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一位患有桑迪弗综合征和食管裂孔疝的成年女性,被误诊为局灶性癫痫发作。

A female adult with Sandifer's syndrome and hiatal hernia misdiagnosed as epilepsy with focal seizures.

机构信息

Department of Neurology and Epilepsy Center, University of Marburg, Germany.

出版信息

Epilepsy Behav. 2012 May;24(1):141-2. doi: 10.1016/j.yebeh.2012.02.016. Epub 2012 Apr 5.

Abstract

Sandifer's syndrome is a rare, probably underdiagnosed, and usually pediatric movement disorder associated with gastroesophageal reflux disease. Often, it is misdiagnosed as epilepsy or paroxysmal dyskinesia. We report the case of an adult female with Sandifer's syndrome initially diagnosed as focal epilepsy and treated inefficiently with anticonvulsants for two years.

摘要

桑迪弗综合征是一种罕见的、可能被低估的、通常与胃食管反流病相关的儿科运动障碍。它经常被误诊为癫痫或阵发性运动障碍。我们报告了一例成年女性桑迪弗综合征的病例,该患者最初被诊断为局灶性癫痫,并在两年内使用抗癫痫药物治疗效果不佳。

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