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A patient with congenital nephrogenic diabetes insipidus due to AVPR2 mutation complicated by persisting polydipsia under hemodialysis treatment.

CEN case reports - 1 May 2021

Iijima Takashi, Mori Takayasu, Sohara Eisei, Suwabe Tatsuya, Hoshino Junichi, Ubara Yoshifumi

Abstract excerpt

A 17-year-old boy was referred to our institution for a re-evaluation of congenital nephrogenic diabetes insipidus. A water restriction test revealed no urine concentration or volume reduction and a subsequent pitressin test revealed a lack of an anti-diuretic response. Nephrogenic diabetes insipidus was confirmed, and the patient was treated using trichlormethiazide 4 mg, indomethacin 175 mg, and desmopressin...

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Share to Adolescent
Share to Diabetes Insipidus, Nephrogenic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Receptors, Vasopressin

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Source

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Identifiers

PMID: 33125666
DOI: 10.1007/s13730-020-00549-8
PMCID: PMC8019439

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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