病例报道:克鲁宗综合征1例  

Case Report:Crouzon Syndrome

作　　者：王静 颜青[1] 何俊平[1] 邱德智[1] 王刚[1] WANG Jing;YAN Qing;HE Junping;QIU Dezhi;WANG Gang(Department of Neurosurgery,Children's Hospital of Nanjing Medical University,Nanjing 210004,China)

机构地区：[1]南京医科大学附属南京儿童医院神经外科,南京市210004

出　　处：《组织工程与重建外科杂志》2020年第1期62-64,共3页Journal of Tissue Engineering and Reconstructive Surgery

摘　　要：报道1例父系遗传的克鲁宗综合征。患儿,女性,4岁,临床表现为颅缝早闭、中面部发育不良、颅内压增高、反颌及突眼畸形,依据其临床资料及影像学表现,诊断为克鲁宗综合征颅面型。于全麻下行颅面重建术,术后患儿头颅外观较前明显改善,突眼好转,眼睑可闭合,视力改善。One case of paternally inherited crouzon syndrome was reported.The female patient was 4 years old,presented with craniosynostosis,midfacial dysplasia,increased intracranial pressure,anti-jaw and exophthalmos.According to the clinical data and imaging findings,the patient was diagnosed as craniofacial type of cruzon syndrome.After craniofacial reconstruction under general anesthesia,the appearance of the head was improved significantly,the protrusion eyes were improved,the eyelids could be closed,and the vision was improved.

关 键 词：克鲁宗综合征 父系遗传 颅面部畸形 

分 类 号：R726.2[医药卫生—儿科]