1·Congenital polycystic kidney disease is a congenital disease.
先天性多囊肾是一种先天性的疾病。
2·Objective Evaluation of CT in the diagnosis of polycystic kidney.
目的探讨多囊肾的CT诊断价值。
3·68% including 16 cases of autosomal recessive polycystic kidney disease ARPKD 34.
包括常染色体隐性遗传多囊肾病ARPKD 16例34。
4·Mechanism of Doppler blood flow ultrasonic spectrum of the polycystic kidney was discussed.
本文还讨论了多囊肾血流多普勒频谱变化的机制。
5·To study the kidney transplantation in the patients with polycystic kidney associated with uremia.
目的研究多囊肾尿毒症患者肾移植术前是否需要切除多囊肾。
6·Methods 12 cases of polycystic kidney receiving transplantation with original renal were retrospectively analyzed.
方法回顾性分析12例多囊肾患者保留原位肾直接进行肾移植术的效果。
7·Objectives To discuss clinical characteristics and early diagnosis of polycystic kidney disease (PKD) in children.
目的探讨小儿多囊肾的临床特点及诊断情况。
8·The oligohydramnios resulted from markedly diminished fetal urine output as a consequence of polycystic kidney disease.
羊水过少是由多囊肾引起胎儿排尿显著减少造成的。
9·Autosomal recessive polycystic kidney disease also known as infantile polycystic kidney disease, polycystic kidney in the rare type.
常染色体隐性遗传性多囊肾又称婴儿型多囊肾，为多囊肾中少见类型。
10·Infantile polycystic kidney disease and autosomal recessive polycystic kidney disease, is the two kind of polycystic kidney in a kind.
婴儿型多囊肾又叫常染色体隐性遗传型多囊肾，是两种多囊肾中的一种。