Symptoms and Testing information for CD2AP Gene Focal Segmental Glomerulosclerosis Type 3 Genetic Test

Symptoms and Testing information for CD2AP Gene Focal Segmental Glomerulosclerosis Type 3 Genetic Test

Focal Segmental Glomerulosclerosis (FSGS) is a disease that attacks the kidney’s filtering units (glomeruli), causing serious scarring which leads to permanent kidney damage and even failure. Among the genetic factors contributing to the development of FSGS, mutations in the CD2AP gene have been identified as a cause for concern. DNA Labs UAE offers a comprehensive genetic test for FSGS Type 3, linked to the CD2AP gene mutation, providing invaluable information for individuals at risk.

Understanding Focal Segmental Glomerulosclerosis Type 3

Focal Segmental Glomerulosclerosis Type 3 is a specific subtype of FSGS, characterized by mutations in the CD2AP gene. This gene plays a crucial role in the functioning of podocytes – cells in the glomeruli that are essential for filtering waste from the blood. Mutations in the CD2AP gene disrupt podocyte function, leading to the symptoms associated with FSGS. Recognizing these symptoms early can be crucial for managing the condition effectively.

Symptoms of CD2AP Gene Focal Segmental Glomerulosclerosis Type 3

The symptoms of FSGS Type 3 can vary widely among individuals but typically include:

  • Proteinuria – high levels of protein in the urine, indicating poor filtration by the kidneys.
  • Swelling in various parts of the body, especially around the eyes, ankles, and feet, caused by fluid retention.
  • Fatigue and weakness, resulting from the body’s inability to properly filter waste.
  • Hypertension (high blood pressure), which can both contribute to and result from kidney damage.
  • Progressive decline in kidney function, potentially leading to kidney failure if left untreated.

It is crucial for individuals experiencing these symptoms to seek medical advice and consider genetic testing, especially if there is a family history of kidney disease.

The Importance of Genetic Testing

Genetic testing for FSGS Type 3 can provide essential insights for individuals and families at risk. By identifying mutations in the CD2AP gene, patients and healthcare providers can better understand the cause of the symptoms and tailor treatment strategies accordingly. Moreover, early detection through genetic testing can lead to interventions that may slow disease progression and improve quality of life.

CD2AP Gene Focal Segmental Glomerulosclerosis Type 3 Genetic Test at DNA Labs UAE

DNA Labs UAE offers a specialized genetic test for detecting mutations in the CD2AP gene associated with FSGS Type 3. The test is conducted using a simple blood sample, with results typically available within a few weeks. The cost of the test is 4400 AED, an investment in health that could provide critical information for managing kidney health and preventing further damage.

Conclusion

Understanding the symptoms of CD2AP Gene Focal Segmental Glomerulosclerosis Type 3 and the importance of genetic testing can be a crucial step in managing and treating this condition. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the CD2AP gene test, to help individuals take control of their kidney health. For more information on the test and how to proceed, please visit DNA Labs UAE.

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