Hyponatremia secondary to reset osmostat in a child with a central nervous system midline defect and a chromosomal abnormality

Journal of Pediatric Endocrinology and Metabolism

Volumn 13, Issue 9, 2000, Pages 1637-1641

  Gupta, P ^a   Mick, G ^a   Fong, C T ^a   Jospe, N ^a   McCormick, K ^a  

^a CHILDREN S HOSPITAL   (United States)

Author keywords

Arginine vasopressin; Hyponatremia; Midline defect; Plasma osmolarity; Reset osmostat; Syndrome of inappropriate anti diuretic hormone (SIADH); Urine osmolarity

Indexed keywords

ARGININE; VASOPRESSIN;

ARTICLE; CASE REPORT; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME DAMAGE; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; HUMAN; HYPONATREMIA; INAPPROPRIATE VASOPRESSIN SECRETION; KARYOTYPE; NEWBORN; PLASMA OSMOLALITY; URINE LEVEL;

EID: 0034518210     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2000.13.9.1637     Document Type: Article

References (11)

1. Vasopressin and its neurophysin
2. Reset osmostat in a healthy patient
3. Chronic reset osmoreceptor response, agenesis of the corpus callosum, and hypothalamic cyst
4. Hyponatremia secondary to reset osmostat
5. Hyponatremia caused by a reset osmostat in a neonate with cleft lip and palate and panhypopituitarism
6. Osmotic thresholds for AVP release with the use of plasma and urine AVP and free water clearance
7. Urinary and metabolic clearances of arginine vasopressin in normal subjects
8. Differentiation of polyuric states by measurement of responses to changes in plasma osmolality induced by hypertonic saline infusions
9. Hypertonic saline test for the investigation of posterior pituitary function
10. Holoprosencephaly associated with diabetes insipidus and syndrome of inappropriate secretion of antidiuertic hormone
11. Lack of inhibition of vasopressin release in midfacial hypoplasia