SLC12A5 Gene Bartter Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer the SLC12A5 Gene Bartter Syndrome Genetic Test. This test is designed to analyze the SLC12A5 gene, which is associated with Bartter syndrome, a rare genetic disorder affecting the kidneys.
Test Components and Price
The SLC12A5 Gene Bartter Syndrome Genetic Test is priced at 4400.0 AED. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA Card.
Report Delivery
After the sample is collected, the report will be delivered within 3 to 4 weeks.
Method
The SLC12A5 Gene Bartter Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sample.
Test Type
This test falls under the categories of Hepatology, Nephrology, and Endocrinology Disorders.
Doctor
The SLC12A5 Gene Bartter Syndrome Genetic Test is recommended by General Physicians.
Test Department
This test is conducted in our Genetics department.
Pre Test Information
Prior to undergoing the SLC12A5 Gene Bartter Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by Bartter syndrome.
Test Details
Bartter syndrome is characterized by an electrolyte imbalance in the body, resulting in symptoms such as excessive urination, dehydration, salt cravings, muscle cramps, and growth problems. The SLC12A5 Gene Bartter Syndrome Genetic Test utilizes NGS technology to identify mutations in the SLC12A5 gene associated with the condition. This test confirms a diagnosis of Bartter syndrome and provides information about the specific genetic variant causing the disorder.
During the test, a blood or saliva sample is collected from the individual. The DNA from the sample is then sequenced to identify any mutations or variations in the SLC12A5 gene. The results of the test can guide treatment decisions and provide information about the risk of passing the condition on to future generations.
It is important to note that NGS genetic testing should be performed by healthcare professionals with expertise in genetic testing and counseling. The test results should be interpreted in the context of the individual’s clinical presentation and family history. Genetic counseling may be recommended to discuss the implications of the results.
| Test Name | SLC12A5 Gene Bartter 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 SLC12A5 Gene Bartter syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A5 Gene Bartter syndrome NGS Genetic DNA Test gene SLC12A5 |
| Test Details |
The SLC12A5 gene is associated with Bartter syndrome, a rare genetic disorder that affects the kidneys. Bartter syndrome is characterized by an imbalance of electrolytes in the body, leading to symptoms such as excessive urination, dehydration, salt cravings, muscle cramps, and growth problems. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze a person’s DNA for specific genetic mutations or variations. In the case of Bartter syndrome, NGS genetic testing can be used to identify mutations in the SLC12A5 gene that are associated with the condition. This test can help confirm a diagnosis of Bartter syndrome and provide information about the specific genetic variant causing the disorder. NGS genetic testing typically involves collecting a blood or saliva sample from the individual undergoing testing. The DNA from the sample is then sequenced, allowing for the identification of any mutations or variations in the SLC12A5 gene. The results of the test can be used to guide treatment decisions and provide information about the risk of passing the condition on to future generations. It is important to note that NGS genetic testing is typically performed by healthcare professionals with expertise in genetic testing and counseling. The test results should be interpreted in the context of the individual’s clinical presentation and family history, and genetic counseling may be recommended to discuss the implications of the results. |
