Polycystic Kidney Disease (cont.)
Polycystic Kidney Disease At A Glance
- The two forms of polycystic kidney disease (PKD) are
- autosomal dominant PKD, a form that usually causes symptoms in adulthood
- autosomal recessive PKD, a rare form that usually causes symptoms in infancy and early childhood
- The symptoms and signs of PKD include
- pain in the back and lower sides
- headaches
- urinary tract infections
- blood in the urine
- cysts in the kidneys and other organs
- Diagnosis of PKD is obtained by
- ultrasound imaging of kidney cysts
- ultrasound imaging of cysts in other organs
- family medical history, including genetic testing
- PKD has no cure. Treatments include
- medicine to control high blood pressure
- medicine and surgery to reduce pain
- antibiotics to resolve infections
- dialysis to replace functions of failed kidneys
kidney transplantation
SOURCE: National Institutes of Health
References: Grantham JJ, Nair V, Winklhoffer F. Cystic diseases of the kidney. In: Brenner BM, ed. Brenner & Rector's The Kidney. Vol. 2. 6th ed. Philadelphia: WB Saunders Company; 2000: 1699-1730.
Last Editorial Review: 5/7/2008