• 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

IIA型口下颌肢体发育不全综合征,舌发育不全-指(趾)发育不全:病例报告

Oromandibular limb hypogenesis syndrome, type IIA, hypoglossia-hypodactylia: a case report.

作者信息

Wadhwani Puneet, Mohammad Shadab, Sahu Ruchi

机构信息

Saraswati Dental College, Oral and Maxillofacial Surgery, Lucknow, Uttar Pradesh, India.

出版信息

J Oral Pathol Med. 2007 Oct;36(9):555-7. doi: 10.1111/j.1600-0714.2007.00570.x.

DOI:10.1111/j.1600-0714.2007.00570.x
PMID:17850440
Abstract

A patient with oromandibular limb hypogenesis syndrome, type IIA hypoglossia-hypodactylia, is reported. The features essential for the diagnosis of this congenital defect include a reduction in tongue size (microglossia), micrognathic mandible and limb abnormalities of varying severity. Parents and the other sibling were normal. Past medical history for exposure of the mother to drugs during pregnancy was positive.

摘要

报告了一例患有IIA型口下颌肢体发育不全综合征(舌下-指趾发育不全)的患者。诊断这种先天性缺陷的关键特征包括舌体缩小(小舌)、小下颌以及不同程度的肢体异常。父母和其他兄弟姐妹均正常。母亲孕期有药物接触史。

相似文献

1
Oromandibular limb hypogenesis syndrome, type IIA, hypoglossia-hypodactylia: a case report.IIA型口下颌肢体发育不全综合征,舌发育不全-指(趾)发育不全:病例报告
J Oral Pathol Med. 2007 Oct;36(9):555-7. doi: 10.1111/j.1600-0714.2007.00570.x.
2
Severe form of hypoglossia-hypodactylia syndrome associated with complex cardiopathy: a case report.与复杂性心脏病相关的严重型舌下发育不全-指(趾)发育不全综合征:一例报告
Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1092-4. doi: 10.1016/j.ijporl.2010.06.011. Epub 2010 Jul 15.
3
Hypoglossia-hypodactylia syndrome: report of a case.
J Osaka Univ Dent Sch. 1980 Dec;20:297-304.
4
Oromandibular-limb hypogenesis syndrome: type II A, hypoglossia-hypodactylia--report of a case.口下颌肢体发育不全综合征:II A型,舌发育不全-指(趾)发育不全——1例报告
Br J Oral Maxillofac Surg. 1992 Dec;30(6):404-6. doi: 10.1016/0266-4356(92)90212-2.
5
Hypoglossia Type 1A: report of a case and review of literature with focus on clinical investigations.1A型舌下神经功能障碍:1例报告及文献复习,重点关注临床研究
Indian J Dent Res. 2012 Mar-Apr;23(2):264-70. doi: 10.4103/0970-9290.100438.
6
Oromandibular limb hypogenesis complex (Hanhart syndrome): a severe adult phenotype.
Am J Med Genet. 1999 Apr 23;83(5):427-9.
7
[Oromandibular-limb hypogenesis spectrum].[口下颌肢体发育不全谱系]
Ryoikibetsu Shokogun Shirizu. 2000(30 Pt 5):224-5.
8
Oromandibular limb hypogenesis and gastroschisis.
J Pediatr Surg. 2001 Jul;36(7):E15. doi: 10.1053/jpsu.2001.24778.
9
Oromandibular limb hypogenesis syndrome.口下颌肢体发育不全综合征
J Philipp Dent Assoc. 1995 Sep-Nov;47(2):29-33.
10
Hypoglossia-hypodactylia (Hanhart's) syndrome with sensorineural hearing loss.伴有感音神经性听力损失的舌下-指发育不全(汉哈特氏)综合征
Turk J Pediatr. 1994 Oct-Dec;36(4):347-52.

引用本文的文献

1
Long-Term Follow-Up of Hypoglossia-Hypodactylia Syndrome: A Case Report.舌下-指趾发育不全综合征的长期随访:一例报告
Cureus. 2023 Jul 2;15(7):e41290. doi: 10.7759/cureus.41290. eCollection 2023 Jul.
2
A Rare Clinical Variant of Oromandibular Limb Hypogenesis Syndrome Type I B.I型B型口下颌肢体发育不全综合征的一种罕见临床变异型。
Int J Clin Pediatr Dent. 2016 Jan-Mar;9(1):78-81. doi: 10.5005/jp-journals-10005-1338. Epub 2016 Apr 22.
3
Oromandibular Limb Hypogenesis Syndrome Type IIB: Case Report of Hypoglossia-Hypodactyly.
IIB型口下颌肢体发育不全综合征:舌发育不全-指(趾)发育不全病例报告
Case Rep Dent. 2013;2013:370695. doi: 10.1155/2013/370695. Epub 2013 Feb 4.
4
Oromandibular-limb Hypogenesis Syndrome Type II C: A Rare Case.II C型口下颌肢体发育不全综合征:1例罕见病例
J Dent Res Dent Clin Dent Prospects. 2010 Fall;4(4):136-9. doi: 10.5681/joddd.2010.033. Epub 2010 Dec 21.