• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

特雷彻·柯林斯综合征、纳格尔综合征和米勒综合征中腭裂的发病机制。

Pathogenesis of cleft palate in Treacher Collins, Nager, and Miller syndromes.

作者信息

Sulik K K, Smiley S J, Turvey T A, Speight H S, Johnston M C

机构信息

Department of Cell Biology and Anatomy, University of North Carolina, Chapel Hill 27599.

出版信息

Cleft Palate J. 1989 Jul;26(3):209-16; discussion 216.

PMID:2758673
Abstract

Abnormalities of the secondary palate were studied in an animal model in which features of Treacher Collins syndrome (TCS) and Nager or Miller syndromes (both of which are facially similar to Treacher Collins, but include limb malformations) were induced by acute maternal exposure to 13-cis-retinoic acid (13-cis-RA, isotretinoin, Accutane). Previous work in our laboratory has illustrated that excessive cell death in the proximal aspect of the maxillary and mandibular prominences of the first visceral arch and in the apical ectodermal ridge of the limb bud probably accounts for the characteristic craniofacial and limb abnormalities observed (Sulik et al, 1987; Sulik and Dehart, 1988). The current study shows that maternal treatment with 400 mg per kilogram 13-cis-RA at 8 days 14 hours (8d14hr) or 9d6hr post fertilization results in abnormalities of the secondary palate that vary in incidence and severity. Following the earlier treatment time, 82 percent (68 of 74) of the 18d fetuses were affected, with, severely hypoplastic, unfused palatal shelves present in 34 percent (25 of 74). The less severely affected fetuses had malformations that involved primarily the posterior aspect of the palatal shelves. This malformation (foreshortening of the posterior portion of the palate) constituted the major developmental alteration that resulted from treatment at the later time, at which time a 52 percent (26 of 50) malformation incidence was seen. The change in pattern of malformations with treatment time is consistent with the changing pattern of programmed cell death, which was observed to occur in the first visceral arch.

摘要

在一个动物模型中研究了继发腭异常,在该模型中,通过母体急性暴露于13 - 顺式维甲酸(13 - cis - RA,异维甲酸,保肤灵)诱导出了特雷彻·柯林斯综合征(TCS)以及纳杰尔或米勒综合征(这两种综合征面部特征均与特雷彻·柯林斯综合征相似,但还包括肢体畸形)的特征。我们实验室之前的研究表明,第一鳃弓上颌和下颌隆起近端以及肢芽顶端外胚层嵴中过多的细胞死亡可能是观察到的典型颅面和肢体异常的原因(苏利克等人,1987年;苏利克和德哈特,1988年)。当前研究表明,在受精后8天14小时(8d14hr)或9天6小时给予母体每千克400毫克13 - 顺式维甲酸治疗,会导致继发腭出现发生率和严重程度各异的异常。在较早的治疗时间点之后,18天胎儿中有82%(74个中的68个)受到影响,其中34%(74个中的25个)出现严重发育不全、未融合的腭板。受影响较轻的胎儿畸形主要累及腭板后部。这种畸形(腭后部缩短)是后期治疗导致的主要发育改变,此时畸形发生率为52%(50个中的26个)。畸形模式随治疗时间的变化与在第一鳃弓中观察到的程序性细胞死亡模式的变化一致。

相似文献

1
Pathogenesis of cleft palate in Treacher Collins, Nager, and Miller syndromes.特雷彻·柯林斯综合征、纳格尔综合征和米勒综合征中腭裂的发病机制。
Cleft Palate J. 1989 Jul;26(3):209-16; discussion 216.
2
Mandibulofacial dysostosis (Treacher Collins syndrome): a new proposal for its pathogenesis.下颌面骨发育不全(特雷彻·柯林斯综合征):关于其发病机制的新观点
Am J Med Genet. 1987 Jun;27(2):359-72. doi: 10.1002/ajmg.1320270214.
3
Processes involved in retinoic acid production of small embryonic palatal shelves and limb defects.小胚胎腭突和肢体缺陷的视黄酸产生所涉及的过程。
Teratology. 1990 Mar;41(3):299-310. doi: 10.1002/tera.1420410307.
4
Etiology of retinoic acid-induced cleft palate varies with the embryonic stage.维甲酸诱导腭裂的病因随胚胎发育阶段而异。
Teratology. 1989 Dec;40(6):533-53. doi: 10.1002/tera.1420400602.
5
Animal models for human craniofacial malformations.人类颅面畸形的动物模型。
J Craniofac Genet Dev Biol. 1991 Oct-Dec;11(4):277-91.
6
Retinoic-acid-induced limb malformations resulting from apical ectodermal ridge cell death.视黄酸诱导的肢体畸形源于顶端外胚层嵴细胞死亡。
Teratology. 1988 Jun;37(6):527-37. doi: 10.1002/tera.1420370602.
7
Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome.患有特雷彻·柯林斯综合征的受试者中牙齿异常、异位萌出及相关口腔畸形的患病率。
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 May;101(5):588-92. doi: 10.1016/j.tripleo.2005.07.016. Epub 2006 Feb 17.
8
Retinoic acid alters epithelial differentiation during palatogenesis.视黄酸在腭发育过程中改变上皮分化。
J Craniofac Genet Dev Biol. 1991 Oct-Dec;11(4):315-25.
9
Strain differences between C57BL/6 and SWV mice in time of palate closure and induction of palatal slit and cleft palate.C57BL/6小鼠和SWV小鼠在腭部闭合时间以及腭部裂隙和腭裂诱导方面的品系差异。
Teratology. 1985 Apr;31(2):279-83. doi: 10.1002/tera.1420310214.
10
[Study on etiology of retinoic acid-induced cleft palate in mouse].[维甲酸诱导小鼠腭裂病因学研究]
Zhonghua Kou Qiang Yi Xue Za Zhi. 2003 May;38(3):185-7.

引用本文的文献

1
Advances in prenatal diagnosis of fetal otocephaly by 3D imaging.三维成像在胎儿头颅畸形产前诊断中的进展。
BMJ Case Rep. 2022 Apr 22;15(4):e249276. doi: 10.1136/bcr-2022-249276.
2
Broad-spectrum next-generation sequencing-based diagnosis of a case of Nager syndrome.基于广谱下一代测序技术对一例纳格综合征病例的诊断
J Clin Lab Anal. 2020 Sep;34(9):e23426. doi: 10.1002/jcla.23426. Epub 2020 Jun 14.
3
A case report: nager acrofacial dysostosis.病例报告:纳杰尔综合征(肢端面部发育不全)
Iran J Otorhinolaryngol. 2012 Winter;24(66):45-50.
4
The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.特雷彻·柯林斯综合征的突变谱显示,产生过早终止密码子的突变占主导地位。
Am J Hum Genet. 1997 Mar;60(3):515-24.
5
Face facts: genes, environment, and clefts.面对现实:基因、环境与腭裂
Am J Hum Genet. 1995 Aug;57(2):227-32.