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ABCD4 Gene Methylmalonic Aciduria CblJ Type Genetic Test Cost

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

-21%

The “ABCD4 Gene Methylmalonic Aciduria CblJ Type Genetic Test” is a specialized diagnostic assessment aimed at identifying mutations in the ABCD4 gene, which are linked to a rare form of methylmalonic aciduria, known as cblJ type. Methylmalonic aciduria is a metabolic disorder that disrupts the body’s ability to process certain fats and proteins, leading to a buildup of methylmalonic acid in the body. This can result in various health issues, including developmental delays, intellectual disabilities, and physical health problems.

The test is specifically designed to detect genetic variations in the ABCD4 gene that are responsible for this condition, enabling healthcare providers to make an accurate diagnosis. Early detection through genetic testing can be crucial for managing symptoms, implementing dietary restrictions, and considering treatment options to improve the quality of life for affected individuals.

This genetic test is available at DNA Labs UAE, a leading facility in the region for genetic testing and analysis. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the specialized expertise required to interpret the results. For families and individuals facing symptoms indicative of methylmalonic aciduria, this test offers a valuable tool for understanding their genetic health and making informed decisions about their care.

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ABCD4 Gene Methylmalonic aciduria CblJ type Genetic Test

Test Name: ABCD4 Gene Methylmalonic aciduria CblJ type Genetic Test

Components:

  • Price: 4400.0 AED
  • Sample Condition: Blood
  • 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 ABCD4 Gene Methylmalonic aciduria CblJ type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonic aciduria CblJ type.

Test Details:

The ABCD4 gene is responsible for producing a protein that is involved in the transport of vitamin B12 into cells. Mutations in this gene can lead to a condition called methylmalonic aciduria CblJ type, which is a rare inherited disorder characterized by the inability to process certain proteins and fats properly.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously. In the context of methylmalonic aciduria CblJ type, NGS genetic testing can be used to identify mutations in the ABCD4 gene that may be causing the condition.

By analyzing the DNA of an individual, NGS genetic testing can identify specific mutations or changes in the ABCD4 gene that are associated with methylmalonic aciduria CblJ type. This information can then be used to provide a diagnosis, assess the risk of passing on the condition to offspring, and guide treatment options for affected individuals and their families.

Test Name ABCD4 Gene Methylmalonic aciduria CblJ type Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 ABCD4 Gene Methylmalonic aciduria CblJ type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonic aciduria CblJ type
Test Details

The ABCD4 gene is responsible for producing a protein that is involved in the transport of vitamin B12 into cells. Mutations in this gene can lead to a condition called methylmalonic aciduria CblJ type, which is a rare inherited disorder characterized by the inability to process certain proteins and fats properly.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously. In the context of methylmalonic aciduria CblJ type, NGS genetic testing can be used to identify mutations in the ABCD4 gene that may be causing the condition.

By analyzing the DNA of an individual, NGS genetic testing can identify specific mutations or changes in the ABCD4 gene that are associated with methylmalonic aciduria CblJ type. This information can then be used to provide a diagnosis, assess the risk of passing on the condition to offspring, and guide treatment options for affected individuals and their families.

SKU: TEST-2541