SLC26A6 Gene Hyperoxaluria SLC26A6 Related Genetic Test sale cost 4400 AED
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SLC26A6 Gene Hyperoxaluria SLC26A6 Related Genetic Test Cost

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

-21%

The SLC26A6 gene plays a crucial role in the regulation of oxalate and chloride ions in the body, impacting the renal handling of oxalate and contributing to the balance of oxalate levels. Mutations or dysfunction in the SLC26A6 gene can lead to hyperoxaluria, a condition characterized by an excessive urinary excretion of oxalate, which can result in kidney stones and, in severe cases, kidney damage. Hyperoxaluria related to the SLC26A6 gene can be either primary, due to genetic factors, or secondary, resulting from dietary factors, other diseases, or additional genetic conditions.

To diagnose and manage this condition effectively, genetic testing for mutations in the SLC26A6 gene is available. In the United Arab Emirates, DNA Labs UAE offers a specific genetic test to identify alterations in the SLC26A6 gene that may contribute to hyperoxaluria. This test is crucial for individuals with a clinical history suggestive of hyperoxaluria or a family history of kidney stones or kidney disease, as it can confirm the genetic basis of the condition, guide treatment decisions, and inform family planning.

The cost of the SLC26A6 related genetic test at DNA Labs UAE is 4400 AED. This investment in genetic testing can provide valuable insights into the genetic underpinnings of hyperoxaluria, facilitating personalized treatment approaches and preventive measures to mitigate the risk of kidney stones and potential kidney damage associated with the condition.

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SLC26A6 Gene Hyperoxaluria Genetic Test

At DNA Labs UAE, we offer the SLC26A6 Gene Hyperoxaluria Genetic Test to diagnose and identify mutations in the SLC26A6 gene that may be causing hyperoxaluria. Hyperoxaluria is a condition characterized by increased levels of oxalate in the urine, which can lead to the formation of kidney stones and other complications.

Test Details

The SLC26A6 gene hyperoxaluria genetic test utilizes next-generation sequencing (NGS) technology to analyze the SLC26A6 gene for any genetic abnormalities. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variants.

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

Prior to the SLC26A6 gene hyperoxaluria genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected with hyperoxaluria, specifically related to the SLC26A6 gene.

Why Choose the SLC26A6 Gene Hyperoxaluria Genetic Test?

By undergoing the SLC26A6 gene hyperoxaluria genetic test, individuals can obtain valuable information about their genetic makeup. This information can aid in the diagnosis of hyperoxaluria, provide insights for genetic counseling, and potentially guide treatment options.

It is important to note that genetic testing for SLC26A6 gene hyperoxaluria may not be available at all healthcare facilities. Therefore, it is recommended to consult with a healthcare professional or genetic counselor to determine the availability and appropriateness of genetic testing for this condition.

Test Name SLC26A6 Gene Hyperoxaluria SLC26A6 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SLC26A6 Gene Hyperoxaluria, SLC26A6 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperoxaluria, SLC26A6 related
Test Details

SLC26A6 gene hyperoxaluria refers to a condition in which mutations in the SLC26A6 gene lead to increased levels of oxalate in the urine, known as hyperoxaluria. This condition can result in the formation of kidney stones and other complications.

To diagnose SLC26A6 gene hyperoxaluria, a next-generation sequencing (NGS) genetic test can be performed. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes, including the SLC26A6 gene, to identify any mutations or variants that may be present.

The NGS genetic test for SLC26A6 gene hyperoxaluria involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to analyze the SLC26A6 gene for any genetic abnormalities.

The results of the NGS genetic test can help determine if there are any mutations or variants in the SLC26A6 gene that may be causing hyperoxaluria. This information can be used for diagnosis, genetic counseling, and potentially guiding treatment options.

It is important to note that genetic testing for SLC26A6 gene hyperoxaluria may not be available at all healthcare facilities. It is recommended to consult with a healthcare professional or genetic counselor to determine the availability and appropriateness of genetic testing for this condition.

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