Investigation of polyuria and polydipsia
Abstract
The causes of polyuria and polydipsia in childhood can be subdivided into three groups; cranial diabetes insipidus, nephrogenic diabetes insipidus and primary polydipsia. A detailed history and examination alone may suggest an underlying explanation for the child's symptoms but a range of baseline and then more extensive investigations are usually required before a diagnosis can be reached. These investigations are not without risk to the patient and it is of paramount importance that they are conducted safely and in a logical manner. In a small number of cases referral to a specialist centre will be required.
Keywords: diabetes insipidus, polyuria, polydipsia, investigation
No full text is available. To read the body of this article, please view the PDF online.
To access this article, please choose from the options below
- f1 Correspondence to: SG. E-mail: susan.glass@ncl.ac.uk
PII: S0957-5839(01)90208-8
doi:10.1054/cupe.2001.0208
© 2001 Harcourt Publishers Ltd. All rights reserved.

