Abstract
Morphological components of craniovertebral junction include bony structures around the foramen magnum, lower brain stem, upper cervical spinal cord, and cerebellar tonsils. Physiological components, which are often overlooked but equally important, consist of cerebrospinal fluid dynamics and motions at the junction. The interplays among these factors may contribute to the pathogenesis of signs and symptoms that are similarly found in Chiari I malformation.
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Tubbs RS, Elton S, Grabb P, Dockery SE, Bartolucci AA, Oakes WJ. Analysis of the posterior fossa in children with the Chiari 0 malformation. Neurosurgery. 2001;48:1050–4.
Bogdanov EI, Heiss JD, Mendelevich EG, et al. Clinical and neuroimaging features of “idiopathic” syringomyelia. Neurology. 2004;62:791–4.
Kyoshima K, Kuroyanagi T, Oya F, et al. Syringomyelia without hindbrain herniation: tight cisterna magna. Report of four cases and a review of the literature. Neurosurgery. 2002;96:239–49.
Iskandar BJ, Hedlund GL, Grabb PA, et al. The resolution of syringohydromyelia without hindbrain herniation after posterior fossa decompression. J Neurosurg. 1998;89:212–6.
Chern JJ, Gordon AJ, Mortazavi MM, et al. Pediatric Chiari malformation type 0: a 12-year institutional experience. J Neurosurg Pediatr. 2011;8:1–5.
Tubbs RS, Iskandar BJ, Bartolucci AA, et al. A critical analysis of the Chiari 1.5 malformation. J Neurosurg (Pediatrics 2). 2004;101:179–83.
Tubbs RS, Beckman J, Naftel RP, et al. Institutional experience with 500 cases of surgically treated pediatric Chiari malformation type I. J Neurosurg Pediatr. 2011;7:248–56.
Greenlee JD, Donovan KA, Hasan DM, et al. Chiari I malformation in the very young child: the spectrum of presentations and experience in 31 children under age 6 years. Pediatrics. 2002;110:1212–9.
Iskandar BJ, Quigley M, Haughton VM. Foramen magnum cerebrospinal fluid flow characteristics in children with Chiari I malformation before and after craniocervical decompression. J Neurosurg. 2004;101(2 suppl):169–78.
Shijman E, Steinbok P. International survey on the management of Chiari I malformation and syringomyelia. Childs Nerv Syst. 2004;20:341–8.
Galarza M, Maritnez-Lage JF, Ham S, et al. Cerebral anomalies and Chiari type I malformation. Pediatr Neurosurg. 2010;46:442–9.
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Mariwalla, N.R., Boydston, W.R., Chern, J.J. (2013). Newer Subsets: Chiari 0 and Chiari 1.5 Malformations. In: Tubbs, R., Oakes, W. (eds) The Chiari Malformations. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6369-6_19
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DOI: https://doi.org/10.1007/978-1-4614-6369-6_19
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