• 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

近亲结婚对巴西人群的遗传影响。

Genetic effects in Brazilian populations due to consanguineous marriages.

作者信息

Freire-Maia N

机构信息

Department of Genetics, Federal University of Paraná, Brazil.

出版信息

Am J Med Genet. 1990 Jan;35(1):115-7. doi: 10.1002/ajmg.1320350121.

DOI:10.1002/ajmg.1320350121
PMID:2301460
Abstract

Estimates of "relative risks" and "attributable risks" are presented for two Brazilian regions with the lowest (F = 0.00030) and the highest (F = 0.00395) inbreeding levels of the country, and for the whole country (F = 0.00088). The abolition of all consanguineous marriages (from second cousins up to and including uncle-niece/aunt-nephew marriages) in Brazil would eliminate only about 0.22, 3.05, and 0.65% of the "total damage," respectively. "Total damage" is defined as including abortions, miscarriages, stillbirths, infant-juvenile mortality (up to the age of 20 years), and anomalies in the survivors. The reduction of prenatal damage would be 0.11, 1.46, and 0.31%, and that of postnatal damage would be 0.49, 6.65, and 1.36%, respectively.

摘要

文中给出了巴西近亲繁殖水平最低(F = 0.00030)、最高(F = 0.00395)的两个地区以及整个巴西(F = 0.00088)的“相对风险”和“归因风险”估计值。在巴西废除所有近亲婚姻(从二级表亲到叔侄/舅甥婚姻)分别只会消除约0.22%、3.05%和0.65%的“总损害”。“总损害”定义为包括流产、死产、死胎、婴幼儿死亡率(至20岁)以及幸存者中的畸形。产前损害的减少分别为0.11%、1.46%和0.31%,产后损害的减少分别为0.49%、6.65%和1.36%。

相似文献

1
Genetic effects in Brazilian populations due to consanguineous marriages.近亲结婚对巴西人群的遗传影响。
Am J Med Genet. 1990 Jan;35(1):115-7. doi: 10.1002/ajmg.1320350121.
2
Effects of consanguineous marriages on morbidity and precocious mortality: genetic counseling.近亲结婚对发病率和过早死亡率的影响:遗传咨询
Am J Med Genet. 1984 Jul;18(3):401-6. doi: 10.1002/ajmg.1320180307.
3
Reproductive wastage and developmental disorders in relation to consanguinity in south India.印度南部近亲结婚导致的生殖损耗与发育障碍
Trop Geogr Med. 1981 Sep;33(3):275-80.
4
[Consanguinity marriages in Brazil].[巴西的近亲婚姻]
Rev Bras Biol. 1990 Nov;50(4):863-6.
5
Consanguinity, fertility, reproductive wastage, infant mortality and congenital malformations in Jordan.约旦的近亲结婚、生育力、生殖损耗、婴儿死亡率及先天性畸形
Saudi Med J. 2000 Feb;21(2):150-4.
6
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births.在一项对238942例连续出生病例的研究中,父母近亲结婚作为出生缺陷发生率增加的一个原因。
Ann Genet. 1999;42(3):133-9.
7
Consanguinity in the Bishopric of Ourense (Galicia, Spain) from 1900 to 1979.1900年至1979年西班牙加利西亚自治区奥伦塞主教辖区的近亲结婚情况。
Ann Hum Biol. 2003 Jul-Aug;30(4):419-33. doi: 10.1080/0301446031000103301.
8
Health effects of consanguinity in Pondicherry.本地治里近亲结婚对健康的影响。
Indian Pediatr. 1992 Jun;29(6):685-92.
9
Consanguinity in Kahramanmaras city, Turkey, and its medical impact.土耳其加济安泰普市的近亲结婚现象及其医学影响。
Saudi Med J. 2004 Dec;25(12):1991-4.
10
Inbreeding coefficients for X-linked and autosomal genes in consanguineous marriages in Spanish populations: the case of Guipúzcoa (Basque Country).西班牙人群近亲婚姻中X连锁基因和常染色体基因的近亲繁殖系数:以吉普斯夸省(巴斯克地区)为例。
Ann Hum Genet. 2009 Mar;73(2):184-95. doi: 10.1111/j.1469-1809.2008.00495.x. Epub 2008 Dec 15.

引用本文的文献

1
The importance of geographic and sociodemographic aspects in the characterization of mucopolysaccharidoses: a case series from Ceará state (Northeast Brazil).地理和社会人口学因素在黏多糖贮积症特征描述中的重要性:来自巴西东北部塞阿拉州的病例系列
J Community Genet. 2024 Oct;15(5):573-580. doi: 10.1007/s12687-024-00718-7. Epub 2024 Aug 19.
2
Brazilian XP-E siblings carrying a novel DDB2 variant developed early-onset melanoma: a case report.巴西 XP-E 同卵双胞胎携带一种新型 DDB2 变异体,引发早发性黑色素瘤:病例报告。
BMC Med Genomics. 2023 Aug 12;16(1):186. doi: 10.1186/s12920-023-01622-8.
3
Analyzing Inbreeding and Estimating Its Related Deficiencies in Northeastern Brazil.
分析巴西东北部的近亲繁殖及其相关缺陷
J Pediatr Genet. 2021 Apr 1;11(4):272-278. doi: 10.1055/s-0041-1725977. eCollection 2022 Dec.
4
So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity.那么,如果不是先天性肾上腺增生症呢?解决未确诊的生殖器模糊病例。
Ital J Pediatr. 2022 Jun 10;48(1):89. doi: 10.1186/s13052-022-01284-9.
5
Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of Piauí, northeastern Brazil?家族性卵磷脂胆固醇酰基转移酶缺乏症:既然如此罕见,为何在巴西东北部皮奥伊州如此常见?
Mol Genet Metab Rep. 2022 Jan 3;30:100840. doi: 10.1016/j.ymgmr.2021.100840. eCollection 2022 Mar.
6
Mucopolysaccharidosis VII in Brazil: natural history and clinical findings.巴西黏多糖贮积症 VII 型:自然病史和临床发现。
Orphanet J Rare Dis. 2021 May 22;16(1):238. doi: 10.1186/s13023-021-01870-w.
7
Gene panel for the diagnosis of epidermolysis bullosa: proposal for a viable and efficient approach.基因panel 用于诊断大疱性表皮松解症:一种可行且有效的方法的建议。
An Bras Dermatol. 2021 Mar-Apr;96(2):155-162. doi: 10.1016/j.abd.2020.05.015. Epub 2021 Feb 2.
8
Clusters of genetic diseases in Brazil.巴西的遗传性疾病集群。
J Community Genet. 2019 Jan;10(1):121-128. doi: 10.1007/s12687-018-0369-1. Epub 2018 Jun 2.
9
Molecular analysis of the CTSK gene in a cohort of 33 Brazilian families with pycnodysostosis from a cluster in a Brazilian Northeast region.对来自巴西东北部一个聚居区的33个患有致密性骨发育不全的巴西家庭的队列进行CTSK基因的分子分析。
Eur J Med Res. 2016 Aug 24;21(1):33. doi: 10.1186/s40001-016-0228-7.
10
Genetics and genomics in Brazil: a promising future.巴西的遗传学与基因组学:前景光明。
Mol Genet Genomic Med. 2014 Jul;2(4):280-91. doi: 10.1002/mgg3.95.