Suppr超能文献

埃勒斯-当洛综合征——病例报告

Ehlers danlos syndrome - a case report.

作者信息

Kaurani Pragati, Marwah Nikhil, Kaurani Mayank, Padiyar Narendra

机构信息

Reader, Department of Prosthodontics, Mahatma Gandhi Dental College and Hospital , Jaipur, India .

Professor, Department of Paedriatic and Preventive Dentistry, Mahatma Gandhi Dental College and Hospital , Jaipur, India .

出版信息

J Clin Diagn Res. 2014 Mar;8(3):256-8. doi: 10.7860/JCDR/2014/4569.4178. Epub 2014 Mar 15.

Abstract

Ehlers Danlos syndrome (EDS) is a hereditary collagen disorder which primarily manifests in the skin and joints. Clinically, it is characterized by hyperelasticity of skin and joint hypermobility. This article has described a rare condition seen in a 10-year-old boy who was diagnosed with EDS, based on the clinical, radiographic and histological findings.

摘要

埃勒斯-当洛综合征(EDS)是一种遗传性胶原蛋白紊乱疾病,主要表现在皮肤和关节。临床上,其特征为皮肤弹性过度和关节活动过度。本文描述了一名10岁男孩中发现的罕见病例,该病例根据临床、影像学和组织学检查结果被诊断为EDS。

相似文献

1
Ehlers danlos syndrome - a case report.埃勒斯-当洛综合征——病例报告
J Clin Diagn Res. 2014 Mar;8(3):256-8. doi: 10.7860/JCDR/2014/4569.4178. Epub 2014 Mar 15.
5
[Ehlers-Danlos syndrome].[埃勒斯-当洛综合征]
Hautarzt. 1999 Apr;50(4):257-65. doi: 10.1007/s001050050898.

本文引用的文献

4
Ehlers-Danlos syndrome (EDS) type IV: review of the literature.IV型埃勒斯-当洛综合征(EDS):文献综述
Clin Oral Investig. 2007 Sep;11(3):183-7. doi: 10.1007/s00784-006-0092-x. Epub 2007 Jan 13.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验