桑迪费尔综合征——食管裂孔疝的一种罕见并发症。病例报告。
Sandifer's syndrome--a rare complication of hiatal hernia. A case report.
作者信息
Hadari A, Azizi E, Lernau O, Nissan S
出版信息
Z Kinderchir. 1984 Jun;39(3):202-3. doi: 10.1055/s-2008-1044208.
PMID:6464565
Abstract
A 13-year-old boy with Sandifer's syndrome whose only symptoms were abnormal posture and movements of the head and neck, underwent a repair of a hiatus hernia. The disappearance of all symptoms following the operation could be explained by the common innervation of the diaphragm and the neck.
摘要
一名患有桑迪费尔综合征的13岁男孩，其唯一症状是头部和颈部姿势及动作异常，接受了食管裂孔疝修补术。术后所有症状消失可通过膈肌和颈部的共同神经支配来解释。
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