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Article

[Dent's disease].

Srpski arhiv za celokupno lekarstvo - 1 Dec 2008

Pavićević Snezana, Bogdanović Radovan, Ludwig Michael, Samardzić Mira

Abstract excerpt

INTRODUCTION: Dent disease is X-linked recessive proximal tubulopathy, due to mutations in the CLCN5 gene. It is characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis and progressive renal failure. CASE OUTLINE: A seven-year-old boy was referred after endocrinological examination where abdominal ultrasound showed nephrocalcinosis. There were anamnestic data neither of oedema,...

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Source

Identifiers

PMID: 20804101
DOI: 10.2298/sarh08s4312p

Genes

CLCN5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.Semantic proximity Read ↗

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