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22q11.2欠失症候群における特徴的顔貌の検討 : 三次元レーザースキャナを用いて
http://hdl.handle.net/10470/25588
http://hdl.handle.net/10470/25588d69ffee6-20a1-43c2-87aa-2b2d6ecfe11f
名前 / ファイル | ライセンス | アクション |
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KJ00006019723.pdf (781.3 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2010-08-10 | |||||
タイトル | ||||||
タイトル | 22q11.2欠失症候群における特徴的顔貌の検討 : 三次元レーザースキャナを用いて | |||||
言語 | ||||||
言語 | jpn | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
別タイトル | ||||||
その他のタイトル | Characteristics of Facial Features in 22q11.2 Deletion Syndromes by Using the Three-Dimensional Curved Surface Measuring Equipment | |||||
著者名 |
山村, 幸江
× 山村, 幸江× 高山, 幹子× 石井, 哲夫× 寺田, 伸一 |
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著者別名 | ||||||
姓名 | YAMAMURA, Yukie | |||||
著者別名 | ||||||
姓名 | TAKAYAMA, Mikiko | |||||
著者別名 | ||||||
姓名 | ISHII, Tetsuo | |||||
著者別名 | ||||||
姓名 | TERADA, Shinichi | |||||
出版者 | ||||||
出版者 | 東京女子医科大学学会 | |||||
受付日付 | ||||||
日付 | 2010-08-10 | |||||
日付タイプ | Created | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0040-9022 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00161368 | |||||
書誌情報 |
東京女子医科大学雑誌 巻 71, 号 2, p. 92-98, 発行日 2001-02-25 |
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著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The DiGeorge syndrome, velo-cardio-facial syndrome and conotruncal anomaly face syndrome have similar but variable phenotypes and share the deletion of 22q11.2. The 22q11.2 deletion syndrome includes the following facial appearance: widely spaced eyes, narrow eyelids, small mouth, prominent apex nasi, flat and widened nasal dorsum. A diagnosis of this syndrome may be made based solely on facial appearance. However, a more accurate and objective evaluation is necessary as facial appearance largely depends on examiner's impressions. A 3-dimensional laser scanner with a slit laser light was used to quantitatively evaluate the facial morphology of the patient, and the effectiveness of this method in diagnosing 22q11.2 deletation syndrome was evaluated. Nine cases of 22q11.2 deletion syndrome were diagnosed from 1994 to 1997 (3 males, 6 females, age range: 4~31 years). We used a 3-dimensional curved surface measuring equipment, to measure the face 3-dimensionally, imputing data digitally. The image obtained with this method showed a reduction in the choroid fissure, with a widened dorsum nasi and the dorsum nasi inclination angle was steeper in the apex nasi than in the radix nasi. In conclusion, the facial appearance of cases of 22q11.2 deletion syndrome, such as reduction in the choroid fissure, a widened dorsum nasi and prominent apex nasi can be evaluated quantitatively. | |||||
著者所属 | ||||||
東京女子医科大学医学部耳鼻咽喉科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部耳鼻咽喉科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部耳鼻咽喉科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部形成外科学 |