Multiple system atrophy

This is a practical guide to diagnosing and managing multiple system atrophy (MSA). We explain the newly published Movement Disorders Society Consensus Diagnostic Criteria, which include new ‘Clinically Established MSA’ and ‘Possible Prodromal MSA’ categories, hopefully reducing time to diagnosis. W...

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Detalles Bibliográficos
Autores principales: Goh, Yee Yen, Saunders, Emma, Pavey, Samantha, Rushton, Emma, Quinn, Niall, Houlden, Henry, Chelban, Viorica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314081/
https://www.ncbi.nlm.nih.gov/pubmed/36927875
http://dx.doi.org/10.1136/pn-2020-002797
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author Goh, Yee Yen
Saunders, Emma
Pavey, Samantha
Rushton, Emma
Quinn, Niall
Houlden, Henry
Chelban, Viorica
author_facet Goh, Yee Yen
Saunders, Emma
Pavey, Samantha
Rushton, Emma
Quinn, Niall
Houlden, Henry
Chelban, Viorica
author_sort Goh, Yee Yen
collection PubMed
description This is a practical guide to diagnosing and managing multiple system atrophy (MSA). We explain the newly published Movement Disorders Society Consensus Diagnostic Criteria, which include new ‘Clinically Established MSA’ and ‘Possible Prodromal MSA’ categories, hopefully reducing time to diagnosis. We then highlight the key clinical features of MSA to aid diagnosis. We include a list of MSA mimics with suggested methods of differentiation from MSA. Lastly, we discuss practical symptom management in people living with MSA, including balancing side effects, with the ultimate aim of improving quality of life.
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spelling pubmed-103140812023-07-02 Multiple system atrophy Goh, Yee Yen Saunders, Emma Pavey, Samantha Rushton, Emma Quinn, Niall Houlden, Henry Chelban, Viorica Pract Neurol Review This is a practical guide to diagnosing and managing multiple system atrophy (MSA). We explain the newly published Movement Disorders Society Consensus Diagnostic Criteria, which include new ‘Clinically Established MSA’ and ‘Possible Prodromal MSA’ categories, hopefully reducing time to diagnosis. We then highlight the key clinical features of MSA to aid diagnosis. We include a list of MSA mimics with suggested methods of differentiation from MSA. Lastly, we discuss practical symptom management in people living with MSA, including balancing side effects, with the ultimate aim of improving quality of life. BMJ Publishing Group 2023-06 2023-03-16 /pmc/articles/PMC10314081/ /pubmed/36927875 http://dx.doi.org/10.1136/pn-2020-002797 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Goh, Yee Yen
Saunders, Emma
Pavey, Samantha
Rushton, Emma
Quinn, Niall
Houlden, Henry
Chelban, Viorica
Multiple system atrophy
title Multiple system atrophy
title_full Multiple system atrophy
title_fullStr Multiple system atrophy
title_full_unstemmed Multiple system atrophy
title_short Multiple system atrophy
title_sort multiple system atrophy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314081/
https://www.ncbi.nlm.nih.gov/pubmed/36927875
http://dx.doi.org/10.1136/pn-2020-002797
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