...多囊肾病(polycystic kidney disease，PKD)是一种常见的遗传性肾脏病，主要表现为双侧肾脏出现多个大小不一的囊肿，囊肿进行性增大，最终破坏肾脏结构和功能，导致终末...
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常染色体显性遗传性多囊肾病(autosomal dominant polycystic kidney disease,ADPKD)是人类最常见的致死性单基因遗传病之一，列遗传性肾病的第一位。
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常染色体显性多囊肾病 ADPKD ; Autosomal dominant polycystic kidney disease
性多囊肾病 ADPKD ; Autosomal dominant polycystic kidney disease ; autosomal recessive polycystic kidney disease
常染色体隐性多囊肾病 ARPKD ; autosomal recessive polycystic kidney disease
多囊肾病基因 polycystic kidney disease gene ; PKD
的多囊肾病 polycystic kidney disease ; PKD
多囊肾病致病基因 polycystic kidney disease gene ; PKD
多囊肾病1型致病基因 polycystic kidney disease gene ; PKD
先天性多囊肾病 polycystic kidney disease ; PKD
型多囊肾病 autosomaldominantpolycystickidneydisease ; ADPKD
包括常染色体隐性遗传多囊肾病ARPKD 16例34。
68% including 16 cases of autosomal recessive polycystic kidney disease ARPKD 34.
目的：研究多囊肾病囊肿衬里上皮的增生与凋亡及相关蛋白表达。
Objective: cyst lining epithelial cell proliferation and apoptosis are implicated in the pathogenesis of cyst formation in autosomal dominant polycystic kidney disease (ADPKD).
CT显示肝实质多个较大包囊，与显性遗传性多囊肾病人的肝脏病变相一致。
This transverse CT scan of the liver demonstrates multiple large cysts in the parenchyma, consistent with polycystic change in the liver of a patient with dominant polycystic kidney disease.
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