基础医学与临床 ›› 2015, Vol. 35 ›› Issue (8): 1145-1147.

• 医学教育 • 上一篇    下一篇

医学遗传学课程教学中“罕见病”教学初探

陈曹逸1,朱新宇2,谭湘陵2,左伋3   

  1. 1. 南通大学
    2. 江苏省南通大学生命科学学院
    3. 复旦大学上海医学院
  • 收稿日期:2015-02-16 修回日期:2015-04-21 出版日期:2015-08-05 发布日期:2015-07-15
  • 通讯作者: 左伋 E-mail:jzuo@shmu.edu.cn
  • 基金资助:
    南通大学2014年度教学改革研究课题;复旦大学基础医学院教学改革研究项目

Preliminary exploration into rare disease teaching in medical genetics

  • Received:2015-02-16 Revised:2015-04-21 Online:2015-08-05 Published:2015-07-15

摘要: 临床上遗传性罕见病存在高误诊、治疗不规范、预防不得力等问题。本文从医学遗传学课程中加强罕见病教学角度,提出精选教学内容,采用多元化教学,参与临床实践等措施,就如何提高医学生罕见病的认知水平进行了初步探讨。

关键词: 罕见病, 医学遗传学, 教学

Abstract: In clinic, rare disease practice faces several problems, such as, frequent diagnosis errors, non-standardized treatment, and ineffective in preventing recurrence. In this paper, from the perspective of strengthening the rare disease teaching, we preliminarily explored how to improve the medical students’ cognitive level of rare disease by taking multiple measures, such as, delivery of selected teaching contents, application of diversity teaching methods and participation in clinical practice.

Key words: rare disease, medical genetics, teaching