镰状细胞性贫血:简介

Smruti R. Sahoo
{"title":"镰状细胞性贫血:简介","authors":"Smruti R. Sahoo","doi":"10.4172/2157-7412.20.11.330","DOIUrl":null,"url":null,"abstract":"Sickle cell disorder (SCD), one of the most common genetic disorders worldwide, is now considered as of global importance and medical significance. SCD is a group of red blood cell disorders inherited from a person’s parents where both the parents are carrier for the gene. Sickle cell anemia is an autosomal linked recessive trait, causing severe associated health problems leading to reduced life span. With the help of improved novel strategies and therapies, it is utmost important that the treatment is availed by the less-resourceful, impoverished countries.","PeriodicalId":89584,"journal":{"name":"Journal of genetic syndromes & gene therapy","volume":"68 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sickle Cell Anemia: A Brief Synopsis\",\"authors\":\"Smruti R. Sahoo\",\"doi\":\"10.4172/2157-7412.20.11.330\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sickle cell disorder (SCD), one of the most common genetic disorders worldwide, is now considered as of global importance and medical significance. SCD is a group of red blood cell disorders inherited from a person’s parents where both the parents are carrier for the gene. Sickle cell anemia is an autosomal linked recessive trait, causing severe associated health problems leading to reduced life span. With the help of improved novel strategies and therapies, it is utmost important that the treatment is availed by the less-resourceful, impoverished countries.\",\"PeriodicalId\":89584,\"journal\":{\"name\":\"Journal of genetic syndromes & gene therapy\",\"volume\":\"68 1\",\"pages\":\"1-2\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of genetic syndromes & gene therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2157-7412.20.11.330\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of genetic syndromes & gene therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2157-7412.20.11.330","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

镰状细胞病(SCD)是世界上最常见的遗传性疾病之一,现在被认为具有全球重要性和医学意义。SCD是一种从父母那里遗传的红细胞疾病,父母双方都是该基因的携带者。镰状细胞性贫血是一种常染色体连锁隐性性状,引起严重的相关健康问题,导致寿命缩短。在改进的新策略和治疗方法的帮助下,最重要的是使资源较少的贫困国家获得这种治疗。
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
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Sickle Cell Anemia: A Brief Synopsis
Sickle cell disorder (SCD), one of the most common genetic disorders worldwide, is now considered as of global importance and medical significance. SCD is a group of red blood cell disorders inherited from a person’s parents where both the parents are carrier for the gene. Sickle cell anemia is an autosomal linked recessive trait, causing severe associated health problems leading to reduced life span. With the help of improved novel strategies and therapies, it is utmost important that the treatment is availed by the less-resourceful, impoverished countries.
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
期刊最新文献
Autoimmune Lymphoproliferative Syndrome T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy Griscelli Syndrome Type 3 (GS3) Smith-Lemli-Opitz Syndrome (SLOS) Niemann-Pick Disease Type C (NPC)
×
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