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Updated: Aug 7, 2026

Spinal Cord Electrophysiology
Published on: January 18, 2010
Hyponatremia secondary to reset osmostat in a child with a central nervous system midline defect and a chromosomal
1Department of Pediatrics, University of Illinois, College of Medicine, Peoria, USA.
Abstract:
A newborn with a CNS midline defect and persistent hyponatremia was diagnosed with a "reset" osmostat using a 3% hypertonic saline test. The diagnosis was established by measuring urinary arginine vasopressin (UAVP) and plasma osmolality (P(Osmoil)). In this infant a chromosome abnormality with the karyotype 46, X, -X, +der(X) t(X;13) (p22.1;q22) was associated with the midline defect and a reset osmostat.
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