【摘要】：正常染色體顯性多囊腎(autosomal dominant polycystic kidney disease,ADPKD)是一種遺傳性單基因疾病,由多囊腎基因1(polycyseic kidneydisease gene,PKD1)、PKD2基因突變所致,稱Ⅰ型ADPKD,Ⅱ型ADPKD。其發(fā)病率很高,1/1 000~1/400,為常見腎臟遺傳病[1-2]。一般成年發(fā)病,又稱成人型多
[Abstract]:Normal chromosomal dominant polycystic kidney disease (ADPKD) is an inherited single gene disease caused by mutation of PKD2 gene of polycystic kidney gene (1 (polycyseic kidneydisease gene PKD1). It is called type I ADPKD, type 鈪，

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