MTATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency NGS Genetic DNA Test
Introduction
The MTATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the MTATP6 gene, which is essential for the proper functioning of mitochondrial ATP synthase. This enzyme plays a critical role in energy production within cells, and deficiencies can lead to severe neurological disorders. Understanding the genetic basis of these conditions is vital for effective management and treatment.
What the Test Measures
This test detects mutations in the MTATP6 gene that may contribute to mitochondrial complex V deficiency. By utilizing Next-Generation Sequencing (NGS) technology, it provides a comprehensive analysis of the gene, ensuring accurate results.
Who Should Consider This Test
Individuals experiencing symptoms such as:
- Muscle weakness
- Neurological issues
- Developmental delays
- Seizures
Should consider this test, especially if there is a family history of mitochondrial disorders or related neurological conditions.
Benefits of Taking the Test
- Early diagnosis of mitochondrial disorders can lead to timely intervention.
- Helps in understanding the genetic risks for family members.
- Guides treatment and management options based on genetic findings.
- Provides peace of mind through clarity on genetic health.
Understanding Your Results
Results from the MTATP6 Gene test will indicate the presence or absence of mutations. It is essential to discuss these results with a qualified healthcare provider, who can provide guidance based on your specific situation and recommend further steps if necessary.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MTATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To schedule your MTATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with your booking and any questions you may have.
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 Genetic Counselling session to draw a pedigree chart of family members affected with MT-ATP6 Gene Mitochondrial Complex V (ATP synthase) deficiency is recommended.
