Literature DB >> 15794178

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

Anna Perretti1, Giancarlo Parenti, Pietro Balbi, Luigi Titomanlio, Lucia Marcantonio, Mariangela Iapoce, Anna Rita Frascogna, Generoso Andria, Lucio Santoro.   

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.

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Year:  2005        PMID: 15794178     DOI: 10.1177/08830738050200020801

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  3 in total

1.  Evoked potentials and neurocognitive functions in pediatric Egyptian Gaucher patients on enzyme replacement therapy: a single center experience.

Authors:  Azza Abdel Gawad Tantawy; Eman Mounir Sherif; Amira Abdel Moneam Adly; Sahar Hassanine; Amina Hafez Awad
Journal:  J Inherit Metab Dis       Date:  2013-03-19       Impact factor: 4.982

2.  Peripheral neural response and sex hormones in type 1 Gaucher disease.

Authors:  Milan B Lakočević; Mirjana M Platiša; Zorica R Šumarac; Nada D Suvajdžić; Lana Đ Mačukanović; Milan S Petakov
Journal:  J Med Biochem       Date:  2020-01-10       Impact factor: 3.402

3.  Analysis of glucocerebrosidase (GBA) gene mutations in Iranian patients with Gaucher disease.

Authors:  Hadi Mozafari; Mohammad Tghikhani; Zohreh Rahimi; Asad Vaisi Raygani; Shahla Ansari; Shohreh Khatami; Mohammad Reza Alaei; Reza Saghiri
Journal:  Iran J Child Neurol       Date:  2021
  3 in total

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