Impaired urinary water excretion in a three-generation family

被引：0

作者：

Y. Tanaka

Kiyoko Sugita

Takako Saito

Koji Muroya

San-e Ishikawa

Midori Awazu

Tsutomu Ogata

机构：

[1] Department of Pediatrics,

[2] Ichikawa General Hospital,undefined

[3] Tokyo Dental College,undefined

[4] 5-11-13 Sugano Ichikawa-shi,undefined

[5] Chiba 272-8513,undefined

[6] Japan. ytanaka7@aol.com,undefined

[7] Department of Endocrinology and Metabolism,undefined

[8] Jichi Medical School,undefined

[9] Tochigi,undefined

[10] Japan,undefined

[11] Department of Pediatrics,undefined

[12] Keio University School of Medicine,undefined

[13] Tokyo,undefined

[14] Japan,undefined

来源：

Pediatric Nephrology | 2001年 / 16卷

关键词：

Keywords Active water resorption; Dominant disorder; AVP; AQP2; SIADH;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

We report on a three-generation family (daughter, mother, and maternal grandmother) with a syndrome of inappropriate secretion of antidiuretic hormone (SIADH)-like condition in the absence of inappropriate ADH secretion. In the three females, a water load test showed severely reduced urinary water excretion, with the ratio of urine volume to the loaded water being 10–33% (normal value: 70.2±7.8%). Urinary AQP2 excretion was normal, as was the DNA sequence of AVPR2 and AQP2. The results suggest the presence of a new dominantly inherited disorder for tubular water resorption.

引用

页码：820 / 822

页数：2

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