Pyruvate Kinase Deficiency: A Near Miss

M. Tullu, Ankita A. Kulkarni, Mukesh Agrawal
{"title":"Pyruvate Kinase Deficiency: A Near Miss","authors":"M. Tullu, Ankita A. Kulkarni, Mukesh Agrawal","doi":"10.21088/ijtep.2348.9987.11219.3","DOIUrl":null,"url":null,"abstract":"Pyruvate kinase deficiency is an inherited disorder that affects red blood cells, which carry oxygen to the body's tissues. People with this disorder have a condition known as chronic hemolytic anemia, in which red blood cells are broken down (undergo hemolysis) prematurely, resulting in a shortage of red blood cells (anemia). Specifically, pyruvate kinase deficiency is a common cause of a type of inherited hemolytic anemia called hereditary nonspherocytic hemolytic anemia. In hereditary nonspherocytic hemolytic anemia, the red blood cells do not assume a spherical shape as they do in some other forms of hemolytic anemia.","PeriodicalId":442130,"journal":{"name":"Indian Journal of Trauma and Emergency Pediatrics","volume":"42 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Trauma and Emergency Pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21088/ijtep.2348.9987.11219.3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

Pyruvate kinase deficiency is an inherited disorder that affects red blood cells, which carry oxygen to the body's tissues. People with this disorder have a condition known as chronic hemolytic anemia, in which red blood cells are broken down (undergo hemolysis) prematurely, resulting in a shortage of red blood cells (anemia). Specifically, pyruvate kinase deficiency is a common cause of a type of inherited hemolytic anemia called hereditary nonspherocytic hemolytic anemia. In hereditary nonspherocytic hemolytic anemia, the red blood cells do not assume a spherical shape as they do in some other forms of hemolytic anemia.
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
丙酮酸激酶缺乏:差一点
丙酮酸激酶缺乏症是一种遗传性疾病,会影响将氧气输送到身体组织的红细胞。患有这种疾病的人患有一种被称为慢性溶血性贫血的疾病,在这种疾病中,红细胞过早被分解(发生溶血),导致红细胞短缺(贫血)。具体来说,丙酮酸激酶缺乏是一种称为遗传性非球型溶血性贫血的遗传性溶血性贫血的常见原因。在遗传性非球形溶血性贫血中,红细胞不像其他形式的溶血性贫血那样呈球形。
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
Hydrocolpos Calcium: Nutrient in Adolescent Girls Prescription Pattern for Acute Diarrheal Disease in Children Between 6 months to 5 years Autonomic Storm" Following Scorpion Sting Exploring Treatment Modalities in Premenstrual Syndrome in Adolescent Girls
×
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