FMO3 Gene Trimethylaminuria NGS Genetic DNA Test
The FMO3 Gene Trimethylaminuria NGS Genetic DNA Test is a crucial diagnostic tool designed to identify mutations in the FMO3 gene, which are responsible for Trimethylaminuria (TMAU), a metabolic disorder characterized by the body’s inability to break down trimethylamine, leading to a fishy odor. This test utilizes Next Generation Sequencing (NGS) technology, allowing for a comprehensive analysis of the FMO3 gene. Early diagnosis through this test is vital for managing symptoms and improving quality of life.
What the Test Measures
This genetic test detects specific mutations in the FMO3 gene that can lead to Trimethylaminuria. By analyzing the DNA, healthcare providers can confirm the presence of these mutations, which is essential for accurate diagnosis and treatment planning.
Who Should Consider This Test?
Individuals who experience symptoms such as a strong fishy body odor, particularly after consuming certain foods, should consider this test. Additionally, those with a family history of metabolic disorders or genetic conditions may benefit from genetic testing. Risk factors include:
- Family history of Trimethylaminuria
- Symptoms of metabolic disorders
Benefits of Taking the Test
Taking the FMO3 Gene Trimethylaminuria NGS Genetic DNA Test offers numerous benefits, including:
- Accurate diagnosis of Trimethylaminuria
- Informed management and treatment options
- Understanding genetic predisposition to metabolic disorders
- Guidance for dietary and lifestyle changes to minimize symptoms
Understanding Your Results
Once the test is completed, results will be analyzed by a qualified healthcare provider. They will guide you through the interpretation of your results, explaining any mutations found and discussing potential next steps for management and treatment.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FMO3 Gene Trimethylaminuria NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the FMO3 Gene Trimethylaminuria NGS Genetic DNA Test, please contact us at +2348110567037 or visit our website. Our team is ready to assist you with any questions and guide you through the booking process.
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 clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Trimethylaminuria.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
