先天性双侧尺桡近端缝膜闭塞1例，22个月大

IF 0.1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING West African Journal of Radiology Pub Date : 2019-01-01 DOI:10.4103/WAJR.WAJR_57_17

O. Alagbe, O. Oyekale, T. O. Adeniyi

{"title":"先天性双侧尺桡近端缝膜闭塞1例，22个月大","authors":"O. Alagbe, O. Oyekale, T. O. Adeniyi","doi":"10.4103/WAJR.WAJR_57_17","DOIUrl":null,"url":null,"abstract":"Congenital radioulnar synostosis is a skeletal abnormality present at birth which may appear clinically as a mild abnormality in the early years. The diagnosis is usually delayed until functional abnormality is noticed. This is a typical case of congenital bilateral proximal radioulnar synostosis diagnosed at about 2 years despite mild upper limb abnormality noticed at birth. The rarity of this condition prompted the report of this case.","PeriodicalId":29875,"journal":{"name":"West African Journal of Radiology","volume":null,"pages":null},"PeriodicalIF":0.1000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"A case report of congenital bilateral proximal radioulnar synostosis in a 22-month-old child\",\"authors\":\"O. Alagbe, O. Oyekale, T. O. Adeniyi\",\"doi\":\"10.4103/WAJR.WAJR_57_17\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Congenital radioulnar synostosis is a skeletal abnormality present at birth which may appear clinically as a mild abnormality in the early years. The diagnosis is usually delayed until functional abnormality is noticed. This is a typical case of congenital bilateral proximal radioulnar synostosis diagnosed at about 2 years despite mild upper limb abnormality noticed at birth. The rarity of this condition prompted the report of this case.\",\"PeriodicalId\":29875,\"journal\":{\"name\":\"West African Journal of Radiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"West African Journal of Radiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/WAJR.WAJR_57_17\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"West African Journal of Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/WAJR.WAJR_57_17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}

引用次数: 2

摘要

先天性尺桡关节闭锁是一种出生时出现的骨骼异常，在临床早期可能表现为轻微的异常。诊断通常延迟到功能异常被注意到。这是一个典型的先天性双侧近端尺桡关节闭锁的病例，尽管在出生时发现了轻微的上肢异常，但在大约2岁时被诊断出来。这种情况的罕见性促使了这个病例的报道。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

A case report of congenital bilateral proximal radioulnar synostosis in a 22-month-old child

Congenital radioulnar synostosis is a skeletal abnormality present at birth which may appear clinically as a mild abnormality in the early years. The diagnosis is usually delayed until functional abnormality is noticed. This is a typical case of congenital bilateral proximal radioulnar synostosis diagnosed at about 2 years despite mild upper limb abnormality noticed at birth. The rarity of this condition prompted the report of this case.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

West African Journal of Radiology RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-

自引率

0.00%

发文量