MTND1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test
Introduction to the Test
The MTND1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to assess genetic mutations associated with mitochondrial complex I deficiency. This condition can lead to a range of neurological disorders, making early detection vital for effective management and treatment.
What the Test Measures
This test specifically measures alterations in the MTND1 gene, which plays a crucial role in mitochondrial function. By identifying mutations in this gene, healthcare providers can better understand the underlying causes of neurological symptoms and disorders.
Who Should Consider This Test?
This test is recommended for individuals who exhibit symptoms such as:
- Unexplained neurological symptoms
- Muscle weakness
- Seizures
- Developmental delays
Additionally, individuals with a family history of mitochondrial disorders or those at risk due to genetic predispositions should consider this test.
Benefits of Taking the Test
- Early and accurate diagnosis of mitochondrial disorders
- Guidance for treatment options and management strategies
- Informed family planning and genetic counseling
- Understanding of potential risks for family members
Understanding Your Results
Results from the MTND1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test will be provided in a clear and concise manner. Patients will receive guidance on the implications of their results, helping them and their healthcare providers make informed decisions regarding their health.
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MTND1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the MTND1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test, please contact us at +2348110567037 via call or WhatsApp. Our team is ready to assist you with the booking process and answer any questions you may have.
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 MT-ND1 Gene Mitochondrial Complex I deficiency is required.
Specialty: Neurology | Department: Genetics | Method: NGS Technology | Disease Type: Neurological Disorders
