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Polycystic Kidney Disease: Overview and Treatment

2017-05-23 09:07

Polycystic Kidney Disease: Overview and TreatmentPolycystic Kidney Disease (PKD) is an inherited disorder that clusters of cysts develop primarily within your kidneys. The cysts are noncancerous round sacs with fluids. Cysts, all contains fluids, various in size, can grow large.

PKD is a genetic disorder that cause multiple cysts grow in kidneys. When it enlarged, it can cause side-effects and reduce the kidney function. What’s more, it can also lead to some symptoms: high blood pressure, back or side pain, headache, increase in the size of your abdomen, blood in urine, frequent urination, kidney stone, kidney failure, urinary tract or kidney infection and etc.

Genetic disorder is the causes and it also means the disease can runs in families. Rarely, a genetic mutation can be the cause of polycystic kidney disease. It can be divided into two type: autosomal dominant polycystic kidney disease (ADPKD)and autosomal recessive polycystic kidney disease(ARPKD).

In some cases, a person with ADPKD has no known family history of the disease. However, it's possible that someone in the affected person's family actually did have the disease, but didn't show signs or symptoms before dying of other causes.

The complications of PKD is high blood pressure, lose of kidney function, pregnancy complications, growth of cysts in the liver, development of an anerysm in the brain and heart valve abnormalities.

Treatment are various, such as dialysis and transplant. Beyond that, we can use natural treatment to improve the kidney condition and release the complications. Toxin-Removing Therapy can help shrink the kidney cysts as well as kidney size. It can also help slow down the development of the kidney disease and provide a better environment for patients want to do transplant.

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Tag: PKD PKD Treatment

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Polycystic Kidney Disease

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