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Generalized Myoclonic Seizures

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Atlas of Epilepsies
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Myoclonic seizures were elegantly described in the nineteenth century by prominent French, English, and German neurologists. The history is detailed in Inoue et al. (2008). During the latter part of the twentieth century, as pediatric epilepsy syndromes were delineated, it became apparent that myoclonic seizures could be found in both benign and severe settings. Generalized myoclonic seizures are covered in this section, but the term generalized does not necessarily imply total body involvement. Rather, the myoclonic activity may be limited to just certain regions, such as proximal limbs or trunk in a more or less symmetric fashion.

Definition

The ILAE glossary defines myoclonus as “sudden brief (<100 ms) involuntary single or multiple contraction(s) of muscle(s) or muscle group of variable topography (axial, proximal limb, distal)” (Blume et al. 2001).

Classification

Myoclonic seizures may be focal or generalized. This section focuses on generalized myoclonic seizures.

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References

  • Blume WT, Luders HO et al. (2001) Glossary of descriptive terminology for ictal semiology: report of the ILAE task force on classification and terminology. Epilepsia 42(9):1212–1218

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  • Inoue Y, Terada K et al. (2008) Generalized myoclonic seizures and negative myoclonus. In: Engel J Jr, Pedley TA (eds) Epilepsy: a comprehensive textbook, vol 1Lippincott Williams & Wilkins, Philadelphia, pp 585–599

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Nordli, D.R. (2010). Generalized Myoclonic Seizures. In: Panayiotopoulos, C.P. (eds) Atlas of Epilepsies. Springer, London. https://doi.org/10.1007/978-1-84882-128-6_51

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  • DOI: https://doi.org/10.1007/978-1-84882-128-6_51

  • Publisher Name: Springer, London

  • Print ISBN: 978-1-84882-127-9

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