GPHN Gene Molybdenum Cofactor Deficiency Type C NGS Genetic DNA Test
Introduction
The GPHN Gene Molybdenum Cofactor Deficiency Type C NGS Genetic DNA Test is a vital diagnostic tool designed to identify genetic mutations associated with Molybdenum Cofactor Deficiency Type C. This condition is a rare metabolic disorder that can lead to severe neurological issues if not diagnosed and managed promptly. The test utilizes Next Generation Sequencing (NGS) technology, providing accurate and comprehensive results.
What the Test Measures
This genetic test analyzes the GPHN gene to detect mutations that could lead to Molybdenum Cofactor Deficiency Type C. By identifying these mutations, healthcare providers can better understand the patient’s condition and tailor appropriate treatment plans.
Who Should Consider This Test
Individuals who may benefit from this test include:
- Patients with unexplained neurological symptoms
- Individuals with a family history of metabolic disorders
- Newborns exhibiting signs of metabolic abnormalities
- Patients undergoing genetic counseling for hereditary conditions
Benefits of Taking the Test
Undergoing the GPHN Gene Molybdenum Cofactor Deficiency Type C NGS Genetic DNA Test offers numerous benefits:
- Early diagnosis of metabolic disorders
- Informed decision-making for treatment options
- Enhanced understanding of family health risks
- Access to specialized care and management strategies
Understanding Your Results
Results from the GPHN Gene Molybdenum Cofactor Deficiency Type C NGS Genetic DNA Test will be provided in a detailed report. It is crucial to discuss these results with a healthcare professional, who can explain the implications and recommend further actions based on the findings.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GPHN Gene Molybdenum Cofactor Deficiency Type C NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To schedule your GPHN Gene Molybdenum Cofactor Deficiency Type C NGS Genetic DNA Test, please contact us at +2348110567037. Our dedicated team is ready to assist you with the booking process and answer any questions you may have.
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 genetic counseling session to draw a pedigree chart of family members affected with Molybdenum cofactor deficiency type C is recommended.
