Suppr超能文献

先天性弯曲综合征的异质性。长骨型和短骨型。

Heterogeneity in the campomelic syndromes. Long-and short-bone varieties.

作者信息

Khajavi A, Lachman R, Rimoin D, Schimke R N, Dorst J, Handmaker S, Ebbin A, Perreault G

出版信息

Radiology. 1976 Sep;120(3):641-7. doi: 10.1148/120.3.641.

Abstract

Analysis of 9 cases of bilateral bent limbs (campomelia) and dwarfism, as well as a review of the literature, indicate that campomelic syndrome appears to be a well-defined distinct disorder which the authors call long-limbed campomelic syndrome. Other neonates with congenital bent-limbed dwarfism can be classified as having short-limbed campomelic syndrome, and among these at least two distinct forms have been delineated--the craniosynostotic and the normocephalic form. Congenital bent bones also occur in a variety of generalized disorders of ossification that must be distinguished from these well-defined types of campomelic dwarfism.

摘要

对9例双侧肢体弯曲(弯肢畸形)和侏儒症病例的分析以及文献综述表明,弯肢综合征似乎是一种明确的独特疾病,作者将其称为长肢弯肢综合征。其他患有先天性肢体弯曲侏儒症的新生儿可归类为短肢弯肢综合征,其中至少已 delineated 出两种不同形式——颅缝早闭型和头型正常型。先天性弯曲骨骼也见于多种全身性骨化障碍,必须将其与这些明确的弯肢侏儒症类型区分开来。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验