Mtfmt Gene Combined Oxidative Phosphorylation Deficiency Type 15 NGS Genetic DNA Test
Introduction
The Mtfmt Gene Combined Oxidative Phosphorylation Deficiency Type 15 NGS Genetic DNA Test is a vital diagnostic tool used to identify genetic mutations associated with mitochondrial disorders. These conditions can lead to severe metabolic dysfunctions affecting various organ systems. Understanding your genetic predisposition through this test can provide crucial insights for early intervention and management.
What the Test Measures
This test specifically detects mutations in the MTFMT gene, which are implicated in oxidative phosphorylation deficiencies. By employing Next-Generation Sequencing (NGS) technology, the test offers a comprehensive analysis of the genetic material, ensuring accurate results.
Who Should Consider This Test?
Individuals who exhibit symptoms related to metabolic disorders, such as:
- Unexplained muscle weakness
- Neurological issues
- Developmental delays in children
- Family history of mitochondrial disorders
are encouraged to consider this test. Additionally, those with risk factors such as a family history of metabolic disorders should also seek testing.
Benefits of Taking the Test
- Early diagnosis of potential metabolic disorders.
- Informed family planning and genetic counseling.
- Personalized healthcare strategies based on genetic insights.
- Peace of mind through understanding genetic health risks.
Understanding Your Results
Results from the Mtfmt Gene Combined Oxidative Phosphorylation Deficiency Type 15 NGS Genetic DNA Test will provide insights into the presence of genetic mutations. A genetic counselor will assist in interpreting these results, guiding you on the next steps and potential health implications.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Booking Information
To schedule your Mtfmt Gene Combined Oxidative Phosphorylation Deficiency Type 15 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in understanding your genetic health and ensuring you receive the best care possible.
Test Details
- 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 Combined Oxidative Phosphorylation Deficiency Type 15.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders