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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 plays a crucial role in the body’s ability to manage minerals and electrolytes, which are vital for bone health and kidney function. Mutations in this gene can lead to a rare condition known as Nephrolithiasis-osteoporosis, hypophosphatemic type 2, characterized by the development of kidney stones and decreased bone density due to an imbalance in phosphate levels. To diagnose this condition, a specific genetic test targeting the SLC9A3R1 gene mutations can be conducted. This test is essential for confirming the diagnosis, understanding the risk of passing the condition to offspring, and guiding treatment options.

At DNA Labs UAE, this specialized genetic test is available for individuals who may be at risk of this condition or are experiencing symptoms related to kidney stones and bone health issues. The test cost is set at 4400 AED, reflecting the comprehensive analysis and the detailed report provided by the lab. Conducting this test at DNA Labs UAE ensures accuracy and reliability, supported by their expertise in genetic diagnostics and counseling services to help patients understand their results and the implications for their health and family.

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SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing laboratory in the UAE. Today, we will be discussing the SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 Genetic Test. This test is designed to identify mutations or variations in the SLC9A3R1 gene that may be responsible for a condition called Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2.

Test Details

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

Our NGS (Next-Generation Sequencing) genetic testing method allows for the analysis of multiple genes simultaneously. In the context of Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2, NGS genetic testing can be used to identify mutations or variations in the SLC9A3R1 gene that may be responsible for the condition. This can greatly assist in the diagnosis and management of individuals with this genetic disorder.

Test Components and Price

Test Name: SLC9A3R1 Gene Nephrolithiasisosteoporosis hypophosphatemic type 2 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA Card for this genetic test.

Report Delivery

Your test report will be delivered within 3 to 4 weeks from the date of sample collection.

Test Type

This test falls under the following categories: Osteology, Dermatology, Immunology Disorders.

Doctor and Test Department

This test is performed by a Dermatologist in our Genetics Test Department.

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 Counselling session will be conducted to draw a pedigree chart of family members affected with SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test gene SLC9A3R1.

Thank you for considering DNA Labs UAE for your genetic testing needs. If you have any further questions or would like to schedule an appointment, please feel free to contact us.

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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
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, brittle bones (osteoporosis) due to low levels of phosphate in the blood (hypophosphatemia).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the context of Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2, NGS genetic testing can be used to identify mutations or variations in the SLC9A3R1 gene that may be responsible for the condition. This can help in the diagnosis and management of individuals with this genetic disorder.

SKU: TEST-3154 Category:

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