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SLC12A3 Gene Gitelman Syndrome Genetic Test Cost

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

-21%

The SLC12A3 gene plays a crucial role in the body’s regulation of mineral balance, particularly involving the reabsorption of sodium and chloride ions in the kidneys. Mutations in this gene can lead to Gitelman syndrome, a rare genetic disorder characterized by low levels of potassium and magnesium in the blood, leading to a range of symptoms such as muscle weakness, cramps, and fatigue.

To diagnose this condition, the Gitelman Syndrome Genetic Test targeting the SLC12A3 gene is available. This test specifically looks for mutations in the SLC12A3 gene that are known to cause Gitelman syndrome. It is a vital tool for confirming the diagnosis in individuals showing symptoms of the syndrome, as well as for genetic counseling purposes for affected families.

The test is offered at DNA Labs UAE, a facility known for its advanced genetic testing services. The cost of the Gitelman Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test provides a reliable diagnosis, aiding in the management and treatment planning for individuals with Gitelman syndrome. It is recommended for individuals with clinical symptoms of the syndrome or those with a family history of the condition.

Description

SLC12A3 Gene Gitelman syndrome Genetic Test

Components: SLC12A3 Gene Gitelman syndrome Genetic Test

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 SLC12A3 Gene Gitelman syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A3 Gene Gitelman syndrome NGS Genetic DNA Test gene SLC12A3

Test Details:

The SLC12A3 gene is associated with Gitelman syndrome, which is a rare genetic disorder that affects the kidneys. This gene provides instructions for producing a protein called the thiazide-sensitive sodium-chloride cotransporter, which is involved in the reabsorption of salt and water in the kidneys.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of genetic variations or mutations in the SLC12A3 gene that may be associated with Gitelman syndrome. This test can help diagnose individuals suspected of having the condition and can also be used for carrier testing in family members.

NGS genetic testing involves collecting a sample of DNA, usually through a blood or saliva sample, and sequencing the entire SLC12A3 gene. The sequencing data is then analyzed to identify any genetic variations or mutations that may be present. This information can help healthcare professionals in making a diagnosis and determining appropriate treatment options for individuals with Gitelman syndrome.

Test Name	SLC12A3 Gene Gitelman 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 SLC12A3 Gene Gitelman syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A3 Gene Gitelman syndrome NGS Genetic DNA Test gene SLC12A3
Test Details	The SLC12A3 gene is associated with Gitelman syndrome, which is a rare genetic disorder that affects the kidneys. This gene provides instructions for producing a protein called the thiazide-sensitive sodium-chloride cotransporter, which is involved in the reabsorption of salt and water in the kidneys. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of genetic variations or mutations in the SLC12A3 gene that may be associated with Gitelman syndrome. This test can help diagnose individuals suspected of having the condition and can also be used for carrier testing in family members. NGS genetic testing involves collecting a sample of DNA, usually through a blood or saliva sample, and sequencing the entire SLC12A3 gene. The sequencing data is then analyzed to identify any genetic variations or mutations that may be present. This information can help healthcare professionals in making a diagnosis and determining appropriate treatment options for individuals with Gitelman syndrome.