Erschienen in:
20.09.2020 | Commentary and Editorial
Mitochondrial disorder should be considered as a differential of late-onset myasthenia gravis
verfasst von:
J. Finsterer, F. A. Scorza, C. A. Scorza, A. C. Fiorini
Erschienen in:
Acta Neurologica Belgica
|
Ausgabe 6/2021
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Excerpt
With interest, we read the article by Oliveria et al. about a 93-year-old female with a 2 months history of generalised weakness, ptosis, double vision, dysarthria, dysphagia, neck pain, and hypophonia, being diagnosed as myasthenia gravis [
1]. The authors concluded that the outcome would be more favourable if the diagnosis would have been established earlier. The study has a number of shortcomings. …