Seizure Types & Mimics — Audia Aurora Glass Neural
Audia • Aurora Glass Neural
Seizure Types, Mimics & EEG Patterns
Not all seizures are epileptic.

Many mimics are treatable once correctly identified (e.g., PNES, metabolic, functional).

EEG is critical, but a normal EEG doesn’t always rule out epilepsy.

Multidisciplinary evaluation is often necessary: neurology, psychiatry, immunology, sleep medicine, genetics.

I. True Epileptic Seizures (EEG-Confirmed)

Involve abnormal cortical discharges.

A. Focal Seizures

  • Focal aware (simple partial)
  • Focal impaired awareness (complex partial)
  • Focal to bilateral tonic-clonic

B. Generalized Seizures

  • Absence (petit mal)
  • Tonic
  • Clonic
  • Tonic-clonic (grand mal)
  • Atonic (drop attacks)
  • Myoclonic

C. Epileptic Syndromes

  • Juvenile Myoclonic Epilepsy (JME)
  • Lennox-Gastaut Syndrome (LGS)
  • Childhood Absence Epilepsy
  • West Syndrome (infantile spasms)
  • Dravet Syndrome
  • Doose Syndrome (myoclonic-atonic epilepsy)

D. Reflex Epilepsies

  • Photosensitive
  • Musicogenic
  • Reading epilepsy
  • Hot-water epilepsy

E. Status Epilepticus

  • Convulsive
  • Non-convulsive (NCSE)

II. Epileptic Encephalopathies & Syndromes

Genetic & Developmental

  • Dravet Syndrome (SCN1A, febrile/myoclonic)
  • Ohtahara Syndrome (tonic spasms, burst suppression)
  • Early Myoclonic Encephalopathy (metabolic/genetic origin)
  • West Syndrome (hypsarrhythmia + spasms)
  • Lennox-Gastaut Syndrome (mixed, cognitive decline)
  • Doose Syndrome (myoclonic-atonic)

Genetic Syndromes (Childhood–Adolescence)

  • Benign Rolandic Epilepsy / BECTS
  • Panayiotopoulos Syndrome (autonomic, occipital EEG spikes)
  • Childhood Absence Epilepsy (3Hz spike-wave)
  • Juvenile Myoclonic Epilepsy
  • Jeavons Syndrome (eyelid myoclonia + photosensitivity)

Focal Structural Epilepsy Syndromes

  • Temporal Lobe Epilepsy (auras, automatisms)
  • Frontal Lobe Epilepsy (nocturnal, bizarre)
  • Occipital Lobe Epilepsy (visual)
  • Parietal Lobe Epilepsy (somatosensory)

III. Progressive Epilepsy Disorders

  • Rasmussen’s Encephalitis (immune-mediated hemiparesis)
  • Lafora Disease (adolescent fatal PME)
  • Unverricht–Lundborg (less severe PME)
  • Batten Disease (CLN/NCLs) (seizures, regression)

IV. Autoimmune & Metabolic Epilepsy

  • Autoimmune Epilepsy (Anti-NMDA, GAD65, VGKC, etc.)
  • FIRES (Febrile Infection-Related Epilepsy Syndrome)
  • Glut1 Deficiency Syndrome (low CSF glucose; keto diet effective)
  • MERRF (Mitochondrial epilepsy)
  • Alpers-Huttenlocher Syndrome (POLG mutation)

🚫 V. Non-Epileptic Events (EEG-Normal)

A. Psychogenic Non-Epileptic Seizures (PNES)

  • Dissociative, trauma-linked
  • Video EEG is diagnostic

B. Medical Mimics

ConditionNotes
SyncopeJerking may occur during brief cerebral hypoxia
HypoglycemiaTremor, collapse
Hypoxia/AnoxiaPost-anoxic myoclonus
Electrolyte imbalanceConfusion, jerks
Toxic encephalopathyBaclofen, lithium, serotonin syndrome
Narcolepsy/CataplexySudden atonia with emotion
Breath-holding spellsSeen in toddlers
HyperventilationTingling, tremor, dizziness

C. Encephalopathies

TypeFeatures
MetabolicUremia, hepatic, diabetic
InfectiousHSV, West Nile, etc.
Autoimmune EncephalitisAnti-NMDA, GAD65, VGKC
Cortical Spreading Depression (CSD)Migraine aura; transient EEG suppression

🧍 VI. Movement Disorders Mimicking Seizures

Motor events without EEG seizure activity.

A. Hyperkinetic Movement Disorders

DisorderFeatures
TicsRepetitive, suppressible (Tourette)
StereotypiesRhythmic, purposeless (autism, IDD)
Myoclonus (non-epileptic)Sleep, metabolic, post-anoxic
ChoreaIrregular, dance-like
BallismusViolent flinging
DystoniaSustained, twisting postures
AthetosisWrithing movements
TremorEssential, parkinsonian, drug-induced
Startle syndromesHyperekplexia, exaggerated reflexes

B. Paroxysmal Dyskinesias

TypeTrigger
PKDSudden motion
PNKDSpontaneous, stress, caffeine
PEDAfter exertion

💤 VII. Sleep-Related Events

Look seizure-like but occur in transitions between sleep stages.

DisorderNotes
Night terrorsScreaming, no recall
REM Behavior Disorder (RBD)Acting out dreams
SleepwalkingComplex behavior, no memory
Rhythmic Movement DisorderHead-banging, body-rocking

🌀 VIII. Other Paroxysmal or Psychiatric Events

Not epileptic, but episodic or seizure-like in appearance.

ConditionFeatures
Autonomic SeizuresPanayiotopoulos: vomiting, eye deviation
Febrile SeizuresAge 6mo–5yr; triggered by fever
Vestibular DisordersVertigo, imbalance, mimic drop attacks
Migraine VariantsAura, hemiplegia, basilar
PANDAS/PANSTics, rage, regression post-infection
Functional Movement DisordersInconsistent, distractible patterns
Narcolepsy/CataplexySleep-attacks, emotional atonia

🧾 IX. EEG Patterns: Interpretation Guide

EEG FindingMeaning
Epileptiform dischargesSpike/sharp waves = epilepsy
Generalized slowingMetabolic/toxic encephalopathy
Focal slowingStructural lesion
Normal EEGDoesn’t exclude epilepsy (esp. PNES, subclinical)
HypsarrhythmiaWest Syndrome (chaotic infantile spasms)