Suppr超能文献

先天性手部畸形分类中短指畸形的位置。

The position of symbrachydactyly in the classification of congenital hand anomalies.

作者信息

Miura T, Nakamura R, Horii E

机构信息

Chukyou University, Toyota City, Japan.

出版信息

J Hand Surg Br. 1994 Jun;19(3):350-4. doi: 10.1016/0266-7681(94)90088-4.

Abstract

The clinical features of 53 cases of intercalated hypoplasia and 113 cases of distal aplasia are reviewed and compared with each other and with 129 cases of syndactyly. Tri-, di- and mono-phalangeal symbrachydactyly, and adactyly with nubbin digits are consecutive anomalies. Transverse deficiency may result if the mesenchyme is damaged severely, and if damage is mild and formation has continued, intercalated transverse deficiency may occur. Webbing in symbrachydactyly may result from failure of the apical ectodermal ridge under the influence of damaged mesenchyme.

摘要

回顾了53例节间发育不全和113例远端发育不全的临床特征,并将它们相互比较,同时与129例并指畸形进行了比较。三指、二指和单指短指畸形以及带有残指的无指畸形是连续的异常情况。如果间充质受到严重损伤,可能会导致横向缺损;如果损伤较轻且发育仍在继续,则可能会出现节间横向缺损。并指畸形中的蹼可能是由于受损间充质影响下顶端外胚层嵴发育失败所致。

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