目的探讨多囊肾的CT诊断价值。
Objective Evaluation of CT in the diagnosis of polycystic kidney.
先天性多囊肾是一种先天性的疾病。
Congenital polycystic kidney disease is a congenital disease.
目的探讨小儿多囊肾的临床特点及诊断情况。
Objectives To discuss clinical characteristics and early diagnosis of polycystic kidney disease (PKD) in children.
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.
羊水过少是由多囊肾引起胎儿排尿显著减少造成的。
The oligohydramnios resulted from markedly diminished fetal urine output as a consequence of polycystic kidney disease.
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).
包括常染色体隐性遗传多囊肾病ARPKD16例34。
68% including 16 cases of autosomal recessive polycystic kidney disease ARPKD 34.
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。
To study the kidney transplantation in the patients with polycystic kidney associated with uremia.
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.
目的探讨超声引导下囊肿内注射消痔灵治疗多囊肝多囊肾的价值。
Objective To study the clinical value of the Xiaozhiling (XZL) injected under ultrasonography guidance (UGG) in the treatment of polycystic liver and kidney.
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).
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.
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。
Methods 12 cases of polycystic kidney receiving transplantation with original renal were retrospectively analyzed.
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）。
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).
该方法为常染色体显性多囊肾疾病行胚胎植入前遗传学诊断提供了依据。
It provide an evidence of using this technique for the PGD for ADPKD.
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。
Infantile polycystic kidney disease and autosomal recessive polycystic kidney disease, is the two kind of polycystic kidney in a kind.
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.
方法回顾性分析23例多囊肾患者的CT表现，并总结其CT表现与肾功能的关系。
Methods CT findings of polycystic kidney in 23 cases were retrospectively analysed , the relationship between CT findings and renal function was evaluated.
多囊性发育不良肾也称为多囊肾发育不良，切开发现，大小不等的囊肿取代了肾实质。
A multicystic dysplastic kidney (also known as cystic renal dysplasia) has been sectioned to reveal the variably sized cysts that replace the renal parenchyma.
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。
Autosomal recessive polycystic kidney disease etiology is mainly because the parents with congenital genetic, so in infancy began to sicken.
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。
Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.
目的研究常染色体显性遗传型多囊肾病肾组织中细胞外基质和多囊蛋白-1的表达及与囊肿发生的关系。
Objective To study the expression of extracellular matrix and polycystin-1 in ADPKD and their relation to cyst formation.
结论CT能准确诊断多囊肾，并可依据其CT征象及临床资料综合评价其肾功能，为临床治疗提供更大帮助。
Conclusion ct is highly accurate to diagnose the polycystic kidney and assess the renal function based on the ct findings and clinical informations.
显性遗传性多囊肾患者的肾脏切面显示：实质为大囊肿取代，和正常的移植肾相比，有囊肿的肾脏多么大啊！
The cut surfaces of these kidneys in a patient with DPKD reveal that the parenchyma is replaced by large cysts. Note how large these kidneys are in relation to the normal sized transplanted kidney.
他们从黄色豌豆中提取豌豆蛋白水解产物，并且每日小剂量用这些产物喂养患有一种名为多囊肾的严重肾病模型的大鼠。
They extracted pea protein hydrolysate from the yellow garden pea and fed a small dose each day to laboratory rats bred to have a severe type of kidney disease called polycystic kidney disease.
他们从黄色豌豆中提取豌豆蛋白水解产物，并且每日小剂量用这些产物喂养患有一种名为多囊肾的严重肾病模型的大鼠。
They extracted pea protein hydrolysate from the yellow garden pea and fed a small dose each day to laboratory rats bred to have a severe type of kidney disease called polycystic kidney disease.
应用推荐