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眼耳脊椎综合征:最新评论

Oculoauriculovertebral spectrum: an updated critique.

作者信息

Cohen M M, Rollnick B R, Kaye C I

机构信息

Department of Oral Biology, Faculty of Dentistry, Dalhousie University, Halifax, NS, Canada.

出版信息

Cleft Palate J. 1989 Oct;26(4):276-86.

PMID:2680167
Abstract

A comprehensive review and critical analysis of oculoauriculovertebral spectrum are provided. Topics discussed include nosologic problems, epidemiology, etiology (chromosomal, monogenic, teratogenic), and pathogenesis (hematoma formation, other vascular mechanisms, overripeness ovopathy). Clinical manifestations are thoroughly reviewed, updated, and documented for craniofacial features, central nervous system characteristics (including the wide spectrum of CNS malformations that make up the so-called "expanded Goldenhar complex"), congenital heart defects, and various other anomalies (kidney, lung, gastrointestinal tract). A number of conditions are discussed that are commonly differentiated from oculoauriculovertebral spectrum but have overlapping relationships, in some instances, with frontonasal dysplasia, branchio-oto-renal (BOR) syndrome, Townes-Brocks syndrome, Wildervanck syndrome, DiGeorge sequence, and several associations (VATER, CHARGE, and MURCS).

摘要

本文对眼耳脊椎综合征进行了全面综述和批判性分析。讨论的主题包括疾病分类问题、流行病学、病因(染色体、单基因、致畸因素)和发病机制(血肿形成、其他血管机制、成熟过度性卵病)。对临床表现进行了全面回顾、更新,并记录了颅面特征、中枢神经系统特征(包括构成所谓“扩展型Goldenhar综合征”的广泛中枢神经系统畸形)、先天性心脏缺陷以及各种其他异常(肾脏、肺部、胃肠道)。还讨论了一些通常与眼耳脊椎综合征相鉴别但在某些情况下与额鼻发育异常、鳃耳肾(BOR)综合征、汤姆斯-布罗克斯综合征、维尔德文克综合征、迪乔治序列以及几种综合征(VATER、CHARGE和MURCS)存在重叠关系的病症。

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