Suppr超能文献

cherubism:科威特一家族中四名患病成员的病例报告

Cherubism: review of four affected members in a Kuwaiti family.

作者信息

Petkovska L, Ramadan S, Aslam M O

机构信息

Radiology Department, Al-Adan Hospital, Safat 5326, Kuwait.

出版信息

Australas Radiol. 2004 Sep;48(3):408-10. doi: 10.1111/j.0004-8461.2004.01329.x.

Abstract

Cherubism is a rare autosomal dominant fibro-osseous disorder of childhood, mostly limited to the maxilla and mandible. Extra-cranial skeletal involvement is rare. Post-pubertal involution of the process and jaw remodeling occurs in adulthood. The aim of this case report is to present four cherubs, a father and his three daughters, in whom the diagnosis was made based on history, physical examination, laboratory tests and typical radiological features. The imaging characteristics are discussed and the published literature is reviewed.

摘要

cherubism是一种罕见的儿童常染色体显性遗传性纤维-骨疾病,主要局限于上颌骨和下颌骨。颅外骨骼受累罕见。青春期后病情会逐渐消退,成年后颌骨会重塑。本病例报告旨在介绍4例cherubism患者,即一位父亲及其3个女儿,他们的诊断是基于病史、体格检查、实验室检查和典型的放射学特征做出的。文中讨论了其影像学特征并回顾了已发表的文献。

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