Our research is focus on congenital nephrogenic diabetes insipidus. 我们所研究的是属于先天遗传性尿崩症。
Identification of mutations in the arginine vasopressin receptor 2 gene in congenital nephrogenic diabetes insipidus patients 先天性肾性尿崩症患者精氨酸加压素受体2基因突变的检测分析
Some suggestions on the time of water deprivation test, the improvement of hypertonic saline solution test and diagnosis of partial nephrogenic diabetes insipidus were made in this paper. 本文还对禁水时间、高渗盐水试验的改进以及部分性肾性尿崩症的诊断提出了看法。
Nephrogenic diabetes insipidus ( NDI ) is a rare disease characterized by the inability of the kidney to concentrate urine. 肾性尿崩症(NDI)就是一种由于肾小管重吸收水的功能障碍而引发的较为严重的泌尿系统疾病。