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.
Original language | English (US) |
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Pages (from-to) | 137-140 |
Number of pages | 4 |
Journal | Practical Neurology |
Volume | 24 |
Issue number | 2 |
DOIs | |
State | Published - Nov 3 2023 |
Keywords
- MUSCLE DISEASE
- MYASTHENIA
- MYOPATHY
- NEUROPATHOLOGY, MUSCLE
ASJC Scopus subject areas
- Clinical Neurology