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


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