Sleep Medicine
Volume 11, Issue 6 , Pages 591-594 , June 2010

Pseudocataplexy in narcolepsy with cataplexy

  • Giuseppe Plazzi

      Affiliations

    • Department of Neurological Sciences, University of Bologna, Bologna, Italy
    • Corresponding Author InformationCorrespondence to: G. Plazzi, Sleep Disorders Center, Department of Neurological Sciences. University of Bologna, Via Ugo Foscolo, 7 - 40123 Bologna, Italy. Tel.: +39 051 2092926; fax: +39 051 2092963.
  • ,
  • Ramin Khatami

      Affiliations

    • Department of Neurology, University Hospital of Zurich, Zurich, Switzerland
  • ,
  • Leonardo Serra

      Affiliations

    • Department of Neurological Sciences, University of Bologna, Bologna, Italy
  • ,
  • Fabio Pizza

      Affiliations

    • Department of Neurological Sciences, University of Bologna, Bologna, Italy
  • ,
  • Claudio L. Bassetti

      Affiliations

    • Department of Neurology, University Hospital of Zurich, Zurich, Switzerland
    • Department of Neurology, Neurocenter (EOC) of Southern Switzerland, Lugano, Switzerland
    • Corresponding Author InformationCorresponding author at: Department of Neurology, UniversistätsSpital Zürich, Frauenklinikstrasse 26, 8091 Zürich, Switzerland. Tel.: +41 044 2555503; fax: +41 044 2554649, Neurology Department, Ospedale Civico, Via Tesserete 46, 6903 Lugano, Switzerland. Tel.: +41 91 811 6658; fax: +41 91 811 6915.

Received 15 December 2009 ,Revised 9 March 2010 ,Accepted 25 March 2010.

Title About Type File Size
Supplementary Video

Segment 1. (Patient 1) Cataplectic attack. While joking and being tickled by her mother, initially there was a transient decrease in cephalic muscle tone accompanied by a slight head nodding, the patient stopped laughing, had sudden loss of knee strength, and 2s later she also lost strength in her arms and trunk, falling to the mat a second later. Ten seconds later, after verbal stimulus from the examiner, the patient started to show initial recovery signs, gradually regaining her muscle tone starting distally, being able to obey orders, eventually sitting up and finally regaining speech (full recovery). The episode lasted a total of 37s. There were no evident positive motor phenomena or EEG abnormalities. Segment 2. (Patient 1) Pseudocataplectic attack. While talking to her mother she gradually and slightly intermittently buckled her knees and fell forward ending supported by her hands and forehead. Initially she did not speak, but after 16s she started crying, and she was capable of verbal response. The episode lasted a total of 37s. There were no positive motor phenomena or EEG abnormalities. This was one of the atypical episodes, as identified by the mother. Segment 3. (Patient 2) Pseudocataplectic attack. The video documentation was part of an experiment to assess emotional modulation of startle reflex in NC. A strong startle reaction was triggered by a loud tone and induced anxious feelings in that patient. Segment 4. (Patient 2) While reporting his emotional reaction to the examiner the patient suddenly reclined, his right arm remained flexed to support his head. When the arm was stretched out by the examiner the patient’s head did not drop. His eyes were closed and he remained conscious throughout the episode. He could not speak, but was able to communicate by uttering noises and nodding or shaking his head. He could not move his arms, open his eyes or speak out loud on command. Slight voluntary movements of the left index finger could be observed. After 50s speech improved and the patient could describe that muscle weakness was gradually resolving. Five seconds later he could open his eyes and after 7s he was able to raise his arms.

	Video
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PII: S1389-9457(10)00148-6

doi: 10.1016/j.sleep.2010.03.004

Sleep Medicine
Volume 11, Issue 6 , Pages 591-594 , June 2010