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Treacher Collins综合征的精准诊断与治疗(基础篇) 被引量:3

Precision diagnosis and treatment for Treacher Collins syndrome:preclinical perspectives
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摘要 1概述 1.1简介 Treacher Collins综合征(Treacher Collins syndrome,TCS),又称Treacher Collins-Franceschetti综合征、Franceschetti-Zwahlen-Klein综合征,是人类下颌面骨发育不全征(mandibulofacial dysostosis disorder)中最常见的一种^([1-4])。目前大多数学者认为其在新生儿中的发病率约为1/50000^([4-5]),也有部分学者认为其发病率介于1/25000~1/50000、1/40000~1/70000或1/10000~1/50000,且无性别差异。
出处 《临床耳鼻咽喉头颈外科杂志》 CAS 北大核心 2018年第16期1207-1212,共6页 Journal of Clinical Otorhinolaryngology Head And Neck Surgery
基金 国家自然科学基金委员会面上项目(No:81271053) 中国罕见病项目(No:2016YFC0901501)
关键词 TREACHER COLLINS综合征 遗传异质性 核糖体病 神经嵴细胞 鳃弓 Treacher Collins syndrome genetic heterogeneity ribosomopathy neural crest cell pharyngeal arch
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  • 2TEBER O A, GILLESSEN-KAESBACH G, FISCH- ER S, et al. Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unex- pected phenotypic variation[J]. Eur J Hum Genet, 2004,12:879--890.
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