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MOCOS Gene Xanthinuria type 2 Genetic Test Cost

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

-21%

The MOCOS gene xanthinuria type 2 genetic test is a specialized diagnostic procedure aimed at detecting mutations in the MOCOS gene, which are responsible for xanthinuria type 2, a rare metabolic disorder. This condition is characterized by an inability to properly metabolize purines, leading to an accumulation of xanthine in the body. Such accumulation can result in various health issues, including kidney stones and potentially leading to kidney failure if left untreated.

The test is performed by DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is set at 4400 AED, reflecting the sophisticated nature of the diagnostic process and the specialized expertise required to accurately interpret the results. This test is crucial for individuals suspected of having xanthinuria type 2 or for those with a family history of the condition, as early detection can significantly improve management and treatment outcomes.

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MOCOS Gene Xanthinuria type 2 Genetic Test

Cost: AED 4400.0

Symptoms and Diagnosis

Xanthinuria type 2 is a rare genetic disorder that affects the metabolism of purines, resulting in the accumulation of xanthine and/or hypoxanthine in the urine. To diagnose this condition, a genetic test called the MOCOS Gene Xanthinuria type 2 Genetic Test can be conducted.

Test Details

The MOCOS gene is associated with xanthinuria type 2. The MOCOS Gene Xanthinuria type 2 Genetic Test utilizes Next-Generation Sequencing (NGS) technology to analyze the DNA sequence of an individual’s genes. This allows for the identification of mutations or variations in the MOCOS gene that may be responsible for the condition.

NGS genetic testing can provide valuable information for the diagnosis, treatment, and management of xanthinuria type 2. It can also be used for carrier testing, genetic counseling, and prenatal testing for individuals with a family history of the condition.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals or genetic counselors who specialize in genetics to ensure accurate and meaningful results.

Test Components and Price

  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: AED 4400.0

Report Delivery

Reports for the MOCOS Gene Xanthinuria type 2 Genetic Test are typically delivered within 3 to 4 weeks.

Test Type and Department

  • Test Type: Metabolic Disorders
  • Test Department: Genetics

Referring Doctor

The MOCOS Gene Xanthinuria type 2 Genetic Test can be requested by a General Physician.

Pre-Test Information

Before undergoing the MOCOS Gene Xanthinuria type 2 Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by Xanthinuria type 2.

Test Name MOCOS Gene Xanthinuria type 2 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 MOCOS Gene Xanthinuria type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Xanthinuria type 2
Test Details

The MOCOS gene is associated with a condition called xanthinuria type 2. Xanthinuria is a rare genetic disorder that affects the metabolism of purines, leading to the accumulation of xanthine and/or hypoxanthine in the urine.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of xanthinuria type 2, NGS genetic testing can be used to identify mutations or variations in the MOCOS gene that may be responsible for the condition.

By analyzing the DNA sequence of the MOCOS gene, NGS genetic testing can help diagnose xanthinuria type 2 and provide valuable information for treatment and management of the condition. This type of testing can also be used for carrier testing, genetic counseling, and prenatal testing for individuals with a family history of xanthinuria type 2.

It’s important to note that genetic testing should be performed and interpreted by healthcare professionals or genetic counselors who specialize in genetics to ensure accurate and meaningful results.

SKU: TEST-2658 Category:

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