| Literature DB >> 16392120 |
Shin J Oh1, Yuki Hatanaka, Shoji Hemmi, Angela M Young, Mia L Scheufele, Sharon P Nations, Liang Lu, Gwen C Claussen, Gil I Wolfe.
Abstract
To better define electrophysiological abnormalities in myasthenia gravis (MG) patients with muscle-specific tyrosine kinase (MuSK) antibodies (Ab), we compared electrophysiological features of 14 MuSK Ab-positive, 73 acetylcholine receptor antibody (AChR Ab)-positive, and 22 MuSK and AChR Ab-negative (seronegative) patients with generalized disease. Repetitive nerve stimulation (RNS) abnormalities were observed in 86% of MuSK Ab-positive and 82% of AChR Ab-positive patients but in only 55% of seronegative patients. RNS decrements in the orbicularis oculi were more common and severe in the MuSK Ab-positive patients than the other two groups. Single-fiber electromyography (SFEMG) of the extensor digitorum communis was abnormal in 90% of MuSK Ab-positive patients. The high frequency of RNS abnormalities in facial muscles in the MuSK Ab-positive population reflects the propensity for facial muscle involvement in this form of MG and emphasizes the importance of including facial muscles in RNS protocols when evaluating these patients.Entities:
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Year: 2006 PMID: 16392120 DOI: 10.1002/mus.20498
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217