Abstract |
Tubular aggregate myopathies comprise a rare group of disorders with characteristic pathological findings and heterogeneous phenotypes, including myasthenic syndrome. We describe a patient with tubular aggregate myopathy who presented with fatiguable weakness improving with pyridostigmine, respiratory involvement and possible cardiac manifestations. We highlight the utility of muscle biopsy in atypical myasthenic syndrome.
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Authors | Qihua Fan, Kelly Gwathmey, Xinli Du, Arjun Seth, Andrea Corse |
Journal | Practical neurology
(Pract Neurol)
(Nov 03 2023)
ISSN: 1474-7766 [Electronic] England |
PMID | 37923376
(Publication Type: Journal Article)
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Copyright | © Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ. |