Suppr超能文献

先天性多发性关节挛缩症:多发性先天性关节挛缩

Arthrogryposis Multiplex Congenita: Multiple Congenital Joint Contractures.

作者信息

Sucuoglu Hamza, Ornek Nurettin Irem, Caglar Cagkan

机构信息

Private Bagcilar Medicine Center, Department of Physical Medicine and Rehabilitation, 34204 Istanbul, Turkey.

Private Safir Medicine Center, Department of Physical Medicine and Rehabilitation, 34265 Istanbul, Turkey.

出版信息

Case Rep Med. 2015;2015:379730. doi: 10.1155/2015/379730. Epub 2015 Oct 28.

Abstract

Arthrogryposis multiplex congenita (AMC) is a syndrome characterized by nonprogressive multiple congenital joint contractures. The etiology of disease is multifactorial; it is most commonly suspected from absent fetal movements and genetic defects. AMC affects mainly limbs; also it might present with other organs involvement. It is crucial that the diagnosis of AMC should be kept in mind by musculoskeletal physicians in newborns with multiple joint contractures and patients must begin rehabilitation in early stage after accurate diagnosis in terms of functional independence. We present the diagnosis, types, clinical features, and treatment approaches of this disease in our case with literature reviews.

摘要

先天性多发性关节挛缩症(AMC)是一种以非进行性多发性先天性关节挛缩为特征的综合征。该病病因是多因素的;最常见的怀疑原因是胎儿活动缺失和基因缺陷。AMC主要影响四肢;也可能伴有其他器官受累。对于患有多发性关节挛缩的新生儿,肌肉骨骼科医生必须牢记AMC的诊断,并且患者在准确诊断后必须尽早开始康复治疗以实现功能独立。我们通过文献综述介绍了我们病例中该病的诊断、类型、临床特征及治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d73/4641175/41a4409048c4/CRIM2015-379730.001.jpg

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