A Possible Case of Hypopituitarism in Neolithic China

被引:6
作者
Hernandez, M. [1 ]
机构
[1] Univ Cambridge, Leverhulme Ctr Human Evolutionary Studies, Dept Biol Anthropol, Cambridge CB2 1QH, England
关键词
China; dwarfism; Neolithic; IDIOPATHIC SHORT STATURE; MULTIPLE EPIPHYSEAL DYSPLASIA; PITUITARY-HORMONE DEFICIENCY; GROWTH-HORMONE; TURNER SYNDROME; ANCIENT-EGYPT; ADULT PATIENTS; DWARFISM; GENE; SHOX;
D O I
10.1002/oa.1266
中图分类号
Q98 [人类学];
学科分类号
030303 ;
摘要
A human skeleton with a possible case of hypopituitarism is reported. The individual (burial M53) is from the site of Guanjia, a Neolithic settlement in northern China, dated to the Late Yangshao period (6000-5500bp). On the basis of the fully erupted third permanent molars and moderate occlusal dental wear resulting in substantial exposure of dentine, the initially estimated age-at-death was placed between 26 and 33years. However, dimensions of the postcranial skeleton fall significantly below and outside the range from contemporaneous adult populations, and along with delayed epiphyseal fusion present throughout the skeleton, the postcranial age is concordant to that of an 11- to 13-year-old child. Most long bone epiphyses display incomplete fusion or are entirely unfused, but a lack of microporosity in the metaphyseal areas near growth plates indicates a cessation of longitudinal bone growth. Because no signs of porotic hyperostosis, cribra orbitalia, periosteal lesions or linear enamel hypoplasia are observed, the restricted growth of this individual is likely caused by a growth hormone disorder and is unrelated to nutritional deficiencies or systemic infection. Copyright (c) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:432 / 446
页数:15
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