临床荟萃
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摘要: 罕见病是指发病率很低的一类疾病。目前种类超过7 000种,80%具有遗传性,以先天性畸形、内分泌代谢及神经系统疾病为主。罕见病的知晓率低、误诊率高、治疗可及性差。伴随基因科技发展,罕见病的诊断与治疗技术取得巨大进步。中国成为罕见病诊治领域进步最快的国家,这标志着中国医疗水平的提高和社会文明的进步。
关键词: 遗传, 畸形, 基因, 罕见病, 诊断, 治疗, 社会保障
Abstract: Rare diseases refer to a type of disease with a very low incidence rate. At present,there are more than 7 000 kinds of rare diseases, 80% of which are hereditary, mainly including congenital malformations, endocrin metabolism, and nervous system diseases. The awareness of rare diseases is low, the rate of misdiagnosis is high, and the accessibility of treatment is poor. With the development of genetic technology, great progress has been made in the diagnosis and treatment of rare diseases. Under the active promotion of the government and various social forces, China has become the country with the fastest progress in the diagnosis and treatment of rare diseases, which marks the improvement of medical level and the progress of social civilization in China.
Key words: heredity, abnormalities;genes, rare disease, diagnosis;therapy, social security
张松筠. 中国罕见病诊疗现状[J]. 临床荟萃, doi: 10.3969/j.issn.1004-583X.2019.03.001.
Zhang Songyun. Diagnosis and treatment of rare diseases in China[J]. Clinical Focus, doi: 10.3969/j.issn.1004-583X.2019.03.001.
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链接本文: https://huicui.hebmu.edu.cn/CN/10.3969/j.issn.1004-583X.2019.03.001
https://huicui.hebmu.edu.cn/CN/Y2019/V34/I3/197