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单纯性下肢镜像运动与脊髓纵裂

Exclusive lower extremity mirror movements and diastematomyelia.

作者信息

Tubbs R Shane, Smyth Matthew D, Dure Leon S, Oakes W Jerry

机构信息

Department of Cell Biology, University of Alabama at Birmingham, Birmingham, Ala., USA.

出版信息

Pediatr Neurosurg. 2004 May-Jun;40(3):132-5. doi: 10.1159/000079856.

DOI:10.1159/000079856
PMID:15367804
Abstract

Mirror movements usually seen in the Klippel-Feil syndrome are most commonly appreciated in the upper extremities. Lower extremity involvement is seen rarely and when observed, is found in conjunction with upper extremity mirror movements. We report what we believe to be the first case of mirror movements found exclusively in the lower extremities in a female patient presenting with tethered cord syndrome. Our hopes are that this report will help elucidate mechanisms involved with these anomalous movements, as currently there is no commonly accepted etiology.

摘要

镜像运动通常见于克-费综合征,最常在上肢出现。下肢受累情况罕见,一旦出现,常与上肢镜像运动同时存在。我们报告了一例我们认为是首例仅在下肢出现镜像运动的女性患者,该患者患有脊髓栓系综合征。我们希望这份报告将有助于阐明这些异常运动所涉及的机制,因为目前尚无普遍认可的病因。

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1
Exclusive lower extremity mirror movements and diastematomyelia.单纯性下肢镜像运动与脊髓纵裂
Pediatr Neurosurg. 2004 May-Jun;40(3):132-5. doi: 10.1159/000079856.
2
Congenital neural abnormalities presenting with mirror movements in a patient with Klippel-Feil syndrome. Case report.先天性神经异常在Klippel-Feil综合征患者中表现为镜像运动。病例报告。
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3
[Isolated mirror-image movements of the upper extremities in Klippel-Feil syndrome].
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Cervical cord tethering and congenital mirror movements: is it an association rather than a coincidence?颈髓拴系与先天性镜像运动:这是一种关联而非巧合吗?
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Diastematomyelia: a case report with review of litratures.脊髓纵裂:一例病例报告并文献复习
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Klippel-Feil syndrome, iniencephalus, anencephalus, hindbrain hernia and mirror movements: overdistention of the neural tube.克-费综合征、无脑畸形、无脑儿、后脑疝和镜像运动:神经管过度扩张。
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