Polycystic kidney disease is also called PKD.
Autosomal dominant Polycystic kidney disease is inherited. This kind of Polycystic kidney disease accounts for about 90 percent of all Polycystic kidney disease cases. The term “Autosomal dominant” means that if one parent has the disease, there is a 50 percent chance that the disease will pass to a child.
Autosomal recessive Polycystic kidney disease is also inherited. This type of Polycystic kidney disease is rare. Parents that do not have the disease can have a child with the disease. How can this happen? If both parents carry the recessive gene and pass the recessive gene to their child, the child will have two recessive genes and develop the disease.
Polycystic Kidney Disease has many symptoms. Individuals with Polycystic kidney disease may not experience all of the symptoms.
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Most people with Polycystic kidney disease can lead a normal life. In most people, Polycystic kidney disease is mild and causes only minor problems. In severe cases, Polycystic kidney disease can cause kidney failure. About 60% of patients develop high blood pressure. High blood pressure can be treated with medication. About 50% of patients with Polycystic kidney disease have kidney failure by age 60. Dialysis and kidney transplants are both effective treatments for kidney failure. Polycystic kidney disease is generally worse in men, African Americans and patients with sickle cell disease.
Maybe. People with Polycystic kidney disease may also have cysts in their liver. However, the cysts in the liver seldom cause problems. Heart valve problems sometimes occur. Other organs that may be affected include the brain, intestines, pancreas, ovaries and spleen.
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