Scientific article
English

"Gourmand syndrome" in a child with pharmacoresistant epilepsy

Published in

Epilepsy & behavior, vol. 13, no. 2, p. 413-415

Publication date

2008

Abstract

We report the case of a 10-year-old boy with pharmacoresistant epilepsy, symptomatic of a right temporoparietal hemorrhagic lesion, who displayed an eating passion as described for the gourmand syndrome (GS) in adults and discuss the role of epilepsy in GS. This patient presented with a significant change in his eating habits (abnormal preoccupation with the preparation and eating of fine-quality food) concordant with the onset of his seizure disorder, without any previous history of eating disorders or psychiatric illness. This observation corroborates the important role of the right cerebral hemisphere in disturbed eating habits, including the relatively benign GS, and, possibly rarely, in less benign eating disorders such as anorexia and obesity.

Keywords

  • Anticonvulsants/therapeutic use
  • Appetite/physiology
  • Cerebral Hemorrhage/complications/physiopathology
  • Child
  • Dominance, Cerebral/physiology
  • Drug Resistance
  • Eating Disorders/diagnosis/drug therapy/physiopathology
  • Epilepsy/diagnosis/drug therapy/physiopathology
  • Feeding Behavior/physiology
  • Humans
  • Male
  • Neuropsychological Tests
  • Parietal Lobe/physiopathology
  • Temporal Lobe/physiopathology

UNIGE research groups

Citation (ISO format)

KURIAN, M. et al. ‘Gourmand syndrome’ in a child with pharmacoresistant epilepsy. In: Epilepsy & behavior, 2008, vol. 13, n° 2, p. 413–415. doi: 10.1016/j.yebeh.2008.04.004

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Article (Accepted version)

Identifiers

Journal ISSN

1525-5050
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Technical informations

Creation

11/03/2009 09:03:00

First validation

11/03/2009 09:03:00

Update

14/03/2023 15:03:14

Status update

14/03/2023 15:03:14

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