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WNK4 Gene Pseudohypoaldosteronism type 2B Genetic Test Cost

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

-21%

The WNK4 Gene Pseudohypoaldosteronism Type 2B Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the WNK4 gene, which are linked to Pseudohypoaldosteronism type 2B (PHA2B). This condition, also known as Gordon’s syndrome, is a rare disorder affecting the body’s ability to properly regulate blood pressure and electrolyte balance. The test involves analyzing the patient’s DNA to detect specific genetic alterations in the WNK4 gene that are responsible for the development of PHA2B.

The importance of this test lies in its ability to provide critical information for the accurate diagnosis and management of individuals with symptoms suggestive of PHA2B. Early detection through genetic testing allows for tailored treatment strategies to manage the electrolyte imbalances and hypertension associated with the condition, improving patient outcomes.

The cost of the WNK4 Gene Pseudohypoaldosteronism Type 2B Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, which includes the collection of a DNA sample, usually through a blood draw or cheek swab, and the subsequent detailed genetic analysis performed in the laboratory. Patients considering this test should consult with their healthcare provider to discuss its relevance and implications based on their individual health profile and family history.

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  • This test is not intended for medical diagnosis or treatment
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WNK4 Gene Pseudohypoaldosteronism type 2B Genetic Test

Welcome to DNA Labs UAE, where we offer the WNK4 Gene Pseudohypoaldosteronism type 2B Genetic Test. This test is designed to analyze the WNK4 gene and detect mutations or variations that may be causing the condition known as pseudohypoaldosteronism, type 2B (PHA2B).

Test Components

The WNK4 Gene Pseudohypoaldosteronism type 2B Genetic Test includes the following 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

Before undergoing the WNK4 Gene Pseudohypoaldosteronism type 2B Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with WNK4 Gene Pseudohypoaldosteronism, type 2B NGS Genetic DNA Test gene WNK4.

Test Details

The WNK4 gene is associated with a condition called pseudohypoaldosteronism, type 2B (PHA2B). This genetic disorder affects the kidneys’ ability to regulate salt and potassium levels in the body, leading to symptoms such as high blood pressure, low potassium levels, and metabolic acidosis.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously to identify any mutations or variations in the DNA sequence. In the context of PHA2B, NGS genetic testing can be used to detect mutations in the WNK4 gene that may be causing the condition.

By identifying specific mutations in the WNK4 gene, NGS testing can help confirm a diagnosis of PHA2B and provide valuable information for managing the condition. It can also be used for genetic counseling, as it can determine if an individual is a carrier of the mutation and at risk of passing it on to their children.

Overall, NGS genetic testing for the WNK4 gene in the context of PHA2B can aid in diagnosis, treatment, and genetic counseling for individuals and families affected by this condition.

Test Name WNK4 Gene Pseudohypoaldosteronism type 2B 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 WNK4 Gene Pseudohypoaldosteronism, type 2B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNK4 Gene Pseudohypoaldosteronism, type 2B NGS Genetic DNA Test gene WNK4
Test Details

The WNK4 gene is associated with a condition called pseudohypoaldosteronism, type 2B (PHA2B). This genetic disorder affects the kidneys’ ability to regulate salt and potassium levels in the body, leading to symptoms such as high blood pressure, low potassium levels, and metabolic acidosis.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously to identify any mutations or variations in the DNA sequence. In the context of PHA2B, NGS genetic testing can be used to detect mutations in the WNK4 gene that may be causing the condition.

By identifying specific mutations in the WNK4 gene, NGS testing can help confirm a diagnosis of PHA2B and provide valuable information for managing the condition. It can also be used for genetic counseling, as it can determine if an individual is a carrier of the mutation and at risk of passing it on to their children.

Overall, NGS genetic testing for the WNK4 gene in the context of PHA2B can aid in diagnosis, treatment, and genetic counseling for individuals and families affected by this condition.

SKU: TEST-3773 Category:

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