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儿童全身性原发性肌张力障碍致寰枢椎脱位。

Atlantoaxial dislocation in a child with generalized primary dystonia.

机构信息

Department of Pediatrics, Maulana Azad Medical College and associated Lok Nayak Hospital, New Delhi, India.

出版信息

J Clin Neurosci. 2011 Jul;18(7):966-8. doi: 10.1016/j.jocn.2010.11.016. Epub 2011 May 6.

Abstract

We describe a 10-year-old boy with generalized dystonia who developed spastic quadriparesis within 1 month of dystonia onset. On neuroimaging, a craniovertebral junction anomaly with atlantoaxial dislocation and compressive myelopathy was present. We postulate that dystonia involving the neck led to atlantoaxial dislocation in this child with a craniovertebral junction anomaly.

摘要

我们描述了一例 10 岁男孩,其在出现全身性肌张力障碍后 1 个月内发展为痉挛性四肢瘫痪。神经影像学显示颅颈交界区异常伴寰枢椎脱位和压迫性脊髓病。我们推测,颈部受累的肌张力障碍导致了该颅颈交界区异常患儿的寰枢椎脱位。

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