• 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

[A case of Wilm's tumor with full symptomatic WAGR syndrome].

作者信息

Januszkiewicz D, Daszkiewicz P

机构信息

I Klinika Chorób Dzieci Instytutu Pediatrii Akademii Medycznej w Poznaniu.

出版信息

Pediatr Pol. 1995 Mar;70(3):255-7.

PMID:8657495
Abstract

The authors of this paper presented a case of a baby with full-symptomatic WAGR syndrome (Wilms tumor, aniridia, genital tract malformation and mental retardation) treated in the I Department of Pediatrics, Institute of Pediatrics, Medical Academy Poznań. The etiology of this syndrome was discussed (deletion of the 13th band of the 11th chromosome short arm). The reason for treatment failure was analysed.

摘要

相似文献

1
[A case of Wilm's tumor with full symptomatic WAGR syndrome].
Pediatr Pol. 1995 Mar;70(3):255-7.
2
Wilm's tumour with WAGR complex.
Indian J Cancer. 1996 Sep;33(3):136-8.
3
[WAGR syndrome: a case report].[WAGR综合征:一例报告]
An Esp Pediatr. 1998 Oct;49(4):381-7.
4
Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias.一名患有无虹膜症的女孩被诊断为WAGR综合征,其哥哥患有尿道下裂。
Genet Couns. 2002;13(2):171-7.
5
Small glomeruli in WAGR (Wilms Tumor, Aniridia, Genitourinary Anomalies and Mental Retardation) syndrome.WAGR(威尔姆斯瘤、无虹膜、泌尿生殖系统异常和智力迟钝)综合征中的小肾小球。
Am J Kidney Dis. 2007 Jun;49(6):793-800. doi: 10.1053/j.ajkd.2007.02.275.
6
Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.通过阵列比较基因组杂交技术对WAGR综合征中11p14 - p12缺失进行特征分析,以鉴定导致智力发育迟缓与自闭症的相关基因。
Cytogenet Genome Res. 2008;122(2):181-7. doi: 10.1159/000172086. Epub 2008 Dec 18.
7
Clinical, cytogenetic and molecular characterization of a patient with combined succinic semialdehyde dehydrogenase deficiency and incomplete WAGR syndrome with obesity.一名患有琥珀酸半醛脱氢酶联合缺乏症、不完全WAGR综合征伴肥胖症患者的临床、细胞遗传学和分子特征
Mol Genet Metab. 2006 Jul;88(3):256-60. doi: 10.1016/j.ymgme.2006.02.003. Epub 2006 Mar 20.
8
WAGR syndrome with tetralogy of Fallot and hydrocephalus.伴有法洛四联症和脑积水的WAGR综合征。
J Pediatr Hematol Oncol. 2011 May;33(4):e174-5. doi: 10.1097/MPH.0b013e3182114e0e.
9
[Sporadic aniridia and Wilm's tumor--a case report and review of recommendation for diagnostic approach in WAGR's syndrome].
Klin Oczna. 2010;112(10-12):321-3.
10
WAGR syndrome: a clinical review of 54 cases.WAGR综合征:54例临床回顾
Pediatrics. 2005 Oct;116(4):984-8. doi: 10.1542/peds.2004-0467.