ABSTRACT
Hypoketotic hypoglycemia, cardiomyopathy cardiac arrhythmia, sudden infant death syndrome (SIDS), myopathy, hyperammonemia, hyperuricemia, elevated creatine kinase, dicarboxylic aciduria, elevated C6 and C8acylcarnitine, deficient activity of medium-chain acylCoA dehydrogenase, and mutation in the ACADM gene, especially A985G.
