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Flashcards

Common Epileptic Syndromes

Amber Castle Eeg R. EEG Inglês 15 flashcards

Flashcards do conjunto (15)

  1. 1What are the three types of seizure onset?Focal, Generalized, unknown onset
  2. 2Benign Epilepsy of Childhood with Central Midtemporal Spikes- BECTSunilateral parethesis of tongue, lips, cheek; possible tonic-clonic activity of tongue/lips/cheek; unilateral central or midtemporal sharp waves; rhythmic spike bursts and spike wave discharges during seizure.
  3. 3Panaylotopoulos syndromeOnset 15 mo-17 years
    blindness, scintillating scotomta, visual hallucinations or illusions
    interictal spike bursts which may be brought on by eye closure
  4. 4Focal Impaired Temporal Lobeloss of awareness, automatisms, staring, deja vu, emotional or thought disturbances, hallucinations
    interictal spike or sharp waves
    activated by sleep deprivation
  5. 5Focal Frontal Lobe- what are the four manifestations?Focal aware primary motor cortex (clonic twitching w/o loc), Focal aware or impaired from supplementary motor cortex (head deviation, raising of one arm with extension of other arm), Focal impaired from superior frontal region (unconsciousness followed by generalized tonic-clonic convulsion), Focal impaired from medial frontal or orbital-frontal areas (body rocking, dystonic posturing, repetitive movements, laughing, crying)
  6. 6What are the EEG patterns of frontal lobe seizures?Interictal discharges and even seizures may be undetected by scalp electrodes, discharges may appear widespread due to deep epileptigenic source
  7. 7Absence seizureno aura, >30 sec, staring, unresponsive, eye blinking, lip smacking, automatisms
    3 Hz generalized spike and wave
    induced by HV
  8. 8Generalized Tonic-ClonicLOC, loss of body tone, stiff muscles, uncontrollable jerking/twitching
    Rapid spikes followed by spike-waves
  9. 9JME (Juvenile Myoclonic Epilepsy)high voltage polyspikes followed by slow waves, often occuring during stage 1 sleep, can be triggered by HV or photic
  10. 10Lennox-Gastautsevere generalized seizures
    EEG shows slow spike and wave complexes
    more than one type of seizure: tonic, atypical absence
    slowed background
  11. 11West Syndrome/Epileptic Spasmsflexor, extensor, or mixed spasms
    usually associated with some degree of developmental delay
    hypsarrythmia
  12. 12Progressive myoclonic epilepsyMyoclonic epilepsies with ragged red fibers, lafora disease, unverricht-lundborg disease, Neuronal ceroid lipofuscinosis, cherry red spot myoclonus syndrom
    characterized by myoclonic seizures, progressive ataxia, and dementia
    generalized polyspike wave or spike wave, background progressively slows
  13. 13Describe Lafora Diseasemyoclonic seizures, GTC seizures, occipital seizures, status epilepticus risk, decline in intellectual function
  14. 14Unverricht-Lunborg DiseaseOnset age 6-15
    Myoclonus
    LOC, muscle rigidity, tonic clonic, ataxia, intention tremor, dysarthia,
  15. 15Landau-Kleffneronset 3-9 years
    Dysphasia, acquired aphasia, 2/3 have seizures
    EEG abnormalities change in abundance, location, and pattern, electrographic status epilepticus

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A review of common epileptic syndromes
Criado por
Amber Castle
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