Literature DB >> 2081683

Familial spastic paraplegia with peroneal amyotrophy. A family with hypersensitivity to pyrexia.

M Serena1, N Rizzuto, G Moretto, G Arrigoni.   

Abstract

We describe 4 siblings with spastic paraparesis and peroneal amyotrophy who were prone to severe pain and painful dysesthesias, tetraparesis and pyramidal signs during pyrexial episodes of variable etiology. These symptoms cleared almost completely in 10-20 days. Nerve conduction velocity was reduced more markedly during the spells of fever. Muscle biopsy specimen was normal. Some transient functional disturbance of membrane equilibrium of the nervous pathways of both central and peripheral nervous systems was probably responsible for the attacks during pyrexial episodes.

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Year:  1990        PMID: 2081683     DOI: 10.1007/BF02337442

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  13 in total

1.  Hereditary (familial) spastic paraplegia.

Authors:  G A SCHWARZ
Journal:  AMA Arch Neurol Psychiatry       Date:  1952-11

2.  Strümpell's familial spastic paraplegia: genetics and neuropathology.

Authors:  W M Behan; M Maia
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-01       Impact factor: 10.154

3.  Classification of the hereditary ataxias and paraplegias.

Authors:  A E Harding
Journal:  Lancet       Date:  1983-05-21       Impact factor: 79.321

4.  Peroneal muscular atrophy with pyramidal features.

Authors:  A E Harding; P K Thomas
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-02       Impact factor: 10.154

5.  A study of posterior column function in familial spastic paraplegia.

Authors:  M R Dimitrijevic; J A Lenman; T Prevec; K Wheatly
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-01       Impact factor: 10.154

6.  The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting.

Authors:  H E Cross; V A McKusick
Journal:  Arch Neurol       Date:  1967-05

7.  Autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Authors:  J P Bouchard; A Barbeau; R Bouchard; R W Bouchard
Journal:  Can J Neurol Sci       Date:  1978-02       Impact factor: 2.104

8.  Myopathy with multiple central cores. A case with hypersensitivity to pyrexia.

Authors:  N Gadoth; D Margalit; Y Shapira
Journal:  Neuropadiatrie       Date:  1978-08

9.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06

10.  Strümpell's familial spastic paraplegia: an electrophysiological demonstration of selective central distal axonopathy.

Authors:  A Uncini; M Treviso; M Basciani; D Gambi
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1987-02
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  1 in total

1.  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

  1 in total

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