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Autor:
Gert W van Dijk, AAD VERRIPS, Michelle FM ten Brinck, Inge WH Verheijen, Jaron van de Wardt, Frouke AP Nijhuis
Publikováno v:
BMJ Neurology Open, Vol 5, Iss 2 (2023)
Background Lambert-Eaton myasthenic syndrome (LEMS) is a neuromuscular junction disorder and the clinical triad consists of proximal muscle weakness, autonomic symptoms and reduced tendon reflexes. Sluggish pupillary reflexes are common but dilated f
Externí odkaz:
https://doaj.org/article/17bac9f518344fb8b36fa0bf715ae593
