Congenital absent radii without thumb aplasia: the first case in Iraq and the early documentation of the condition in the literature

Aamir Jalal Al-Mosawi
{"title":"Congenital absent radii without thumb aplasia: the first case in Iraq and the early documentation of the condition in the literature","authors":"Aamir Jalal Al-Mosawi","doi":"10.15406/mojcr.2020.10.00340","DOIUrl":null,"url":null,"abstract":"Background: The vast majority of the reported cases of congenital absent radii without thumb aplasia were associated with congenital thrombocytopenia or thrombocytopenia occurring early life. The occurrence of congenital absent radii without thumb aplasia and without evidence congenital thrombocytopenia or thrombocytopenia occurring early life is extremely rare and has not been reported in Iraq. Patients and methods: An Iraqi newborn infant with congenital absent radii without evidence of congenital thrombocytopenia during the first week is presented, and the relevant literatures were reviewed with aim of describing the early documentation of the condition in the medical literature. Results: A newborn infant with congenital absence of the radii without thumb aplasia. The neonate was followed for one week without the occurrence of thrombocytopenia. The rest of physical examination was normal and no other abnormalities could be detected. The parents were consanguineous, but family history was negative for a similar condition. Conclusion: The extremely rare occurrence congenital absence of the radii without thumb aplasia without evidence of thrombocytopenia during the first week of life is reported in an Iraqi newborn.","PeriodicalId":93339,"journal":{"name":"MOJ clinical & medical case reports","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MOJ clinical & medical case reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/mojcr.2020.10.00340","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Background: The vast majority of the reported cases of congenital absent radii without thumb aplasia were associated with congenital thrombocytopenia or thrombocytopenia occurring early life. The occurrence of congenital absent radii without thumb aplasia and without evidence congenital thrombocytopenia or thrombocytopenia occurring early life is extremely rare and has not been reported in Iraq. Patients and methods: An Iraqi newborn infant with congenital absent radii without evidence of congenital thrombocytopenia during the first week is presented, and the relevant literatures were reviewed with aim of describing the early documentation of the condition in the medical literature. Results: A newborn infant with congenital absence of the radii without thumb aplasia. The neonate was followed for one week without the occurrence of thrombocytopenia. The rest of physical examination was normal and no other abnormalities could be detected. The parents were consanguineous, but family history was negative for a similar condition. Conclusion: The extremely rare occurrence congenital absence of the radii without thumb aplasia without evidence of thrombocytopenia during the first week of life is reported in an Iraqi newborn.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
先天性桡骨缺失无拇指发育不全:第一例在伊拉克和早期文献条件
背景:绝大多数报道的先天性桡骨缺失伴拇指发育不全的病例与先天性血小板减少症或早期发生的血小板减少症有关。无拇指发育不全的先天性桡骨缺失和无证据的先天性血小板减少症或早期发生的血小板减少症极为罕见,在伊拉克尚未报道。患者和方法:一个伊拉克新生儿先天性桡骨缺失,在第一周内没有先天性血小板减少症的证据,并对相关文献进行了回顾,目的是描述医学文献中对这种疾病的早期记录。结果:1例新生儿先天性桡骨缺失无拇指发育不全。新生儿随访1周,未发生血小板减少症。其余体格检查均正常,未发现其他异常。父母是近亲,但家族史没有类似的疾病。结论:极为罕见的先天性桡骨缺失无拇指发育不全无血小板减少的证据,在生命的第一周报告在伊拉克新生儿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Epiploic appendagitis, a infrequent cause of abdominal pain Surgical management of rare benign tumors of the sternum. Tympanic membrane perforation, otitis media and labyrinthitis caused by otomycosis confirmed by intravenous gadolinium 1.5 tesla MRI-a case report Inebriated liver causing mesangial turmoil Complications of refractory juvenile dermatomyositis: a case report and literature review
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1