Very long chain acyl-CoA dehydrogenase deficiency (Q93436): Difference between revisions

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Latest revision as of 08:32, 16 August 2026

Acyl-CoA dehydrogenase very long chain (VLCAD) deficiency is an inborn error of mitochondrial long-chain fatty acid oxidation with variable presentation including a severe form with recurrent episodes of hypoketotic hypoglycaemia, often associated with hypertrophic cardiomyopathy with pericardial effusion, or arrythmia, which can lead to a cardiorespiratory arrest in neonates or infants.

Language	Label	Description	Also known as
default for all languages	ID_907810567
English	Very long chain acyl-CoA dehydrogenase deficiency	Acyl-CoA dehydrogenase very long chain (VLCAD) deficiency is an inborn error of mitochondrial long-chain fatty acid oxidation with variable presentation including a severe form with recurrent episodes of hypoketotic hypoglycaemia, often associated with hypertrophic cardiomyopathy with pericardial effusion, or arrythmia, which can lead to a cardiorespiratory arrest in neonates or infants.