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Polycystic Kidney Disease

Read|Author:|Published:2016-04-13

Polycystic kidney includes two types,one is autosome recessive genotype PKD(infantilism),with attack in infancy,rarely seen clinically.The other is autosome dominant genotype PKD(adult),commonly with attact in youth and middle age,but it can be any age.Polycystic kidney is a common genetic neohropathy,main clinical manifestation is bilateral kidney emerging with various sized cysts,which keeps progressively increasing,finally detroy kidney structure and function and leads to end-stage renal failure.

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