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Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing

BACKGROUND: Over the past decade increasing scientific progress in the field of autoantibody–mediated neurological diseases was achieved. Movement disorders are a frequent and often prominent feature in such diseases which are potentially treatable. MAIN BODY: Antibody-mediated movement disorders en...

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Autores principales: Gövert, Felix, Leypoldt, Frank, Junker, Ralf, Wandinger, Klaus-Peter, Deuschl, Günther, Bhatia, Kailash P., Balint, Bettina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650144/
https://www.ncbi.nlm.nih.gov/pubmed/33324912
http://dx.doi.org/10.1186/s42466-020-0053-x
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author Gövert, Felix
Leypoldt, Frank
Junker, Ralf
Wandinger, Klaus-Peter
Deuschl, Günther
Bhatia, Kailash P.
Balint, Bettina
author_facet Gövert, Felix
Leypoldt, Frank
Junker, Ralf
Wandinger, Klaus-Peter
Deuschl, Günther
Bhatia, Kailash P.
Balint, Bettina
author_sort Gövert, Felix
collection PubMed
description BACKGROUND: Over the past decade increasing scientific progress in the field of autoantibody–mediated neurological diseases was achieved. Movement disorders are a frequent and often prominent feature in such diseases which are potentially treatable. MAIN BODY: Antibody-mediated movement disorders encompass a large clinical spectrum of diverse neurologic disorders occurring either in isolation or accompanying more complex autoimmune encephalopathic diseases. Since autoimmune movement disorders can easily be misdiagnosed as neurodegenerative or metabolic conditions, appropriate immunotherapy can be delayed or even missed. Recognition of typical clinical patterns is important to reach the correct diagnosis. CONCLUSION: There is a growing number of newly discovered antibodies which can cause movement disorders. Several antibodies can cause distinctive phenotypes of movement disorders which are important to be aware of. Early diagnosis is important because immunotherapy can result in major improvement. In this review article we summarize the current knowledge of autoimmune movement disorders from a point of view focused on clinical syndromes. We discuss associated clinical phenomenology and antineuronal antibodies together with alternative etiologies with the aim of providing a diagnostic framework for clinicians considering underlying autoimmunity in patients with movement disorders.
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spelling pubmed-76501442020-12-14 Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing Gövert, Felix Leypoldt, Frank Junker, Ralf Wandinger, Klaus-Peter Deuschl, Günther Bhatia, Kailash P. Balint, Bettina Neurol Res Pract Review BACKGROUND: Over the past decade increasing scientific progress in the field of autoantibody–mediated neurological diseases was achieved. Movement disorders are a frequent and often prominent feature in such diseases which are potentially treatable. MAIN BODY: Antibody-mediated movement disorders encompass a large clinical spectrum of diverse neurologic disorders occurring either in isolation or accompanying more complex autoimmune encephalopathic diseases. Since autoimmune movement disorders can easily be misdiagnosed as neurodegenerative or metabolic conditions, appropriate immunotherapy can be delayed or even missed. Recognition of typical clinical patterns is important to reach the correct diagnosis. CONCLUSION: There is a growing number of newly discovered antibodies which can cause movement disorders. Several antibodies can cause distinctive phenotypes of movement disorders which are important to be aware of. Early diagnosis is important because immunotherapy can result in major improvement. In this review article we summarize the current knowledge of autoimmune movement disorders from a point of view focused on clinical syndromes. We discuss associated clinical phenomenology and antineuronal antibodies together with alternative etiologies with the aim of providing a diagnostic framework for clinicians considering underlying autoimmunity in patients with movement disorders. BioMed Central 2020-02-20 /pmc/articles/PMC7650144/ /pubmed/33324912 http://dx.doi.org/10.1186/s42466-020-0053-x Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Gövert, Felix
Leypoldt, Frank
Junker, Ralf
Wandinger, Klaus-Peter
Deuschl, Günther
Bhatia, Kailash P.
Balint, Bettina
Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
title Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
title_full Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
title_fullStr Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
title_full_unstemmed Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
title_short Antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
title_sort antibody-related movement disorders – a comprehensive review of phenotype-autoantibody correlations and a guide to testing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650144/
https://www.ncbi.nlm.nih.gov/pubmed/33324912
http://dx.doi.org/10.1186/s42466-020-0053-x
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