克鲁宗综合征：一例病例报告及文献综述。
Crouzon syndrome: A case report and review of literature.
作者信息
Kaur Harroop, Singh Waraich Harmeet, Sharma Chander Mohan
机构信息
Dept of Opthomology, I.G.Medical College, Shimla.
出版信息
Indian J Otolaryngol Head Neck Surg. 2006 Oct;58(4):381-2. doi: 10.1007/BF03049602.
Abstract
Crouzon syndrome, also called craniofacial dysostosis is an autosomal dominant disorder characterized by premature closure of cranial sutures, midfacial hypoplasia and orbital defects. Herein we report a case of this rare entity who presented with brachycephaly, maxillary hypoplasia, wide parrot beaked nose, repaired bilateral cleft lip and cleft palate along with dental and orbital abnormalities.
摘要
克鲁宗综合征，也称为颅面骨发育不全，是一种常染色体显性疾病，其特征为颅缝过早闭合、面中部发育不全和眼眶缺陷。在此，我们报告一例这种罕见疾病的病例，该患者表现为短头畸形、上颌骨发育不全、鹦鹉嘴样宽鼻、双侧唇腭裂修补术后，同时伴有牙齿和眼眶异常。
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