天津医药

天津医药 ›› 2019, Vol. 47 ›› Issue (3): 290-292.doi: 10.11958/20181796

• 临床研究 • 上一篇    下一篇

新生儿第一二鳃弓综合征一例报告

宋立，刘洋，王丹   

  1. 1天津市儿童医院新生儿科（邮编300134）；2天津医科大学研究生院
  • 收稿日期:2018-11-16 修回日期:2019-01-17 出版日期:2019-03-15 发布日期:2019-04-24
  • 通讯作者: 宋立 E-mail:etyysll@163.com

One case of first and second branchial arch syndrome in neonates

SONG Li,LIU Yang,WANG Dan   

  1. 1 Department of New Pediatrics, Tianjin Children’s Hospital, Tianjin 300134, China;2 Graduate School of Tianjin Medical University
  • Received:2018-11-16 Revised:2019-01-17 Published:2019-03-15 Online:2019-04-24
  • Contact: SONG Li E-mail:etyysll@163.com

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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。

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

Abstract: 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.

Key words: congenital abnormalities, branchioma, karyotyping, chromosomes, case reports, infant, newborn