新生儿第一二鳃弓综合征一例报告  

One case of first and second branchial arch syndrome in neonates

作　　者：宋立[1,2] 刘洋 王丹[1] SONG Li;LIU Yang;WANG Dan(Department of New Pediatrics,Tianjin Children’s Hospital,Tianjin 300134,China;Graduate School of Tianjin Medical University)

机构地区：[1]天津市儿童医院新生儿科,300134 [2]天津医科大学研究生院

出　　处：《天津医药》2019年第3期290-292,共3页Tianjin Medical Journal

摘　　要：新生儿第一二鳃弓综合征,又称为半侧颜面短小畸形(HFM)。HFM是一种先天性颅面部畸形,病因及发病机制尚不明确,可依靠详细的体格检查及影像学检查来确诊。通过手术及非手术治疗,可以改善面部结构和功能,促进心身健康发展。The first and second branchial arch syndrome,also known as the hemifacial microsomia(HFM) is a congenital craniofacial deformity. Its etiology and pathogenesis are still unclear. It can rely on the detailed physical examination and imaging examination to diagnose. Surgical and non-surgical treatment can improve facial structure and function, and promote the development of psychosomatic health.

关 键 词：先天畸形 鳃原瘤 核型分析 染色体 病例报告 婴儿 新生 

分 类 号：R722.19[医药卫生—儿科]