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肢体纵向缺损与体节。对378例沙利度胺诱发的肢体发育异常畸形的分析。

Longitudinal limb deficiencies and the sclerotomes. An analysis of 378 dysmelic malformations induced by thalidomide.

作者信息

McCredie J, Willert H G

机构信息

Royal Prince Alfred Hospital, Sydney, Australia.

出版信息

J Bone Joint Surg Br. 1999 Jan;81(1):9-23. doi: 10.1302/0301-620x.81b1.8448.

Abstract

The pathogenesis of longitudinal reduction deformities of the limbs, or dysmelia, is still a matter of debate. Their morphological pattern was defined from a large collection of radiographs of children with dysmelia following the thalidomide disaster. We compared radiographs of 378 of these limbs with the sclerotomes which are areas of segmental sensory innervation of the limb skeleton defined by the radiation of referred pain. The pattern of dysmelia matched the sclerotomes closely in 279 limbs (73.5%). The principles of skeletal reduction in dysmelia are explained by the arrangement of the sclerotomes. The congruence between two separate and independent data sets shows that both patterns are expressions of the underlying segmental sensory innervation of the skeleton, and that the sensory nervous system is involved in the process of limb morphogenesis and teratogenesis.

摘要

肢体纵向缩短畸形(即肢体发育不全)的发病机制仍是一个有争议的问题。在沙利度胺灾难后,通过收集大量肢体发育不全儿童的X光片确定了其形态模式。我们将其中378个肢体的X光片与硬骨节进行了比较,硬骨节是由牵涉痛放射所定义的肢体骨骼节段性感觉神经支配区域。在279个肢体(73.5%)中,肢体发育不全的模式与硬骨节紧密匹配。肢体发育不全中骨骼缩减的原理可通过硬骨节的排列来解释。两个独立数据集之间的一致性表明,这两种模式都是骨骼潜在节段性感觉神经支配的表现,并且感觉神经系统参与了肢体形态发生和致畸过程。

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