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LAMA5 Gene Focal Segmental Glomerulosclerosis LAMA5 Related Genetic Test Cost

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

-21%

The LAMA5 gene plays a crucial role in the development and maintenance of the kidney’s filtering units, known as glomeruli. Mutations in the LAMA5 gene can lead to a condition known as Focal Segmental Glomerulosclerosis (FSGS), a severe disease characterized by scarring (sclerosis) in the glomeruli. This condition can lead to significant kidney damage and, ultimately, kidney failure.

DNA Labs UAE offers a specialized genetic test aimed at detecting mutations in the LAMA5 gene that are associated with FSGS. This test is critical for individuals with a family history of FSGS or those exhibiting symptoms of the disease, as early detection can significantly impact the management and treatment options available.

The cost of the LAMA5-related genetic test at DNA Labs UAE is 4400 AED. This investment can provide invaluable information for affected individuals and their families, guiding treatment decisions and offering insights into the risk of FSGS for future generations.

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LAMA5 Gene Focal Segmental Glomerulosclerosis Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing provider. In this blog, we will discuss the LAMA5 gene and its association with focal segmental glomerulosclerosis (FSGS). We will also provide details about the LAMA5-related genetic test, including its cost, symptoms, diagnosis, and more.

Test Name: LAMA5 Gene Focal Segmental Glomerulosclerosis LAMA5-related Genetic Test

  • Components: LAMA5 gene analysis
  • 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: Hepatology Nephrology Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient

Test Details

The LAMA5 gene codes for the laminin alpha-5 subunit protein, which is crucial for the structural support of various tissues in the body, including the kidneys. Focal segmental glomerulosclerosis (FSGS) is a kidney disorder characterized by scarring and damage to the glomeruli, the tiny blood vessels responsible for filtering waste and excess fluid from the blood.

LAMA5-related FSGS is a specific subtype of FSGS caused by mutations in the LAMA5 gene. These mutations can lead to a defective or non-functional laminin alpha-5 protein, resulting in abnormal kidney development and function.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the LAMA5 gene. This test can detect mutations or variations in the LAMA5 gene that may be associated with the development of FSGS.

NGS genetic testing is valuable for diagnosing LAMA5-related FSGS, predicting disease progression, and guiding treatment decisions. It is important to note that this test is typically performed in individuals with a suspected or confirmed diagnosis of FSGS, as well as their family members to identify individuals at risk of developing the condition.

Genetic counseling is highly recommended before and after genetic testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

Conclusion

The LAMA5 gene plays a crucial role in the development and function of the kidneys. Mutations in this gene can lead to LAMA5-related FSGS, a specific subtype of FSGS. NGS genetic testing allows for the identification of these mutations and helps in diagnosing and managing the condition. At DNA Labs UAE, we offer the LAMA5 Gene Focal Segmental Glomerulosclerosis LAMA5-related Genetic Test at a cost of 4400.0 AED. If you or your family members have a suspected or confirmed diagnosis of FSGS, we recommend considering this test and seeking genetic counseling for a comprehensive understanding of your genetic health.

Test Name LAMA5 Gene Focal segmental glomerulosclerosis LAMA5 related 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LAMA5 Gene Focal segmental glomerulosclerosis, LAMA5 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LAMA5 Gene Focal segmental glomerulosclerosis, LAMA5 related NGS Genetic DNA Test gene LAMA5
Test Details

The LAMA5 gene is a gene that codes for the laminin alpha-5 subunit protein. This protein is an important component of the extracellular matrix, which provides structural support to various tissues in the body, including the kidneys.

Focal segmental glomerulosclerosis (FSGS) is a kidney disorder characterized by scarring and damage to the glomeruli, which are the tiny blood vessels in the kidneys responsible for filtering waste and excess fluid from the blood. FSGS can lead to kidney dysfunction and eventually kidney failure.

LAMA5-related FSGS is a specific subtype of FSGS that is caused by mutations in the LAMA5 gene. These mutations can result in a defective or non-functional laminin alpha-5 protein, leading to abnormal kidney development and function.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the LAMA5 gene. This test can detect mutations or variations in the LAMA5 gene that may be associated with the development of FSGS. NGS genetic testing can help in diagnosing LAMA5-related FSGS, predicting disease progression, and guiding treatment decisions.

It is important to note that genetic testing for LAMA5-related FSGS is typically performed in individuals with a suspected or confirmed diagnosis of FSGS, as well as in their family members to identify individuals at risk of developing the condition. Genetic counseling is often recommended before and after genetic testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

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