Polycystic kidney disease
a genetic disorder characterized by the growth of numerous fluid-filled cysts in the kidneys
Polycystic kidney disease (PKD) is a genetic disorder that causes numerous cysts to grow in the kidneys. These cysts can gradually replace healthy kidney tissue, causing the kidneys to become enlarged and lose function over time. There are two forms of PKD: autosomal dominant PKD, which is inherited from one parent, and autosomal recessive PKD, which is inherited from both parents.
Symptoms of PKD may include:
– Pain in the back or sides
– Headaches
– High blood pressure
– Frequent urinary tract infections
– Blood in the urine
– Kidney stones
– Enlarged abdomen
– Fatigue
– Loss of appetite
Treatment for PKD typically involves managing symptoms and preventing complications. This may include:
– Pain management with medications
– High blood pressure medication to protect the kidneys
– Antibiotics to treat infections
– Surgery to remove cysts or to treat complications such as kidney stones
In some cases, patients with PKD may need to undergo dialysis or kidney transplantation if their kidneys fail. It is important for individuals with PKD to receive regular monitoring from a healthcare professional and to follow a healthy lifestyle, including regular exercise and a balanced diet.
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