• 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

罗宾序列和复合体：病因异质性及发病机制/表型变异性

Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability.

作者信息

Cohen M M

出版信息

Am J Med Genet. 1999 Jun 4;84(4):311-5.

PMID:10340643
Abstract

Robin sequence has been the subject of numerous general papers and has also been cited in specific syndrome articles. Evidence is provided that the condition is not only causally heterogeneous but also pathogenetically and phenotypically variable, necessitating the use of the terms "Robin sequences" and "Robin complexes."

摘要

罗宾序列征一直是众多综述文章的主题，也在特定综合征文章中被引用。有证据表明，这种情况不仅病因异质性，而且在发病机制和表型上也存在差异，因此有必要使用“罗宾序列征”和“罗宾复合体”这两个术语。

相似文献

1
Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability.罗宾序列和复合体：病因异质性及发病机制/表型变异性
Am J Med Genet. 1999 Jun 4;84(4):311-5.
2
[Early hyperplasia of the mandible (Pierre-Robin syndrome): report of a case].[下颌骨早期增生（皮埃尔 - 罗宾综合征）：一例报告]
Stomatol Mediterr. 1986 Oct-Dec;6(4):541-4.
3
Interface between Robin sequence and ordinary cleft palate.罗宾序列征与普通腭裂之间的关联
Am J Med Genet. 2001 Jul 1;101(3):288. doi: 10.1002/ajmg.1377.
4
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneity.远端关节挛缩症、智力障碍、吹口哨面容与皮埃尔·罗宾序列征的关联：疾病分类异质性的证据
Am J Med Genet. 1991 Mar 15;38(4):557-61. doi: 10.1002/ajmg.1320380412.
5
Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.男性患者中的常染色体隐性矮小症、罗宾序列征、下颌骨裂、轴前/轴后手部异常以及马蹄内翻足。
Am J Med Genet. 1993 Oct 1;47(5):707-9. doi: 10.1002/ajmg.1320470524.
6
[Paradoxal evolution of the Robin syndrome].[罗宾综合征的反常演变]
Orthod Fr. 1976;47(0):139-47.
7
Pierre Robin syndrome: an update.皮埃尔·罗宾综合征：最新进展。
Niger Postgrad Med J. 2007 Jun;14(2):140-5.
8
Mandibular distraction osteogenesis for Pierre Robin sequence: what percentage of neonates need it?下颌骨牵张成骨术治疗Pierre Robin序列征：新生儿中需要该治疗的比例是多少？
J Craniofac Surg. 2008 Sep;19(5):1237-43. doi: 10.1097/SCS.0b013e3181843293.
9
Pierre Robin sequence: a series of 117 consecutive cases.皮埃尔·罗宾序列征：117例连续病例系列研究
J Pediatr. 2001 Oct;139(4):588-90. doi: 10.1067/mpd.2001.117784.
10
The mandibular catch-up growth controversy in Pierre Robin sequence.皮埃尔·罗宾序列中下颌骨追赶生长的争议
Am J Orthod Dentofacial Orthop. 2001 Sep;120(3):280-5. doi: 10.1067/mod.2001.115038.

引用本文的文献

1
Micrognathia and cleft palate as a cause of obstructive sleep apnoea in infants.小颌畸形和腭裂作为婴儿阻塞性睡眠呼吸暂停的一个病因
Acta Paediatr. 2025 Jun;114(6):1169-1178. doi: 10.1111/apa.17540. Epub 2024 Dec 5.
2
Non-Surgical Respiratory Management in Relation to Feeding and Growth in Patients with Robin Sequence; a Prospective Longitudinal Study.与罗宾序列征患者喂养及生长相关的非手术呼吸管理：一项前瞻性纵向研究
Cleft Palate Craniofac J. 2023 Sep 20;62(1):10556656231199840. doi: 10.1177/10556656231199840.
3
Construction of fetal inferior facial angle and hemi-mandible length reference ranges at 18-21 weeks' gestation in an Australian population.
澳大利亚人群中孕18至21周胎儿下颌下角度和半侧下颌骨长度参考范围的构建。
Australas J Ultrasound Med. 2017 Oct 7;20(4):168-173. doi: 10.1002/ajum.12066. eCollection 2017 Nov.
4
An innovative method for manufacturing the Tuebingen palatal plate for infants with Robin sequence.用于制造 Robin 序列婴儿的图宾根腭托的创新方法。
BMC Pediatr. 2020 Mar 4;20(1):103. doi: 10.1186/s12887-020-2009-2.
5
Pierre Robin Sequence in a Child With Ectopic Kidney, Polysyndactyly, And Short Stature: A Case Report.一名患有异位肾、多指（趾）畸形和身材矮小儿童的Pierre Robin序列征：病例报告
Cureus. 2019 Dec 27;11(12):e6475. doi: 10.7759/cureus.6475.
6
Hyaluronic acid is required for palatal shelf movement and its interaction with the tongue during palatal shelf elevation.透明质酸是腭褶运动所必需的，并且在腭褶提升过程中与舌相互作用。
Dev Biol. 2020 Jan 1;457(1):57-68. doi: 10.1016/j.ydbio.2019.09.004. Epub 2019 Sep 14.
7
Characterization of the perinatal mandible growth pattern: preliminary results.围产期下颌骨生长模式的特征：初步结果。
Surg Radiol Anat. 2018 Jun;40(6):667-679. doi: 10.1007/s00276-018-2030-4. Epub 2018 Apr 25.
8
Treatment of infants with Syndromic Robin sequence with modified palatal plates: a minimally invasive treatment option.采用改良腭板治疗患有综合征性罗宾序列的婴儿：一种微创治疗选择。
Head Face Med. 2017 Mar 30;13(1):4. doi: 10.1186/s13005-017-0137-1.
9
Polysomnographic findings in infants with Pierre Robin sequence.患有皮埃尔·罗宾序列征婴儿的多导睡眠图检查结果
Ann Thorac Med. 2017 Jan-Mar;12(1):25-29. doi: 10.4103/1817-1737.197770.
10
Clinical and Molecular Characterisation of Children with Pierre Robin Sequence and Additional Anomalies.患有皮埃尔·罗宾序列征及其他异常的儿童的临床与分子特征
Mol Syndromol. 2016 Nov;7(6):322-328. doi: 10.1159/000449115. Epub 2016 Sep 15.