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原发性中线发育区。I. 临床和流行病学特征。

Primary midline developmental field. I. Clinical and epidemiological characteristics.

作者信息

Martínez-Frías M L

机构信息

ECEMC, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

出版信息

Am J Med Genet. 1995 May 8;56(4):374-81. doi: 10.1002/ajmg.1320560406.

DOI:10.1002/ajmg.1320560406
PMID:7604845
Abstract

Opitz [BD:OAS XXIX(1):3-37, 1993] has postulated that during early blastogenesis the entire embryo represents a single morphogenetic unit, the primary field. During this period, beginning gastrulation, the most important events are the formation of the midline and the mesoderm. Consequently, one could expect that dysmorphogenetic reactions of the primary field are likely to disturb more than one of the essential events of blastogenesis, such as fusion, lateralization, decussation, segmentation, morphogenetic movements, asymmetry formation, etc. I have used the 20,891 liveborn malformed infants identified by the Spanish Collaborative Study of Congenital Malformations (ECEMC) to analyze the concept of the primary field defect (DFD). The malformed children were separated into 4,679 children with only midline defects, 1,592 children with midline plus other non-midline anomalies, and 14,620 babies without midline defects. Sex, twinning, neonatal death, parental consanguinity, and other malformed first degree relatives in the family were analyzed in each group. Different defects were selected as indicators of specific morphogenetic events of blastogenesis. Cardiac and neural tube defect were selected as indicators of fusion anomalies; agenesis/hypoplasia of the corpus callosum were included as example of decussation defect; cyclopia as representation of the alteration of lateralization; vertebral defects as indicators of anomalies of segmentation; intestinal malrotation and omphalocele as representatives of the alteration of the morphogenetic movement; and, finally, infants with asplenia, polysplenia, dextrocardias, transposition of great vessels, visceral transposition, and situs inversus totalis were grouped to allow an analysis of alteration of the normal body asymmetry.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

奥皮茨(1993年,《出生缺陷原始文献汇编》第XXIX卷第1期,第3 - 37页)曾推测,在早期胚胎形成过程中,整个胚胎代表一个单一的形态发生单位,即原基。在此期间,从原肠胚形成开始,最重要的事件是中线和中胚层的形成。因此,可以预期原基的形态发生异常反应可能会干扰胚胎形成过程中不止一个基本事件,比如融合、侧化、交叉、分割、形态发生运动、不对称形成等。我利用西班牙先天性畸形协作研究(ECEMC)识别出的20,891例活产畸形婴儿来分析原基缺陷(DFD)的概念。畸形儿童被分为仅患有中线缺陷的4,679名儿童、患有中线加其他非中线异常的1,592名儿童以及无中线缺陷的14,620名婴儿。对每组中的性别、双胎情况、新生儿死亡、父母近亲结婚以及家庭中其他畸形的一级亲属进行了分析。选择不同的缺陷作为胚胎形成特定形态发生事件的指标。心脏和神经管缺陷被选作融合异常的指标;胼胝体发育不全/发育不良被作为交叉缺陷的例子;独眼畸形作为侧化改变的代表;脊柱缺陷作为分割异常的指标;肠旋转不良和脐膨出作为形态发生运动改变的代表;最后,将患有无脾症、多脾症、右位心、大血管转位、内脏转位和完全性内脏反位的婴儿归为一组,以便分析正常身体不对称性的改变。(摘要截选至250词)

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