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Mimics and chameleons in motor neurone disease

The progression of motor neurone disease (MND) is currently irreversible, and the grave implications of diagnosis naturally fuels concern among neurologists over missing a potential mimic disorder. There is no diagnostic test for MND but in reality there are few plausible mimics in routine clinical...

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Autores principales: Turner, Martin R, Talbot, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664389/
https://www.ncbi.nlm.nih.gov/pubmed/23616620
http://dx.doi.org/10.1136/practneurol-2013-000557
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author Turner, Martin R
Talbot, Kevin
author_facet Turner, Martin R
Talbot, Kevin
author_sort Turner, Martin R
collection PubMed
description The progression of motor neurone disease (MND) is currently irreversible, and the grave implications of diagnosis naturally fuels concern among neurologists over missing a potential mimic disorder. There is no diagnostic test for MND but in reality there are few plausible mimics in routine clinical practice. In the presence of a progressive pure motor disorder, signs such as florid fasciculations, bilateral tongue wasting, the ‘split hand’, head drop, emotionality, and cognitive or behavioural impairment carry high positive predictive value. MND is clinically heterogeneous, however, with some important chameleon-like presentations and considerable variation in clinical course. Lack of confidence about the scope of such variation, or an approach to diagnosis emphasising investigations over clinical common sense, has the potential to exacerbate diagnostic delay in MND and impede timely planning of the care which is essential to maximising quality of life.
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spelling pubmed-36643892013-05-31 Mimics and chameleons in motor neurone disease Turner, Martin R Talbot, Kevin Pract Neurol Reviews The progression of motor neurone disease (MND) is currently irreversible, and the grave implications of diagnosis naturally fuels concern among neurologists over missing a potential mimic disorder. There is no diagnostic test for MND but in reality there are few plausible mimics in routine clinical practice. In the presence of a progressive pure motor disorder, signs such as florid fasciculations, bilateral tongue wasting, the ‘split hand’, head drop, emotionality, and cognitive or behavioural impairment carry high positive predictive value. MND is clinically heterogeneous, however, with some important chameleon-like presentations and considerable variation in clinical course. Lack of confidence about the scope of such variation, or an approach to diagnosis emphasising investigations over clinical common sense, has the potential to exacerbate diagnostic delay in MND and impede timely planning of the care which is essential to maximising quality of life. BMJ Publishing Group 2013-06 /pmc/articles/PMC3664389/ /pubmed/23616620 http://dx.doi.org/10.1136/practneurol-2013-000557 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/3.0/ and http://creativecommons.org/licenses/by-nc/3.0/legalcode
spellingShingle Reviews
Turner, Martin R
Talbot, Kevin
Mimics and chameleons in motor neurone disease
title Mimics and chameleons in motor neurone disease
title_full Mimics and chameleons in motor neurone disease
title_fullStr Mimics and chameleons in motor neurone disease
title_full_unstemmed Mimics and chameleons in motor neurone disease
title_short Mimics and chameleons in motor neurone disease
title_sort mimics and chameleons in motor neurone disease
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664389/
https://www.ncbi.nlm.nih.gov/pubmed/23616620
http://dx.doi.org/10.1136/practneurol-2013-000557
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