背景与目的：常染色体隐性遗传性多囊肾(Autosomal recessive polycystic kidney disease，ARPKD)是婴幼儿和儿童的一种以肾脏囊性改变为特征常见遗传性疾病，据 孕36周,怀疑多囊肾,孩子该生还是?
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背景与目的：常染色体隐性遗传性多囊肾(Autosomal recessive polycystic kidney disease，ARPKD)是婴幼儿和儿童的一种以肾脏囊性改变为特征常见遗传性疾病，据 孕36周,怀疑多囊肾,孩子该生还是?
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...蛋白在ADPKD肾脏中的表达及意义 韩乐天 【摘要】： 目的常染色体显性多囊肾(autosomal dominant polycystic kidney disease, ADPKD)是由于PKD基因异常导致的单基因遗传病,是导致终末期肾病的重要疾病之一,发病率约为1：400～1：1..
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【摘要】：正常染色体显性遗传性多囊肾(autosomal domi-nant polycystic kidney disease,ADPKD)是一种较常见的遗传疾病,该病发病率为1/1000～1/400,为我国终末期肾..
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常染色体显性多囊肾 autosomal dominant polycystic kidney ; ADPKD ; 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
常染色体隐性多囊肾病 ARPKD ; autosomal recessive polycystic kidney disease
显性遗传性多囊肾 DPKD
先天性多囊肾 congenital polycystic kidney
天性多囊肾 polycystic kidney
先天性多囊肾病 polycystic kidney disease ; PKD
遗传性多囊肾病 autosomal recessive polycystic kidney disease ; ARPKD
在本例，肉眼和组织学表现均符合隐性遗传性多囊肾。
The histologic appearance in this case, coupled with the gross appearance. , was consistent with recessive polycystic kidney disease (RPKD).
隐性遗传性多囊肾镜下见囊肿布满了实质，很难找到肾小球。
Here is the microscopic appearance of recessive polycystic kidney disease (RPKD). Note that the cysts fill most of the parenchyma, and it is hard to find glomeruli.
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。
Autosomal recessive polycystic kidney disease also known as infantile polycystic kidney disease, polycystic kidney in the rare type.
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