NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test
Introduction to the Test
The NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test is a specialized genetic test that plays a crucial role in diagnosing mitochondrial disorders, particularly those related to the NDUFAF3 gene. This test utilizes Next Generation Sequencing (NGS) technology to analyze the genetic makeup of individuals, providing valuable insights into potential genetic predispositions to neurological disorders.
What the Test Measures
This test specifically measures variations in the NDUFAF3 gene, which is essential for the proper functioning of mitochondrial complex I. Deficiencies in this gene can lead to severe neurological conditions, making early detection vital for effective management.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Those with a family history of mitochondrial disorders.
- Patients exhibiting symptoms such as muscle weakness, developmental delays, or neurological issues.
- Individuals with unexplained metabolic or neurological symptoms.
Benefits of Taking the Test
Taking the NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test offers several benefits:
- Early diagnosis of mitochondrial disorders.
- Informed decision-making regarding treatment options.
- Guidance for family planning and genetic counseling.
- Understanding potential health risks associated with genetic variations.
Understanding Your Results
Results from the NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test will be interpreted by a qualified genetic counselor or neurologist. They will help you understand the implications of your results, including any necessary follow-up actions or treatments.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +2348110567037. Our team is ready to assist you with the booking process and provide any additional information you may need.
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 NDUFAF3 Gene Mitochondrial Complex I deficiency.
For further inquiries or to schedule a consultation, feel free to reach out to us!
