1) Infantile polycystic kidney disease
婴儿型多囊肾
2) infantile polycystic kidner disease (IPCKD)
婴儿多囊肾病
3) 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
5) baby
[英]['beɪbi] [美]['bebɪ]
小型物婴儿
6) Polycystic kidney
多囊肾
1.
Clinic study on 169 cases of polycystic kidney;
169例多囊肾临床研究
2.
Expression of matrix metalloproteinases-1/tissue inhibitor of metalloproteinase-1 in kidney of patients with autosomal dominant polycystic kidney disease;
基质金属蛋白酶1/组织金属蛋白酶抑制因子1在常染色体显性遗传性多囊肾组织中的表达
3.
Sirolimus slows down disease progression in rats with autosomal dominant polycystic kidney disease and renal dysfunction;
西罗莫司延缓肾功能不全常染色体显性遗传性多囊肾病大鼠的疾病进程
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。
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