Polycystic Kidney Disease
What is polycystic kidney disease (PKD)?
Polycystic kidney disease (PKD) is a rare genetic disorder. It causes numerous cysts filled with fluid to grow in the kidneys. PKD cysts can reduce kidney function, leading to kidney failure. PKD is the 4th leading cause of 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.
What are the different types of PKD?
There are 2 primary inherited forms of PKD and 1 noninherited form:
Autosomal dominant PKD (inherited)
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, and that both males and females are equally affected. These cases usually are diagnosed in adulthood.
Autosomal dominant PKD is often called the adult polycystic kidney disease. Symptoms usually develop between age 30 and 40. But they can begin as early as childhood. They may include the following:
Autosomal dominant PKD may occur with other conditions including:
The symptoms of autosomal dominant PKD may look like other conditions or medical problems. Always check with your child’s healthcare provider for a diagnosis.
Diagnosis of autosomal dominant PKD may include:
Your child’s healthcare provider will figure out a treatment plan for autosomal dominant PKD after careful consideration of the child’s symptoms and medical history. Treatment may include:
Autosomal recessive PKD (inherited)
Autosomal recessive PKD is a rare, inherited form of polycystic kidney disease. It is thought to be caused by a particular genetic flaw that is different from the genetic flaw that causes autosomal dominant PKD. Parents who don’t 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 before birth using a fetal ultrasound.
Symptoms of autosomal recessive PKD can begin before birth. In most cases, the earlier symptoms start, the more severe the outcome. There are 4 different types of autosomal recessive PKD, depending on the child’s age when symptoms become evident:
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 look like other conditions or medical problems. Always check 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. Ultrasound exam of kidneys of relatives may also be helpful.
Your child’s healthcare provider will figure out a treatment plan for autosomal recessive PKD after careful consideration of the child’s symptoms and medical profile. Treatment may include:
Acquired cystic kidney disease, or ACKD (noninherited)
Acquired cystic kidney disease may develop in association with long-term kidney problems, especially in people who have kidney failure and who have been on dialysis for a long time. Therefore, it tends to occur 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.
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