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SLC12A2 Gene Bartter Syndrome Genetic Test Cost

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

-21%

The SLC12A2 gene plays a crucial role in the body’s regulation of electrolyte balance. Mutations in this gene are associated with a rare condition known as Bartter syndrome, which affects the kidneys and leads to a range of symptoms including salt wasting, frequent urination, dehydration, and electrolyte imbalances. To diagnose this condition accurately, genetic testing is performed to identify mutations in the SLC12A2 gene.

DNA Labs UAE offers a specialized genetic test for Bartter syndrome focusing on the SLC12A2 gene. The test is designed to provide a definitive diagnosis by analyzing the patient’s DNA for mutations that are known to cause the disorder. This is particularly important for guiding treatment decisions and for understanding the risk of passing the condition on to future generations.

The cost of the SLC12A2 gene Bartter syndrome genetic test at DNA Labs UAE is 4400 AED. This investment covers the full process of collecting a DNA sample, usually through a blood draw or a cheek swab, conducting the genetic analysis in the laboratory, and providing a detailed report of the findings. The test is conducted by experienced professionals using the latest technology to ensure accurate and reliable results.

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SLC12A2 Gene Bartter Syndrome Genetic Test

Are you or someone you know experiencing symptoms of Bartter syndrome? Genetic testing can help provide valuable insights into the genetic basis of the disorder and guide treatment and management strategies. At DNA Labs UAE, we offer the SLC12A2 Gene Bartter Syndrome Genetic Test at a cost of AED 4400.0.

Test Details

The SLC12A2 gene is associated with Bartter syndrome, a rare genetic disorder that affects the kidneys. This syndrome is characterized by abnormalities in the reabsorption of certain ions in the kidney, leading to excessive urination, dehydration, and electrolyte imbalances. Our NGS (Next-Generation Sequencing) technology allows for the simultaneous sequencing of multiple genes or even the entire genome.

Components

  • Test Name: SLC12A2 Gene Bartter Syndrome 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: Hepatology, Nephrology, Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to the SLC12A2 Gene Bartter Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by Bartter syndrome.

Benefits of NGS Genetic Testing for Bartter Syndrome

NGS genetic testing for Bartter syndrome can help with diagnosis and provide information about the specific genetic mutation involved. This information is valuable for determining the inheritance pattern of the disorder within a family, as well as for genetic counseling and family planning.

Conclusion

The SLC12A2 Gene Bartter Syndrome Genetic Test offered at DNA Labs UAE is a valuable tool for diagnosing and managing Bartter syndrome. By analyzing the SLC12A2 gene using NGS technology, we can provide insights into the genetic basis of the disorder and guide treatment strategies. If you or someone you know is experiencing symptoms of Bartter syndrome, consider getting tested to gain a better understanding of the condition and plan for the future.

Test Name SLC12A2 Gene Bartter syndrome 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 SLC12A2 Gene Bartter syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A2 Gene Bartter syndrome NGS Genetic DNA Test gene SLC12A2
Test Details

The SLC12A2 gene is associated with Bartter syndrome, a rare genetic disorder that affects the kidneys. Bartter syndrome is characterized by abnormalities in the reabsorption of certain ions in the kidney, leading to excessive urination, dehydration, and electrolyte imbalances.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of Bartter syndrome, NGS genetic testing can be used to analyze the SLC12A2 gene and identify any genetic mutations or variations that may be causing the disorder.

NGS genetic testing for Bartter syndrome can help with diagnosis, as well as providing information about the specific genetic mutation involved. This information can be useful for determining the inheritance pattern of the disorder within a family, as well as for genetic counseling and family planning.

Overall, NGS genetic testing for the SLC12A2 gene in Bartter syndrome can provide valuable insights into the genetic basis of the disorder and help guide treatment and management strategies.

SKU: TEST-3585 Category:

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