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SLC3A1 Gene Cystinuria Genetic Test Cost

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

-21%

The SLC3A1 Gene Cystinuria Genetic Test is a specialized diagnostic examination designed to identify mutations in the SLC3A1 gene, which is primarily associated with the development of cystinuria. Cystinuria is an inherited disorder that leads to the formation of cystine stones in the kidneys, bladder, and urinary tract, potentially causing pain, urinary tract infections, and kidney damage. The test is crucial for individuals with a family history of cystinuria or those exhibiting symptoms related to kidney stones, as early detection can aid in managing the condition effectively through dietary changes, medication, and lifestyle adjustments.

Conducted at DNA Labs UAE, a leading facility in genetic and molecular diagnostics, the test offers a comprehensive analysis of the SLC3A1 gene. DNA Labs UAE utilizes advanced genetic sequencing technologies to ensure accurate and reliable results. The cost of the SLC3A1 Gene Cystinuria Genetic Test is 4400 AED, reflecting the sophisticated nature of the genetic analysis and the invaluable insights it provides into managing cystinuria. By opting for this test, individuals gain critical information that can help in tailoring specific treatment plans and preventive measures, significantly improving quality of life for those affected by cystinuria.

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  • This test is not intended for medical diagnosis or treatment
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SLC3A1 Gene Cystinuria Genetic Test

Are you concerned about cystinuria and its genetic implications? DNA Labs UAE offers the SLC3A1 Gene Cystinuria Genetic Test at an affordable cost of AED 4400.0.

Test Details

The SLC3A1 gene is associated with cystinuria, a hereditary disorder characterized by the kidneys’ inability to reabsorb the amino acid cystine. This leads to the formation of cystine stones in the urinary tract.

Our SLC3A1 Gene Cystinuria Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes. By examining the SLC3A1 gene, this test can identify any mutations or variations that may be responsible for cystinuria.

Not only does this test help in diagnosing cystinuria, but it also provides valuable information about the genetic cause of the disease and the risk of passing it on to future generations.

Test Components

  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop of 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 SLC3A1 Gene Cystinuria NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the SLC3A1 gene. This will aid in identifying potential carriers of the genetic mutation.

Don’t wait any longer. Take control of your genetic health and get the SLC3A1 Gene Cystinuria Genetic Test today at DNA Labs UAE.

Test Name SLC3A1 Gene Cystinuria 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 SLC3A1 Gene Cystinuria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC3A1 Gene Cystinuria NGS Genetic DNA Test gene SLC3A1
Test Details

The SLC3A1 gene is associated with a condition called cystinuria. Cystinuria is an inherited disorder characterized by the inability of the kidneys to reabsorb the amino acid cystine, leading to the formation of cystine stones in the urinary tract.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the case of cystinuria, NGS genetic testing can be used to identify mutations or variations in the SLC3A1 gene that may be responsible for the condition. This type of testing can help diagnose cystinuria, determine the genetic cause of the disease, and provide information about the risk of passing the condition on to future generations.