Polycystic Kidney Disease
What is polycystic kidney disease (PKD)?
Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts filled with fluid in the kidneys. PKD cysts can reduce kidney function. This leads to kidney failure. People with PKD can also have cysts in the liver and problems in other organs, such as the heart and blood vessels in the brain.
PKD is the fourth leading cause of kidney failure and affects approximately 600,000 people in the U.S., according to the National Kidney Foundation (NKF). The NKF states that about 50% of people with autosomal dominant form of PKD progress to kidney failure by age 60 and about 60% will have kidney failure by age 70.
What are the different types of PKD?
There are 2 primary inherited forms of PKD and one noninherited form:
This is the most common inherited form of polycystic kidney disease, accounting for about 90% of all PKD cases. Autosomal dominant means that if one parent has the disease, there is a 50% chance that the disease will pass to a child. Both males and females are equally affected. These cases are usually diagnosed in adulthood.
Autosomal dominant PKD is often called the adult polycystic kidney disease. Symptoms usually develop between age 30 and 40. They can begin as early as childhood and may include the following:
Autosomal dominant PKD may happen with other conditions including:
The symptoms of PKD sometimes look like other conditions or medical problems. Always see your healthcare provider for a diagnosis.
Diagnosis of autosomal dominant PKD may include the use of imaging techniques to detect cysts on the kidney and other organs and a review of the family history of autosomal dominant PKD. There are 3 different dominant genes that have been identified and further subdivide autosomal dominant PKD into PKD1, PKD2, and PKD3.
A healthcare provider will establish a treatment plan for autosomal dominant PKD only after careful consideration of the child's symptoms and medical history. Treatment may include:
Autosomal recessive PKD is a rare, inherited form of polycystic kidney disease thought to be caused by a particular genetic flaw. This is different from the genetic flaw that causes autosomal dominant PKD. Parents who do not have the disease can have a child with the disease if both parents carry the abnormal gene and both pass the gene to their child. Carrier parents have a 25% chance with each pregnancy to have a child with this type of PKD. Males and females are equally affected. Autosomal recessive PKD is sometimes detected prenatally (before birth) using a fetal ultrasound.
Children born with autosomal recessive PKD may develop kidney failure within a few years and often experience the following:
The disease also usually affects the liver, spleen, and pancreas. This results in low blood cell counts, varicose veins, and hemorrhoids.
The symptoms of autosomal recessive PKD may resemble other conditions or medical problems. Always talk with your child's healthcare provider for a diagnosis.
Diagnosis often includes ultrasound imaging of the fetus or newborn to reveal cysts in the kidneys. An ultrasound exam of kidneys of relatives may also be helpful.
Your child's healthcare provider will establish a treatment protocol for autosomal recessive PKD only after careful consideration of the child's symptoms and medical profile. Treatment may include:
Acquired cystic kidney disease (ACKD) may develop in association with long-term kidney problems. This is especially so in people who have kidney failure and who have been on dialysis for a long time. Therefore, it tends to happen later in life and is an acquired, not inherited, form of PKD. Often there are cysts in other organs, such as the liver and the pancreas.