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Acquired neuromyotonia following upper respiratory tract infection: a case report

We present a 37-year-old male subject who presented with burning sensations in his hands and feet with generalised twitching of his limbs, trunk and face. His symptoms developed 2 weeks after an upper respiratory tract infection. There was associated facial flushing and disturbed night sleep but no...

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Detalles Bibliográficos
Autores principales: Imam, Ibrahim, Edwards, Simon, Hanemann, C Oliver
Formato: Texto
Lenguaje:English
Publicado: Cases Network Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769391/
https://www.ncbi.nlm.nih.gov/pubmed/19918441
http://dx.doi.org/10.4076/1757-1626-2-7952
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author Imam, Ibrahim
Edwards, Simon
Hanemann, C Oliver
author_facet Imam, Ibrahim
Edwards, Simon
Hanemann, C Oliver
author_sort Imam, Ibrahim
collection PubMed
description We present a 37-year-old male subject who presented with burning sensations in his hands and feet with generalised twitching of his limbs, trunk and face. His symptoms developed 2 weeks after an upper respiratory tract infection. There was associated facial flushing and disturbed night sleep but no memory impairment or generalised sweating. Examination showed generalised myokymia and fasciculations and electromyography revealed widespread continuous semi-rhythmic doublets and triplets of low frequency with interspersed silent periods. Anti voltage gated potassium channel antibodies, antinuclear antibodies, anti-acetylcholine receptor antibodies and the anti-neuronal antibodies anti Hu, anti Yo and anti Ri were all negative. His symptoms improved slightly on lamotrigine and amitriptyline.
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spelling pubmed-27693912009-11-16 Acquired neuromyotonia following upper respiratory tract infection: a case report Imam, Ibrahim Edwards, Simon Hanemann, C Oliver Cases J Case report We present a 37-year-old male subject who presented with burning sensations in his hands and feet with generalised twitching of his limbs, trunk and face. His symptoms developed 2 weeks after an upper respiratory tract infection. There was associated facial flushing and disturbed night sleep but no memory impairment or generalised sweating. Examination showed generalised myokymia and fasciculations and electromyography revealed widespread continuous semi-rhythmic doublets and triplets of low frequency with interspersed silent periods. Anti voltage gated potassium channel antibodies, antinuclear antibodies, anti-acetylcholine receptor antibodies and the anti-neuronal antibodies anti Hu, anti Yo and anti Ri were all negative. His symptoms improved slightly on lamotrigine and amitriptyline. Cases Network Ltd 2009-09-08 /pmc/articles/PMC2769391/ /pubmed/19918441 http://dx.doi.org/10.4076/1757-1626-2-7952 Text en © 2009 Imam et al.; licensee Cases Network Ltd. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Imam, Ibrahim
Edwards, Simon
Hanemann, C Oliver
Acquired neuromyotonia following upper respiratory tract infection: a case report
title Acquired neuromyotonia following upper respiratory tract infection: a case report
title_full Acquired neuromyotonia following upper respiratory tract infection: a case report
title_fullStr Acquired neuromyotonia following upper respiratory tract infection: a case report
title_full_unstemmed Acquired neuromyotonia following upper respiratory tract infection: a case report
title_short Acquired neuromyotonia following upper respiratory tract infection: a case report
title_sort acquired neuromyotonia following upper respiratory tract infection: a case report
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769391/
https://www.ncbi.nlm.nih.gov/pubmed/19918441
http://dx.doi.org/10.4076/1757-1626-2-7952
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