NDUFA11 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test
Introduction
The NDUFA11 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to detect mutations in the NDUFA11 gene, which plays a critical role in mitochondrial function. Mitochondrial disorders, particularly those affecting Complex I, can lead to severe neurological impairments and other systemic issues. This test is vital for early diagnosis and management of such conditions, providing patients and healthcare providers with essential information for treatment planning.
What the Test Measures
This test specifically analyzes the NDUFA11 gene to identify any pathogenic variants that may lead to mitochondrial Complex I deficiency. By utilizing Next Generation Sequencing (NGS) technology, the test can provide a comprehensive overview of the genetic landscape related to this disorder.
Who Should Consider This Test
Individuals who exhibit symptoms of mitochondrial dysfunction, such as:
- Neurological disorders
- Muscle weakness
- Developmental delays
- Seizures
- Unexplained metabolic issues
Additionally, those with a family history of mitochondrial disorders or known NDUFA11 mutations should also consider this test.
Benefits of Taking the Test
- Early diagnosis of mitochondrial diseases can lead to timely interventions.
- Understanding genetic risks helps in making informed health decisions.
- Assists in family planning and genetic counseling.
- Provides clarity for patients and families regarding the nature of the disorder.
Understanding Your Results
Results from the NDUFA11 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test will be interpreted by qualified geneticists or neurologists. A positive result indicates the presence of a pathogenic variant, while a negative result suggests no known mutations are detected. It is essential to discuss the results with a healthcare professional to understand their implications fully.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| NDUFA11 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To ensure you or your loved ones receive the best care, consider booking the NDUFA11 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test today. For appointments, please call or WhatsApp us at +2348077798758.
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 who is going for the test and a genetic counseling session to draw a pedigree chart of family members affected with NDUFA11 Gene Mitochondrial Complex I deficiency is required.
