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Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants

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タイトル: Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants
その他のタイトル: maxillofacial features of Apert syndrome
著者: Kakutani, Hitomi 著作を一覧する
Sato, Yoshiaki 著作を一覧する
Tsukamoto-Takakusagi, Yuri 著作を一覧する
Saito, Fumio 著作を一覧する
Oyama, Akihiko 著作を一覧する
Iida, Junichiro 著作を一覧する
キーワード: Apert syndrome
maxillary hypoplasia
skeletal Class III jaw-base relationship
発行日: 2017年 1月
出版者: Wiley-Blackwell
誌名: Congenital Anomalies
巻: 57
号: 1
開始ページ: 15
終了ページ: 23
出版社 DOI: 10.1111/cga.12180
抄録: Apert syndrome is a rare craniosynostosis syndrome characterized by irregular craniosynostosis, midface hypoplasia, and syndactyly of the hands and feet. Previous studies analyzed individuals with Apert syndrome and reported some facial and intraoral features caused by severe maxillary hypoplasia. However, these studies were performed by analyzing both individuals who had and those had not received a palate repair surgery, which had a high impact on the maxillary growth and occlusion. To highlight the intrinsic facial and intraoral features of Apert syndrome, five Japanese individuals with Apert syndrome from 5 years and 2 months to 9 years and 10 months without cleft palate were analyzed in this study. A concave profile and a skeletal Class III jaw-base relationship caused by severe maxillary hypoplasia were seen in all patients. The patients exhibited anterior and posterior crossbites possibly due to a small dental arch of Maxilla.
Rights: This is the peer reviewed version of the following article: Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants, which has been published in final form at http://doi.org/10.1111/cga.12180. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
資料タイプ: article (author version)
URI: http://hdl.handle.net/2115/68023
出現コレクション:雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

提供者: 角谷 瞳

 

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