Ahmed Imtiaz, Afzal Ambreen
Department of Orthodontics, Dr. Ishrat-ul-Ebad Khan Institute of Oral Health Sciences (DIKIOHS), Dow University of Health Sciences, Karachi.
J Coll Physicians Surg Pak. 2009 May;19(5):318-20.
Crouzon syndrome is an autosomal dominant condition characterized by craniosynostosis with associated dentofacial anomalies. This report describes the different clinical features in two affected individuals of different families with particular reference to characteristic findings of this syndrome.
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。本报告描述了两个来自不同家庭的患病个体的不同临床特征，并特别提及了该综合征的特征性表现。
