Polycystic kidney disease (PKD) is one of the most common life threatening genetic disorder

PKD Treatment

As the cysts of PKD increase in number and become enlarged, they destroy kidney function, and renal failure develops. Autosomal dominant polycystic kidney disease (ADPKD) is the most common form, while autosomal recessive polycystic kidney disease (ARPKD) is rare and is one of the leading causes of childhood end-stage renal disease.In addition to the kidneys, PKD can affect other organs, including, most commonly, the liver, where cysts can also develop.

Polycystic kidney disease (PKD) is one of the most common life threatening genetic disorder and affects many people worldwide. Polycystic kidney disease Treatment is a gradually progressing condition that may eventually lead to death unless a kidney transplant is received. Natural approaches to PKD can help preserve kidney function and delay the need for more invasive treatment.
PKD Treatment is a genetic disorder characterized by the growth of numerous fluid – filled cysts on the kidneys which dramatically enlarge kidneys which severely compromises kidneys function. PKD is prevalent, inherited condition for which there is currently no effective specific clinical therapy. The cysts are derived from renal tubular epithelial cells which gradually compress the parenchyma and compromise renal function.

Polycystic kidney disease Treatment (PKD) is a genetic disease in which multiple cysts grow on the kidneys.(1) As the cysts expand in size, they impinge on the normal structure of the kidney, and there is a decrease in kidney function.(1, 2) In people with severe forms of the disease, this leads to a condition called end-stage renal disease (ESRD), which refers to such low kidney filtering function that dialysis and kidney transplantation become necessary.


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