期刊
JOURNAL OF NEURO-OPHTHALMOLOGY
卷 29, 期 4, 页码 296-299出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/WNO.0b013e3181c25390
关键词
-
资金
- Research to Prevent Blindness, Inc., New York, NY
After rapid correction of severe hyponatremia, a 36-year-old man developed osmotic demyelination syndrome (ODS), manifested neurologically by impaired cognition, extremity weakness, bilateral third cranial nerve palsies, and gaze-evoked upbeat and rotary nystagmus. Brain MRI showed restricted diffusion in the rostral midbrain and temporal and parietal lobes but not in the pons. Over several weeks, all neurologic and imaging deficits resolved. This is the first report to document ocular motor abnormalities associated with midbrain dysfunction in ODS.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据