Book contents
- Neuromuscular Disease: A Case-Based Approach
- Neuromuscular Disease
- Copyright page
- Contents
- Contributors
- Foreword
- Preface to 2nd Edition
- Part I Evaluation and Treatment of Patients with a Neuromuscular Disorder
- Part II Neuromuscular Cases
- Disorders of the Anterior Horn Cell
- Peripheral Neuropathies
- Disorders of the Neuromuscular Junction
- Case 31 Myasthenia Gravis with Acetylcholine Receptor Antibodies (AChR MG)
- Case 32 Myasthenia Gravis with Muscle-Specific Kinase Antibodies (MuSK MG)
- Case 33 Drug-Induced Myasthenia Gravis: Immune Checkpoint Inhibitor (ICI)-Related
- Case 34 Lambert–Eaton Myasthenic Syndrome (LEMS)
- Case 35 Congenital Myasthenic Syndromes (CMS): Dok7
- Myopathies
- Video legends
- Index
- References
Case 34 - Lambert–Eaton Myasthenic Syndrome (LEMS)
from Disorders of the Neuromuscular Junction
Published online by Cambridge University Press: aN Invalid Date NaN
- Neuromuscular Disease: A Case-Based Approach
- Neuromuscular Disease
- Copyright page
- Contents
- Contributors
- Foreword
- Preface to 2nd Edition
- Part I Evaluation and Treatment of Patients with a Neuromuscular Disorder
- Part II Neuromuscular Cases
- Disorders of the Anterior Horn Cell
- Peripheral Neuropathies
- Disorders of the Neuromuscular Junction
- Case 31 Myasthenia Gravis with Acetylcholine Receptor Antibodies (AChR MG)
- Case 32 Myasthenia Gravis with Muscle-Specific Kinase Antibodies (MuSK MG)
- Case 33 Drug-Induced Myasthenia Gravis: Immune Checkpoint Inhibitor (ICI)-Related
- Case 34 Lambert–Eaton Myasthenic Syndrome (LEMS)
- Case 35 Congenital Myasthenic Syndromes (CMS): Dok7
- Myopathies
- Video legends
- Index
- References
Summary
A 33-year-old-woman who was diagnosed with chronic fatigue syndrome several years ago noticed a ‘heavy feeling’ and progressive weakness of the upper legs over a period of four months. Climbing stairs became very difficult, and eventually she could no longer walk independently. She did not complain about weakness in her arms. There were no sensory complaints. During the past months, her voice had changed. Especially if she was tired, she would speak ‘like a drunk’. There were no complaints about double vision, drooping eyelids, or swallowing. There were no clear symptoms of autonomic dysfunction. She did not drink alcohol but had smoked at least a pack of cigarettes per day for over 10 years.
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- Neuromuscular DiseaseA Case-Based Approach, pp. 165 - 167Publisher: Cambridge University PressPrint publication year: 2024