Symptoms and Testing information for PAX2 Gene Focal Segmental Glomerulosclerosis Type 7 Genetic Test

Symptoms and Testing information for PAX2 Gene Focal Segmental Glomerulosclerosis Type 7 Genetic Test

Focal Segmental Glomerulosclerosis (FSGS) is a complex kidney disorder characterized by scarring (sclerosis) in the kidney’s filtering units (glomeruli). This condition can lead to severe kidney damage and even kidney failure. One specific subtype of this disease, known as FSGS Type 7, has been genetically linked to mutations in the PAX2 gene. Understanding the symptoms and genetic underpinnings of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for this condition, providing essential insights for affected individuals and their families.

Symptoms of PAX2 Gene Focal Segmental Glomerulosclerosis Type 7

The symptoms of FSGS Type 7, caused by mutations in the PAX2 gene, can vary widely among individuals. However, some common signs and symptoms should prompt individuals to consider genetic testing. These include:

  • Proteinuria: Excessive levels of protein in the urine, which can be an early sign of kidney damage.
  • Hematuria: The presence of blood in the urine, indicating a possible kidney or urinary tract problem.
  • Edema: Swelling, particularly in the legs and feet, due to fluid retention caused by compromised kidney function.
  • Hypertension: High blood pressure, often a consequence of kidney dysfunction.
  • Reduced Kidney Function: Decreased kidney performance, which may progress to kidney failure if left untreated.

It is important to note that these symptoms can also be indicative of other kidney disorders. Therefore, genetic testing for the PAX2 gene mutation can be a crucial step in achieving an accurate diagnosis.

Genetic Test for PAX2 Gene Focal Segmental Glomerulosclerosis Type 7

DNA Labs UAE offers a specific genetic test to identify mutations in the PAX2 gene associated with FSGS Type 7. This test is an essential tool for individuals experiencing symptoms of kidney disease or those with a family history of FSGS. The test involves a simple blood draw or saliva sample, making it a non-invasive procedure.

The genetic test not only aids in the diagnosis of FSGS Type 7 but also helps in tailoring a personalized treatment plan. Understanding the genetic basis of the disease can guide healthcare providers in selecting the most effective treatment strategies, potentially improving outcomes for individuals with this condition.

Test Cost

The cost of the PAX2 gene Focal Segmental Glomerulosclerosis Type 7 genetic test at DNA Labs UAE is 4400 AED. While the cost may seem significant, it is important to consider the value of a precise diagnosis and the potential for a personalized treatment plan that can address the specific needs of individuals with this condition.

For more information about the test and to schedule an appointment, visit DNA Labs UAE.

Conclusion

FSGS Type 7, associated with mutations in the PAX2 gene, is a serious kidney disorder that can lead to significant health issues if left undiagnosed and untreated. Recognizing the symptoms early and undergoing genetic testing can be crucial steps in managing the disease effectively. DNA Labs UAE provides a comprehensive genetic test for this condition, offering hope and direction for individuals and families affected by this challenging diagnosis. With the right information and support, it is possible to navigate the complexities of FSGS Type 7 and achieve better health outcomes.

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