VARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 20 NGS Genetic DNA Test
Introduction to the Test
The VARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 20 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the VARS2 gene, which are associated with metabolic disorders. This test employs Next Generation Sequencing (NGS) technology to provide comprehensive insights into genetic health, allowing for early detection and management of potential health issues.
What the Test Measures
This genetic test specifically detects variations in the VARS2 gene that can lead to oxidative phosphorylation deficiencies. These deficiencies are linked to mitochondrial dysfunction, which can manifest in various metabolic disorders. By analyzing the genetic makeup, healthcare professionals can better understand the underlying causes of symptoms and tailor treatment plans accordingly.
Who Should Consider This Test?
Individuals experiencing symptoms related to mitochondrial dysfunction, such as:
- Unexplained muscle weakness
- Neurological issues
- Developmental delays
- Recurrent metabolic crises
Additionally, those with a family history of metabolic disorders or who have undergone genetic counseling should consider this test.
Benefits of Taking the Test
- Early diagnosis of metabolic disorders linked to the VARS2 gene.
- Informed decision-making regarding treatment options.
- Understanding genetic predispositions that may affect family members.
- Access to genetic counseling for better management of health.
Understanding Your Results
Upon completion of the test, results will be provided in a clear and comprehensible format. It is essential to consult with a healthcare professional to interpret the results accurately. They will guide you through the implications of the findings and discuss potential next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the VARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 20 NGS Genetic DNA Test, contact us at +2348077798758 or visit our website.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient and a Genetic Counseling session to draw a pedigree chart of family members affected with Combined Oxidative Phosphorylation Deficiency Type 20.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
Take control of your health today by understanding your genetic makeup. Book your test now!
