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long-chain acyl-CoA dehydrogenase deficiency (LCAD deficiency)
Pathology: non-ketotic hypoglycemia
Genetics: associated with defects in ACADL
Laboratory:
- serum glucose hypoglycemia
- serum ketones, non-ketotic
General
lipid metabolism, inborn error; lipid storage disease; lipidosis
Database Correlations
OMIM 201460
References
OMIM :accession 201460