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KCNJ1 Gene Bartter Syndrome Type 2 Genetic Test Cost

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

-21%

The KCNJ1 gene Bartter Syndrome Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the KCNJ1 gene. This gene is crucial for the proper function of kidney cells involved in electrolyte and fluid balance. Mutations in the KCNJ1 gene are directly linked to Bartter Syndrome Type 2, a rare inherited condition that affects the kidney’s ability to reabsorb sodium, leading to imbalances in electrolytes and various clinical symptoms such as dehydration, frequent urination, and growth retardation.

The test is conducted using a sample of the patient’s blood or saliva, through which DNA is extracted and analyzed for specific mutations in the KCNJ1 gene. This genetic test is pivotal for the early diagnosis and management of Bartter Syndrome Type 2, allowing for tailored treatment plans that can mitigate symptoms and improve the quality of life for affected individuals.

The cost of the KCNJ1 gene Bartter Syndrome Type 2 Genetic Test at DNA Labs UAE is 4400 AED. This investment in health care is essential for families with a history of the syndrome or those exhibiting symptoms, providing them with crucial information for managing the condition.

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KCNJ1 Gene Bartter Syndrome Type 2 Genetic Test

At DNA Labs UAE, we offer the KCNJ1 Gene Bartter Syndrome Type 2 Genetic Test for individuals who suspect they may have this rare genetic disorder affecting the kidneys. This test can provide valuable information about the specific genetic changes that may be causing Bartter syndrome type 2.

Test Details

The KCNJ1 gene is associated with Bartter syndrome type 2, a condition characterized by the inability of the kidneys to reabsorb certain electrolytes, leading to imbalances in the body’s salt and fluid levels. Our NGS (Next-Generation Sequencing) technology allows us to analyze the DNA sequence of a person’s genes, helping to identify mutations or variations in the KCNJ1 gene that may be responsible for the disorder.

Components and Price

  • Test Name: KCNJ1 Gene Bartter Syndrome Type 2 Genetic Test
  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card for this test.

Report Delivery

Your test results will be delivered within 3 to 4 weeks from the date of sample submission.

Method

We utilize NGS technology for the KCNJ1 Gene Bartter Syndrome Type 2 Genetic Test.

Test Type

This test falls under the categories of Hepatology, Nephrology, and Endocrinology Disorders.

Doctor

Your test will be conducted by a General Physician.

Test Department

This test is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the KCNJ1 gene.

It is crucial to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Bartter syndrome type 2. They can provide guidance on the testing process, interpretation of results, and any potential implications for the individual and their family.

Test Name KCNJ1 Gene Bartter syndrome type 2 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 KCNJ1 Gene Bartter syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNJ1 Gene Bartter syndrome type 2 NGS Genetic DNA Test gene KCNJ1
Test Details

The KCNJ1 gene is associated with Bartter syndrome type 2, which is a rare genetic disorder affecting the kidneys. Bartter syndrome is characterized by the inability of the kidneys to reabsorb certain electrolytes, leading to imbalances in the body’s salt and fluid levels.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. In the context of Bartter syndrome type 2, NGS genetic testing can be used to identify mutations or variations in the KCNJ1 gene that may be responsible for the disorder.

By analyzing the DNA sequence, NGS testing can provide valuable information about the specific genetic changes that may be causing Bartter syndrome type 2. This information can help with diagnosis, treatment decisions, and genetic counseling for affected individuals and their families.

It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Bartter syndrome type 2. They can provide guidance on the testing process, interpretation of results, and any potential implications for the individual and their family.

SKU: TEST-3590 Category:

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