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发育波动不对称与发育起源性疾病

Fluctuating asymmetry and disorders of developmental origin.

作者信息

Naugler C T, Ludman M D

机构信息

Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Am J Med Genet. 1996 Dec 2;66(1):15-20. doi: 10.1002/(SICI)1096-8628(19961202)66:1<15::AID-AJMG4>3.0.CO;2-V.

Abstract

Environmental and/or genetic stresses may cause a breakdown in developmental homeostasis, resulting in increased bilateral asymmetry of morphological traits. The degree of these deviations (termed "fluctuating asymmetry") is thought to correlate with the severity of the stress. If these stresses also play a role in the appearance of developmental disorders, then increased morphological asymmetry may serve as a risk marker for disorders of developmental origin. This would be possible if 1) the environmental stress that caused a breakdown in developmental stability also contributed to the appearance of the disorder, and/or 2) the genetic predisposition (liability) to the disorder and increased susceptibility to fluctuating asymmetry have a common cause. Although a number of authors have reported associations between increased fluctuating asymmetry and disorders of presumed developmental origin, the usefulness of fluctuating asymmetry as a risk marker has not been established. One obstacle to this assessment is the lack of odds ratios reported by previous authors.

摘要

环境和/或基因压力可能导致发育稳态的破坏,从而导致形态特征的双侧不对称性增加。这些偏差的程度(称为“波动不对称性”)被认为与压力的严重程度相关。如果这些压力也在发育障碍的出现中起作用,那么形态不对称性的增加可能作为发育起源性障碍的风险标志物。如果1)导致发育稳定性破坏的环境压力也促成了该障碍的出现,和/或2)该障碍的遗传易感性(易患性)以及对波动不对称性的易感性增加有共同的原因,那么这将是有可能的。尽管许多作者报告了波动不对称性增加与推测为发育起源性障碍之间的关联,但波动不对称性作为风险标志物的有用性尚未确立。进行这种评估的一个障碍是先前作者未报告比值比。

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