Hyperventilation will often reproduce the event

(( Absence seizures)): generalized seizures , manifest as brief staring spells, sometimes with automatisms.
:point_right:t2: onset age , commonly between 5 and 8 years , :bulb:may be overlooked for prolonged periods due to their very brief duration.
:point_right:t2:Hyperventilation will often reproduce the event.
:point_right:t2:Diagnosis is by characteristic 3 Hz spike-and-slow-wave complexes on the EEG.

:brain::brain: ((Myoclonic seizures)):
:point_right:t2:vary in prognosis and neurodevelopmental outcome.
:point_right:t2:Infantile spasms are the most serious variant.
:point_right:t2:Symptoms commonly begin between 4 and 7 months of age with clusters of rapid ”jackknifing” contractions of the neck, trunk, and limbs followed by a brief sustained tonic contraction.
:point_right:t2:Hypsarrhythmia is the characteristic finding on EEG.
:point_right:t2:EEG is necessary to distinguish infantile spasms from 1⃣benign myoclonus of infancy (a benign involuntary movement) and 2⃣a myoclonic epilepsy (which vary in severity and outcome).

:brain::brain:(( Epileptic spasms )):(which includes infantile spasms) are classified as an unknown seizure type because they do not fit well into the generalized or focal subsets.

:brain::brain: ((alternating hemiplegia of childhood)): Intermittent episodes of hemiplegia (which may alternate between sides of the body) .
:point_right:t2:Onset : infancy , attacks are flaccid in young infants and more dystonic in older ones.
:point_right:t2:Episodes range from minutes to weeks.
:point_right:t2:Other involuntary movements, nystagmus, or autonomic disturbances may accompany the episodes.

:brain::brain:((Benign paroxysmal vertigo )) : commonly occurs in toddlers.
:point_right:t2:Children experience brief episodes of sudden imbalance. frightened by the episodes and fall to the floor, refusing to stand or walk.
:point_right:t2:Consciousness and speech are preserved.
:point_right:t2:Nystagmus is usually evident.
:point_right:t2:Neurologic evaluation (including imaging and EEG) is normal, except for abnormal vestibular function noted on ice water caloric testing.
:point_right:t2: considered a migraine variant and a likely precursor to migraine headaches.

:brain::brain:((spasmus nutans )) :Paroxysmal head-nodding, torticollis (head tilt), and nystagmus
:point_right:t2:consciousness is preserved.
:point_right:t2:Onset : first few months of life , resolves by 5 years.
:point_right:t2:Neuroimaging recommended to rule out tumors.

:brain::brain: Repetitive purposeless movements are exhibited by autistic or handicapped children,in environments with a low level of stimulation.may be difficult to distinguish clinically from seizure activity.
:brain::brain:Syncopal convulsions may be self-induced by performing the Valsalva maneuver.
:brain::brain:Masturbation in young children also mistaken as seizures by parents.

:brain::brain: ((Involuntary movements)) : occur as isolated entities or as a component of more complex movement disorders;
:point_right:t2:chorea, dystonia, hypokinesia, myoclonus are examples.

:point_right:t2:Tics and stereotypic movements described as involuntary movements even though affected individuals may have some ability to suppress those motions.

:point_right:t2:Some electroclinical (epilepsy) syndromes are characterized by both seizures and involuntary movements,
:point_right:t2: movement disorders alone can be difficult to distinguish from seizures when manifest as abrupt or paroxysmal involuntary movements.
:point_right:t2: movement disorders1⃣ do not manifest during sleep, 2⃣more stereotypical than seizures, 3⃣not associated with loss of consciousness 4⃣ no abnormal EEG findings.

:brain::brain:((Benign childhood epilepsy with centrotemporal spikes)) : (previously called benign rolandic epilepsy)
:point_right:t2: presents as a brief hemifacial seizure (parents may describe the child’s face as “twisted”) awakens the child from sleep.
:point_right:t2:Generalization rarely.
:point_right:t2: Drooling and an inability to speak are common, :bulb: preserved consciousness
:point_right:t2: EEG :characteristic centrotemporal spikes.
:point_right:t2: Onset : 3 _13 years of age , resolution in adolescence.
:point_right:t2: family history often positive for epilepsy.

:brain::brain:(( Narcolepsy )) : recurrent short sleep attacks. often accompanied by cataplexy (a sudden collapse due to loss of muscle tone but with preserved consciousness)
:point_right:t2: induced by laughter, excitement, or startle.
:point_right:t2:Vivid hallucinations (e.g., visual, auditory, tactile) with transition to and from sleep; sleep paralysis may accompany them.
:point_right:t2:Disturbed nighttime sleep is common.

:brain::brain:((Night terrors)): sudden partial arousal from non-REM sleep,
:point_right:t2:occurring 2 hours after sleep onset,
:point_right:t2:accompanied by inconsolable screaming and crying.
:point_right:t2:occur mostly in preschoolers and early school-aged children.
:point_right:t2:Children appear awake but not recognize people , no memory of the event.
:point_right:t2:Confusional arousals are similar, less extreme events , more gradual onset, child is less likely to try to get out of bed.

:brain::brain:Rarely, prolonged episodes of hyperventilation may result in loss of consciousness and some seizure activity.