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Article

[Type 1 primary hyperoxaluria: From childhood to adult, how to manage adequately medical therapy compliance?]

Nephrologie & therapeutique - 1 May 2018

Leflot Marie, Krzesinski Jean-Marie, Collard Laure, Thomas Alexandre, Ghuysen Marie-Sophie

Abstract excerpt

We report the cases of three young patients suffering from type 1 primary hyperoxaluria, a metabolic genetic disorder characterized by intracellular accumulation of oxalate and which may result in end-stage renal disease with systemic impairment. A number of effective conservative therapeutic means are available for early management of affected children particularly when he is growing older. Despite the...

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Identifiers

PMID: 29198962
DOI: 10.1016/j.nephro.2017.06.004

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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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