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骨发育异常中的模式识别

Pattern recognition in bone dysplasias.

作者信息

Spranger J

出版信息

Prog Clin Biol Res. 1985;200:315-42.

PMID:4080742
Abstract

Genetically different bone dysplasias may manifest themselves in similar patterns of skeletal abnormalities. It is proposed to group these similar dysplasias in 'families' for two reasons: 1 The knowledge of developmental patterns shared by different genetic disorders cautions the diagnostician and encourages a two-step procedure: a) provisional recognition of a pattern and b) more careful analysis of the pattern to reach a final, specific diagnosis. 2 Families of bone dysplasias may be the result of similar pathogenetic mechanisms. Once the mechanism is discovered in one member of the family, a search for similar mechanisms in others may be rewarding. An example of such a pattern is dysostosis multiplex. It is found in a family of disorders caused by defects of complex carbohydrate degradation. The present study delineates four more patterns and their families: the achondroplasia pattern, spondyloepiphyseal dysplasia congenita pattern, the Larsen/OPD pattern and the Stickler/Kniest pattern.

摘要

基因不同的骨发育异常可能以相似的骨骼异常模式表现出来。出于两个原因,建议将这些相似的发育异常归为“家族”:1. 不同遗传疾病共有的发育模式知识提醒诊断医生,并鼓励采用两步程序:a)初步识别模式,b)更仔细地分析模式以得出最终的具体诊断。2. 骨发育异常家族可能是相似致病机制的结果。一旦在家族中的一个成员身上发现了这种机制,在其他成员中寻找相似机制可能会有收获。这种模式的一个例子是多发性骨发育不全。它出现在由复杂碳水化合物降解缺陷引起的一组疾病中。本研究描绘了另外四种模式及其家族:软骨发育不全模式、先天性脊柱骨骺发育异常模式、拉森/骨发育异常模式和斯蒂克勒/克尼斯特模式。

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