UMOD Gene Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Genetic Test
At DNA Labs UAE, we offer the UMOD Gene Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Genetic Test. This diagnostic test uses Next-Generation Sequencing (NGS) technology to analyze the UMOD gene for mutations associated with glomerulocystic kidney disease, hyperuricemia, and isosthenuria.
Test Details
The UMOD gene glomerulocystic kidney disease with hyperuricemia and isosthenuria NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the UMOD gene for mutations associated with glomerulocystic kidney disease, hyperuricemia, and isosthenuria. Glomerulocystic kidney disease is a rare genetic disorder characterized by the formation of small cysts within the kidney’s glomeruli, which are responsible for filtering waste products from the blood. This condition can lead to impaired kidney function and the development of other complications.
Hyperuricemia is a condition characterized by high levels of uric acid in the blood. It can lead to the formation of uric acid crystals in the joints and other tissues, causing gout and kidney stones. Isosthenuria refers to the inability of the kidneys to concentrate or dilute urine appropriately. It can result in excessive water loss or retention and impaired kidney function.
The UMOD gene provides instructions for producing a protein called uromodulin, which is primarily produced in the kidneys and plays a role in regulating urine concentration and kidney function. Mutations in the UMOD gene can disrupt the normal function of uromodulin, leading to the development of glomerulocystic kidney disease, hyperuricemia, and isosthenuria.
Test Components and Price
- Test Name: UMOD Gene Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Genetic Test
- 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 UMOD Gene Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session may be conducted to draw a pedigree chart of family members affected with UMOD Gene Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria NGS Genetic DNA Test gene UMOD.
Importance of Genetic Testing
The NGS genetic test analyzes the UMOD gene for any mutations or genetic variants that may be associated with glomerulocystic kidney disease, hyperuricemia, and isosthenuria. This test can help diagnose individuals with these conditions, allowing for appropriate management and treatment strategies to be implemented.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and counseling based on the test results.
| Test Name | UMOD Gene Glomerulocystic kidney disease with hyperuricemia and isosthenuria 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 UMOD Gene Glomerulocystic kidney disease with hyperuricemia and isosthenuria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UMOD Gene Glomerulocystic kidney disease with hyperuricemia and isosthenuria NGS Genetic DNA Test gene UMOD |
| Test Details | UMOD gene glomerulocystic kidney disease with hyperuricemia and isosthenuria NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the UMOD gene for mutations associated with glomerulocystic kidney disease, hyperuricemia, and isosthenuria. Glomerulocystic kidney disease is a rare genetic disorder characterized by the formation of small cysts within the kidney’s glomeruli, which are responsible for filtering waste products from the blood. This condition can lead to impaired kidney function and the development of other complications. Hyperuricemia is a condition characterized by high levels of uric acid in the blood. It can lead to the formation of uric acid crystals in the joints and other tissues, causing gout and kidney stones. Isosthenuria refers to the inability of the kidneys to concentrate or dilute urine appropriately. It can result in excessive water loss or retention and impaired kidney function. The UMOD gene provides instructions for producing a protein called uromodulin, which is primarily produced in the kidneys and plays a role in regulating urine concentration and kidney function. Mutations in the UMOD gene can disrupt the normal function of uromodulin, leading to the development of glomerulocystic kidney disease, hyperuricemia, and isosthenuria. The NGS genetic test analyzes the UMOD gene for any mutations or genetic variants that may be associated with these conditions. It can help diagnose individuals with glomerulocystic kidney disease, hyperuricemia, and isosthenuria, allowing for appropriate management and treatment strategies to be implemented. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and counseling based on the test results. |
