1) infantile polycystic kidner disease (IPCKD)
婴儿多囊肾病
2) Infantile polycystic kidney disease
婴儿型多囊肾
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) polycystic kidney disease.
多囊性肾病
5) infantile encephalopathy
婴儿脑病
6) infantile myopathy
婴儿肌病
补充资料：婴儿型多囊肾
婴儿型多囊肾
infantile polycystic ki?〖JP〗dney
是常染色体隐性遗传，均伴肝脏病变，虽然主要见于年幼儿，但也可发生于年龄较大的儿童及成人。根据症状出现时年龄，婴儿型多囊肾可分为四个临床类型：①围生期型；②新生儿型；③婴儿型；④童年型。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条