人类性别多态性与人类骨骼性别指标形态变异预测范围。

IF 2 2区 生物学 Q1 ANTHROPOLOGY
Claudia Marie Astorino
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引用次数: 0

摘要

目的:虽然生物学家通常认为人类是两性二态的,但人类在性别特征上的差异比一般认为的要大。双性人,或那些具有传统上被认为是男性、女性和/或非典型特征的特征组合的人,代表了这种变化的一部分。虽然已经有很多研究致力于描述性别差异和估计人类骨骼的性别,但阴阳人的骨骼性别特征的变化是未知的。材料和方法:对九种双性人的骨骼性别指标表达的相对水平进行知情预测,使用最近的内分泌学文本,其中一节侧重于双性人的变化。骨骼性别指标在标准性别指标中的表达预测被定义为低、中、高。结果:结果预测,阴阳人完全雄激素不敏感(CAIS)、X单体和XY性腺发育不良的个体,骨骼性别指标的表达可能较低;中间体为5α-还原酶(5α-RD)、部分雄激素不敏感(PAIS)、先天性肾上腺增生(CAH)(21-羟化酶变异)、勒氏杆菌发育和XXY;而对于CAH (11β-羟化酶变异)和尿道下裂的双性人来说,这一比例更高。结论:这些预测可能用于测试关于双性人骨骼变异的假设,当骨骼遗骸和/或数据在双性人同意的情况下可获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Human Sexual Polymorphism and Predicted Ranges of Morphological Variation in Human Skeletal Sex Indicators

Human Sexual Polymorphism and Predicted Ranges of Morphological Variation in Human Skeletal Sex Indicators

Objective

Humans, while most often considered to be sexually dimorphic by biologists, exhibit a greater range of variation in sex traits than is generally acknowledged. Intersex individuals, or those with a combination of traits traditionally considered male, female, and/or atypical for either, represent some of this variation. While much study has been devoted to characterizing sex differences and estimating sex in the human skeleton, skeletal variation in sex traits is unknown for intersex individuals.

Materials and Methods

Informed predictions of the relative level of skeletal sex indicator expression for nine forms of intersex were created using a recent endocrinological text with a section focused on intersex variations. Predictions of skeletal sex indicator expression in standard sex indicators were defined as low, intermediate, or high.

Results

Results predicted that skeletal sex indicator expression is expected to be low for individuals whose form of intersex is complete androgen insensitivity (CAIS), monosomy X, and XY gonadal dysgenesis; intermediate for those whose form of intersex is 5α-reductase (5α-RD), partial androgen insensitivity (PAIS), congenital adrenal hyperplasia (CAH) (21-hydroxylase variations), Müllerian agenesis, and XXY; and high for those whose form of intersex is CAH (11β-hydroxylase variations) and hypospadias.

Conclusions

These predictions may be used for testing hypotheses on intersex skeletal variation when skeletal remains and/or data are accessible with the consent of intersex individuals.

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