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COL6A2 Gene Ullrich Congenital Muscular Dystrophy Genetic Test Cost

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

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The COL6A2 gene is crucial for the production of collagen VI, a vital component of the extracellular matrix in muscle tissues. Mutations in this gene are associated with Ullrich Congenital Muscular Dystrophy (UCMD), a severe genetic disorder characterized by muscle weakness, joint hypermobility, and skin abnormalities. The condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

To diagnose UCMD and identify mutations in the COL6A2 gene, genetic testing is available. DNA Labs UAE offers a specialized test for this purpose. The test involves analyzing the patient’s DNA, obtained through a blood sample, to look for mutations in the COL6A2 gene that are known to cause UCMD. This test is crucial for accurate diagnosis, guiding treatment options, and providing information for family planning.

The cost of the COL6A2 gene test for Ullrich Congenital Muscular Dystrophy at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic mutations associated with the disorder, providing essential information for patients and their families.

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COL6A2 Gene Ullrich Congenital Muscular Dystrophy Genetic Test

Are you or a loved one experiencing muscle weakness and joint stiffness? It could be a sign of Ullrich congenital muscular dystrophy (UCMD), a rare genetic disorder. To get a definitive diagnosis and understand the specific genetic changes responsible for UCMD, consider getting the COL6A2 Gene Ullrich congenital muscular dystrophy Genetic Test at DNA Labs UAE.

Test Details

The COL6A2 gene is associated with Ullrich congenital muscular dystrophy (UCMD). This genetic disorder is characterized by muscle weakness and joint stiffness. UCMD is caused by mutations in the COL6A1, COL6A2, or COL6A3 genes, which encode the collagen VI protein. The COL6A2 Gene Ullrich congenital muscular dystrophy Genetic Test uses NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously.

Components

  • Test Name: COL6A2 Gene Ullrich congenital muscular dystrophy Genetic Test
  • 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the COL6A2 Gene Ullrich congenital muscular dystrophy Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with COL6A2 Gene Ullrich congenital muscular dystrophy. This information will help in the accurate interpretation of the test results.

Why Choose NGS Genetic Testing?

NGS genetic testing offers several advantages in diagnosing UCMD. By analyzing multiple genes simultaneously, NGS can identify mutations in the COL6A2 gene and other related genes. This comprehensive approach provides important information about the specific genetic changes responsible for UCMD in an individual.

Implications and Next Steps

Once the test results are available, it is recommended to consult with a healthcare professional or a genetic counselor to discuss the implications of the findings. The information obtained from NGS genetic testing can aid in diagnosis, genetic counseling, and potentially guide treatment options for UCMD.

Don’t let the symptoms of muscle weakness and joint stiffness go undiagnosed. Contact DNA Labs UAE today to schedule the COL6A2 Gene Ullrich congenital muscular dystrophy Genetic Test and gain valuable insights into your genetic makeup.

Test Name COL6A2 Gene Ullrich congenital muscular dystrophy Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for COL6A2 Gene Ullrich congenital muscular dystrophy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with COL6A2 Gene Ullrich congenital muscular dystrophy
Test Details

The COL6A2 gene is associated with Ullrich congenital muscular dystrophy (UCMD), a rare genetic disorder characterized by muscle weakness and joint stiffness. UCMD is caused by mutations in the COL6A1, COL6A2, or COL6A3 genes, which encode the collagen VI protein.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of UCMD, NGS can be used to identify mutations in the COL6A2 gene and other related genes.

NGS genetic testing can provide important information about the specific genetic changes responsible for UCMD in an individual. This information can help with diagnosis, genetic counseling, and potentially guide treatment options.

It is important to consult with a healthcare professional or a genetic counselor to discuss the specific details and implications of NGS genetic testing for UCMD.

SKU: TEST-2098 Category:

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