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SLC12A1 Gene Bartter Syndrome Type 1 Genetic Test Cost

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

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The SLC12A1 gene plays a crucial role in the body’s ability to manage electrolyte balance and blood pressure. Mutations in this gene can lead to Bartter Syndrome Type 1, a rare inherited condition characterized by kidney dysfunction, frequent urination, thirst, and electrolyte imbalances from an early age. Bartter Syndrome Type 1 can have significant health implications if not diagnosed and managed properly.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the SLC12A1 gene, helping in the diagnosis of Bartter Syndrome Type 1. This test is crucial for individuals showing symptoms of the syndrome or those with a family history of the condition, as it can provide a definitive diagnosis, allowing for appropriate management and treatment plans to be established.

The test costs 4400 AED and involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the lab for the presence of mutations in the SLC12A1 gene. The results from this test can guide healthcare providers in creating a tailored treatment plan that may include nutritional support, medications, and regular monitoring of electrolyte levels and kidney function.

By offering this genetic test, DNA Labs UAE plays a vital role in the early detection and management of Bartter Syndrome Type 1, ultimately improving the quality of life for affected individuals.

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SLC12A1 Gene Bartter Syndrome Type 1 Genetic Test

Introduction

The SLC12A1 gene is associated with Bartter syndrome type 1, a rare genetic disorder that affects the kidneys’ ability to reabsorb certain electrolytes. DNA Labs UAE offers a comprehensive NGS (Next-Generation Sequencing) genetic test specifically designed to detect mutations or variations in the SLC12A1 gene that are known to cause Bartter syndrome type 1.

Test Details

The SLC12A1 Gene Bartter Syndrome Type 1 Genetic Test is performed using NGS technology, which allows for the sequencing of multiple genes simultaneously. This comprehensive analysis of an individual’s genetic makeup helps in confirming a diagnosis of Bartter syndrome type 1 and provides information about the specific genetic variant causing the condition.

Components and Price

  • Test Name: SLC12A1 Gene Bartter Syndrome Type 1 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition and Report Delivery

The test requires a blood sample or extracted DNA. Alternatively, one drop of blood on an FTA card can also be used as a sample. The report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The SLC12A1 Gene Bartter Syndrome Type 1 Genetic Test falls under the category of Hepatology, Nephrology, and Endocrinology Disorders. It is recommended to consult a General Physician for this test.

Test Department and Pre-Test Information

The test is conducted in the Genetics department. It is essential to provide the clinical history of the patient who is undergoing the SLC12A1 Gene Bartter Syndrome Type 1 NGS Genetic DNA Test. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected with Bartter syndrome type 1 and the SLC12A1 gene.

Benefits of Genetic Testing for Bartter Syndrome Type 1

Genetic testing for Bartter syndrome type 1 can be beneficial for the following reasons:

  • Confirming a diagnosis of Bartter syndrome type 1
  • Providing information about the specific genetic variant causing the condition
  • Identifying individuals with symptoms suggestive of Bartter syndrome type 1
  • Evaluating family members who may be at risk of inheriting the genetic mutation
  • Assisting in genetic counseling and family planning

Conclusion

It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor. They can help interpret the test results and provide appropriate recommendations and support based on the individual’s genetic makeup.

Test Name SLC12A1 Gene Bartter syndrome type 1 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 SLC12A1 Gene Bartter syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC12A1 Gene Bartter syndrome type 1 NGS Genetic DNA Test gene SLC12A1
Test Details

The SLC12A1 gene is associated with Bartter syndrome type 1, a rare genetic disorder that affects the kidneys’ ability to reabsorb certain electrolytes. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the sequencing of multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup.

The SLC12A1 gene Bartter syndrome type 1 NGS genetic test specifically looks for mutations or variations in the SLC12A1 gene that are known to cause Bartter syndrome type 1. This test can help confirm a diagnosis of Bartter syndrome type 1 and provide information about the specific genetic variant causing the condition.

Genetic testing for Bartter syndrome type 1 can be useful for individuals with symptoms suggestive of the condition, as well as for family members of affected individuals who may be at risk of inheriting the genetic mutation. It can also be helpful for genetic counseling and family planning purposes.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor, who can help interpret the results and provide appropriate recommendations and support.

SKU: TEST-3589 Category:

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