Lennox – gastaut syndrom some typical characteristics and clinical prognostic aspects
Abstract
In epileptology, Lennox - Gasto syndrome identification is extremely complex and difficult, because of the lack of modern complex treatment schemes, one of the top priorities in the current problems.
Experts admit that studying the clinical picture of 10 lennox gastro syndrome patients means knowing all child neurology, and children with lennox gastro syndrome are rarely recorded, so situations need to be addressed more correctly.
References
Shields WD. Diagnosis of Infantile Spasms, Lennox-Gastaut Syndrome, and Progressive Myoclonic Epilepsy. Epilepsia. 2004;45:2–4.
Crumrine PK. Lennox-Gastaut syndrome. J Child Neurol. 2002:70–75.
Markand ON. Lennox-Gastaut syndrome (childhood epileptic encephalopathy) J Clin Neurophysiol. 2003;20:426–441.
Heiskala H. Community-based study of Lennox-Gastaut syndrome. Epilepsia. 1997;38:526–531.
Trevathan E. Infantile Spasms and Lennox-Gastaut Syndrome. J Child Neurol. 2002;17:9–22.
Gastaut H, Roger J, Soulayrol R, Tassinari CA, Regis H, Dravet C. Childhood epileptic encephalopathy of children with diffuse slow spike-waves (otherwise known as "petit mal variant") or Lennox syndrome. Epilepsia. 1966;7:139–179.
Chevrie JJ, Aicardi J. Childhood epileptic encephalopathy with slow spike-wave: a statistical study of 80 cases. Epilepsia. 1972;13:259–271.
Gastaut H, Gastaut JL, Goncalves e Silva GE, Fernandez Sanchez GR. Relative frequency of different types of epilepsy: a study employing the classification of the International League Against Epilepsy. Epilepsia. 1975;16:457–461.
Keywords
epileptology
cryptogenic
symptomatic Леннокс - гастро-синдром
Эпилептология
криптоген
симптоматический Lennoks – qasto sindromu
epileptologiya
kriptogen
simptomatik