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Article

Differential diagnosis of hereditary nephrogenic diabetes insipidus with desmopressin infusion test.

Indian journal of pediatrics - 1 Nov 2010

Bircan Zelal, Mutlu Hatice, Cheong Hae Il

Abstract excerpt

PURPOSE: The causes of hereditary nephrogenic diabetes insipidus (HNDI) are the mutations in the arginine vasopressin V2 receptor gene (AVPR2) (90%) and aquaporin 2 gene (AQP2) (10%). Although it is possible to perform mutation analysis where available, differentional diagnosis at clinical bases...

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Topics

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Share to Aquaporin 2
Share to Deamino Arginine Vasopressin
Share to Diabetes Insipidus, Nephrogenic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diagnosis, Differential

Share to AVPR2 gene

Share to Infant

Share to Mutation

Share to Receptors, Vasopressin

Source

Identifiers

PMID: 20814834
DOI: 10.1007/s12098-010-0181-3

Genes

AQP2
AVPR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20814834-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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