Article Text
Statistics from Altmetric.com
As non-neurophysiologists we enjoyed this informative review of electromyography (EMG), and benefit enormously from the service provided by our local colleagues. We suggest, however, that EMG is neither ‘essential’ nor ‘diagnostic’ for motor neurone disease (MND). Rather, for at least the 85% of cases with classical amyotrophic lateral sclerosis, MND is a clinical diagnosis.
The average delay in diagnosis of MND from the onset of symptoms has stubbornly remained around 1 year over the last two decades.1 Over-reliance on investigations, including neurophysiology, excluding implausible mimic conditions may be a contributory factor. The first …
Footnotes
Response to: Whittaker RG. The fundamentals of electromyography. Pract Neurol 2012;12:187–94
-
Contributors MRT drafted the letter and KT edited the letter.
-
Funding Medical Research Council & Motor Neurone Disease Association UK Lady Edith Wolfson Fellowship.
-
Competing interests None.
-
Provenance and peer review Not commissioned; externally peer reviewed.
Read the full text or download the PDF:
Other content recommended for you
- An evaluation of neurophysiological criteria used in the diagnosis of motor neuron disease
- Mimics and chameleons in motor neurone disease
- A rapidly progressive neuropathy
- Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study
- Outcome of ventilatory support for acute respiratory failure in motor neurone disease
- Cause of death and clinical grading criteria in a cohort of amyotrophic lateral sclerosis cases undergoing autopsy from the Scottish Motor Neurone Disease Register
- Motor neuron disease
- Advances in molecular pathology, diagnosis, and treatment of amyotrophic lateral sclerosis
- Motor neuron disease mimics in practice: a case series
- Structural MRI reveals cortical thinning in amyotrophic lateral sclerosis