肾性尿崩症致严重肾积水1例

发布时间：2018-03-26 16:54

  本文选题：肾性尿崩　切入点：肾积水　出处：《中国实用内科杂志》2017年03期

【摘要】：正肾性尿崩症是肾脏对抗利尿激素(antidiuretic hormone,ADH)反应缺陷所致,病因可分为遗传性和继发性两种,继发性肾性尿崩症多因各种疾病或药物(如庆大霉素、链霉素等)导致的肾小管损害和代谢紊乱所致;而遗传性肾性尿崩症主要表现为AVPR2受体基因的突变,且多伴有一定的家族史,发病年龄较小,以男性居多。现将我院收治的1例患者报道如下。1病历资料患者男,19岁,于2015-10-09因"口干多饮多尿
[Abstract]:Positive renal diabetes insipidus is caused by the deficiency of renal response to the diuretic hormone homeostasis, which can be divided into two types: hereditary and secondary. Secondary renal diabetes insipidus is caused by various diseases or drugs such as gentamicin. The hereditary renal diabetes insipidus was mainly characterized by mutation of AVPR2 receptor gene, accompanied by a certain family history, and the onset of renal diabetes insipidus at a younger age, and the renal tubule damage and metabolic disorder were caused by streptomycin (streptomycin, et al). Most of them are men. One patient in our hospital is reported as follows. 1 the patient was 19 years old because of "dry mouth and polyuria" in 2015-10-09.
【作者单位】： 南京中医药大学;江苏省中医院;
【分类号】：R692

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