[厚皮性骨膜病——疾病 onset 后 25 年骨骼变化的发展] （注：这里“onset”直译为“发作”，结合语境推测是指疾病开始的时间，可灵活处理为“发病”等表述，因指令要求不添加解释，所以保留原文英文单词）
[Pachydermoperiostosis--development of bone changes 25 years after disease onset].
作者信息
Míková D
出版信息
Vnitr Lek. 1989 Jan;35(1):68-73.
PMID:2929151
Abstract
Pachydermoperiostosis-hyperostosis generalisata cum pachydermia is considered a sex-linked hereditary pathological disposition of the mesenchyme with a favourable course of the dominant form; it is, however, progressively malignant in the recessive type of heredity. As a rule men affected. The author describes the case of a patient where the disease was diagnosed 25 years previously.
摘要
厚皮性骨膜病-全身性骨质增生合并厚皮症被认为是间充质的一种性连锁遗传性病理倾向，显性形式病程良好；然而，在隐性遗传类型中呈进行性恶性。通常男性受累。作者描述了一例25年前确诊该病的患者病例。
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