课题基金 / 基金详情

PHENOTYPE AND GENOTYPE IN CONGENITAL NEPHROGENIC DIABETES INSIPIDUS

PHENOTYPE AND GENOTYPE IN CONGENITAL NEPHROGENIC DIABETES INSIPIDUS
先天性肾性尿崩症的表型和基因型
批准号：
6275281
负责人：
GARY L. ROBERTSON
金额：
$2.26万
依托单位：
NORTHWESTERN UNIVERSITY AT CHICAGO
依托单位国家：
美国
项目类别：
财政年份：
1997
资助国家：
美国
项目状态：
已结题
起止时间：
1997-12-01 至 1998-11-30
来源：
https://reporter.nih.gov/project-details/6275281
关键词：
clinical research congenital kidney disorder genotype human subject nephrogenic diabetes insipidus phenotype vasopressins

项目摘要

项目成果

GARY L. ROBERTSON的其他基金

相关文献

中文摘要
翻译
先天性肾源性尿崩症是一种先天性疾病 由肾脏对加压素的抗利尿作用不敏感引起。 临床表现为多尿、烦渴和反复发作 脱水，通常表现在几天或几周内， 出生在某些情况下，可以改善多尿和烦渴。的 本项目的目标是确定变量之间的关系 CNDI基因型和临床表型。
英文摘要
Congenital nephrogenic diabetes insipidus (CNDI) is an inborn disorder caused by renal insensitivity to the antidiuretic effects of vasopressin. It is character-ized clinically by polyuria, polydipsia, and recurrent dehydration which usually manifest themselves within days or weeks of birth. In some cases, the polyuria and polydipsia can be ameliorated. The goal of this project is to determine the relationships between variations in genotype and clinical phenotype in CNDI.
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会议论文
Effect of the Oral Vasopressin Receptor Antagonist CI-1025
PATHOGENESIS AND PATHOPHYSIOLOGY OF FAMILIAL NEUROHYPOPHYSEAL DIABETES
EFFECTS OF VPA 985 AND PLACEBO IN TREATMENT OF HYPONATREMIA
PHENOTYPE AND GENOTYPE IN CONGENITAL NEPHROGENIC DIABETES INSIPIDUS