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.
作者
宋立
刘洋
王丹
SONG Li;LIU Yang;WANG Dan(Department of New Pediatrics,Tianjin Children’s Hospital,Tianjin 300134,China;Graduate School of Tianjin Medical University)
出处
《天津医药》
CAS
北大核心
2019年第3期290-292,共3页
Tianjin Medical Journal
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
congenital abnormalities
branchioma
karyotyping
chromosomes
case reports
infant,newborn