DisorderOrgan or system affectedSigns of metabolic instabilityNeurodevelopmental effects (if not treated)
Carnitine transport defectCNS, cardiovascularLow carnitine levelsDevelopmental delay, motor deficits, muscle weakness
Citrullinemia type I (carnitine palmityl transferase type I deficiency)CNSHypoglycemiaDevelopmental delay, motor deficits
Citrullinemia type II (carnitine palmityl transferase type II deficiency)CNS, cardiovascularHypoglycemiaNeonatal presentation: severe mental retardation or death
Later onset: muscle weakness
Glutaric acidemia type IICNSHypoglycemiaSevere motor deficits or mental retardation
Short-chain acyl-CoA dehydrogenase deficiencyCNSHypoglycemia, acidosisDevelopmental delay, motor deficits, potential for mental retardation
Medium-chain acyl-CoA dehydrogenase deficiencyCNSHypoglycemia, acidosisDevelopmental delay, motor deficits, potential for mental retardation
Long-chain acyl-CoA dehydrogenase deficiencyCNS, eye, cardiovascularHypoglycemiaDevelopmental delay, motor deficits, potential for mental retardation, poor vision
Very long-chain acyl-CoA dehydrogenase deficiencyCNS, cardiovascularHypoglycemiaDevelopmental delay, motor deficits, potential for mental retardation