Polycystic kidney disease diagnosis

Polycystic kidney disease might lead to various symptoms, often signs of other kidney-related issues, including kidney cancer, pyelonephritis, and glomerulonephritis. So, a proper diagnosis of PKD remains necessary in creating the best management and treatment strategy. The diagnosis-verifying process begins with the patient’s conversation with medical practitioners, evaluation and detection of the disease’s symptoms, and general health check-ups. Next, the nephrologist came up with a list of necessary lab tests and other diagnostic procedures. Complete blood count and inflammation blood tests help exclude many chronic and some acute diseases and conditions from the list of potential causes. Tests that help evaluate the function of kidneys and measure electrolytes help to understand more about the current state of these organs and come up with the best recommendations. Various medical imaging tests help to verify the diagnosis of polycystic kidney disease via indirect images of the organ. Ultrasound, MRI, and CT scans are among the most valuable and widely used methods. Also, in some cases, doctors might order genetic testing for polycystic kidney disease, which might help prevent this disease in your kids and verify your diagnosis.