重症肌无力
多神经根神经病
医学
弱点
病态的
儿科
格林-巴利综合征
免疫学
病理
外科
作者
Kazue Kimura,A Nezu,Seiji Kimura,Noriyuki Otsuki,Takayoshi Kobayashi,Yuichiro Nomura,Masafumi Segawa
出处
期刊：Neuropediatrics
[Thieme Medical Publishers (Germany)]
日期：1998-04-01
卷期号：29 (02): 108-112
被引量：28
标识
DOI：10.1055/s-2007-973544
摘要
We report a 14-year-old girl who developed chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) during the course of myasthenia gravis. Myasthenia gravis, which was clinically of ocular type, but with waning phenomenon of the extremities, occurred at 2 years and 4 months of age. Muscle weakness of the lower extremities gradually developed over the next 6 years.
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