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SCNN1G Gene Pseudohypoaldosteronism type 1 autosomal recessive Genetic Test

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

-21%

The SCNN1G gene plays a critical role in the regulation of sodium balance in the body. Mutations in this gene can lead to a rare genetic disorder known as pseudohypoaldosteronism type 1 (PHA1), specifically the autosomal recessive form. This condition is characterized by the body’s inability to properly respond to the hormone aldosterone, leading to issues such as salt loss, dehydration, and electrolyte imbalances.

To diagnose this condition, a genetic test targeting the SCNN1G gene can be conducted. DNA Labs UAE offers this specialized test, providing a comprehensive analysis to identify any mutations within the gene that could be responsible for PHA1. The test is priced at 4400 AED, offering a crucial diagnostic tool for individuals exhibiting symptoms of PHA1 or those with a family history of the condition. Through this genetic testing, affected individuals can receive accurate diagnosis, enabling timely and appropriate management of the disorder.

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SCNN1G Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive Genetic Test

Genetic testing is an important tool in diagnosing and understanding genetic disorders. One such disorder is SCNN1G Gene Pseudohypoaldosteronism type 1, which is inherited in an autosomal recessive manner.

Test Name

SCNN1G 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 SCNN1G Gene Pseudohypoaldosteronism type 1 autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCNN1G Gene Pseudohypoaldosteronism type 1 autosomal recessive NGS Genetic DNA Test gene SCNN1G.

Test Details

SCNN1G gene pseudohypoaldosteronism type 1 is a genetic disorder that is inherited in an autosomal recessive manner. This means that both copies of the SCNN1G gene, one inherited from each parent, must have mutations in order for an individual to develop the disorder.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of SCNN1G gene pseudohypoaldosteronism type 1, NGS genetic testing would involve sequencing the SCNN1G gene to identify any mutations or variations that may be present.

This type of genetic testing can be helpful in diagnosing individuals with suspected pseudohypoaldosteronism type 1 and can also be used for carrier testing in individuals with a family history of the disorder. It can provide valuable information about the specific genetic mutations present, which can aid in understanding the underlying cause of the disorder and potentially guide treatment options.

It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics, as the results can have significant implications for individuals and their families. Genetic counseling is often recommended both before and after testing to help individuals understand the implications of the results and make informed decisions about their healthcare.

Test Name SCNN1G 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 SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test gene SCNN1G
Test Details

SCNN1G gene pseudohypoaldosteronism, type 1 is a genetic disorder that is inherited in an autosomal recessive manner. This means that both copies of the SCNN1G gene, one inherited from each parent, must have mutations in order for an individual to develop the disorder.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of SCNN1G gene pseudohypoaldosteronism, type 1, NGS genetic testing would involve sequencing the SCNN1G gene to identify any mutations or variations that may be present.

This type of genetic testing can be helpful in diagnosing individuals with suspected pseudohypoaldosteronism, type 1 and can also be used for carrier testing in individuals with a family history of the disorder. It can provide valuable information about the specific genetic mutations present, which can aid in understanding the underlying cause of the disorder and potentially guide treatment options.

It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics, as the results can have significant implications for individuals and their families. Genetic counseling is often recommended both before and after testing to help individuals understand the implications of the results and make informed decisions about their healthcare.

SKU: TEST-3772 Category:

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