Polycystic Kidney Disease

Polycystic Kidney Diseases

What is PKD?

Polycystic Kidney Disease (PKD) is a genetic disorder where numerous fluid-filled cysts grow in the kidneys, impairing their ability to filter blood. PKD is the fourth leading cause of chronic kidney disease and can also cause cysts in other organs such as the liver.

Incidence PKD affects about 1 in 1,000 people worldwide and is equally common in males and females. Approximately 5% of chronic kidney disease patients requiring dialysis or transplantation have PKD.

Effects on Kidneys In autosomal dominant PKD, cysts of varying sizes develop in both kidneys, causing kidney enlargement and potentially leading to chronic kidney failure. This damage often results in hypertension, protein loss in urine, and reduced kidney function.

Symptoms

Progression Not all patients will develop kidney failure. About 50% will experience kidney failure by age 60, and 60% by age 70. Risk factors include larger cyst size, early diagnosis, hypertension, proteinuria, and certain genetic mutations.

Diagnosis
Prevention
Treatment

PKD is manageable with proper care and monitoring to delay progression and address symptoms effectively.