多囊肾又名Potter(Ⅰ)综合征、Perlmann综合征、先天性肾囊肿瘤病、囊胞肾、双侧肾发育不全综合征、肾脏良性多房性囊瘤、多囊病。我国1941年朱宪彝首先报道，本病临床并不少见。多囊肾有两种类型，常染色体隐性遗传型（婴儿型）多囊肾，发病于婴儿期，临床较罕见；常染色体显性遗传型（成年型）多囊肾，常于青中年时期被发现，也可在任何年龄发病。
多囊肾(polycystic kidney)是遗传性疾病，其病变特征是双肾本质有平常的囊肿变成，系胚胎发育过程中肾小管与集结管间连绵不良，我不知道null。
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常染色体显性多囊肾 autosomal dominant polycystic kidney ; ADPKD ; autosomal dominant polycystic kidney disease
多囊肾病 PKD ; polycystic kidney disease ; MCDK ; autosomal dominant polycystic kidney disease
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
性多囊肾 ARPKD ; autosomal recessive polycystic kidney disease ; Autosomal dominant polycystic kidney disease ; ADPKD
多囊肾蛋白2抗体 Anti-Polycystin ; Polycystin
多囊肾疾病 Polycystic Kidney Diseases ; autosomal dominant polycystic kidney disease ; PKD ; autosomal recessive polycystic kidney disease
常染色体多囊肾疾病 ADPKD
多囊肾蛋白1抗体 Anti-Polycystin
Met hods Depression and pedicled omental packing was carried out for 16 patients with polycystic kidney.
方法 采用去顶减压加带蒂大网膜包裹术治疗成人多囊肾患者 16例。
参考来源 - 去顶减压加带蒂大网膜包裹治疗成人多囊肾·2,447,543篇论文数据，部分数据来源于NoteExpress
目的探讨多囊肾的CT诊断价值。
Objective Evaluation of CT in the diagnosis of polycystic kidney.
左肾为多囊肾和发育不良，乙状结肠极度扩张。
The left kidney was multicystic dysplastic. The sigmoid colon was extremely distended.
本文还讨论了多囊肾血流多普勒频谱变化的机制。
Mechanism of Doppler blood flow ultrasonic spectrum of the polycystic kidney was discussed.
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