MTTN Gene Mitochondrial Complex I Deficiency MTTN Related NGS Genetic DNA Test
Introduction
The MTTN Gene Mitochondrial Complex I Deficiency MTTN Related NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic mutations associated with mitochondrial disorders. These disorders can significantly impact a patient’s health by affecting energy production in cells, leading to a variety of neurological symptoms. Understanding these genetic factors is essential for accurate diagnosis and effective management of the condition.
What the Test Measures
This test specifically measures mutations in the MTTN gene that are linked to mitochondrial complex I deficiency. By utilizing Next Generation Sequencing (NGS) technology, the test provides comprehensive insights into the genetic makeup of the patient, allowing for precise identification of potential genetic issues.
Who Should Consider This Test
Individuals who experience symptoms such as muscle weakness, neurological issues, or unexplained fatigue should consider this test. Additionally, those with a family history of mitochondrial disorders may benefit from genetic testing to understand their risk factors and potential hereditary implications.
Benefits of Taking the Test
- Accurate diagnosis of mitochondrial disorders.
- Informed treatment decisions based on genetic findings.
- Understanding of hereditary risks for family members.
- Access to specialized care from neurologists and geneticists.
Understanding Your Results
Results from the MTTN Gene Mitochondrial Complex I Deficiency test will indicate whether any mutations are present. A genetic counseling session is recommended to help interpret the results and discuss the implications for treatment and family planning.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the MTTN Gene Mitochondrial Complex I Deficiency MTTN Related NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and provide any additional information you may need.
Turnaround time for results is estimated at 3 to 4 weeks. The sample type required includes blood or extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history and a genetic counseling session are recommended to draw a pedigree chart of family members affected by mitochondrial disorders.
Don’t wait to get the answers you need about your health. Book your test today!
