全部

1·Congenital polycystic kidney disease is a congenital disease.

先天性多囊肾是一种先天性的疾病。

2·68% 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。

3·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。

4·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。

5·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。

6·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。

7·The histologic appearance in this case, coupled with the gross appearance. , was consistent with recessive polycystic kidney disease (RPKD).

在本例，肉眼和组织学表现均符合隐性遗传性多囊肾。

8·Autosomal recessive polycystic kidney disease etiology is mainly because the parents with congenital genetic, so in infancy began to sicken.

常染色体隐性遗传型多囊肾的病因主要是因为父母先天性的遗传，所以在婴儿期就开始发病。

9·The ratio of urinary tract infections for patients within the polycystic kidney disease group was remarkably higher than for those within control group (P< 0.05).

多囊肾组患者术后的泌尿系感染的发生率高于对照组（P<0.05）。

10·Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.

目的：研究华东地区汉族人常染色体显性遗传性多囊肾病(adpkd)基因型与临床表现型的关系。