45. Some juvenile epilepsy syndroms and some of their typical characteristics

  1. West syndrom (Infantile spasms): EEG typically shows slow spike-wave complexes?
  2. West syndrom (Infantile spasms): is typically treated with adrenocorticotrophic hormone (ACTH), oral prednisone, or vigabatrin ?
  3. Absence seizures (Petit mal): EEG shows a very characteristic pattern with generalized 4–6 Hz polyspike and slow wave discharges?
  4. Lennox–Gastaut syndrome (LGS): characterized by a triad of signs – frequent seizures of multiple types, a distinctive EEG pattern and mental retardation?
  5. Juvenile myoclonic epilepsy (JME): patients usually have normal intelligence?
  6. Juvenile myoclonic epilepsy (JME): EEG shows hypsarrhythmia?

  1. F
  2. T
  3. F
  4. T
  5. F
  6. F

44. Seizure types

Differences between terminology in the old* and the new** classification of epilepsy:

  1. Generalized —> Generalized. (T/F?)
  2. Simple –> Aware. (T/F?)
  3. Complex –> Impaired awareness. (T/F?)
  4. Partial –> Focal. (T/F?)
  5. Simple partial –> Focal aware. (T/F?)
  6. Complex partial –> Focal impaired awareness. (T/F?)
  7. Secondarily generalized tonic-clonic –> Focal to bilateral tonic-clonic. (T/F?)

*”Proposal for revised clinical and electroencephalographic classification of epileptic seizures”, from the Commission on Classification and Terminology of the International League Against Epilepsy, 1981.

**”2017 Revised Classification of Seizures”, International League Against Epilepsy (ILAE)

  1. T
  2. T
  3. T
  4. T
  5. T
  6. T
  7. T