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A part of "Essential Concepts for the R.EEG.T Exam" – Includes Tables, Diagrams, and Illustrations. Table of contents: 44 pages - Filters, time constant. common mode rejection and digital EEG setting parameters - Montages - Normal varients - Artifacts - Increasing beta/fast activities - N2 sleep and Arousal pattern - Pediatric EEG and syndrome by age group - Neonatal sleep wake pattern - Pediatric epilepsy syndrome by interictal pattern - Differential of sleep provoked seizure - Photic stimulation - Hyperventilation - Lateralization - Severity of encephalopathy and EEG pattern - Rhythmic delta - Clinical seizure correlate with EEG - Seizure semiology s
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Episode during NREM Continuous Spikes and Waves during Slow-Wave Sleep (CSWS) Disorder of arousal (Confusion arousal, Night terror, Somnambulism) Nocturna l Frontal Lobe Epilepsy (NFLE) Ictal scalp EEG Continuous spike-wave discharges: if SWI >85% of NREM is called Electrical Status Epilepticus in Sleep ( ESES ). It is sleeping disorder not seizure: Normal EEG but increase autonomic -EKG, respiratory rate Most are normal or rarely frontal SWs which obscured with muscle artifacts Clinical corelate Subtle (Electrographic seizure) Impair cognitive esp. declarative memory Landau-Kleffner Syndrome (LKS) is language deficit subtype Confusion arousal: minimal, cause confusion during episode and day- time sleepiness Night terror: fear Somnambulism: complex motor ie walking, eating Mimic presentation of arousal disorder but last shorter than few minutes. Day-time sleepiness from disrupted sleep. Family History + ++ +++ (AD) Prognosis ESES peak at age 4-8 and remit at age 8-12 : seizure subside along with ESES but cognitive impair remained Peak in childhood 4-12 and most are resolved when growing up Onset any age up to 20s life-long but not progress. Rx -Carbamazepine: target Ach receptor mutation.