Absolute |
Carnitine deficiency (primary) |
Carnitine palmitoyltransferase (CPT) I or II deficiency |
Carnitine translocase deficiency |
β‐oxidation defects |
Medium‐chain acyl dehydrogenase deficiency (MCAD) |
Long‐chain acyl dehydrogenase deficiency (LCAD) |
Short‐chain acyl dehydrogenase deficiency (SCAD) |
Long‐chain 3‐hydroxyacyl‐CoA deficiency |
Medium‐chain 3‐hydroxyacyl‐CoA deficiency. |
Pyruvate carboxylase deficiency |
Porphyria |
Relative |
Inability to maintain adequate nutrition |
Surgical focus identified by neuroimaging and video‐EEG monitoring |
Parent or caregiver noncompliance |
Propofol concurrent use (risk of propofol infusion syndrome may be higher) |