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Atypical Benign Partial Epilepsy of Childhood

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Atlas of Epilepsies

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Atypical benign partial epilepsy (ABPE) is an epileptic disorder characterized by seizures typical of benign childhood epilepsy with centrotemporal spikes (BCECTS), bilateral or segmental focal atonic seizures, and atypical absences. Awake EEG shows focal paroxysms resembling BCECTS associated with bursts of generalized paroxysms and with a marked activation of slow spike wave activity in non-REM sleep reproducing an “electric status epilepticus during sleep (ESES)” EEG pattern. This condition, firstly described by Aicardi and Chevrie (1982), was named ABPE because of the benign prognosis of epilepsy and cognitive function.

The term “pseudo-lennox syndrome” was also used because of the multiple daily falls occurring in these patients mimicking semiological findings of the Lennox-Gastaut syndrome (LGS). Persistent mental handicap after remission of epilepsy occur in 56% of patients. ABPE has been shown to present broad overlap with BCECTS, continuous spike-waves during...

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Abbreviations

BCECTS:

Benign Childhood Epilepsy with Centrotemporal Spikes

CSWS:

Continuous Spike-Waves During Sleep Syndrome

ENM:

Epileptic Negative Myoclonus

ESES:

Electric Status Epilepticus During Sleep

LGS:

Lennox-Gastaut Syndrome

LKS:

Landau-Kleffner Syndrome

MAE:

Myoclonic Astatic Epilepsy

References

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Gobbi, G., Grosso, S. (2010). Atypical Benign Partial Epilepsy of Childhood. In: Panayiotopoulos, C.P. (eds) Atlas of Epilepsies. Springer, London. https://doi.org/10.1007/978-1-84882-128-6_133

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  • DOI: https://doi.org/10.1007/978-1-84882-128-6_133

  • Publisher Name: Springer, London

  • Print ISBN: 978-1-84882-127-9

  • Online ISBN: 978-1-84882-128-6

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