The pathogenesis of Chiari I malformation and syringomyelia

Raymond F. Sekula, Gregory Arnone, Christine Crocker, Khaled M. Aziz, Noam Alperin

Research output: Contribution to journalReview article

16 Citations (Scopus)

Abstract

Objective: The pathogeneses of Chiari malformation type I and syringomyelia are incompletely understood. In this article, the authors attempt to review the current theories on the pathogeneses of Chiari I malformation and syringomyelia. Methods: A literature review for articles pertaining to Chiari I malformation or syringomyelia before August 2010 was conducted; in addition, the author's own experience in treating Chiari I malformation and syringomyelia is included. Results: Chiari I malformation has been defined radiographically as cerebellar tonsillar herniation or ectopia 5 mm or greater below the foramen magnum. By this narrow definition, Chiari I malformation (i.e. cerebellar tonsillar herniation or ectopia 5 mm or greater below the foramen magnum) likely encompasses a heterogeneous grouping of disorders caused by different mechanisms. Molecular and genetic studies have been helpful in furthering our understanding of Chiari I malformation. Conclusion: A review of the pathogeneses of Chiari I malformation and syringomyelia is reported.

Original languageEnglish (US)
Pages (from-to)232-239
Number of pages8
JournalNeurological Research
Volume33
Issue number3
DOIs
StatePublished - Apr 1 2011

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Syringomyelia
Encephalocele
Foramen Magnum
Arnold-Chiari Malformation
Molecular Biology

All Science Journal Classification (ASJC) codes

  • Neurology
  • Clinical Neurology

Cite this

Sekula, Raymond F. ; Arnone, Gregory ; Crocker, Christine ; Aziz, Khaled M. ; Alperin, Noam. / The pathogenesis of Chiari I malformation and syringomyelia. In: Neurological Research. 2011 ; Vol. 33, No. 3. pp. 232-239.
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The pathogenesis of Chiari I malformation and syringomyelia. / Sekula, Raymond F.; Arnone, Gregory; Crocker, Christine; Aziz, Khaled M.; Alperin, Noam.

In: Neurological Research, Vol. 33, No. 3, 01.04.2011, p. 232-239.

Research output: Contribution to journalReview article

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