MOCOS Gene Xanthinuria Type 2 NGS Genetic DNA Test
Introduction
The MOCOS Gene Xanthinuria Type 2 NGS Genetic DNA Test is a specialized genetic test designed to detect mutations in the MOCOS gene, which are responsible for Xanthinuria Type 2. This metabolic disorder affects the body’s ability to process certain substances, leading to the accumulation of xanthine in the urine. Understanding your genetic predisposition to this condition is vital for effective management and treatment.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to analyze the MOCOS gene. It identifies any pathogenic variants that may contribute to Xanthinuria Type 2, providing a comprehensive view of your genetic health.
Who Should Consider This Test
Individuals who may benefit from this test include:
- Those with a family history of metabolic disorders, particularly Xanthinuria Type 2.
- Patients exhibiting symptoms such as kidney stones or recurrent urinary issues.
- Individuals seeking genetic counseling for planning future pregnancies.
Benefits of Taking the Test
Taking the MOCOS Gene Xanthinuria Type 2 NGS Genetic DNA Test offers numerous benefits:
- Early diagnosis of potential metabolic disorders.
- Informed management and treatment options based on genetic insights.
- Guidance for family planning and risk assessment for future generations.
Understanding Your Results
Results from the MOCOS Gene Xanthinuria Type 2 NGS Genetic DNA Test will be provided with a detailed report. It is essential to consult with a healthcare professional to interpret these results accurately and discuss the implications for your health and that of your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MOCOS Gene Xanthinuria Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To schedule your MOCOS Gene Xanthinuria Type 2 NGS Genetic DNA Test, please contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you with the booking process and any questions you may have.
Pre-Test Instructions
Prior to taking the test, it is recommended to undergo a genetic counseling session to chart a pedigree of family members affected by Xanthinuria Type 2. Additionally, a clinical history of the patient is necessary for accurate results.
Test Details
- Turnaround Time: 3 to 4 weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
