Vermeij-Keers C, Mazzola R F, Van der Meulen J C, Strickler M
Cleft Palate J. 1983 Apr;20(2):128-45.
A macro- and/or microscopical study on the normal and abnormal development of the forebrain with the eyes, nose, and cranium, was performed in 139 mouse embryos, 120 normal and 19 abnormal human embryos and fetuses, and in about 2,300 human skulls. The results suggest that from the embryological point of view, a distinction should be made between facial defects involving the brain and/or the neural elements of the eyes, i.e., the cerebro-craniofacial dysplasias, and malformations of the face and cranium only, called the craniofacial dysplasias. Both groups can be subdivided into early or primary defects (in embryos less than or equal to 17 mm C-RL) and late or secondary defects (in embryos greater than or equal to 17 mm C-RL). Almost all of the primary defects can be considered to originate from disorders occurring during the transformation of the brain and face. The secondary defects concern defective differentiation of neurectoderm and of the mesenchyme into bone centers, cartilage, and muscles. All of the defects in question can be explained by insufficient cell proliferation, degeneration, and/or differentiation. New terminology is proposed.
对139个小鼠胚胎、120个正常人类胚胎和胎儿以及19个异常人类胚胎和胎儿,以及约2300个人类颅骨进行了关于前脑与眼睛、鼻子和颅骨正常及异常发育的宏观和/或微观研究。结果表明,从胚胎学角度来看,应区分涉及大脑和/或眼睛神经成分的面部缺陷,即脑颅面发育异常,以及仅涉及面部和颅骨的畸形,即颅面发育异常。这两组都可细分为早期或原发性缺陷(在头臀长小于或等于17毫米的胚胎中)和晚期或继发性缺陷(在头臀长大于或等于17毫米的胚胎中)。几乎所有原发性缺陷都可被认为源于大脑和面部转变过程中发生的紊乱。继发性缺陷涉及神经外胚层和间充质向骨中心、软骨和肌肉的分化缺陷。所有这些缺陷都可以用细胞增殖不足、退化和/或分化来解释。提出了新的术语。