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先天性C2至C6发育异常。

Congenital dysplasia of C2--6.

作者信息

Archer E, Batniztky S, Franken E A, Muller J, Hale B

出版信息

Pediatr Radiol. 1977 Sep 1;6(2):121-2. doi: 10.1007/BF00973536.

DOI:10.1007/BF00973536
PMID:896351
Abstract

Neural arch dysplasia of the cervical vertebrae is a rare occurrence. The authors present a case with dysplasia of cervical bodies and posterior arch elements at multiple levels. The embryogenesis of these anomalies is discussed.

摘要

颈椎神经弓发育异常较为罕见。作者报告了一例多个节段椎体及后弓结构发育异常的病例。并对这些异常的胚胎发生进行了讨论。

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引用本文的文献

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Developmental anomalies of the lateral portion of the cervical neural arch: Multimodal imaging and clinical implications.颈椎神经弓外侧部分的发育异常:多模态成像及临床意义。
Neuroradiol J. 2020 Jun;33(3):252-258. doi: 10.1177/1971400920923284. Epub 2020 May 13.
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Absent congenital cervical pedicle nearly misdiagnosed as a facet dislocation: A case report.先天性颈椎椎弓根缺如险些误诊为小关节脱位:一例报告
Interdiscip Neurosurg. 2017 Sep;9:20-23. doi: 10.1016/j.inat.2016.04.003.
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The role of CT imaging in the congenital absence of a cervical spine pedicle: a case report and review of the literature.
CT成像在先天性颈椎椎弓根缺如中的作用:一例病例报告及文献复习
J Radiol Case Rep. 2009;3(5):7-10. doi: 10.3941/jrcr.v3i5.181. Epub 2009 May 1.
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Congenital defect of the posterior arch of cervical spine : report of three cases and review of the current literature.颈椎后弓先天性缺陷:三例报告并复习当前文献
J Korean Neurosurg Soc. 2010 Sep;48(3):294-7. doi: 10.3340/jkns.2010.48.3.294. Epub 2010 Sep 30.
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Absent cervical spine pedicle and associated congenital spinal abnormalities - a diagnostic trap in a setting of acute trauma: case report.颈椎椎弓根缺失及相关先天性脊柱异常 - 急性创伤环境中的诊断陷阱:病例报告。
BMC Med Imaging. 2010 Nov 9;10:25. doi: 10.1186/1471-2342-10-25.
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Congenital absence of a cervical spine pedicle : report of two cases and review of the literature.先天性颈椎椎弓根缺如:两例报告并文献复习
J Korean Neurosurg Soc. 2008 Dec;44(6):389-91. doi: 10.3340/jkns.2008.44.6.389. Epub 2008 Dec 31.
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Skeletal Radiol. 2007 Aug;36(8):773-7. doi: 10.1007/s00256-007-0276-8. Epub 2007 Feb 14.
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Posterior arch defects of the cervical spine.颈椎后弓缺损
Skeletal Radiol. 1982;8(2):135-9. doi: 10.1007/BF00349580.
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Case report 332: A complex anomaly of the craniovertebral junction representing a regressive malformation with agenesis of the neural arch of C-2, hypomorphogenesis at C5-C6 and instability of the upper cervical spine.病例报告332:颅颈交界区复杂畸形,表现为C2神经弓发育不全的退行性畸形、C5-C6发育不全及上颈椎不稳。
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