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儿科病理学中的发育领域概念——尤其是关于腓骨发育不全/发育不良和迪格奥尔格综合征。

The developmental field concept in pediatric pathology--especially with respect to fibular a/hypoplasia and the DiGeorge anomaly.

作者信息

Opitz J M, Lewin S O

出版信息

Birth Defects Orig Artic Ser. 1987;23(1):277-92.

PMID:3580552
Abstract

Identical anomalies produced by different causes such as aneuploidy, gene mutation, teratogenic chemicals, and certain surgical procedures are a clear indication that embryonic primordia respond as units in the production of developmental anomalies of anatomic structure. Hence, they must also act as units during normal ontogeny. The presence of identical malformations in different mammalian species identifies developmental and anatomic homology by virtue of descent from a common ancestor. These dys- and orthomorphogenetically reactive units are the equivalents of the classic experimental embryologist's epimorphic fields, which are those units of the embryo in which the development of complex structures appropriate to the species is determined and controlled in a spatially coordinated, temporarily synchronous, and epimorphically hierarchical manner that expresses both species-nonspecific (that is, phylogenetic) and species-specific genetically coded developmental information. Thus, it is as important for pathologists as it is for clinical geneticists to steep themselves in the art and science of phenotype analysis and to be able to do all of those studies, including anthropometry, dermatoglyphics, and growth analysis, that are required to arrive at inferences of cause and pathogenesis from the phenotype. There is probably one other incentive besides the ethical and intellectual ones to do this and to do it as well as possible, namely, the medico-legal consequences. If pathologists fail to illuminate the causal genesis of a given case to aid in preventing recurrence, then, in short order, they might be held equally as liable as clinicians for missing high recurrence risk genetic diagnoses. These depressing considerations aside, it is important to close on a positive note. As at the outset, we want to emphasize once more that, without question, this is the most exciting time to be working in the field of developmental pathology. In this specialty a marriage is occurring of several types of investigational methods, ranging from humble morphologic studies to metabolic analysis to the most sophisticated designs of molecular biology, to produce new interdisciplinary approaches to the solution of the oldest intellectual problem confronting medicine--how does the "fabric of the human body" (in the immortal words of Vesalius) come about?(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

由不同原因(如非整倍体、基因突变、致畸化学物质和某些外科手术)产生的相同异常,清楚地表明胚胎原基在产生解剖结构发育异常时作为一个整体做出反应。因此,它们在正常个体发育过程中也必定作为一个整体发挥作用。不同哺乳动物物种中相同畸形的存在,凭借共同祖先的遗传确定了发育和解剖学上的同源性。这些发育异常和正常形态发生反应性单位等同于经典实验胚胎学家的形态发生场,即胚胎中的那些单位,其中适合该物种的复杂结构的发育是以空间协调、暂时同步且形态发生层次的方式确定和控制的,这种方式表达了物种非特异性(即系统发育)和物种特异性的遗传编码发育信息。因此,对于病理学家来说,像临床遗传学家一样深入研究表型分析的艺术和科学,并能够进行所有那些研究,包括人体测量学、皮纹学和生长分析,以便从表型推断病因和发病机制,这同样重要。除了伦理和学术方面的动机外,可能还有另一个动机促使人们尽可能做好这件事,即医学法律后果。如果病理学家未能阐明特定病例的因果起源以帮助预防复发,那么很快他们可能会因遗漏高复发风险的基因诊断而与临床医生承担同样的责任。抛开这些令人沮丧的考虑不谈,以积极的态度结束是很重要的。正如一开始那样,我们想再次强调,毫无疑问,这是从事发育病理学领域工作最令人兴奋的时期。在这个专业领域,正在发生几种研究方法的融合,从简单的形态学研究到代谢分析,再到最复杂的分子生物学设计,以产生新的跨学科方法来解决医学面临的最古老的学术问题——“人体结构”(用维萨里不朽的话说)是如何形成的?(摘要截取自250字)

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Birth Defects Orig Artic Ser. 1987;23(1):277-92.
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Pediatr Cardiol. 1996 May-Jun;17(3):143-9. doi: 10.1007/BF02505203.
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