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MVK Gene Mevalonic Aciduria Genetic Test Cost

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

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The MVK Gene Mevalonic Aciduria Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the MVK gene, which are known to cause Mevalonic Aciduria (MVA), a rare genetic disorder. This condition is part of the mevalonate kinase deficiency spectrum, which also includes Hyper-IgD Syndrome. Mevalonic Aciduria is characterized by a range of symptoms including developmental delay, recurrent fever, failure to thrive, and dysmorphic facial features, among others. The disorder results from a deficiency in mevalonate kinase, an enzyme crucial for cholesterol and isoprenoid biosynthesis.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in a laboratory setting. By examining the genetic makeup of the MVK gene, this test can confirm the presence of mutations that lead to the enzyme deficiency causing the disorder. Early diagnosis through genetic testing is vital for managing symptoms and improving the quality of life for affected individuals.

The MVK Gene Mevalonic Aciduria Genetic Test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, which reflects the comprehensive analysis and detailed report provided by the lab. DNA Labs UAE employs state-of-the-art technology and adheres to international standards to ensure accurate and reliable results. This test is an essential tool for families seeking answers to unexplained symptoms that may be linked to genetic disorders, offering a pathway towards targeted treatment and management strategies.

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MVK Gene Mevalonic aciduria Genetic Test

Cost: 4400.0 AED

Test Components:

  • 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:

A Genetic Counselling session is required to draw a pedigree chart of family members affected with Mevalonic aciduria. It is important to provide the clinical history of the patient who is going for the MVK Gene Mevalonic aciduria NGS Genetic DNA Test.

Test Details:

The MVK gene Mevalonic aciduria NGS genetic test is a genetic test that specifically looks for mutations in the MVK gene associated with Mevalonic aciduria. Mevalonic aciduria is a rare genetic disorder characterized by the deficiency of the enzyme mevalonate kinase, which is encoded by the MVK gene. The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the MVK gene, to identify any genetic variations or mutations.

This test helps in the diagnosis of Mevalonic aciduria by detecting mutations in the MVK gene that may be causing the disease. Genetic testing for Mevalonic aciduria can be beneficial for individuals with suspected or confirmed symptoms of the condition, as well as for their family members who may be at risk of inheriting the disease. Early diagnosis through genetic testing can help in the management and treatment of Mevalonic aciduria, as well as provide information for family planning and genetic counseling.

Test Name MVK Gene Mevalonic aciduria 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 MVK Gene Mevalonic aciduria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mevalonic aciduria
Test Details

MVK gene Mevalonic aciduria NGS genetic test is a genetic test that specifically looks for mutations in the MVK gene associated with Mevalonic aciduria. Mevalonic aciduria is a rare genetic disorder characterized by the deficiency of the enzyme mevalonate kinase, which is encoded by the MVK gene.

The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the MVK gene, to identify any genetic variations or mutations. This test helps in the diagnosis of Mevalonic aciduria by detecting mutations in the MVK gene that may be causing the disease.

Genetic testing for Mevalonic aciduria can be beneficial for individuals with suspected or confirmed symptoms of the condition, as well as for their family members who may be at risk of inheriting the disease. Early diagnosis through genetic testing can help in the management and treatment of Mevalonic aciduria, as well as provide information for family planning and genetic counseling.

SKU: TEST-2545 Category:

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