ABSTRACT
Megalencephaly; acute encephalitis-like crises; neurodegenerative disorder with spasticity, dystonia, choreoathetosis, and dyskinesia; seizures; characteristic temporal hypoplasia, acute subdural hemorrhages or subdural fluid collections and striatal degeneration; glutaric aciduria and 3-hydroxyglutaric aciduria; and deficient activity of glutaryl CoA dehydrogenase.
