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[人类鼻额芽的神经嵴病。筛骨综合征(鼻中隔筛骨发育不全和过度发育)(作者译)]

[Neurocristopathies of the human nasofrontal bud. Ethmoidal syndromes (hypo- and hyper-septoethmoidism) (author's transl)].

作者信息

Couly G

出版信息

Rev Stomatol Chir Maxillofac. 1981;82(4):213-25.

PMID:6944757
Abstract

Knowledge of human brain development biology has increased rapidly over the last decade due to fundamental acquisitions in the fields of organogenesis, fetal development, and post-natal growth. The role of the neural crests during cephalic organogenesis, recently studied by Mme Nicole Le Douarin, has given new biological dimensions to the head : it is an organic complex, globally neural in character, and of encephalofacial territorialization. The cervicocephalic region derives this original segmentation from the migratory property of this contingent of the neural crests. In this perspective, the nasofrontal bud is therefore an embryonic cephalic segment, in which appears the pro-encephalon, the eyes, the olfactory bulb, and the median facial zones (bone, cartilage, teeth). Any morphogenetic anomaly in this original craniofacial segment creates associated malformation of the brain, the base of the skull, and the face (eyes and olfactory bulbs) : the neurocristopathies. In this respect, and from the semiological point of view, the face is the "predicate" of the brain. A new classification of these malformations is proposed, based on the clinical study of the ethmoid, a cartilaginous median organ which is accessible clinically. Epigenesis lasts for 18 months in this organ, which forms a part of the face and the neurocranium, and which is known to play a "motor" morphogenetic role on the osteomembranous face : the ethmoidal syndromes (hypo- and hyper-septoethmoidism). Future reports will discuss the neurocristopathies of the branchial arches.

摘要

在过去十年中,由于器官发生、胎儿发育和出生后生长领域取得的基础性成果,人类大脑发育生物学知识迅速增长。妮可·勒杜兰夫人最近对神经嵴在头部器官发生过程中的作用进行了研究,这为头部赋予了新的生物学维度:它是一个整体具有神经特征且存在脑面区域化的有机复合体。颈头部区域从这群神经嵴的迁移特性中获得了这种原始的分段特征。从这个角度来看,鼻额芽因此是一个胚胎头部节段,其中出现了前脑、眼睛、嗅球和面部正中区域(骨骼、软骨、牙齿)。这个原始颅面部节段中的任何形态发生异常都会导致大脑、颅底和面部(眼睛和嗅球)出现相关畸形:即神经嵴病。在这方面,从症状学角度来看,面部是大脑的“谓语”。基于对筛骨的临床研究,提出了这些畸形的一种新分类方法。筛骨是一个临床可触及的软骨性正中器官,其个体发生持续18个月,它是面部和神经颅的一部分,并且已知在骨膜性面部发挥“驱动”形态发生作用:即筛骨综合征(筛骨发育不全和过度发育)。未来的报告将讨论鳃弓的神经嵴病。

相似文献

1
[Neurocristopathies of the human nasofrontal bud. Ethmoidal syndromes (hypo- and hyper-septoethmoidism) (author's transl)].[人类鼻额芽的神经嵴病。筛骨综合征(鼻中隔筛骨发育不全和过度发育)(作者译)]
Rev Stomatol Chir Maxillofac. 1981;82(4):213-25.
2
[Cephalic neural crests and disorders of craniofacial morphogenesis. Neurocristopathies (author's transl)].[头部神经嵴与颅面形态发生障碍。神经嵴病(作者译)]
Rev Stomatol Chir Maxillofac. 1980;81(6):332-48.
3
The facial features of holoprosencephaly in anencephalic human specimens. II. Craniofacial anatomy.无脑儿标本中前脑无裂畸形的面部特征。II. 颅面解剖学
Teratology. 1981 Jun;23(3):305-15. doi: 10.1002/tera.1420230305.
4
[Development of the face in the embryo].
Rev Prat. 1991 Jan 1;41(1):7-15.
5
Median facial malformations and their implications for brain malformations.面部正中畸形及其对脑畸形的影响。
Birth Defects Orig Artic Ser. 1975;11(7):155-81.
6
[Associated morphological anomalies of the face and brain in infants].
Arch Fr Pediatr. 1988 Feb;45(2):99-104.
7
[Serious cerebral malformations (corpus callosum aplasia, prosencephalic cyst), internal carotid canal and facial malformations due to neural crest abnormalities, associated with choleosteatoma].
Minerva Pediatr. 2007 Aug;59(4):403-8.
8
[The human cartilaginous mesethmoid (author's transl)].[人类软骨性鼻中隔(作者译)]
Rev Stomatol Chir Maxillofac. 1980;81(3):135-51.
9
Classification of facial malformations.面部畸形的分类。
Int J Oral Surg. 1981;10(Suppl 1):267-72.
10
[Malformations of the nasal fossa and paramedian facial clefts. New perspectives].[鼻窝畸形与面部正中裂。新视角]
Ann Otolaryngol Chir Cervicofac. 1996;113(7-8):373-8.

引用本文的文献

1
Dysgenesis of the internal carotid artery associated with transsphenoidal encephalocele: a neural crest syndrome?与经蝶骨脑膨出相关的颈内动脉发育不全:一种神经嵴综合征?
AJNR Am J Neuroradiol. 1999 Jun-Jul;20(6):1154-7.
2
Separation of neural and surface ectoderm after closure of the rostral neuropore.在头侧神经孔闭合后神经外胚层与表面外胚层的分离。
Anat Embryol (Berl). 1990;182(5):455-63. doi: 10.1007/BF00178910.