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  • Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy

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Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy

Authors

  • Menatalla Elwan Department of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Andrew M Schaefer Department of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne, UKWellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK PubMed articlesGoogle scholar articles
  • Kate Craig Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK PubMed articlesGoogle scholar articles
  • Sila Hopton Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK PubMed articlesGoogle scholar articles
  • Gavin Falkous Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK PubMed articlesGoogle scholar articles
  • Emma L Blakely Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK PubMed articlesGoogle scholar articles
  • Robert W Taylor Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UKNHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle University, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Naomi Warren Department of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Naomi Warren; naomiwarren{at}nhs.net
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Citation

Elwan M, Schaefer AM, Craig K, et al
Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy
BMJ Neurology Open 2022;4:e000352. doi: 10.1136/bmjno-2022-000352

Publication history

  • Accepted November 22, 2022
  • First published December 8, 2022.
Online issue publication 
December 08, 2022

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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.