NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 NGS Genetic DNA Test
Introduction
The NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 NGS Genetic DNA Test is a groundbreaking diagnostic tool designed to identify genetic mutations that lead to metabolic disorders. By utilizing Next-Generation Sequencing (NGS) technology, this test provides a comprehensive analysis of the NARS2 gene, which plays a crucial role in mitochondrial function and energy production in cells.
What the Test Measures
This genetic test detects mutations in the NARS2 gene associated with combined oxidative phosphorylation deficiency type 24. It evaluates the integrity of mitochondrial function, offering insights into potential metabolic dysfunctions that could affect overall health.
Who Should Consider This Test?
Individuals who exhibit symptoms of metabolic disorders, such as unexplained muscle weakness, neurological issues, or developmental delays, should consider this test. Additionally, those with a family history of metabolic conditions or genetic disorders may also benefit from testing to assess their risk.
Benefits of Taking the Test
- Accurate identification of genetic mutations related to metabolic disorders.
- Guidance for personalized treatment options based on genetic findings.
- Informed family planning decisions through genetic counseling.
- Early intervention and management of potential health issues.
Understanding Your Results
Results from the NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 NGS Genetic DNA Test will provide insights into the presence of any genetic mutations. A healthcare professional will assist in interpreting the results, explaining their implications for health and potential next steps in management.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Our team is ready to assist you with scheduling your test and answering 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: 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 24.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
