Peeters Hilde, Devriendt Koen
Department of Human Genetics, University Hospital Gasthuisberg, University of Leuven, Herestraat 49, B-3000 Leuven, Belgium.
Eur J Med Genet. 2006 Sep-Oct;49(5):349-62. doi: 10.1016/j.ejmg.2005.12.003. Epub 2006 Jan 3.
Heterotaxia is a group of congenital disorders characterized by a misplacement of one or more organs according to the left-right axis. Bilateral asymmetry of internal organs is conserved among all vertebrate species. Analyses in animal models such as mouse, chicken, frog and zebrafish allowed for a remarkable progress of knowledge on the embryonic and genetic mechanisms underlying internal left-right asymmetry. In this review we focus on the insights from these model organisms that are useful for a better understanding of the etiology and pathogenesis of human heterotaxia. The known causes of human heterotaxia are reviewed and situated within the conceptual framework that originates from vertebrate model organisms. Furthermore, we attempt to apply the rapidly increasing insights gained from both animal models and human genetics to clinical practice in order to contribute to a more accurate conceptual classification, genetic diagnosis and counseling.
内脏逆位是一组先天性疾病,其特征是一个或多个器官相对于左右轴位置异常。所有脊椎动物物种的内脏双侧不对称现象都是保守的。对小鼠、鸡、青蛙和斑马鱼等动物模型的分析使我们对内脏左右不对称的胚胎学和遗传学机制有了显著的认识进展。在这篇综述中,我们重点关注这些模式生物的见解,这些见解有助于更好地理解人类内脏逆位的病因和发病机制。我们回顾了人类内脏逆位的已知病因,并将其置于源自脊椎动物模式生物的概念框架内。此外,我们试图将从动物模型和人类遗传学中迅速增加的见解应用于临床实践,以便更准确地进行概念分类、基因诊断和咨询。