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SLC9A3R1 Gene Nephrolithiasisosteoporosis Hypophosphatemic Type 2 Genetic Test Cost

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

-21%

The SLC9A3R1 gene is associated with a rare genetic condition known as Nephrolithiasis-Osteoporosis, Hypophosphatemic Type 2. This condition is characterized by the development of kidney stones, reduced bone density leading to osteoporosis, and hypophosphatemia, which is an abnormally low level of phosphate in the blood. These symptoms result from mutations in the SLC9A3R1 gene, which plays a crucial role in phosphate regulation and bone mineralization.

To diagnose this condition, a specific genetic test is available at DNA Labs UAE. The test involves analyzing the patient’s DNA to identify mutations in the SLC9A3R1 gene that are indicative of Nephrolithiasis-Osteoporosis, Hypophosphatemic Type 2. This genetic test is crucial for confirming the diagnosis, understanding the disease’s progression, and guiding treatment and management strategies.

The cost of the SLC9A3R1 gene nephrolithiasis-osteoporosis hypophosphatemic type 2 genetic test at DNA Labs UAE is 4400 AED. Given the complexity and specificity of this test, it represents a critical step towards personalized medicine for patients exhibiting symptoms or having a family history of this rare condition. By identifying the genetic basis of the disease, healthcare providers can offer more targeted and effective interventions to manage and mitigate the symptoms associated with this disorder.

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SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 Genetic Test

Welcome to DNA Labs UAE, where we offer the SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 Genetic Test. This test can help diagnose individuals with Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 and provide valuable information for treatment and management strategies.

Test Details

The SLC9A3R1 gene is associated with a condition called Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2. This condition is characterized by the formation of kidney stones (nephrolithiasis) and weak bones (osteoporosis) due to low levels of phosphate in the blood (hypophosphatemia).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously for genetic variations or mutations. In the case of Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2, NGS genetic testing can be used to identify any genetic variations or mutations in the SLC9A3R1 gene that may be causing the condition.

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

Before undergoing the SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2.

Conclusion

The SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 Genetic Test offered by DNA Labs UAE can help diagnose individuals with Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 and provide valuable information for treatment and management strategies. It can also be used for genetic counseling and family planning purposes.

Test Name SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 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 SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test gene SLC9A3R1
Test Details

The SLC9A3R1 gene is associated with a condition called Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2. This condition is characterized by the formation of kidney stones (nephrolithiasis) and weak bones (osteoporosis) due to low levels of phosphate in the blood (hypophosphatemia).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously for genetic variations or mutations. In the case of Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2, NGS genetic testing can be used to identify any genetic variations or mutations in the SLC9A3R1 gene that may be causing the condition.

By identifying these genetic variations or mutations, NGS genetic testing can help in diagnosing individuals with Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 and provide valuable information for treatment and management strategies. It can also be used for genetic counseling and family planning purposes.

SKU: TEST-3717 Category:

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