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Article

Late-onset MADD: a rare cause of cirrhosis and acute liver failure?

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology - 1 Mar 2020

Soldath Patrick, Lund Allan, Vissing John

Abstract excerpt

Late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) is a severe inborn error of fat metabolism. In late-onset MADD, hepatopathy in the form of steatosis is commonplace and considered a benign and stable condition that does not progress to more advanced stages of liver disease, however, progression to cirrhosis and acute liver failure (ALF) has been reported in two previous case reports. Here, we report a...

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Identifiers

PMID: 32607475
DOI: 10.36185/2532-1900-003
PMCID: PMC7315895

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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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