Case report: Hypodipsia and hypernatremia in congenital hydrocephalus

R. Franco-Saenz, B. K. Wolffing, R. J. Rivers

Research output: Contribution to journalArticlepeer-review

Abstract

The authors describe a case of hypodipsia and severe hypernatremia most probably secondary to hydrocephalus in a 22-year-old man in the absence of abnormalities of ADH secretion or metabolism. The patient became hypernatremic only in situations when the decreased spontaneous fluid intake was insufficient to replace that lost caused by sweating or vomiting. Adequate hydration returned the sodium value to normal.

Original languageEnglish (US)
Pages (from-to)385-386
Number of pages2
JournalAmerican Journal of the Medical Sciences
Volume297
Issue number6
DOIs
StatePublished - Jan 1 1989
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)

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