Turner综合征伴听力障碍发病机制的研究进展  

Advance in Pathogenesis of Turner Syndrome Accompanied by Otological Problems

作　　者：于秀妍[1] 臧鸿斌[1] 贺薇[1] 

机构地区：[1]中国医科大学,七年制辽宁沈阳110001

出　　处：《中国现代医生》2010年第21期14-15,17,共3页China Modern Doctor

摘　　要：Turner综合征(Turner Syndrome,TS)是常见的染色体病之一,典型的临床特征有身材矮小、性腺发育不良等。听力障碍也是其常见的症状之一,它主要包括中耳炎和感觉神经性耳聋这两种类型。其发病机制可能涉及雌激素、染色体、基因等方面。Turner Syndrome is one of common chromosomal disease, with typical clinical features such as short stature,gonadal dysgenesis and so on. Hearing problem can also be one of its common symptoms,including otitis media and sensorineural hearing loss. Its pathogenesis may involve estrogen,chromosomes,genes and so on.

关 键 词：TURNER综合征 听力障碍 x染色体缺失 雌激素 

分 类 号：R596.1[医药卫生—内科学]