| Literature DB >> 19533655 |
T Ueda1, F Kanda, H Kobessho, H Hamaguchi, M Motomura.
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.Entities:
Mesh:
Year: 2009 PMID: 19533655 DOI: 10.1002/mus.21301
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217