2015年1月22日星期四

PKD Treatment is an incurable genetic disorder characterized


 PKD Treatment
PKD is a hereditary kidney disorder, which implicates that there are already cysts present at birth and usually in both kidneys. PKD cannot be diagnosed by a single blood test. However, in some situations where it is important to have a diagnosis (for example, if a family member wants to donate a kidney to an affected parent or sibling, and ultrasound and CT scans are normal), special blood tests on at least three family members can be done to get a diagnosis in the at-risk individual. This form of testing is called gene linkage analysis.
PKD Treatment is an incurable genetic disorder characterized by the formation of fluid-filled cysts in the kidneys of affected individuals. These cysts multiply over time.
These cysts are cavities filled with fluids that originate from normal kidney tissue. In kittens these cavities are in the majority of cases very small (1 to 2 mm). As the animal matures these cavities will become larger In one kidney there can be as many as 20 to 200 cysts present.
PKD is also a well known kidney disorder in humans which affects over 5 million people worldwide.
PKD Treatment was originally believed that the cysts eventually caused kidney failure by crowding out the healthy kidney tissue. It is now thought that the kidney damage seen in PKD is actually the result of the body's immune system. The immune system, in its attempts to rid the kidney of the cysts, instead progressively destroys the formerly healthy kidney tissue.

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