B. Karacabey, Nur Aydınlı, Mine Çalışkan
{"title":"MTHFR A1298C Homozigot Gen Polimorfizmi Olan Süt Çocuğunda Akut İskemik İnme: Olgu Sunumu","authors":"B. Karacabey, Nur Aydınlı, Mine Çalışkan","doi":"10.26650/JCHILD.2020.1.0007","DOIUrl":null,"url":null,"abstract":"Acute ischemic stroke is rare in children, but it is one of the important causes of neurological morbidity. The etiology of AIS in childhood includes cardiac pathologies, cerebral arteriopathies, hypercoagulation, chemicals, drugs, inflammatory and autoimmune causes. In this article, we present an infant who has a genetic predisposition to hypercoagulation and comes with AIS clinic when multifactorial risk factors are added. The diagnosis, the underlying etiology, the risk factors affecting the process, the treatment of acute phase, the secondary treatment and the associated preventive approach on prognosis were discussed.","PeriodicalId":86257,"journal":{"name":"The Journal of child psychiatry","volume":"55 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of child psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26650/JCHILD.2020.1.0007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

急性缺血性脑卒中在儿童中罕见,但却是神经系统疾病的重要病因之一。儿童期AIS的病因包括心脏病变、脑动脉病变、高凝、化学物质、药物、炎症和自身免疫性原因。在这篇文章中,我们提出了一个婴儿谁有遗传易感性的高凝血和AIS临床时,多因素的危险因素增加。本文就该病的诊断、病因、影响病程的危险因素、急性期治疗、二次治疗及相关预防措施对预后的影响进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MTHFR A1298C Homozigot Gen Polimorfizmi Olan Süt Çocuğunda Akut İskemik İnme: Olgu Sunumu
Acute ischemic stroke is rare in children, but it is one of the important causes of neurological morbidity. The etiology of AIS in childhood includes cardiac pathologies, cerebral arteriopathies, hypercoagulation, chemicals, drugs, inflammatory and autoimmune causes. In this article, we present an infant who has a genetic predisposition to hypercoagulation and comes with AIS clinic when multifactorial risk factors are added. The diagnosis, the underlying etiology, the risk factors affecting the process, the treatment of acute phase, the secondary treatment and the associated preventive approach on prognosis were discussed.
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
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信