2015年2月7日星期六

Category Division of Polycystic Kidney Disease (PKD)

Among Chronic Kidney Diseases, Polycystic Kidney Disease (PKD) belongs to a very hard and hereditary disease. According to the Genetics, PKD can be categorized as autosomal dominant and recessive PKD. And autosomal dominant PKD is more universal amid patients.
Patients of this kind usually present features as family disease, in other words, man and woman can suffer from it and the risk to get disease for them is equal. This disease could happen to generations successively.
ADPKD is also known as adult PKD, which is very common. With the gradual penetration to this disease, prognosis for this disease gets improved apparently. ARPKD is an initial for autosomal recessive Polycystic Kidney Disease, which is also known as fetus PKD. Fetus’ parents rarely have disease history. This occupies only a minority parts among patients, most of them will die soon after their birth, only very few of them can survive till to childhood even adulthood.

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