Literature DB >> 6305662

Leber's disease with spastic paraplegia and peripheral neuropathy. Case report with nerve biopsy study.

M Pagès, A M Pagès.   

Abstract

A 43-year-old patient with familial Leber's optic atrophy suffered from spastic paraplegia. Physical examination disclosed cerebellar and pyramidal signs and signs of peripheral neuropathy. On sural nerve biopsy, there were few large myelinated fibers, signs of axonal degeneration and thin myelin sheets. This case suggests an overlap syndrome with central and peripheral nervous system features of Leber's disease, spinocerebellar degeneration and peroneal muscular atrophy.

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Year:  1983        PMID: 6305662     DOI: 10.1159/000115557

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  3 in total

1.  Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).

Authors:  C Weiller; A Ferbert
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

2.  Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy.

Authors:  A Federico; L Manneschi; M Meloni; C Alessandrini; A M Bardelli; M T Dotti; P Sabatelli
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous. Report of nerve biopsy in four cases and review of the literature.

Authors:  F Gemignani; D Guidetti; P Bizzi; P Preda; G Cenacchi; A Marbini
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

  3 in total

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