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SCNN1G Gene Liddle Syndrome Genetic Test

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

-21%

The SCNN1G gene plays a crucial role in the regulation of sodium reabsorption in the kidney. Mutations in this gene are associated with Liddle syndrome, a rare genetic disorder characterized by early-onset hypertension, low plasma renin activity, and hypokalemia. The condition mimics symptoms of hyperaldosteronism but does not respond to conventional treatments, making accurate diagnosis crucial for effective management.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the SCNN1G gene, providing a definitive diagnosis of Liddle syndrome. This test is particularly important for individuals with a family history of the condition or those presenting with clinical features suggestive of the syndrome. Early detection through genetic testing allows for targeted treatment strategies, significantly improving patient outcomes.

The test is priced at 4400 AED and involves a simple procedure where a sample of the patient’s DNA, typically obtained through a blood draw or cheek swab, is analyzed for specific mutations in the SCNN1G gene. Results from this test can guide healthcare providers in customizing treatment plans that may include dietary modifications and specific medications to manage symptoms effectively.

By offering the SCNN1G gene Liddle syndrome genetic test, DNA Labs UAE provides a crucial service for the accurate diagnosis and management of this rare condition, supporting patients and their families in navigating the challenges associated with Liddle syndrome.

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SCNN1G Gene Liddle Syndrome Genetic Test

At DNA Labs UAE, we offer the SCNN1G Gene Liddle Syndrome Genetic Test at a cost of AED 4400.0.

Test Components

The 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

Prior to the SCNN1G Gene Liddle Syndrome Genetic Test, it is important to provide the clinical history of the patient who is undergoing the test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by SCNN1G Gene Liddle Syndrome.

Test Details

The SCNN1G gene is responsible for encoding the subunit of the epithelial sodium channel (ENaC), which plays a role in regulating sodium transport across epithelial tissues. Mutations in the SCNN1G gene have been linked to a rare genetic disorder known as Liddle Syndrome.

Liddle Syndrome is an autosomal dominant disorder characterized by early-onset hypertension (high blood pressure) and low potassium levels in the blood. It is caused by mutations in the SCNN1G gene, which result in increased activity of the ENaC channel and enhanced sodium reabsorption in the kidneys.

NGS (Next-Generation Sequencing) genetic testing is a cutting-edge genetic test that allows for the analysis of multiple genes simultaneously. It is a more efficient and cost-effective method compared to traditional sequencing methods. In the case of SCNN1G gene NGS genetic testing, the SCNN1G gene is sequenced to identify any mutations or variants associated with Liddle Syndrome.

The SCNN1G Gene Liddle Syndrome Genetic Test can help confirm a diagnosis of Liddle Syndrome and guide appropriate treatment and management strategies.

Test Name SCNN1G Gene Liddle 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 SCNN1G Gene Liddle syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCNN1G Gene Liddle syndrome NGS Genetic DNA Test gene SCNN1G
Test Details

SCNN1G is a gene that encodes for the subunit of the epithelial sodium channel (ENaC), which is involved in regulating sodium transport across epithelial tissues. Mutations in the SCNN1G gene have been associated with a rare genetic disorder called Liddle syndrome.

Liddle syndrome is an autosomal dominant disorder characterized by early-onset hypertension (high blood pressure) and low potassium levels in the blood. It is caused by mutations in the SCNN1G gene, which lead to increased activity of the ENaC channel and enhanced sodium reabsorption in the kidneys.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the identification of genetic mutations in a more efficient and cost-effective manner compared to traditional sequencing methods.

Therefore, an SCNN1G gene NGS genetic test would involve sequencing the SCNN1G gene to identify any mutations or variants that may be associated with Liddle syndrome. This test can help in confirming a diagnosis of Liddle syndrome and guiding appropriate treatment and management strategies.

SKU: TEST-3697 Category:

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