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SCNN1A Gene Pseudohypoaldosteronism type 1 autosomal recessive Genetic Test

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

-21%

The SCNN1A gene plays a crucial role in regulating the balance of sodium and fluids in the body. Mutations in this gene can lead to a condition known as pseudohypoaldosteronism type 1 (PHA1), an autosomal recessive disorder. This condition is characterized by the body’s inability to properly respond to aldosterone, a hormone that helps regulate sodium, potassium, and fluid levels. As a result, individuals with PHA1 experience salt wasting, dehydration, and high levels of potassium in the blood, which can lead to serious health issues if not properly managed.

To diagnose this condition accurately, genetic testing is employed to identify mutations in the SCNN1A gene. In the United Arab Emirates, DNA Labs UAE offers a specialized genetic test for this purpose. The test is designed to detect mutations in the SCNN1A gene that are associated with pseudohypoaldosteronism type 1 autosomal recessive. This precise genetic testing is crucial for confirming the diagnosis, which can then guide appropriate treatment and management strategies for affected individuals.

The cost of the SCNN1A gene pseudohypoaldosteronism type 1 autosomal recessive genetic test at DNA Labs UAE is 4400 AED. This investment is vital for families seeking answers to their loved ones’ health issues, as it not only confirms the diagnosis but also helps in planning for the necessary medical care and lifestyle adjustments to manage the condition effectively.

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SCNN1A Gene Pseudohypoaldosteronism type 1 autosomal recessive Genetic Test

At DNA Labs UAE, we offer the SCNN1A Gene Pseudohypoaldosteronism type 1 autosomal recessive Genetic Test at a cost of AED 4400.0.

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

Before undergoing the SCNN1A Gene Pseudohypoaldosteronism type 1 autosomal recessive 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 with SCNN1A Gene Pseudohypoaldosteronism type 1 autosomal recessive NGS Genetic DNA Test gene SCNN1A.

Test Details

The SCNN1A gene is associated with a condition called pseudohypoaldosteronism type 1 (PHA1). PHA1 is a rare genetic disorder characterized by salt-wasting and high levels of potassium in the blood. It is inherited in an autosomal recessive manner, meaning that both copies of the mutated gene must be inherited (one from each parent) to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of PHA1, an NGS genetic test can be used to identify mutations in the SCNN1A gene, confirming the diagnosis of autosomal recessive PHA1.

By identifying the specific genetic mutation causing PHA1, NGS testing can also provide information about the inheritance pattern, potential risks for family members, and help guide appropriate treatment and management strategies. It is crucial to consult with a genetic counselor or healthcare professional to understand the implications of the test results and determine the appropriate course of action.

Test Name SCNN1A Gene Pseudohypoaldosteronism type 1 autosomal recessive 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 SCNN1A Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCNN1A Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test gene SCNN1A
Test Details

The SCNN1A gene is associated with a condition called pseudohypoaldosteronism type 1 (PHA1). PHA1 is a rare genetic disorder characterized by salt-wasting and high levels of potassium in the blood. It is inherited in an autosomal recessive manner, which means that an individual must inherit two copies of the mutated gene (one from each parent) to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of PHA1, an NGS genetic test can be used to identify mutations in the SCNN1A gene, which can confirm the diagnosis of autosomal recessive PHA1.

By identifying the specific genetic mutation causing PHA1, NGS testing can also provide information about the inheritance pattern, potential risks for family members, and help guide appropriate treatment and management strategies. It is important to consult with a genetic counselor or healthcare professional to understand the implications of the test results and the appropriate course of action.

SKU: TEST-3770 Category:

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