Hyperoxaluria Type 2, also known as Primary Hyperoxaluria Type II (PH2), is a rare genetic condition characterized by the overproduction of oxalate, a substance that, when in excess, can lead to kidney stones and other serious kidney problems. This condition is caused by mutations in the GRHPR gene, which plays a crucial role in the metabolic process that prevents the accumulation of oxalate. Understanding the symptoms of this condition is vital for early diagnosis and treatment, which can significantly improve the quality of life for those affected. In this regard, DNA Labs UAE offers a comprehensive GRHPR Gene Hyperoxaluria Type 2 Genetic Test aimed at identifying the mutations responsible for this condition.
Symptoms of Hyperoxaluria Type 2
The symptoms of Hyperoxaluria Type 2 can vary widely among individuals. However, there are several common signs that may indicate the presence of this condition. These symptoms are often related to the formation of calcium oxalate stones in the kidneys and can include:
- Pain in the back, side (flank pain), or abdomen
- Blood in the urine (hematuria)
- Frequent urination or the need to urinate more often than usual
- Painful urination
- Nausea and vomiting
- Urinary tract infections (UTIs)
It’s important to note that these symptoms can also be associated with other conditions, making it crucial to undergo genetic testing for a definitive diagnosis.
The Importance of Genetic Testing
Genetic testing for Hyperoxaluria Type 2 is essential for individuals who exhibit symptoms or have a family history of the condition. The GRHPR Gene Hyperoxaluria Type 2 Genetic Test offered by DNA Labs UAE is a reliable method for diagnosing this genetic disorder. This test specifically looks for mutations in the GRHPR gene that are known to cause the condition. Identifying these mutations can help in developing a personalized treatment plan that can mitigate the symptoms and prevent further complications such as kidney damage.
Test Cost and Procedure
The cost of the GRHPR Gene Hyperoxaluria Type 2 Genetic Test at DNA Labs UAE is 4400 AED. The test involves a simple and non-invasive procedure where a sample of saliva or blood is collected from the patient. This sample is then analyzed in our state-of-the-art laboratory for the presence of mutations in the GRHPR gene. The results of this test can provide valuable information for the diagnosis, treatment, and management of Hyperoxaluria Type 2.
Conclusion
Hyperoxaluria Type 2 is a condition that, if left undiagnosed and untreated, can lead to severe kidney problems. Recognizing the symptoms early and undergoing genetic testing is critical for those at risk. DNA Labs UAE’s GRHPR Gene Hyperoxaluria Type 2 Genetic Test is a valuable tool in the diagnosis and management of this rare genetic disorder. With a cost of 4400 AED, this test offers a pathway to understanding and managing the condition effectively, ultimately leading to a better quality of life for those affected.
For more information on the GRHPR Gene Hyperoxaluria Type 2 Genetic Test and to schedule an appointment, please visit our website.
