Polycystic kidney disease (PKD) is a genetic disorder characterized by the development of fluid-filled cysts in the kidneys. Unlike harmless simple kidney cysts, PKD is a serious form of chronic kidney disease that can have significant health complications. The cysts in PKD can grow in size, causing the kidneys to enlarge and disrupt their ability to effectively filter waste from the blood, resulting in a progressive decline in kidney function.
Polycystic kidney disease comes in two types:
Consequently, most individuals affected by PKD will eventually require dialysis or a kidney transplant to sustain their kidney function.
Symptoms of polycystic kidney disease include:
It is important to be aware that polycystic kidney disease can often go undetected for extended periods. If any signs or symptoms associated with this condition arise, seeking medical attention is recommended. Individuals with a first-degree relative such as a parent, sibling, or child who has polycystic kidney disease should consult a healthcare professional to discuss the possibility of screening for this disorder.
Polycystic kidney disease is brought on by abnormal genes, which implies that it typically runs in families. Sometimes a gene will change spontaneously, leaving neither parent with a copy of the modified gene. But occasionally, genes will randomly change or mutate. PKD can affect people of various ages, races, and ethnicities. Both men and women can get it.
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