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特雷彻·柯林斯综合征、阿佩尔综合征和克鲁宗综合征中的耳部形态。

Ear morphology in Treacher Collins', Apert's, and Crouzon's syndromes.

作者信息

Farkas L G

出版信息

Arch Otorhinolaryngol. 1978 Mar 3;220(1-2):153-7. doi: 10.1007/BF00456310.

Abstract

Size, proportions, level, inclination and shape of the ears were assessed by anthrompometric methods in eight patients with Treacher Collins' syndrome, eleven with Apert's, and 25 with Crouzon's syndrome. The ears were most severely damaged in Treacher Collins' syndrome, in which they were microtic or disproportionally long; many were low-set and with great inclination. All patients with Apert's syndrome had low-set ears and a tendency to disproportion, with widening and small inclination of the longitudinal axis. The ears were least affected in Crouzon's syndrome; in two-thirds of the patients there were mild growth variations leading to disproportion in width (wide ears), or low-set ears, or both.

摘要

采用人体测量方法对8例特雷彻·柯林斯综合征患者、11例阿佩尔综合征患者和25例克鲁宗综合征患者的耳朵大小、比例、位置、倾斜度和形状进行了评估。耳朵在特雷彻·柯林斯综合征中受损最为严重,表现为小耳畸形或不成比例地长;许多耳朵位置较低且倾斜度大。所有阿佩尔综合征患者的耳朵位置都较低,且有不成比例的倾向,纵轴变宽且倾斜度小。耳朵在克鲁宗综合征中受影响最小;三分之二的患者有轻微的生长差异,导致宽度不成比例(耳朵宽)、耳朵位置低或两者皆有。

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