Chapter 5 Sz Flashcards
automatisms
temporal lobe epilepsy
3 hx spike and wave
absence
4-6 hz polyspikes
JME
autoinduction of metabolism
carbamazepine
nephrolithiasis
topiramate and zonisamide
Steven johnsons syndrome
Lamotrigine
Hypsarrhythmia
infantile spasms
fencer’s posture
supplementary motor area contralateral to arm extension
figure of 4 sign
supplementary motor area
Doose’s Syndrome
Myoclonic-astatic epilepsy
Dravet’s Syndrome
Severe myoclonic epilepsy of infancy
Ohtahara’s syndrome
early infantile epileptic encephalopathy
West’s syndrome
Triad of infantile spasms, hypsarrhythmia, psychomotor delay
Panayiotopoulos syndrome
occipital epilepsy withtonic eye deviations, ictal vomiting and visual seizures
Lennox-Gastaut Syndrome
multiple seizure types, slow spike wave complexes, psychomotor delay/regression
Landay-Kleffner syndrome
epilepsy with multiple seizure types and acquired aphasia
Nocturnal hypermotor seizures
AD nocturnal frontal lobe epilepsy
Gelastic/Dacrystic Seizures
hypothalamic hamartoma
Head version
contralateral frontal lobe
dystonic posture
contralateral temporal lobe
EPM1 and cystatin B
Unverricht-lundborg syndrome
EPM2A
Lafora Body disease
Progressive myoclonic epilepsy and cherry red spot
sialidosis
PME and mitochondrial disease
MERRF
Ab to glutamate receptor 3
Rasmussen’s encephalitis
Triphasic waves
metabolic encephalopathy
Temporal PLEDS (LPDs)
HSV encephalitis, structural abnormality
k complex and sleep spindles
stage 2 sleep
REMS and atonia
REM
apnea with no respiratory effort
central apnea
apnea with respiratory effort
OSA
low hypocretin
narcolepsy
low ferritin
RLS
REM sleep behavorial disorders
alpha-synucleinopathies
