Very long chain acyl-CoA dehydrogenase deficiency (Q93436)
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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 |
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| 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. |
Statements
CID11:ID_907810567
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dki-india-ID_907810567
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Concluído
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15 August 2026
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