• 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

巴林儿童轻度智力障碍的病因:一项基于社区的病例对照研究。

Etiology of mild mental retardation among Bahraini children: a community-based case control study.

作者信息

al-Ansari A

机构信息

Arabian Gulf University, College of Medicine and Medical Sciences, Department of Community Medicine and Human Behavior, State of Bahrain.

出版信息

Ment Retard. 1993 Jun;31(3):140-3.

PMID:8326872
Abstract

The etiology of and suspected risk factors leading to mild mental retardation were analyzed in unselected series of 109 Bahraini school children with this condition born between 1967 and 1982. The cause was considered to be prenatal in 38.5% of the children; perinatal (asphyxia and prematurity), in 11.9%; and postnatal, in 7.4%. In 42% the cause was untraceable. Predisposing background factors associated with mild mental retardation were compared with characteristics of a matched control group from community schools. An illiterate father, consanguinity, and a relative with mental retardation were significantly more common among the sample with mild mental retardation. These results are not consistent with the view that mild retardation is predominantly cultural-familial and not pathological in nature.

摘要

对1967年至1982年间出生的109名患有轻度智力发育迟缓的巴林学童进行了分析,这些儿童未经挑选,分析了导致轻度智力发育迟缓的病因及疑似风险因素。病因被认为是产前的儿童占38.5%;围产期(窒息和早产)的占11.9%;产后的占7.4%。42%的病因无法查明。将与轻度智力发育迟缓相关的诱发背景因素与来自社区学校的匹配对照组的特征进行了比较。在轻度智力发育迟缓样本中,文盲父亲、近亲结婚以及有智力发育迟缓亲属的情况明显更为常见。这些结果与轻度智力发育迟缓主要是文化家族性而非病理性的观点不一致。

相似文献

1
Etiology of mild mental retardation among Bahraini children: a community-based case control study.巴林儿童轻度智力障碍的病因:一项基于社区的病例对照研究。
Ment Retard. 1993 Jun;31(3):140-3.
2
[An epidemiological study on etiology of mental retardation].[智力发育迟缓病因的流行病学研究]
Zhonghua Yi Xue Za Zhi. 1994 Mar;74(3):134-7, 189.
3
Incidence of obesity among school children with mental retardation in Japan.日本智障学童的肥胖发生率。
Am J Ment Retard. 1994 Nov;99(3):283-8.
4
Mild mental retardation in northern Finland.
Ups J Med Sci Suppl. 1987;44:47-51.
5
Mental retardation in a birth cohort, 1976-1980, Rochester, Minnesota.
Am J Ment Retard. 1996 Jan;100(4):335-44.
6
[Mental retardation in children. Prevalence and etiology].
Tidsskr Nor Laegeforen. 1992 Feb 28;112(6):749-51.
7
Preventable fraction of mental retardation: analysis based on individuals with severe mental retardation.智力迟钝的可预防比例:基于重度智力迟钝个体的分析
Ment Retard. 1996 Jun;34(3):182-8.
8
Severe mental retardation in a Swedish county. II. Etiologic and pathogenetic aspects of children born 1959--1970.
Neuropadiatrie. 1977 Aug;8(3):293-304. doi: 10.1055/s-0028-1091525.
9
[Epidemiology of mental deficiency. The study of Safor (I): prevalence and etiology].[智力缺陷流行病学。萨福尔研究(I):患病率与病因]
An Esp Pediatr. 1991 May;34(5):365-71.
10
Review of recent epidemiological studies of mental retardation: prevalence, associated disorders, and etiology.
Am J Ment Retard. 1987 Nov;92(3):243-54.

引用本文的文献

1
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration.AIMP1基因中的错义变异与无神经退行性变的常染色体隐性智力障碍有关。
Eur J Hum Genet. 2016 Mar;24(3):392-9. doi: 10.1038/ejhg.2015.148. Epub 2015 Jul 15.
2
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.常染色体隐性智力低下:纯合子作图确定 27 个单连锁区间,至少 14 个新位点和几个突变热点。
Hum Genet. 2011 Feb;129(2):141-8. doi: 10.1007/s00439-010-0907-3. Epub 2010 Nov 10.