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dc.contributor.authorTubbs, RS
dc.contributor.authorShoja, MM
dc.contributor.authorArdalan, MR
dc.contributor.authorShokouhi, G
dc.contributor.authorLoukas, M
dc.date.accessioned2018-08-26T08:56:55Z
dc.date.available2018-08-26T08:56:55Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54508
dc.description.abstractHerniation of the hindbrain outside of the setting of intracranial hypertension, trauma, and brain tumors is an uncommon phenomenon with estimated incidence of less than 1%. In the late 1890's, Hans Chiari, a German pathologist, classified hindbrain herniation into three forms. This classification was then extended to include six types. We reviewed the current literature for the proposed embryological theories as well as the potential genetic mutations/syndromes associated with the hindbrain herniation or Chiari malformation. The review is illustrated by a unique cadaver with Chiari type I malformation (i.e. herniation of the cerebellar tonsils through the foramen magnum). Finally, it seems that no single theory could explain all forms of the Chiari malformation, and that this malformation might be a heterogeneous entity.
dc.language.isoEnglish
dc.relation.ispartofItalian Journal of Anatomy and Embryology
dc.subjectanimal
dc.subjectArnold Chiari malformation
dc.subjectarticle
dc.subjectcase report
dc.subjectcerebellum
dc.subjectclassification
dc.subjectcongenital malformation
dc.subjectforamen magnum
dc.subjectgenetic predisposition
dc.subjectgenetics
dc.subjecthuman
dc.subjecthydrocephalus
dc.subjectmutation
dc.subjectpathophysiology
dc.subjectposterior fossa
dc.subjectrhombencephalon
dc.subjectAnimals
dc.subjectArnold-Chiari Malformation
dc.subjectCerebellum
dc.subjectCranial Fossa, Posterior
dc.subjectForamen Magnum
dc.subjectGenetic Predisposition to Disease
dc.subjectHumans
dc.subjectHydrocephalus
dc.subjectMutation
dc.subjectRhombencephalon
dc.titleHindbrain herniation: A review of embryological theories
dc.typeBook Chapter
dc.citation.volume113
dc.citation.issue1
dc.citation.spage37
dc.citation.epage46
dc.citation.indexScopus


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