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SLC12A7 Gene Bartter Syndrome Genetic Test Cost

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

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The SLC12A7 gene plays a critical role in the proper functioning of the kidneys, particularly in the regulation of electrolyte and fluid balance. Mutations in this gene can lead to a rare condition known as Bartter syndrome, which is characterized by a set of symptoms including salt wasting, hypokalemic metabolic alkalosis, hypercalciuria, and elevated renin and aldosterone levels. This condition often presents in infancy or childhood with symptoms such as dehydration, frequent urination, and growth retardation.

To diagnose Bartter syndrome and specifically identify mutations in the SLC12A7 gene, a genetic test is available at DNA Labs UAE. This test involves analyzing the patient’s DNA to look for mutations in the SLC12A7 gene that are known to cause the condition. The test is crucial for confirming the diagnosis of Bartter syndrome, which can then guide treatment and management strategies to mitigate symptoms and prevent complications.

The cost of the SLC12A7 Gene Bartter Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted in a state-of-the-art laboratory setting by experienced geneticists and technicians, ensuring accurate and reliable results. The test not only aids in the diagnosis of Bartter syndrome but also helps in the assessment of the risk of passing the condition to future generations, making it an invaluable tool for affected families.

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SLC12A7 Gene Bartter Syndrome Genetic Test

Components

  • Test Name: SLC12A7 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

Clinical History of Patient who is going for SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test gene SLC12A7.

Test Details

The SLC12A7 gene is associated with Bartter syndrome, a rare genetic disorder that affects the kidneys. Bartter syndrome is characterized by an imbalance of electrolytes in the body, leading to symptoms such as excessive urination, dehydration, salt cravings, and muscle weakness.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of Bartter syndrome, NGS can be used to identify mutations or variations in the SLC12A7 gene that may be responsible for the disorder. This type of genetic testing can help confirm a diagnosis of Bartter syndrome and provide information about the specific genetic cause of the condition.

NGS genetic testing for Bartter syndrome typically involves obtaining a DNA sample, usually through a blood sample or saliva collection, and sequencing the SLC12A7 gene. The DNA sequence is then compared to a reference sequence to identify any genetic variations or mutations that may be present.

The results of the NGS genetic test can help healthcare providers determine the most appropriate treatment and management strategies for individuals with Bartter syndrome. Additionally, genetic testing can provide valuable information for family members who may be at risk of inheriting the condition.

It’s important to note that genetic testing for Bartter syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.

Test Name SLC12A7 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 SLC12A7 Gene Bartter syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A7 Gene Bartter syndrome NGS Genetic DNA Test gene SLC12A7
Test Details

The SLC12A7 gene is associated with Bartter syndrome, a rare genetic disorder that affects the kidneys. Bartter syndrome is characterized by an imbalance of electrolytes in the body, leading to symptoms such as excessive urination, dehydration, salt cravings, and muscle weakness.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of Bartter syndrome, NGS can be used to identify mutations or variations in the SLC12A7 gene that may be responsible for the disorder. This type of genetic testing can help confirm a diagnosis of Bartter syndrome and provide information about the specific genetic cause of the condition.

NGS genetic testing for Bartter syndrome typically involves obtaining a DNA sample, usually through a blood sample or saliva collection, and sequencing the SLC12A7 gene. The DNA sequence is then compared to a reference sequence to identify any genetic variations or mutations that may be present.

The results of the NGS genetic test can help healthcare providers determine the most appropriate treatment and management strategies for individuals with Bartter syndrome. Additionally, genetic testing can provide valuable information for family members who may be at risk of inheriting the condition.

It’s important to note that genetic testing for Bartter syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.

SKU: TEST-3588 Category:

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