Glossary

Recognizing types of seizures

Use the common trends you are seeing in your loved one to determine what type of seizure they may be experiencing. Use things such as the time of day, length of time, affected body part, and awareness levels to help narrow your search.

The materials included on this website are for informational purposes only—not intended as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other healthcare provider regarding any questions on a medical condition or treatment. Never disregard professional medical advice or delay in seeking it because of something you have read or seen on this website.

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Awareness

Awareness

Key part of the body

Eyes
Mouth
Head
Body
Hands & Arms
Behavior
Speech
Age

Timing/duration

Timing/duration

Absence/petit mal seizures

(ab-sans/pe-tē-mal)

  • Previously known as petit mal seizures
  • Causes a short period of “blanking out” or staring into space
  • During the seizure, the person's motor symptoms are minimal except for subtle ones such as eyelid flutter
  • Usually affect only a person’s awareness of what is going on at that time, with immediate recovery
Less typical with LGS
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Woman with blank look - Absence seizure

Atonic seizures

(a-taa-nik)

  • May be referred to as a “drop attack” or “drop seizure”
  • Person has a sudden loss of muscle tone and goes limp
  • Mild seizures look like a head nod or drop, while severe seizures can cause a person to fall to the ground
  • People with these types of seizures may wear helmets to protect from injuries
Typical with LGS
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Man in wheel chair with head slumped - atonic seizure

Atypical absence seizures

(a-TIP-i-kul/ab-sans)

  • Period of "blanking out" or staring into space as also seen during typical absence seizures
  • Referred to as "atypical" as the person may exhibit small movements such as chewing or lip smacking, and/or finger or hand rubbing
  • May begin and end more gradually compared to typical absence seizures
Typical with LGS
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Man with blank spaced look- Atypical absence seizure

Clonic seizures

(klä-nik)

  • Associated with repeated, rhythmic jerking movements lasting a few seconds to a minute that cannot be stopped by restraining or repositioning the arms or legs
  • Hemiclonic seizures occur when sustained rhythmic jerking rapidly involves one side of the body at seizure onset
  • Most commonly occur in babies
  • Often seen as part of a tonic-clonic seizure and may be difficult to distinguish from a myoclonic seizure; however, the jerking is more regular and sustained during a clonic seizure
  • May also be associated with jerking that follows stiffening of muscles, as in a tonic-clonic seizure, and can last seconds to 1 to 2 minutes
Less typical with LGS
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Man with head falling back with jerking movement- clonic seizures

Focal impaired awareness/complex partial seizures

(fō-kǝl im-'perd ǝ-'wer-nǝs/käm-,pleks pär-shǝl)

  • Used to be called complex partial seizures
  • Person loses awareness, may not respond, and may have no memory of the seizure


Experiences vary, but can include:

  • Starting with a blank stare, followed by chewing/lip smacking
  • Random activity like picking at the air or clothes, attempting to pick up objects, removing clothing, repeating words or phrases, etc
Less typical with LGS
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Woman with speech bubbles around her showing loss of awareness- focal impaired awareness seizure

Generalized tonic-clonic/grand mal seizures

(jen-rǝ-,līzd tän-i(k)-'klä-nik/grän(d)-,mäl)

  • Formerly known as “grand mal” seizures. This seizure type is what most people think of when they hear the word “seizure”
  • Person loses consciousness or awareness, muscles extend and become rigid, and then jerk rhythmically on both sides of the body
Typical with LGS
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Woman lying down with jerky motion - generalized tonic- clonic-grand mal seizure

Infantile spasms/epileptic spasms

(in-fǝn-,tī(-ǝ)l/e-pǝ-'lep-tik spa-zǝms)

  • Typically occurs within first year of life, usually by 4 to 8 months
  • Typically seen as a sudden stiffening of the body and brief bending forward or backward of the arms, legs, and head (can occur with limbs coming inwards toward chest, but not always)
  • Face may grimace or look surprised
  • Some infants arch their backs as they extend their arms and legs
  • Some infants may experience head drops
  • Frequently occur in clusters upon awakening or going to sleep
  • May look like a startle reflex in infants
Typical with LGS
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Baby on mat with startled look- infantile spasms

More to explore:

Learn about a treatment option for LGS

Treatment option

Talk to your doctor about LGS

Meeting with your doctor

Glossary/Tab/Desktop
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Autism
  • A neurodevelopmental disorder that can exhibit characteristics such as deficits in social communication, repetitive behaviors, and restricted interests 
  • Autism is more common in males than females, with an estimated ratio of around 3:1 
Cerebral palsy
  • A neuromotor disorder caused by an injury to the developing brain before or shortly following birth 
  • Development of movement, muscle tone, and posture can be affected 
Developmental delays
  • Refers to when a child does not achieve developmental milestones in comparison to peers of the same age range 
  • Examples include lack of engagement with age-appropriate toys, speech delays, or other delays identified by a doctor 
Electroencephalogram (EEG)
  • A diagnostic test that measures electrical activity in the brain using small electrodes attached to the scalp 
  • It is commonly used to detect abnormalities related to epilepsy and other neurological disorders 
Epileptologist
  • A neurologist who has undergone specific training in the diagnosis and management of epilepsy 
  • Epileptologists focus on the management of patients with epilepsy 
Genetic mutation
  • A permanent alteration in the DNA sequence that makes up a gene 
  • Some genetic mutations are hereditary, while others occur spontaneously 
  • Certain mutations are linked to specific medical conditions, including some forms of epilepsy 
Immune disorders
  • Disorders that result from a dysfunction in the immune system, which may be overactive or underactive 
  • Some immune disorders are thought to contribute to the development of epilepsy and other neurological conditions 
Lennox-Gastaut syndrome (LGS)
  • Lennox-Gastaut syndrome (LGS) is a rare form of epilepsy that usually begins in childhood and is associated with multiple kinds of seizures
Metabolic disorders
  • A group of disorders that affect the body's ability to convert food into energy 
  • These disorders can be genetic and may lead to a variety of health issues, including developmental delays and neurological symptoms 
Neurologist
  • A medical specialist who diagnoses, manages, and treats disorders of the nervous system, including the brain, spinal cord, nerves, neuromuscular junction, and muscles 
  • Neurologists often serve as the first point of contact for patients with neurological symptoms 
Paroxysmal fast rhythms
  • Paroxysmal fast rhythms, also known as generalized paroxysmal fast activity (GPFA), are patterns of neural activity consisting of 8–26 Hz bursts of generalized rhythmic discharges 
  • Paroxysmal fast rhythms have traditionally been associated with Lennox-Gastaut syndrome 
Refractory epilepsy
  • May also be referred to as “uncontrolled,” “intractable,” or “drug-resistant” epilepsy 
  • Occurs when a person has failed to become (and stay) seizure free with adequate trials of 2 appropriately selected antiseizure medications 
Refractory Epilepsy Screening Tool for LGS (REST-LGS)
  • A questionnaire-based tool developed by experts to improve both the identification and treatment of patients with Lennox-Gastaut syndrome (LGS)
  • Helps providers to assess the likelihood that a patient has LGS based on four major symptoms and four minor features commonly associated with LGS 
Slow spike-wave pattern (SSW)
  • Refers to a pattern seen on an electroencephalogram (EEG) characterized by slow, high-amplitude spike-and-wave discharges 
  • This pattern is often associated with specific types of epilepsy, including Lennox-Gastaut syndrome (LGS)
Tuberous sclerosis complex (TSC)
  • Tuberous sclerosis complex (TSC) is a genetic condition characterized by the development of noncancerous tumors that may cause a range of symptoms, including seizures