1) Adult polycystic kidney disease
成人多囊肾病
1.
Objective To investigate the polymorphisms of four microsatellites,D4S1534, D4S1563,D4S423 and D4S414, which are tightly linked to polycystic kidney disease 2 (PKD2) gene, and hence to provide a basis for studying the heterogeneity of adult polycystic kidney disease (APKD).
目的 分析与成人多囊肾病 PKD2基因紧密连锁的 4种微卫星 DNA D4S15 34、D4S15 6 3、D4S42 3和 D4S414在中国汉族人群中的多态性 ,为该病的异质性研究奠定基础。
2) autosomal dominant polycystic kidney disease
成人型多囊肾
1.
Genetic detection and prenatal diagnosis of autosomal dominant polycystic kidney disease in a family
一成人型多囊肾家系的遗传检测及产前诊断
3) polycystic kidney disease
多囊肾病
1.
Morphology of renal tissue in Han:SPRD,a rat model of autosomal dominant polycystic kidney disease;
常染色体显性多囊肾病Han:SPRD大鼠肾脏病理观察及其意义
2.
Gene diagnosis of autosomal dominant polycystic kidney disease type 2 using microsatellite DNA tightly linked to polycystic kidney disease gene 2;
用与PKD2紧密连锁的微卫星DNA对2型常染色体显性多囊肾病进行基因诊断
3.
N-(4-hydroxyphenyl) retinamide induced apoptosis in autosomal dominant polycystic kidney disease cyst-lining epithelial cells;
4-羟苯基维甲酸诱导常染色体显性遗传性多囊肾病囊肿衬里上皮细胞凋亡
4) adult polycystic liver disease
成人多囊肝病
1.
Value of clinical classification of adult polycystic liver disease for selection of treatments
成人多囊肝病临床分期对治疗方式选择的价值
5) polycystic kidney disease.
多囊性肾病
补充资料：婴儿型多囊肾病
婴儿型多囊肾病
infantile polycystic renal disease
是常染色体隐性遗传病，病因不明。两侧肾脏弥漫性病变。皮质似海绵状，扩张的集合管在髓质内形成大小不等的小囊肿，并呈放射状排列到皮质，间质纤维化，肾盂被胀大的肾实质挤压。本病与髓质海绵肾不同，可鉴别诊断。常并发肝纤维化，其并发症是门静脉高压症和胆道感染。在胎儿期已可确诊，并发严重羊水过少和肺发育不全。出生前受母体胎盘的透析，但出生后几天内死于严重肾功能衰竭或呼吸功能不全。如加强呼吸管理及血液透析可延长生命。预后不良。
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参考词条