Literature DB >> 1865233

Multisystem involvement of the central nervous system in Strümpell's disease. A neurophysiological and neuropsychological study.

G Tedeschi1, S Allocca, A Di Costanzo, S Carlomagno, F Merla, V Petretta, A Toriello, G Tranchino, G Ambrosio, V Bonavita.   

Abstract

The multisystem involvement of the central nervous system (CNS) in familial spastic paraplegia (FSP) has not been fully investigated by means of complete neurophysiological and neuropsychological examinations. The classification which distinguishes pure and complicated forms of FSP, is based on clinical features and does not take into account the possibility that clinically silent lesions of the CNS can be identified by means of adequate tests. The study was intended to assess the subclinical and multisystem involvement of the CNS in a group of 11 patients affected by FSP, clinically distinguished in 7 pure forms and 4 complicated forms. Neurophysiological tests included saccadic eye movements analysis, visual and auditory brain stem evoked responses. Neuropsychological examination was devised by means of a special purpose mental deterioration battery. Our results, showing a high incidence of multisystemic subclinical involvement of the CNS, confirm and extend the concept that FSP is a multisystemic degenerative disease of the CNS, and that the existence of "pure" forms should be reconsidered.

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Year:  1991        PMID: 1865233     DOI: 10.1016/0022-510x(91)90284-e

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  6 in total

Review 1.  Hereditary spastic paraparesis: a review of new developments.

Authors:  C McDermott; K White; K Bushby; P Shaw
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-08       Impact factor: 10.154

2.  Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.

Authors:  J E Nielsen; K Krabbe; P Jennum; P Koefoed; L N Jensen; K Fenger; H Eiberg; L Hasholt; L Werdelin; S A Sørensen
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-01       Impact factor: 10.154

3.  A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.

Authors:  E Reid; A M Dearlove; M Rhodes; D C Rubinsztein
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

4.  Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.

Authors:  O Heinzlef; C Paternotte; F Mahieux; J F Prud'homme; J Dien; M Madigand; J Pouget; J Weissenbach; E Roullet; J Hazan
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

Review 5.  Hereditary spastic paraplegia.

Authors:  John K Fink
Journal:  Curr Neurol Neurosci Rep       Date:  2006-01       Impact factor: 5.081

6.  Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Authors:  L N Jensen; T Gerstenberg; E B Kallestrup; P Koefoed; J Nordling; J E Nielsen
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-11       Impact factor: 10.154

  6 in total

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