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Congenital Nephrogenic Diabetes Insipidus in a Baby Girl

Overview
Journal Arch Dis Child
Specialty Pediatrics
Date 1978 Nov 1
PMID 215090
Citations 4
Authors
R L Schreiner
P R Skafish
S K Anand
J D NORTHWAY
Affiliations
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Abstract

A 6-week-old girl with fever, hypernatraemia, dehydration, and polyuria failed to concentrate urine in response to exogenous vasopressin administration. There was no family history of nephrogenic diabetes insipidus. When she was 15 months old, the infusion of vasopressin did not produce an increase in urinary cyclic-AMP.

Citing Articles

Nephrogenic diabetes insipidus: identification of the genetic defect.

Knoers N, van den Ouweland A, Dreesen J, Verdijk M, Monnens L, van Oost B Pediatr Nephrol. 1993; 7(5):685-8.

PMID: 8251344 DOI: 10.1007/BF00852579.

Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.

van Lieburg A, Verdijk M, Schoute F, Ligtenberg M, van Oost B, Waldhauser F Hum Genet. 1995; 96(1):70-8.

PMID: 7607658 DOI: 10.1007/BF00214189.

Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatment.

Knoers N, Monnens L Pediatr Nephrol. 1992; 6(5):476-82.

PMID: 1457333 DOI: 10.1007/BF00874020.

Congenital nephrogenic diabetes insipidus.

Koepp P Arch Dis Child. 1979; 54(10):807.

PMID: 507907 PMC: 1545653. DOI: 10.1136/adc.54.10.807.

References
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