Study of multimodal evoked potentials in patients with type 1 Gaucher's disease

Anna Perretti, Giancarlo Parenti, Pietro Balbi, Luigi Titomanlio, Lucia Marcantonio, Mariangela Iapoce, Anna Rita Frascogna, Generoso Andria, Lucio Santoro

Research output: Contribution to journalArticle

Abstract

To detect early subclinical nervous dysfunction in Gaucher's disease type 1, we carried out motor, brainstem auditory, visual, and somatosensory evoked potentials in 17 patients with Gaucher's disease type 1. Central motor evoked potential abnormalities were found in nine patients (69.2%), consisting of an increased motor threshold in all, with prolonged central motor conduction time in two patients. Brainstem auditory evoked potentials were abnormal in five patients (31.2%), and the most frequent abnormality was a bilateral increased I-III interpeak latency. Visual evoked potentials showed a delayed latency of the P100 wave in four patients (25%). Somatosensory evoked potential abnormalities were found in three patients (18.7%), consisting of an increased N13-N20 interval in two patients and a not reproducible N13 wave in one patient. Our findings suggest that the multimodal evoked potential approach provides information about nervous subclinical damage in Gaucher's disease type 1; transcranial magnetic stimulation proved to be the most sensitive tool. Early detection of subclinical neurologic dysfunction can be useful in view of more effective therapeutic strategies.

Original languageEnglish
Pages (from-to)124-128
Number of pages5
JournalJournal of Child Neurology
Volume20
Issue number2
Publication statusPublished - Feb 2005

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health

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    Perretti, A., Parenti, G., Balbi, P., Titomanlio, L., Marcantonio, L., Iapoce, M., Frascogna, A. R., Andria, G., & Santoro, L. (2005). Study of multimodal evoked potentials in patients with type 1 Gaucher's disease. Journal of Child Neurology, 20(2), 124-128.