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Over 40 Different Types Of Seizures - Revised

Sun, 03/25/2007 - 03:04

It has been said repeatedly that there are over 40 different types of seizures with more or less only the most 'popular' listed. Let's see if we can locate the ones that aren't. These types of seizures affect someone and I feel need to be noted. I'm curious to see how many can be located. Anyone interested in helping me find them, please list what you find here along with their description. Thank you! Take care and have a good day! -Spiz This thread is a revision of the first one in order to make changes and additions.

A Note from epilepsy.com's Editors (August 2017)

This forum post was originally created in 2007. Over the years, many of the links provided in the comments have expired or may not have been updated. To find reliable, expert-verified information, visit the following sections of this site:

In late 2016, the International League Against Epilepsy (ILAE) approved a new way of organizing seizures that reflects recent advances in our understanding of the brain and seizures. This new system will make diagnosis and classification of seizures easier and more accurate. Learn more here.

These terms don’t change what occurs during a seizure, but offer a different way of naming seizures. More accurate ways of naming seizures can lead to more appropriate treatment.

We also want to take this opportunity to remind site visitors...

Comments

Autosomal Dominant Nocturnal

Submitted by spiz on Wed, 2007-04-04 - 22:26
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE) :This is a recently described syndrome that appears to be a genetic localization-related epilepsy.Seizures are nocturnal and occur in clusters, mimicking parasomnias. They mostly are brief tonic seizures and rare tonic-clonic convulsions, often preceded by a nonspecific aura... Mesial Temporal Lobe Epilepsy :Seizures typically are complex partial with automatisms, often preceded by a simple partial phase with sensory symptoms (ie, aura). Auras commonly observed in temporal lobe epilepsy are epigastric (abdominal) and psychic auras, including déja-vu or jamais-vu and fear. Neocortical Seizures :Neocortical seizures may be simple partial or complex partial, with symptoms depending on the area of cortex affected. Frontal discharges can spread rapidly and mimic "primary" generalized spike-wave complexes. This is referred to as "secondary bilateral synchrony" (with interictal epileptiform discharges that appear to be generalized but are in reality "secondarily generalized" focal discharges)... Idiopathic Epilepsies :While generally idiopathic means "of unknown cause," idiopathic epilepsies are not truly of unknown cause. This terminology most likely will be corrected in the upcoming classification system of the International League Against Epilepsy (ILAE). Idiopathic epilepsies are determined genetically and have no apparent structural cause, with seizures as the only manifestation of the condition. Localization - Related Epilepsies :Because of dramatic differences in electroclinical semiology and management, localization-related epilepsies usually are divided into mesiotemporal and neocortical. The most common localization-related epilepsy in adults is mesiotemporal lobe epilepsy, but, in neonates and young children, this is less common than neocortical epilepsy... Janz Syndrome (JME) :A primary generalized epilepsy syndrome, usually beginning between ages 5 to 17 years, characterized by myoclonic (muscle-jerk) seizures and possibly also absence and tonic-clonic seizures; responds well to valproate... Symptomatic Myoclonic Epilepsy :This is less frequent than the idiopathic (ie, cryptogenic) variety, and the age of onset is usually between a few months and 2-3 years. Clinical features include psychomotor retardation, and neuroimaging frequently demonstrates brain atrophy. Myoclonic jerks can occur alone, but they more commonly are associated with generalized clonic seizures. Rhythmic jerks can occur during sleep, with associated dystonic posturing during wakefulness. The prognosis for meaningful cognitive function is poor, although the myoclonic jerks may be controlled medically. Cryptogenic Myoclonic Epilepsy :This group includes all patients with idiopathic seizures who display primarily recurrent myoclonic attacks. Some patients have infrequent generalized tonic-clonic seizures. Most myoclonic seizures are axial, which sometimes results in falls. The outcome in these patients is usually favorable, although about half the patients may have behavioral or cognitive dysfunction. This has sometimes been termed "benign myoclonic epilepsy." Myoclonic Variant of Lennox-Gastaut Syndrome :All patients have myoclonic seizures associated with recurrent brief attacks of varying types. Examples of these attacks include atonic seizures, atypical absence, partial seizures, and brief tonic seizures. This is sometimes termed the myoclonic variant of Lennox-Gastaut syndrome. The outcome is worse than in the cryptogenic myoclonic epilepsy group; more patients have cognitive dysfunction, and a significant proportion of those have severe mental retardation. However, the outcome is better than in patients with Lennox-Gastaut syndrome... Severe Myoclonic Epilepsy :Occurs in a significant proportion of severe childhood epilepsies. The age of onset of seizures is between 4 and 11 months, and the seizures are initially unilateral or generalized clonic movements (or rarely, generalized tonic-clonic movements). *Seizures are usually long lasting, from 10-90 minutes in duration, and mostly associated with fever or minor infections. *Myoclonic seizures appear by the second or third year and are often photosensitive. *Atypical absence seizures may be seen without an electrographic correlate. *Initially, development may be normal; later, cognitive delays become evident and are usually moderate to severe. Most patients have fluctuating ataxia and erratic myoclonus. *The myoclonic seizures may resolve after a few years, but other seizures tend to be persistent... Neonatal Myoclonic Epilepsy :This syndrome presents in the first 4 weeks of life with prominent myoclonic seizures. *The seizures usually result from a severe metabolic disorder, including that associated with elevated glycine levels in the cerebrospinal fluid (CSF), although they may be associated with any condition that produces severe brain dysfunction. *Distinguishing neonatal myoclonic epilepsy from benign neonatal sleep myoclonus is important. The latter condition is seen in healthy infants and occurs only in sleep... Early Myoclonic Encephalopathy :Myoclonic seizures can occur in many types of epilepsy; but in infancy and early childhood, they may occur as the dominant seizure type. The outlook and treatment of this condition differ from those of the more severe Lennox-Gastaut syndrome, which also may have myoclonic seizures as an important component. At times in this heterogenous group, nonmyoclonic seizures may dominate the clinical picture... Myoclonic SE :Myoclonic seizures are characterized by quick, often repetitive, jerks that randomly involve the limbs. *Seizures often are repetitive and, in some cases, may be unabated for lengthy periods. *Some patients with myoclonic epilepsies may sustain repetitive myoclonus that persists for days with or without altered consciousness...

Re: Autosomal Dominant Nocturnal

Submitted by spiz on Mon, 2007-04-16 - 17:42
Here is some information on Simple Partial Seizures: History: The ICES lists 18 categories of SPS . All types of SPS can be seen with subsequent complex partial secondarily generalized seizures . The suspicion of SPS is based on the history of typical, reproducible patterns as outlined here. * Motor simple partial seizures o Clonic discharges in the sensorimotor cortex cause jerky, rhythmic movements that may remain restricted to one body segment or spread by “jacksonian march.” o Benign focal epilepsy of childhood accounts for 15-25% of childhood epilepsy and eventually remits by age 16 years. + Typical seizures are simple and motor, affect the face or arm, and occur soon after falling asleep or awakening. + As it usually remits by age 16 years, this syndrome does not always require treatment. o Another subtype, epilepsia partialis continua (ie, Kojewnikoff syndrome) , includes stereotypical periodic to semiperiodic clonic activity that may persist for years and is often refractory to treatment. + Clonic jerking usually involves the thumb or great toe, and may or may not spread to other body parts. + This activity has been associated with stroke, tumor, trauma, hypoxia, Rasmussen encephalitis, syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke (MELAS), subacute sclerosing panencephalitis (SSPE), and adult nonketotic hyperglycinemia. o Tonic-supplementary motor area (SMA) and premotor region discharges produce sustained contractions and unusual postures of a limb. + In 72% of cases SMA seizures are not associated with impaired consciousness. + Versive-smooth or jerky, tonic contractions of head and eye muscles, usually on the side contralateral to the discharge, often are followed by a secondarily generalized tonic-clonic seizure. + Phonatory activation of the primary or supplementary motor cortex produces vocalizations, speech arrest, or aphasia. * Sensory simple partial seizures o Somatosensory-primary sensory cortex seizures usually elicit positive or negative sensations contralateral to the discharge. o Symptoms associated with seizures from the postcentral gyrus include tingling, numbness, pain, heat, cold, agnosia, phantom sensations, or sensations of movement. o Abdominal pain usually originates from the temporal lobe, and genital pain from the mesial parietal sensory cortex. o The posterior parietal cortex is the likely origin of limb agnosia. o Supplemental sensory-secondary sensory cortex seizures may have ipsilateral or bilateral positive or negative sensations or vague axial or diffuse sensations. o Visual-calcarine cortex discharges produce elemental hallucinations including scintillations, scotomata, colored lights, visual field deficits, or field inversion. o The visual association cortex is the probable location of origin of complex visual hallucinations and photopsias. o Auditory SPS from the auditory cortex typically are perceived as simple sounds, rather than words or music. o Olfactory-uncinate seizures originate from the orbitofrontal cortex and the mesial temporal area. Perceived odors are usually unpleasant, often with a burning quality. o Gustatory seizures usually are associated with temporal lobe origin, although the insula and parietal operculum also have been implicated. Perceived tastes are typically unpleasant, often with a metallic component. o Vestibular seizures originate from various areas, including frontal and temporal-parietal-occipital junction. Symptoms include vertigo, a tilting sensation, and vague dizziness. o Psychic SPS arise predominantly from the temporal and limbic region, including the amygdala, hippocampus, and parahippocampal gyrus. Perceptual hallucinations or illusions are usually complex, visual or auditory, and are rarely bimodal. + Includes the déj - vu and jamais vu phenomena + Emotional: Fear is usual, but SPS can elicit happiness, sexual arousal, anger, and similar responses. + Cognitive: These responses include feelings of depersonalization, unreality, forced thinking, or feelings that may defy description. * Autonomic simple partial seizures o Abdominal sensation phenomena + These are common in mesial temporal epilepsy but can arise from the operculum and occipital region. + Symptoms include nausea, pain, hunger, warmth, and “epigastric rising” sensations, and may be associated with piloerection (ie, gooseflesh). o Cardiovascular sensations + The most common cardiac manifestation of any seizure is sinus tachycardia with arrhythmias, with bradycardia occurring infrequently. + Some patients have chest pain or a sensation of palpitation that mimics cardiac disease. + Respiratory inhibition has been reported with electrical stimulation of the temporal regions. o Pupillary symptoms - Miosis, mydriasis, hippus, and unilateral pupillary dilatation o Urogenital symptoms + Seizures from the superior portion of the posterior central gyrus can result in genital sensations, while sexual auras arise more from the limbic or temporal regions. + Ictal orgasms have been reported, although rarely, in association with seizures arising from various cerebral locations. o Other autonomic symptoms - Rarely perspiration, lacrimation, ictal enuresis, or flushing * Postictal neurological deficits can occur after an SPS as a negative manifestation of the function affected by the seizure (eg, Todd paralysis). Physical: The physical examination may show subtle or obvious neurological focality. * Immediately following a SPS, the focality may become more pronounced owing to postictal inhibition (eg, Todd paralysis). * If an examination is performed during a SPS, no impairment of awareness or responsiveness is observed. o Preservation of awareness implies that a person is able to recount simple events that happen during the ictus. This is best established by giving a specific, uncommon 2-syllable word to the patient during the SPS and asking for its recall soon after the seizure has resolved. o Preservation of responsiveness implies that a person is able to carry out simple commands or directed volitional actions. o Responsiveness may appear to be impaired because of interference by the motor manifestations of the SPS. o This is best established by asking the patient to perform simple, unilateral and bilateral neurological functions during the SPS. o If the patient is unable to perform a task because of the manifestations of the SPS, recollection of the instructions implies responsiveness was preserved. * Motor, sensory, special sensory, psychic, and autonomic manifestations may begin in a small anatomical area and spread to a larger area of the body. This has been termed as “jacksonian march,” and it typically progresses along contiguous parts of the body in a reproducible pattern.

Sleep Disorders

Submitted by spiz on Sat, 2007-04-21 - 17:00
Sleep Disorders (Nonepileptic unless specified) Cataplexy :a medical condition which often affects people who have narcolepsy, a disorder whose principal signs are EDS (Excessive Daytime Sleepiness), sleep attacks, and disturbed night-time sleep. Cataplexy is sometimes confused with epilepsy, where a series of flashes or other stimuli cause superficially similar seizures... Narcolepsy :a neurological condition most characterized by Excessive Daytime Sleepiness (EDS). A narcoleptic will most likely experience disturbed nocturnal sleep, confused with insomnia, and disorder of REM or rapid eye movement sleep. It is a type of dyssomnia...Narcolepsy is often mistaken for depression, epilepsy, or the side effects of medications... Hypersomnia :also known as excessive daytime sleepiness (EDS), is excessive amount of sleepiness...Medical conditions including multiple sclerosis, depression, encephalitis, epilepsy, or obesity may contribute to the disorder... Dyssomnia :primary disorders of initiating or maintaining sleep or of excessive sleepiness and are characterized by a disturbance in the amount, quality, or timing of sleep... Sleep Paralysis :a condition characterized by temporary paralysis of the body shortly after waking up (known as hypnopompic paralysis) or, less often, shortly before falling asleep (known as hypnagogic paralysis)...Sleep paralysis occurs when the brain is awakened from a REM state into essentially a normal fully awake state, but the bodily paralysis is still occurring. This causes the person to be fully aware, but unable to move...Many people who commonly enter sleep paralysis also suffer from narcolepsy. However, various studies suggest that many or most people will experience sleep paralysis at least once or twice in their lives... Hypnogogia & Hypnopompia :the experiences a person can go through in the hypnagogic (or hypnogogic) state, the period of falling asleep. Hypnopompia are the experiences a person may go through in the hypnopompic state, the period of waking up...An experience of the hypnagogic state is not an uncommon occurrence with 30 to 40 percent of people experiencing it at least once in their lives.[citation needed] However, it could be a sign of a sleep disorder, such as narcolepsy and insomnia, or associated with temporal lobe epilepsy... Automatic Behavior :the spontaneous production of often purposeless verbal or motor behavior without conscious self-control or self-censorship. This condition can be observed in a variety of contexts, including schizophrenia, psychogenic fugue, complex partial seizure, epilepsy, narcolepsy or in response to a traumatic event. The individual does not recall the behavior... Nocturnal Myoclonus :Periodic Limb Movement Disorder (PLMD), also called nocturnal myoclonus, is a sleep disorder where the patient moves limbs involuntarily during sleep and has symptoms or problems related to the movement... Approximately 80-90% of people with Restless Leg Syndrome (RLS) also have PLMD, Periodic Limb Movement Disorder, which causes slow "jerks" or flexions of the affected body part. These occur during sleep (PLMS = Periodic Limb Movement while Sleeping) or while awake (PLMW - Periodic Limb Movement while Waking)... Delayed Sleep Phase Syndrome :a chronic disorder of sleep timing. People with DSPS tend to fall asleep at very late times, and also have difficulty waking up in the morning...People with DSPS tend to be extreme night owls. They feel most alert and say they function best and are most creative in the evening and at night. DSPS patients cannot simply force themselves to sleep early...There have been a few cases of DSPS developing into non 24-hour sleep-wake syndrome, a more severe and debilitating disorder in which the individual sleeps later each day... Non-24-Hour Sleep-Wake Syndrome :In people with this disorder, the person's body essentially insists that the day is longer than 24 hours. This tends to not allow socially accepted sleeping patterns, and makes it difficult for the sufferer to sleep at "normal" times...Left untreated, non-24-hour sleep-wake syndrome causes a person's sleep-wake cycle to change every day, the degree determined by how much over 24 hours the cycle lasts. The cycle may go around the clock, eventually returning to "normal" for one or two days before going "off" again...

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