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Treatable Hyperkinetic Movement Disorders Not to Be Missed

Hyperkinetic movement disorders are characterized by the presence of abnormal involuntary movements, comprising most notably dystonia, chorea, myoclonus, and tremor. Possible causes are numerous, including autoimmune disorders, infections of the central nervous system, metabolic disturbances, geneti...

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Autores principales: Méneret, Aurélie, Garcin, Béatrice, Frismand, Solène, Lannuzel, Annie, Mariani, Louise-Laure, Roze, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671871/
https://www.ncbi.nlm.nih.gov/pubmed/34925200
http://dx.doi.org/10.3389/fneur.2021.659805
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author Méneret, Aurélie
Garcin, Béatrice
Frismand, Solène
Lannuzel, Annie
Mariani, Louise-Laure
Roze, Emmanuel
author_facet Méneret, Aurélie
Garcin, Béatrice
Frismand, Solène
Lannuzel, Annie
Mariani, Louise-Laure
Roze, Emmanuel
author_sort Méneret, Aurélie
collection PubMed
description Hyperkinetic movement disorders are characterized by the presence of abnormal involuntary movements, comprising most notably dystonia, chorea, myoclonus, and tremor. Possible causes are numerous, including autoimmune disorders, infections of the central nervous system, metabolic disturbances, genetic diseases, drug-related causes and functional disorders, making the diagnostic process difficult for clinicians. Some diagnoses may be delayed without serious consequences, but diagnosis delays may prove detrimental in treatable disorders, ranging from functional disabilities, as in dopa-responsive dystonia, to death, as in Whipple's disease. In this review, we focus on treatable disorders that may present with prominent hyperkinetic movement disorders.
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spelling pubmed-86718712021-12-16 Treatable Hyperkinetic Movement Disorders Not to Be Missed Méneret, Aurélie Garcin, Béatrice Frismand, Solène Lannuzel, Annie Mariani, Louise-Laure Roze, Emmanuel Front Neurol Neurology Hyperkinetic movement disorders are characterized by the presence of abnormal involuntary movements, comprising most notably dystonia, chorea, myoclonus, and tremor. Possible causes are numerous, including autoimmune disorders, infections of the central nervous system, metabolic disturbances, genetic diseases, drug-related causes and functional disorders, making the diagnostic process difficult for clinicians. Some diagnoses may be delayed without serious consequences, but diagnosis delays may prove detrimental in treatable disorders, ranging from functional disabilities, as in dopa-responsive dystonia, to death, as in Whipple's disease. In this review, we focus on treatable disorders that may present with prominent hyperkinetic movement disorders. Frontiers Media S.A. 2021-12-01 /pmc/articles/PMC8671871/ /pubmed/34925200 http://dx.doi.org/10.3389/fneur.2021.659805 Text en Copyright © 2021 Méneret, Garcin, Frismand, Lannuzel, Mariani and Roze. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Méneret, Aurélie
Garcin, Béatrice
Frismand, Solène
Lannuzel, Annie
Mariani, Louise-Laure
Roze, Emmanuel
Treatable Hyperkinetic Movement Disorders Not to Be Missed
title Treatable Hyperkinetic Movement Disorders Not to Be Missed
title_full Treatable Hyperkinetic Movement Disorders Not to Be Missed
title_fullStr Treatable Hyperkinetic Movement Disorders Not to Be Missed
title_full_unstemmed Treatable Hyperkinetic Movement Disorders Not to Be Missed
title_short Treatable Hyperkinetic Movement Disorders Not to Be Missed
title_sort treatable hyperkinetic movement disorders not to be missed
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671871/
https://www.ncbi.nlm.nih.gov/pubmed/34925200
http://dx.doi.org/10.3389/fneur.2021.659805
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