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Severe progression of a young-onset non-paraneoplastic Lambert-Eaton myasthenic syndrome.
Acta Neurol Belg
October 2024
Serviço de Neurologia, Departamento de Neurociências e de Saúde Mental, Unidade Local de Saúde de Santa Maria, Lisboa, Portugal.
Article Synopsis
- * A case report details a 21-year-old woman with LEMS who initially improved with treatment but developed psychotic symptoms leading to steroid discontinuation and later experienced worsening health, including respiratory distress and difficulties with swallowing.
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Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy.
Neurol Sci
December 2024
Neurodegeneration Research Laboratory, NDAL-KUTTAM, School of Medicine, Suna and Inan Kıraç Foundation, Koc University, Istanbul, Turkey.
Fatigue and associated factors in myasthenia gravis: a nationwide registry study.
J Neurol
August 2024
Department of Neurology with Institute of Translational Neurology, University Hospital Münster, 48149, Münster, Germany.
Fatigue is commonly associated with myasthenia gravis (MG), but factors contributing to fatigue development in MG are incompletely understood. This nationwide cross-sectional registry study included 1464 patients diagnosed with autoimmune MG, recruited between February 2019 and April 2023. Frequency and severity of fatigue was assessed at study inclusion using the patient-reported Chalder Fatigue Questionnaire (CFQ).
View Article and Find Full Text PDFEfgartigimod infusion in the treatment regimen for myasthenic crisis: A case report.
Muscle Nerve
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Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Myasthenic crises are associated with negative long-term outcomes in myasthenia gravis.
J Neurol
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Department of Neurology, Justus Liebig University, Klinikstrasse 33, 35392, Giessen, Germany.
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