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

作者信息

Serena M, Rizzuto N, Moretto G, Arrigoni G

机构信息

Ospedale Civile di Treviso.

出版信息

Ital J Neurol Sci. 1990 Dec;11(6):583-8. doi: 10.1007/BF02337442.

DOI:10.1007/BF02337442
PMID:2081683
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.

摘要

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引用本文的文献

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.伴有遗传性痉挛性截瘫的腓骨肌萎缩症(遗传性运动感觉神经病V型)在病理上具有异质性。4例神经活检报告及文献综述。
Acta Neuropathol. 1992;83(2):196-201. doi: 10.1007/BF00308479.

本文引用的文献

1
Hereditary (familial) spastic paraplegia.遗传性(家族性)痉挛性截瘫。
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A study of posterior column function in familial spastic paraplegia.家族性痉挛性截瘫后柱功能的研究
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Peroneal muscular atrophy with pyramidal features.伴有锥体束征的腓骨肌萎缩症
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The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting.特罗耶综合征。一种伴有远端肌肉萎缩的隐性痉挛性截瘫形式。
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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.伴有腓骨肌萎缩的下运动神经元和初级感觉神经元疾病。II. 各种神经元变性的神经学、遗传学和电生理发现。
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Strümpell's familial spastic paraplegia: an electrophysiological demonstration of selective central distal axonopathy.施特吕姆佩尔家族性痉挛性截瘫:选择性中枢性远端轴索性神经病的电生理证明
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Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves.腓骨肌萎缩症(PMA)及相关疾病。II. 腓肠神经的组织学发现
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay.夏尔沃-萨格奈常染色体隐性遗传性痉挛性共济失调
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