Suppr超能文献

一名智力正常但有听力缺陷男孩的组氨酸血症(作者译)

[Histidinemia in a normal intelligent boy with hearing defect (author's transl)].

作者信息

Plöchl E, Tasser C, Jarosch E

出版信息

Padiatr Padol. 1978;13(3):303-9.

PMID:673435
Abstract

Amino acid screening in an institute for children with hearing defects led to the detection of a 14 years male with histidinuria. Further investigations established the diagnosis histidinemia. In this normal intelligent patient audiologic tests showed bilateral internal ear hearing defect. It is accepted that the hearing defect is the reason for speech abnormities in form of diminished articulation. But it is not clear how far the inborn error of histidine metabolism is directly responsible for the hearing loss. This observation suggests that the well known speech defects in histidinemics are partly caused by hearing disability.

摘要

在一所针对听力缺陷儿童的机构中进行的氨基酸筛查,发现一名14岁男性患有组氨酸尿症。进一步检查确诊为组氨酸血症。在这名智力正常的患者中,听力测试显示双侧内耳听力缺陷。人们认为听力缺陷是导致发音清晰度降低形式的言语异常的原因。但尚不清楚组氨酸代谢的先天性缺陷在多大程度上直接导致听力损失。这一观察结果表明,组氨酸血症患者中众所周知的言语缺陷部分是由听力障碍引起的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验