• 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

Multicentric study on genetic causes of mental retardation in India. ICMR Collaborating Centres & Central Co-ordinating Unit.

出版信息

Indian J Med Res. 1991 Apr;94:161-9.

PMID:1879891
Abstract

A study on 1314 children with mental retardation (MR) without an obvious environmental cause was carried out at Bangalore, Bombay, Delhi and Lucknow to determine the extent and pattern of genetic causes of mental retardation in different parts of India. In all, 42.3 per cent patients had mild, 25.3 per cent moderate, 19.2 per cent severe and 13.1 per cent profound mental retardation. Among 1314 patients, the chromosomal anomalies were found in 23.7 per cent, metabolic defects in 5.0 per cent and an identificable genetic syndrome in 11.6 per cent of the patients. In the remaining 59.7 per cent patients, no known genetic cause could be identified. However, 66.5 per cent of these patients had one or more of the following conditions: (i) congenital malformation with or without neurological deficit, (ii) history of consanguinity, (iii) positive family history of mental retardation or (iv) a positive screening test but without a confirmed diagnosis of metabolic defect (suggesting that there may be additional unidentified genetic causes of mental retardation).

摘要

相似文献

1
Multicentric study on genetic causes of mental retardation in India. ICMR Collaborating Centres & Central Co-ordinating Unit.
Indian J Med Res. 1991 Apr;94:161-9.
2
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.
3
Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patients.智力发育迟缓及/或多发先天性异常患者的染色体结构异常:24例新病例系列研究
Genet Couns. 2012;23(2):289-96.
4
Genetic screening for mental retardation in Michigan.
Am J Ment Defic. 1981 Jan;85(4):335-40.
5
The aetiology of intellectual disability in Western Australia: a community-based study.
Dev Med Child Neurol. 1991 Nov;33(11):963-73. doi: 10.1111/j.1469-8749.1991.tb14812.x.
6
Subtle chromosomal rearrangements in children with unexplained mental retardation.不明原因智力发育迟缓儿童的细微染色体重排。
Lancet. 1999 Nov 13;354(9191):1676-81. doi: 10.1016/S0140-6736(99)03070-6.
7
Epidemiological study of child & adolescent psychiatric disorders in urban & rural areas of Bangalore, India.印度班加罗尔城乡儿童及青少年精神疾病的流行病学研究。
Indian J Med Res. 2005 Jul;122(1):67-79.
8
[Clinico-genetic diagnosis of severe mental retardation].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1979;79(10):1418-23.
9
The incidence of developmental and other genetic abnormalities.
Guys Hosp Rep. 1973;122(1-2):53-63.
10
Cytogenetics study in severely mentally retarded patients.重度智力发育迟缓患者的细胞遗传学研究。
Saudi Med J. 2001 May;22(5):444-9.

引用本文的文献

1
High Risk Stratified Neonatal Screening.高危分层新生儿筛查。
Indian J Pediatr. 2018 Dec;85(12):1050-1054. doi: 10.1007/s12098-017-2545-4. Epub 2018 Mar 15.
2
Metabolic screening and its impact in children with nonsyndromic intellectual disability.代谢筛查及其对非综合征性智力障碍儿童的影响。
Neuropsychiatr Dis Treat. 2017 Apr 19;13:1065-1070. doi: 10.2147/NDT.S130196. eCollection 2017.
3
Inborn errors of metabolism (IEM) - an Indian perspective.先天性代谢缺陷(IEM)——印度视角
Indian J Pediatr. 2005 Apr;72(4):325-332. doi: 10.1007/BF02724016.
4
Radio-imaging for detecting congenitally defective metabolic pathways: A review.用于检测先天性代谢途径缺陷的放射成像:综述
Australas Med J. 2011;4(9):480-4. doi: 10.4066/AMJ.2011.822. Epub 2011 Sep 30.
5
Detection of inherited metabolic diseases in children with mental handicap.对智力障碍儿童遗传性代谢疾病的检测。
Indian J Clin Biochem. 2008 Jan;23(1):10-6. doi: 10.1007/s12291-008-0004-8. Epub 2008 Mar 6.
6
Aetiologic spectrum of mental retardation & developmental delay in India.印度精神发育迟缓和发育迟缓的病因谱。
Indian J Med Res. 2012 Sep;136(3):436-44.
7
Diagnosis of major organic acidurias in children: two years experience at a tertiary care centre.儿童主要有机酸尿症的诊断:在一家三级医疗中心的两年经验
Indian J Clin Biochem. 2011 Oct;26(4):347-53. doi: 10.1007/s12291-011-0111-9. Epub 2011 Feb 1.
8
Organic acidurias: an updated review.有机酸尿症:最新综述
Indian J Clin Biochem. 2011 Oct;26(4):319-25. doi: 10.1007/s12291-011-0134-2. Epub 2011 Apr 29.
9
Genetics of autism and mental retardation: A spoonful from the sea!自闭症与智力障碍的遗传学:沧海一粟!
Indian J Hum Genet. 2009 Sep;15(3):85-7. doi: 10.4103/0971-6866.60181.
10
Preliminary report on neonatal screening for congenital hypothyroidism, congenital adrenal hyperplasia and glucose-6-phosphate dehydrogenase deficiency: a Chandigarh experience.新生儿先天性甲状腺功能减退症、先天性肾上腺皮质增生症和葡萄糖-6-磷酸脱氢酶缺乏症筛查的初步报告:昌迪加尔经验。
Indian J Pediatr. 2010 Sep;77(9):969-73. doi: 10.1007/s12098-010-0150-x. Epub 2010 Aug 27.