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dc.contributor.authorTubbs, RS
dc.contributor.authorLyerly, MJ
dc.contributor.authorLoukas, M
dc.contributor.authorShoja, MM
dc.contributor.authorOakes, WJ
dc.date.accessioned2018-08-26T08:28:41Z
dc.date.available2018-08-26T08:28:41Z
dc.date.issued2007
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51586
dc.description.abstractBackground Both the diagnosis and treatment regimens for the Chiari I malformation (CIM) are varied and controversial. The present paper analyzes the literature regarding this form of hindbrain herniation in regard to definition, anatomy, pathobiology, symptoms, findings, treatment, and outcomes. Discussions Appropriate literature germane to the CIM is reviewed and discussed. There is variation in the reported anatomy, outcome, and treatment for children with CIM. Based on the literature, most patients have preoperative symptoms or findings (e.g., syringomyelia) improve no matter what surgical technique is utilized. However, standardized treatment paradigms based on randomized controlled studies are still necessary to elucidate the optimal selection and treatment criteria.
dc.language.isoEnglish
dc.relation.ispartofCHILDS NERVOUS SYSTEM
dc.subjecttonsillar ectopia
dc.subjecthindbrain hernia
dc.subjectneurosurgery
dc.titleThe pediatric chiari i malformation: A review
dc.typeReview
dc.citation.volume23
dc.citation.issue11
dc.citation.spage1239
dc.citation.epage1250
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1007/s00381-007-0428-0


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