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Article

Five years results after intrafamilial kidney post-transplant in a case of familial hypomagnesemia due to a claudin-19 mutation.

Jornal brasileiro de nefrologia - 1 Jan 2000

Almeida Jorge Reis, Machado Gabriel de Almeida, dos Santos Márcia Maria Guimarães, Lopes Patricia de Fátima, de Matos Jorge Paulo Strogoff, Neves Aderbal Cypriano, Lugon Jocemir Ronaldo

Abstract excerpt

INTRODUCTION: Familial Hypomagnesaemia with hypercalciuria and nephrocalcinosis, with severe ocular impairment secondary to claudin-19 mutation, is a rare recessive autossomic disorder. Its spectrum includes renal Mg2+ wasting, medullary nephrocalcinosis and progressive chronic renal failure in y...

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Identifiers

PMID: 25317625
DOI: 10.5935/0101-2800.20140057

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25317625-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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