Literature DB >> 12365065

Fibrillation and sharp-waves: do we need them to diagnose ALS?

M de Carvalho1, C Bentes, T Evangelista, M L Luís.   

Abstract

BACKGROUND: Fibrillation/sharp-waves (fibs-sw) are considered an essential neurophysiological marker in Amyotrophic Lateral Sclerosis (ALS). We investigated how frequently an initial electrophysiological (EMG) evaluation, performed in ALS patients, revealed no fibs-sw.
METHODS: The initial EMG studies from 68 ALS patients were analysed. The presence of fibs-sw in at least two muscles of each limb and two cranial-innervated muscles was assessed.
RESULTS: We observed no fibs-sw in cranial-innervated muscles, and 7/15 bulbar-onset patients had no fibs-sw in limb muscles. Two of 28 upper-limb-onset patients, who had a short history before EMG, showed no fibs-sw. All lower-limb-onset patients had fibs-sw. Generally patients with no fibs-sw had diffuse abundant fasciculations.
CONCLUSIONS: The absence of fibs-sw should not necessarily preclude the neurophysiological diagnosis of ALS in bulbar-onset patients. Early affected upper-limb-onset patients might show no fibs-sw, but profuse fasciculations associated with mild to moderate denervation-reinnervation in weak muscles are found.

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Mesh:

Year:  1999        PMID: 12365065     DOI: 10.1080/146608299300079501

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord        ISSN: 1466-0822


  2 in total

1.  Corticomotoneuronal function and hyperexcitability in acquired neuromyotonia.

Authors:  Steve Vucic; Benjamin C Cheah; Con Yiannikas; Angela Vincent; Matthew C Kiernan
Journal:  Brain       Date:  2010-08-23       Impact factor: 13.501

2.  Mimicking Amyotrophic Lateral Sclerosis: A Case of a Spinal Dural Arteriovenous Fistula.

Authors:  Mónica Santos; Sofia Reimão; Mamede de Carvalho
Journal:  Case Rep Neurol       Date:  2021-12-27
  2 in total

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