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This article is part of the supplement: 48th Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida .

Open AccessOral Presentation

Neuropsychological assessment of cerebellar malformation in Spina Bifida

Anja Vinck email, Ben Maassen, Reinier Mullaart and Jan Rotteveel

Interdisciplinary Child Neurology Centre 945, University Medical Centre St Radboud, Nijmegen, The Netherlands

author email corresponding author email

from 48th Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida
Dublin, Ireland. 23–26 June 2004

Cerebrospinal Fluid Research 2004, 1(Suppl 1):S7doi:10.1186/1743-8454-1-S1-S7

The electronic version of this abstract is the complete one and can be found online at: http://www.cerebrospinalfluidresearch.com/content/1/S1/S7

Published: 23 December 2004

Background

It is widely agreed that the typical cognitive profile of children with spina bifida is influenced by medical variables such as hydrocephalus, the height of the lesion and other physical complications [1]. However, very little is known about the specific contribution of the Arnold-Chiari malformation (ACM) in the information processing of these children. The aim of this study is to delineate in the cognitive profile the specific contribution of the ACM by comparing within a group of children with spina bifida among those with and without ACM.

Materials and Methods

Fifty-five children between 6 and 14 years of age were recruited from the spina bifida team of the Radboud University Nijmegen, Medical Centre. Of the whole group of children, those with a well documented presence or absence of ACM were included for further analysis (complete group). To eliminate the confounding influence of IQ a selection was made on the criteria of a total IQ of above 70 (non-retarded group). Table 1 presents the patient characteristics of the different subgroups. All children underwent a neuropsychological assessment which consisted of tests on a wide range of cognitive functions, comprising verbal, performal, and general intelligence, visuo-motor processing, selective and sustained attention, simultaneous and sequential memory, word fluency, and speed of information processing. To address the cerebellar cognitive functions, some tasks were included which are expected to measure cerebellar information processing [2,3].

Table 1. Patient characteristics

Results

Results reveal significant differences in information processing among the children with and those without ACM. In the complete group, children with ACM performed significantly worse on the following cognitive functions: perception, visual-motor integration, verbal functioning, sequential memory, (non)verbal speed, and arithmetics. For the non-retarded group the data reveals a different cognitive profile. In this group, children with ACM showed impairments on tasks which require perception, imprinting and verbal memory, and verbal fluency.

Discussion

In the complete group, a cognitive profile of strengths and weaknesses was found that resembles the one associated with hydrocephalus and spina bifida as presented in the literature. However, this typical cognitive profile was not found for the non-retarded group. The non-retarded ACM group showed impairments on cognitive tasks which are hypothesized to be mediated by the cerebellum and can be compared to cognitive deficits related to cerebellar pathology.

This study is part of the multidisciplinary research program 'Prognosis of Spina Bifida' of the Radboud University Nijmegen (The Netherlands).

References

  1. Wills KE: Neuropsychological functioning in children with Spina Bifida and/ or Hydrocephalus.

    J Clin Child Psychol 1993 , 22:247-265. OpenURL

  2. Leiner HC, Leiner AL, Dow RS: Cognitive and language functions of the human cerebellum [Review].

    Trends Neurosci 1993 , 16:444-447. PubMed Abstract | Publisher Full Text OpenURL

  3. Schmahmann JD, Sherman JC: The cerebellar cognitive affective syndrome.

    Brain 1998 , 121:561-579. PubMed Abstract | Publisher Full Text OpenURL

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