Singer S L, Walpole I, Brogan W F, Goldblatt J
Princess Margaret Hospital, Perth, Western Australia.
Aust Dent J. 1997 Feb;42(1):11-7. doi: 10.1111/j.1834-7819.1997.tb00089.x.
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.
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。
