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ID 52012
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Author
Sugimoto, Yoshihisa Kaken ID
Takigawa, Tomoyuki ORCID Kaken ID researchmap
Tetsunaga, Tomoko
Abstract
Craniometaphyseal dysplasia is a rare genetic condition characterized by progressive thickening of bones in the skull and metaphyseal abnormalities in the long bones. This disorder often causes progressively symptomatic cranial nerve compression, but in rare cases foramen magnum stenosis may lead to quadriplegia. Chiari I malformation with craniometaphyseal dysplasia is extremely rare. The authors report on a 25-year-old woman with myelopathy due to Chiari I malformation along with craniometaphyseal dysplasia. There are only four previous case reports of this condition. The authors present here the fifth case report of this rare condition and summarize its characteristics.
Keywords
craniometaphyseal dysplasia
Chiari malformation
cervicomedullary compression
Amo Type
Case Report
Published Date
2013-12
Publication Title
Acta Medica Okayama
Volume
volume67
Issue
issue6
Publisher
Okayama University Medical School
Start Page
385
End Page
389
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
英語
Copyright Holders
CopyrightⒸ 2013 by Okayama University Medical School
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT