一例克鲁宗综合征家族的牙颌面特征。病例报告。

Dentofacial features of a family with Crouzon syndrome. Case reports.

作者信息

Singer S L, Walpole I, Brogan W F, Goldblatt J

机构信息

Princess Margaret Hospital, Perth, Western Australia.

出版信息

Aust Dent J. 1997 Feb;42(1):11-7. doi: 10.1111/j.1834-7819.1997.tb00089.x.

DOI:10.1111/j.1834-7819.1997.tb00089.x

PMID:9078640

Abstract

Crouzon syndrome is an autosomal dominant condition characterized by craniosynostosis with associated dentofacial anomalies. This paper describes the variable clinical features in affected individuals over two generations of a family with particular reference to the dentofacial deformities and discussion of management strategies.

摘要

克鲁宗综合征是一种常染色体显性疾病，其特征为颅缝早闭并伴有牙颌面异常。本文描述了一个家族两代受影响个体的可变临床特征，特别提及牙颌面畸形，并讨论了治疗策略。