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Article

Renal dysfunction in methylmalonic acidurias: review for the pediatric nephrologist.

Pediatric nephrology (Berlin, Germany) - 1 Feb 2013

Morath Marina A, Hörster Friederike, Sauer Sven W

Abstract excerpt

Methylmalonic acidurias are a heterogeneous group of inborn errors of branched-chain amino acid metabolism. Depending on the underlying etiology, acute or chronic renal disease constitutes major (long-term) complications. In recent decades, overall survival has improved due to optimized treatment strategies based on the use of standardized emergency protocols and dialysis techniques. The majority of these...

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Identifiers

PMID: 22814947
DOI: 10.1007/s00467-012-2245-2

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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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