• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major.引入产前诊断对重型地中海贫血高危家庭生殖行为的影响。
Br Med J. 1980 Jun 7;280(6228):1347-50. doi: 10.1136/bmj.280.6228.1347.
2
Reproductive behaviour of families segregating for Cooley's anaemia before and after the availability of prenatal diagnosis.在产前诊断可用前后,患库利贫血的家系的生殖行为。
J Med Genet. 1991 Aug;28(8):523-9. doi: 10.1136/jmg.28.8.523.
3
Reproductive patterns and thalassaemia major.生殖模式与重型地中海贫血
J Biosoc Sci. 1986 Jul;18(3):285-95. doi: 10.1017/s0021932000016254.
4
Counselling for prenatal diagnosis of sickle cell disease and beta thalassaemia major: a four year experience.镰状细胞病和重型β地中海贫血产前诊断的咨询:四年经验
J Med Genet. 1988 Nov;25(11):769-72. doi: 10.1136/jmg.25.11.769.
5
Prenatal diagnosis of thalassaemia major resulting from Lepore/ beta-thalassaemia genotype.Lepore/β地中海贫血基因型导致的重型地中海贫血的产前诊断。
J Med Genet. 1981 Dec;18(6):476-8. doi: 10.1136/jmg.18.6.476.
6
Sociocultural challenges of beta-thalassaemia major birth in carriers of beta-thalassaemia in Iran.伊朗β-地中海贫血携带者中重型β-地中海贫血患儿出生所面临的社会文化挑战。
J Med Screen. 2012 Sep;19(3):109-11. doi: 10.1258/jms.2012.012038.
7
Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry.孕期地中海贫血基因筛查中的知情选择:来自一项全国性保密调查的审计
BMJ. 2000 Feb 5;320(7231):337-41. doi: 10.1136/bmj.320.7231.337.
8
Long-term effect of prospective detection of high genetic risk on couples' reproductive life: data for thalassaemia.前瞻性检测高遗传风险对夫妇生殖生活的长期影响:地中海贫血的数据
Prenat Diagn. 2000 Jun;20(6):469-74. doi: 10.1002/1097-0223(200006)20:6<469::aid-pd857>3.0.co;2-v.
9
Antenatal diagnosis of thalassaemia major.重型地中海贫血的产前诊断。
Br Med J. 1978 Feb 11;1(6109):350-3. doi: 10.1136/bmj.1.6109.350.
10
Prenatal control of severe thalassaemia: Chiang Mai strategy.重度地中海贫血的产前控制:清迈策略。
Prenat Diagn. 2000 Mar;20(3):229-34.

引用本文的文献

1
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.地中海贫血、镰状细胞病、囊性纤维化和泰萨二氏病的孕前风险评估。
Cochrane Database Syst Rev. 2021 Oct 11;10(10):CD010849. doi: 10.1002/14651858.CD010849.pub4.
2
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.地中海贫血、镰状细胞病、囊性纤维化和泰-萨克斯病的孕前风险评估。
Cochrane Database Syst Rev. 2018 Mar 14;3(3):CD010849. doi: 10.1002/14651858.CD010849.pub3.
3
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.地中海贫血、镰状细胞病、囊性纤维化和泰-萨克斯病的孕前风险评估。
Cochrane Database Syst Rev. 2015 Aug 12;2015(8):CD010849. doi: 10.1002/14651858.CD010849.pub2.
4
Survival analysis and its associated factors of Beta thalassemia major in hamadan province.哈马丹省重型β地中海贫血的生存分析及其相关因素
Iran J Med Sci. 2015 May;40(3):233-9.
5
Red blood cell parameters in antenatal nonsickling hemoglobinopathy screening.产前非镰状血红蛋白病筛查中的红细胞参数
Int J Womens Health. 2015 Apr 8;7:379-84. doi: 10.2147/IJWH.S73362. eCollection 2015.
6
A holistic approach to education programs in thalassemia for a multi-ethnic population: consideration of perspectives, attitudes, and perceived needs.针对多民族人群的地中海贫血教育项目的整体方法:对观点、态度和感知需求的考量
J Community Genet. 2011 Jun;2(2):71-9. doi: 10.1007/s12687-011-0039-z. Epub 2011 Feb 24.
7
Haemoglobinopathies in Greece: prevention programme over the past 35 years.希腊的血红蛋白病:过去 35 年的预防计划。
Indian J Med Res. 2011 Oct;134(4):572-6.
8
Prenatal diagnosis by amniocentesis and chorionic villus biopsy.通过羊膜穿刺术和绒毛取样进行产前诊断。
Can Fam Physician. 1986 Jan;32:105-8.
9
A stochastic model to evaluate options for antenatal genetic screening.一种用于评估产前基因筛查方案的随机模型。
Health Care Manag Sci. 2006 May;9(2):111-24. doi: 10.1007/s10729-006-7660-0.
10
Iranian national thalassaemia screening programme.伊朗国家地中海贫血筛查项目。
BMJ. 2004 Nov 13;329(7475):1134-7. doi: 10.1136/bmj.329.7475.1134.

本文引用的文献

1
Obstetric aspects of midtrimester fetal blood sampling by needling or fetoscopy.孕中期经针刺或胎儿镜进行胎儿采血的产科相关问题。
Br J Obstet Gynaecol. 1980 Feb;87(2):87-99. doi: 10.1111/j.1471-0528.1980.tb04499.x.
2
Development of a quantitative immunoassay for the cystic fibrosis gene.
Lancet. 1980 Feb 16;1(8164):330-1. doi: 10.1016/s0140-6736(80)90882-x.
3
Incidence of -thalassaemia trait among Cypriots in London.伦敦塞浦路斯人当中β地中海贫血特征的发病率。
Br Med J. 1972 Sep 23;3(5829):737-8. doi: 10.1136/bmj.3.5829.737.
4
In utero diagnosis of hemoglobinopathies. Technic for obtaining fetal blood.血红蛋白病的宫内诊断。获取胎儿血液的技术。
N Engl J Med. 1974 May 9;290(19):1065-7. doi: 10.1056/NEJM197405092901908.
5
Fetal blood-sampling in utero.宫内胎儿采血
Lancet. 1974 Jan 19;1(7847):79-80. doi: 10.1016/s0140-6736(74)92293-4.
6
Continuous subcutaneous administration of deferoxamine in patients with iron overload.对铁过载患者持续皮下给予去铁胺。
N Engl J Med. 1977 Aug 25;297(8):418-23. doi: 10.1056/NEJM197708252970804.
7
Management of thalassaemia major.
Br Med Bull. 1976 Sep;32(3):270-6. doi: 10.1093/oxfordjournals.bmb.a071374.
8
Antenatal diagnosis of thalassaemia major.重型地中海贫血的产前诊断。
Br Med J. 1978 Feb 11;1(6109):350-3. doi: 10.1136/bmj.1.6109.350.
9
Prenatal diagnosis of hemoglobinopathies and other hematologic diseases.血红蛋白病及其他血液系统疾病的产前诊断。
J Pediatr. 1979 Oct;95(4):501-3. doi: 10.1016/s0022-3476(79)80753-2.
10
Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells.通过羊水细胞的DNA分析进行镰状细胞贫血的产前诊断。
Lancet. 1978 Oct 28;2(8096):910-2. doi: 10.1016/s0140-6736(78)91629-x.

引入产前诊断对重型地中海贫血高危家庭生殖行为的影响。

Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major.

作者信息

Modell B, Ward R H, Fairweather D V

出版信息

Br Med J. 1980 Jun 7;280(6228):1347-50. doi: 10.1136/bmj.280.6228.1347.

DOI:10.1136/bmj.280.6228.1347
PMID:7388536
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1601817/
Abstract

Families who were at risk of producing a child with thalassaemia major were studied to determine the sequential effects on their reproductive behaviour of knowing the risk and, subsequently, of knowing that antenatal diagnosis was available. Knowing the risk caused them virtually to stop reproduction and to seek termination of 70% of pregnancies, most of which were accidental. The introduction of antenatal diagnosis in 1975 permitted the resumption of nearly normal reproduction by at-risk families, with fewer than 30% of pregnancies being terminated for thalassaemia major. All couples at risk for thalassaemia major should be detected and counselled before they produce an affected child; responsibility for either choosing or refusing antenatal diagnosis should be theirs alone.

摘要

对有生出重型地中海贫血患儿风险的家庭进行了研究,以确定知晓风险以及随后知晓可进行产前诊断对其生育行为的一系列影响。知晓风险实际上导致他们停止生育,并寻求终止70%的妊娠,其中大多数是意外怀孕。1975年引入产前诊断后,有风险的家庭得以恢复几乎正常的生育,因重型地中海贫血而终止的妊娠不到30%。所有有重型地中海贫血风险的夫妇都应在生出患病孩子之前被检测出来并接受咨询;选择或拒绝产前诊断的责任应完全由他们自己承担。