Suppr超能文献

穆尔-费德曼综合征与肢端短小发育不良:它们是同一病症吗?

Moore-Federman syndrome and acromicric dysplasia: are they the same entity?

作者信息

Winter R M, Patton M A, Challener J, Mueller R F, Baraitser M

机构信息

Kennedy Galton Centre, Northwick Park Hospital, London.

出版信息

J Med Genet. 1989 May;26(5):320-5. doi: 10.1136/jmg.26.5.320.

Abstract

Four unrelated patients are reported with short stature, stiffness of the joints, short fingers, inability to make a fist, and thickened skin on the forearms. Investigations have failed to show a lysosomal storage disorder and radiographs show non-specific changes with a delayed carpal bone age. The clinical features in the four children are very similar to the recently described acromicric dysplasia. There are also similarities to Moore-Federman syndrome which has only been described in one family. The case is made that acromicric dysplasia and Moore-Federman syndrome are the same entity.

摘要

报告了4例无血缘关系的患者,他们身材矮小、关节僵硬、手指短小、无法握拳且前臂皮肤增厚。检查未发现溶酶体贮积症,X线片显示非特异性改变且腕骨年龄延迟。这4名儿童的临床特征与最近描述的肢端短小发育不良非常相似。与仅在一个家族中被描述过的穆尔-费德曼综合征也有相似之处。有理由认为肢端短小发育不良和穆尔-费德曼综合征是同一病症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e5/1015599/12e67e1d0166/jmedgene00055-0032-a.jpg

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