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Benign partial epilepsy of childhood: a longitudinal neuropsychological and EEG study of cognitive function

Published online by Cambridge University Press:  03 October 2000

Thierry Deonna
Affiliation:
Neuropaediatric Unit, Children's University Hospital and Clinical Neurophysiology Unit, Lausanne, Switzerland.
Pascal Zesiger
Affiliation:
Neuropaediatric Unit, Children's University Hospital and Clinical Neurophysiology Unit, Lausanne, Switzerland.
Veronique Davidoff
Affiliation:
Neuropaediatric Unit, Children's University Hospital and Clinical Neurophysiology Unit, Lausanne, Switzerland.
Malin Maeder
Affiliation:
Neuropaediatric Unit, Children's University Hospital and Clinical Neurophysiology Unit, Lausanne, Switzerland.
Claire Mayor
Affiliation:
Neuropaediatric Unit, Children's University Hospital and Clinical Neurophysiology Unit, Lausanne, Switzerland.
Elaine Roulet
Affiliation:
Neuropaediatric Unit, Children's University Hospital and Clinical Neurophysiology Unit, Lausanne, Switzerland.
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Abstract

The study combined prospective neuropsychological and EEG results of 22 children presenting with typical benign partial epilepsy with rolandic spikes (19 participants) and occipital spikes (three participants). The aims were to assess the types of cognitive problems which may be encountered in this population, to evaluate the course of cognitive and learning capacities during the active phase of epilepsy, and to see if there was a correlation with paroxysmal activity on the EEG. Average age at entry in the study was 8.4 years and each child was seen 2 to 4 times over a period of 1 to 3 years. EEGs showed persistent spike foci in most cases that worsened in three cases, but there were no continuous spike–waves during sleep. No child had persistent stagnation, marked fluctuations, or a regression in cognitive abilities. Of 22 children, 21 had average IQ (>80). Eight children had school difficulties requiring special adjustment. No single cognitive profile was identified. Four children had delayed language development and eight children had transient weak scores in one isolated domain (verbal, visuospatial, memory) which improved or normalized during the course of the study with concomitant EEG improvement or normalization. In two of the three children with aggravation of the paroxysmal EEG activity, clinical changes were documented. A proportion of children with typical benign partial epilepsy with rolandic spikes showed mild, varied, and transient cognitive difficulties during the course of their epilepsy and in most cases this probably had a direct relation with the paroxysmal EEG activity.

Type
Original Articles
Copyright
© 2000 Mac Keith Press

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