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FMO3 Gene Trimethylaminuria Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

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The FMO3 gene trimethylaminuria genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FMO3 gene, which are responsible for the condition known as trimethylaminuria, or more commonly referred to as “fish odor syndrome.” This genetic disorder impairs the body’s ability to break down trimethylamine (TMA), a compound derived from the diet that has a strong fishy odor. As a result, individuals with trimethylaminuria accumulate TMA in their bodies, leading to the emission of a fish-like odor through breath, sweat, and urine, which can significantly impact their social and psychological well-being.

The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific mutations in the FMO3 gene. Identifying these mutations can confirm the diagnosis of trimethylaminuria, enabling healthcare providers to offer appropriate management strategies and dietary advice to help minimize symptoms.

In the United Arab Emirates, this genetic test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the FMO3 gene trimethylaminuria genetic test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the FMO3 gene, providing crucial information for individuals suspecting they might have this condition or for those seeking confirmation of their diagnosis.

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FMO3 Gene Trimethylaminuria Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing laboratory. Today, we will be discussing the FMO3 Gene Trimethylaminuria Genetic Test and its cost.

Test Details

The FMO3 gene is responsible for producing an enzyme called flavin-containing monooxygenase 3 (FMO3). This enzyme plays a crucial role in the metabolism of certain compounds, including trimethylamine (TMA). Trimethylaminuria, also known as fish odor syndrome, is a rare genetic disorder caused by mutations in the FMO3 gene.

People with trimethylaminuria are unable to properly break down TMA, resulting in a strong body odor resembling that of rotten fish. To diagnose this condition, we offer the FMO3 Gene Trimethylaminuria Genetic Test using NGS (Next-Generation Sequencing) technology.

NGS is a type of genetic testing that allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. By analyzing the FMO3 gene for mutations associated with trimethylaminuria, our test can help confirm a diagnosis and provide information about the specific genetic mutation(s) present.

Test Components and Price

The FMO3 Gene Trimethylaminuria Genetic Test is priced at 4400.0 AED. The test requires a sample of either blood, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery

Once the sample is collected, the report will be delivered within 3 to 4 weeks. Our team of experts will analyze the data and provide a detailed report of the findings.

Test Type and Doctor

The FMO3 Gene Trimethylaminuria Genetic Test falls under the category of Metabolic Disorders. Our team of experienced General Physicians will oversee the testing process and provide expert guidance.

Test Department

The FMO3 Gene Trimethylaminuria Genetic Test is conducted in our Genetics department. Our skilled geneticists and technicians ensure accurate and reliable results.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the FMO3 Gene Trimethylaminuria NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by Trimethylaminuria. This information helps in understanding the inheritance pattern and potential risk factors.

Implications and Future Considerations

The results of the FMO3 Gene Trimethylaminuria Genetic Test can be used for genetic counseling, family planning, and potentially for personalized treatment options in the future. However, it is crucial to consult with a healthcare professional or genetic counselor to fully understand the implications of the results and discuss any potential treatment options.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule an appointment for the FMO3 Gene Trimethylaminuria Genetic Test and take a step towards better health.

Test Name FMO3 Gene Trimethylaminuria Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FMO3 Gene Trimethylaminuria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Trimethylaminuria
Test Details

The FMO3 gene is responsible for producing an enzyme called flavin-containing monooxygenase 3 (FMO3). This enzyme is involved in the metabolism of certain compounds, including trimethylamine (TMA).

Trimethylaminuria, also known as fish odor syndrome, is a rare genetic disorder caused by mutations in the FMO3 gene. People with this condition are unable to properly break down TMA, resulting in a strong body odor resembling that of rotten fish.

NGS (Next-Generation Sequencing) is a type of genetic testing that can be used to analyze the FMO3 gene for mutations associated with trimethylaminuria. This technique allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup.

The FMO3 gene trimethylaminuria NGS genetic test involves collecting a sample of DNA, typically through a blood or saliva sample, and analyzing it using NGS technology. The test can identify mutations in the FMO3 gene that may be causing trimethylaminuria.

The results of the test can help confirm a diagnosis of trimethylaminuria and provide information about the specific genetic mutation(s) present. This information can be used for genetic counseling, family planning, and potentially for personalized treatment options in the future.

It is important to note that while genetic testing can provide valuable information, it is always recommended to consult with a healthcare professional or genetic counselor to fully understand the implications of the results and discuss any potential treatment options.

SKU: TEST-2645 Category:

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