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[先天性感音神经性耳聋及相关综合征]

[Congenital sensorineural deafness and associated syndromes].

作者信息

Moatti L, Garabedian E N, Lacombe H, Spir-Jacob C

机构信息

Service d'ORL et Chirurgie Cervico-Faciale, Hôpital Trousseau, Paris.

出版信息

Ann Otolaryngol Chir Cervicofac. 1990;107(3):181-6.

PMID:2188546
Abstract

The etiology of perceptive deafness, especially the congenital variety, requires investigation. The presence of a variety of signs associated with deafness constitutes an "associated syndrome" and helps to define a possible genetic origin. These syndromes only represent a small percentage of overall causes of deafness in children, since at most they account for only 10% of cases. Certain syndromes are encountered more often or are well known, others are extremely rare or have only been described recently. The authors report six of these very rare syndromes discovered among their patients: a KID syndrome, a Leopard syndrome, a Norrie syndrome, a Jervell and Lange Nielsen syndrome, a recently described entity called CEE with deafness and an External Neuro-Cochleo-Pancreatic syndrome which would not appear to have been previously described.

摘要

感音神经性耳聋的病因,尤其是先天性耳聋的病因,需要进行调查。与耳聋相关的各种体征的存在构成了一种“相关综合征”,有助于确定可能的遗传起源。这些综合征仅占儿童耳聋总体病因的一小部分,因为它们最多仅占病例的10%。某些综合征较为常见或广为人知,其他的则极为罕见或最近才被描述。作者报告了在他们的患者中发现的六种非常罕见的综合征:一种KID综合征、一种豹皮综合征、一种诺里综合征、一种耶尔韦尔和朗格·尼尔森综合征、一种最近描述的名为伴有耳聋的CEE的实体以及一种似乎以前未被描述过的外部神经-耳蜗-胰腺综合征。

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