Symptoms of WT1 Gene Wilms Tumor Type 1 Familial Genetic Test Price 4400 AED
Wilms tumor, also known as nephroblastoma, is a rare kidney cancer that primarily affects children. It is associated with mutations in the WT1 gene, which plays a crucial role in kidney development. Recognizing the symptoms early can lead to timely diagnosis and treatment, significantly improving outcomes. DNA Labs UAE offers a comprehensive genetic test for the WT1 gene, aiding in the identification of familial predisposition to Wilms tumor.
Understanding Wilms Tumor
Wilms tumor can occur in one or both kidneys and is most commonly diagnosed in children aged 3 to 4 years. The WT1 gene mutation can be sporadic or inherited. Familial cases, although less common, suggest a genetic predisposition that can be identified through genetic testing.
Key Symptoms and Signs
- Abdominal Swelling or Lump: One of the first signs of Wilms tumor is often a noticeable swelling or lump in the abdomen, which may or may not be accompanied by pain.
- Blood in Urine: Hematuria, or blood in the urine, is another symptom that can occur, though it is less common.
- High Blood Pressure: Increased blood pressure can be associated with Wilms tumor due to the tumor’s effect on kidney function.
- Fever: Unexplained fevers that do not result from an infection can be a sign of cancer, including Wilms tumor.
- Loss of Appetite and Weight Loss: Unintentional weight loss and a decrease in appetite can be symptoms of Wilms tumor.
- Fatigue: Persistent tiredness that doesn’t improve with rest may also be a warning sign.
The Importance of Genetic Testing
Genetic testing for the WT1 gene is crucial for families with a history of Wilms tumor. It helps identify individuals at risk, enabling early surveillance and intervention. The test is particularly recommended for children with a family history of Wilms tumor or congenital anomalies associated with WT1 mutations, such as certain urogenital malformations and syndromes.
WT1 Gene Wilms Tumor Type 1 Familial Genetic Test at DNA Labs UAE
DNA Labs UAE offers a specialized genetic test for the WT1 gene to assess the risk of Wilms tumor. The test is performed using a blood sample, and the process is straightforward and minimally invasive. It provides families with critical information about their risk of developing Wilms tumor, facilitating early detection and treatment strategies.
Test cost
The cost of the WT1 Gene Wilms Tumor Type 1 Familial Genetic Test is 4400 AED. For more information about the test and to schedule an appointment, please visit https://dnalabsuae.com/tests/wt1-gene-wilms-tumor-type-1-familial-genetic-test/.
Conclusion
Early detection of Wilms tumor through genetic testing can significantly improve the prognosis for affected children. Understanding the symptoms and having access to comprehensive genetic testing like the WT1 Gene Wilms Tumor Type 1 Familial Genetic Test offered by DNA Labs UAE can empower families to take proactive steps in managing their health. If you have a family history of Wilms tumor or related congenital anomalies, consider discussing genetic testing options with a healthcare provider.
