Polycystic Disease Of The Kidneys

Polycystic Kidney Disease (PKD) is a genetic disorder characterized by the growth of multiple cysts in the kidneys, which lead to kidney failure and other urinary problems. This is one of the most common congenital malformations of the genitourinary system, which can occur in any type of kidney and occur with varying degrees of disease severity.

Polycystic kidney disease is a genetically inherited disease, meaning it is transmitted by passing genes from one generation to the next through an autosomal dominant pattern. The only risk factor that increases the likelihood of developing the disease is having a parent with the disease.

Symptoms of polycystic kidney disease can appear at different periods of a person's life. In general, symptoms may include hematuria (blood in the urine), urinary tract infections, and problems related to hypertension. The disease usually manifests itself between the ages of 20 and 40. However, the vast majority of people with this disease can live long and healthy lives. However, having the disease may increase your risk of developing kidney failure or other kidney problems.

There is no cure for polycystic kidney disease, but there are treatments designed to relieve symptoms of the disease and keep a person with the disease healthy. Treatment may include antibiotics, diet, lifestyle changes, and surgery when possible.