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苗勒管异常及相关听觉缺陷。

Müllerian tract abnormalities and associated auditory defects.

作者信息

Letterie G S, Vauss N

机构信息

Department of Obstetrics and Gynecology, Tripler Army Medical Center, Honolulu, Hawaii 96859-5000.

出版信息

J Reprod Med. 1991 Nov;36(11):765-8.

PMID:1765952
Abstract

Fifteen women with müllerian defects and a control population of 15 with normal müllerian systems underwent dynamic audiometric testing. The rate of auditory defects in women with müllerian abnormalities (33%) was significantly higher (P less than .05) than in the control population (0%). Those patients manifested mild, moderate and severe sensorineural defects in the high-frequency range. The defects were not accounted for by age or occupation and were associated with renal agenesis in 60% of the cases. One patient with normal audiometric testing and a septate uterus had a family history significant for an identical twin sister with unilateral renal agenesis, ipsilateral congenital deafness and an unevaluated müllerian tract. The results of the study suggest that a spectrum of auditory changes may exist in association with müllerian defects, ranging from previously described congenital deafness to more subtle hearing defects not clinically evident.

摘要

15名患有苗勒管缺陷的女性和15名苗勒管系统正常的对照人群接受了动态听力测试。患有苗勒管异常的女性中听觉缺陷发生率(33%)显著高于对照人群(0%)(P小于0.05)。这些患者在高频范围内表现出轻度、中度和重度感音神经性缺陷。这些缺陷与年龄或职业无关,60%的病例与肾发育不全有关。一名听力测试正常但有纵隔子宫的患者有家族病史,其同卵双胞胎姐妹有单侧肾发育不全、同侧先天性耳聋且苗勒管未评估。研究结果表明,与苗勒管缺陷相关的可能存在一系列听觉变化,从先前描述的先天性耳聋到临床上不明显的更细微的听力缺陷。

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