Abstract |
A 67-year-old man was admitted with a 2-year history of dropped head. Neurological examination revealed ptosis, dysarthria, neck weakness, hyporeflexia of all limbs, and autonomic failure. Electrophysiologic study showed a 400% increment response to high-rate repetitive nerve stimulation. Serum anti-P/Q-voltage-gated calcium channel antibody was positive, confirming the diagnosis of Lambert-Eaton myasthenic syndrome (LEMS). His symptoms and electrophysiological abnormalities improved with oral prednisolone following plasmapheresis. This is the first report of LEMS as a cause of dropped head syndrome.
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Authors | T Ueda, F Kanda, H Kobessho, H Hamaguchi, M Motomura |
Journal | Muscle & nerve
(Muscle Nerve)
Vol. 40
Issue 1
Pg. 134-6
(Jul 2009)
ISSN: 0148-639X [Print] United States |
PMID | 19533655
(Publication Type: Case Reports, Journal Article)
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Topics |
- Aged
- Head Movements
- Humans
- Lambert-Eaton Myasthenic Syndrome
(complications, pathology)
- Male
- Movement Disorders
(etiology, pathology)
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