このエントリーをはてなブックマークに追加
ID 52012
JaLCDOI
フルテキストURL
Thumnail 67_6_385.pdf 2.32 MB
著者
Tanaka, Masato Department of Orthopaedic Surgery, Okayama University Hospital
Arataki, Shinya Department of Orthopaedic Surgery, Okayama University Hospital
Sugimoto, Yoshihisa Department of Orthopaedic Surgery, Okayama University Hospital
Takigawa, Tomoyuki Department of Orthopaedic Surgery, Okayama University Hospital ORCID Kaken ID researchmap
Tetsunaga, Tomoko Department of Orthopaedic Surgery, Okayama University Hospital
Ozaki, Toshifumi Department of Orthopaedic Surgery, Okayama University Hospital Kaken ID publons researchmap
抄録
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.
キーワード
craniometaphyseal dysplasia
Chiari malformation
cervicomedullary compression
Amo Type
Case Report
発行日
2013-12
出版物タイトル
Acta Medica Okayama
67巻
6号
出版者
Okayama University Medical School
開始ページ
385
終了ページ
389
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
English
著作権者
CopyrightⒸ 2013 by Okayama University Medical School
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT