NDUFS8 Gene Leigh Syndrome NGS Genetic DNA Test
Introduction
The NDUFS8 Gene Leigh Syndrome NGS Genetic DNA Test is an advanced diagnostic tool designed to detect mutations in the NDUFS8 gene, which are associated with Leigh syndrome, a severe neurological disorder. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive genetic analysis, helping to identify individuals at risk and guiding clinical management.
What the Test Measures
This genetic test specifically measures mutations in the NDUFS8 gene, which plays a critical role in mitochondrial function. By analyzing the genetic material, the test can detect alterations that may lead to Leigh syndrome, allowing for early diagnosis and intervention.
Who Should Consider This Test?
Individuals who exhibit symptoms of Leigh syndrome or have a family history of neurological disorders should consider this test. Symptoms may include developmental delays, loss of motor skills, and neurological impairments. Risk factors include a family history of mitochondrial diseases and unexplained neurological symptoms.
Benefits of Taking the Test
- Early diagnosis of Leigh syndrome can significantly improve management and treatment options.
- Identifying genetic mutations helps in understanding the condition and planning for future care.
- Genetic counseling can be provided to affected families, aiding in informed decision-making.
- Access to targeted therapies and interventions based on genetic findings.
Understanding Your Results
Results from the NDUFS8 Gene Leigh Syndrome NGS Genetic DNA Test will be discussed in detail with a genetic counselor or healthcare provider. It is essential to understand the implications of the findings, including potential health risks and family planning considerations.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the NDUFS8 Gene Leigh Syndrome NGS Genetic DNA Test or for more information, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment 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 and a genetic counseling session to draw a pedigree chart of family members affected with NDUFS8 Gene Leigh syndrome is required.
Consult with a neurologist or genetic specialist to understand the necessity of this test in your health journey.
