Abstract
Juvenil Myoclonic Epilepsy (JME) is a subtype of the group of Idiopathic Generalized Epilepsy that does not present apparent abnormalities on conventional Magnetic Resonance Imaging.However, proton Magnetic Resonance Spectroscopy (MRS) studies revealed conflicting metabolic alterations, especially regarding the decrease of marker N-acetyl aspartate (NAA) in the frontal lobe of patients.Co…