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对亨廷顿舞蹈症患者及其家族的人体测量评估。

An anthropometric assessment of Huntington's disease patients and families.

作者信息

Farrer L A, Meaney F J

出版信息

Am J Phys Anthropol. 1985 Jul;67(3):185-94. doi: 10.1002/ajpa.1330670304.

Abstract

An anthropometric investigation was designed to evaluate patterns of physical deterioration in Huntington's disease (HD). In this study a comprehensive set of measurements was taken including height, weight, body circumferences, skinfold thickness, and craniofacial, linear, and breadth components of the body, on 44 normal, 26 affected, and 70 at-risk individuals between 14 and 88 years of age. The anthropometric data were converted to z-scores using standards to adjust for age and sex differences. These scores were then adjusted for inter-family variation. There were significant differences among normal and affected individuals for all dimensions of body mass, as well as for several craniofacial and linear components of the body. Several significant differences were also found between normals and particular age cohorts of at-risk persons. HD gene carrier status was further assessed by factor analysis of the adjusted scores.

摘要

一项人体测量学调查旨在评估亨廷顿舞蹈症(HD)患者身体机能衰退的模式。在这项研究中,对44名正常个体、26名患病个体以及70名14至88岁的高危个体进行了全面的测量,包括身高、体重、身体周长、皮褶厚度以及身体的颅面、线性和宽度部分。人体测量数据通过使用标准转换为z分数,以调整年龄和性别差异。然后对这些分数进行调整以消除家庭间的差异。正常个体和患病个体在所有身体质量维度以及身体的几个颅面和线性部分存在显著差异。在正常个体与特定年龄组的高危人群之间也发现了一些显著差异。通过对调整分数的因子分析进一步评估了HD基因携带者状态。

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