Volume 17, Issue 1 pp. 95-96
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Mixed myoclonic-absence status epilepticus in juvenile myoclonic epilepsy

Philippe Gélisse

Corresponding Author

Philippe Gélisse

Epilepsy Unit, Hôpital Gui de Chauliac, Montpellier

Correspondence: Philippe Gélisse Epilepsy Unit, Hôpital Gui de Chauliac, 80 avenue Fliche, 34295 Montpellier cedex 05, France [email protected]Search for more papers by this author
Arielle Crespel

Arielle Crespel

Research Unit URCMA (Unité de recherche sur les comportements et mouvements anormaux), INSERM, U661 Montpellier, France

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First published: 13 April 2015
Citations: 12

Abstract

Myoclonic status epilepticus or mixed absence-myoclonic status is uncommon in juvenile myoclonic epilepsy (JME), often precipitated by sleep deprivation, withdrawal of medication, or inadequate antiepileptic drugs (Thomas et al., 2006; Crespel et al., 2013). Such episodes respond well to benzodiazepines or valproate (Crespel et al., 2013). We present the video-EEG of a 24-year-old woman with JME and bipolar disorder. She had a confusional state five days after withdrawal of clonazepam (14 mg/d) and introduction of oxazepam (200 mg/d), followed by catatonic stupor with subtle myoclonus of the face and the arms. The EEG showed absence status (figures 1, 2), which stopped after IV injection of clonazepam (1 mg) (figure 3). Consciousness returned to normal [Published with video sequence and figures].

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