from the NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test will indicate the presence or absence of mutations in the NDUFA10 gene. A genetic counselor can assist in interpreting these results and discussing potential implications for health and family planning.
Test Details and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to gain insights into your genetic health. Book the NDUFA10 Gene Leigh Syndrome NGS Genetic DNA Test today by calling or sending a WhatsApp message to +2348077798758. Our team at DNA Labs Nigeria is ready to assist you with your testing needs.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Ensure to provide a clinical history and attend a genetic counseling session to draw a pedigree chart of family members affected with NDUFA10 Gene Leigh syndrome.
Specialty: Neurology | Department: Genetics | Method: NGS Technology | Disease Type: Neurological Disorders
